List projects.

Fields

id (integer)

Primary key.

Expansions

To activate relation expansion add the desired fields as a comma separated list to the expand query parameter like this:

?expand=<field>,<field>,<field>,...

The following relational fields can be expanded:

  • organization
  • category
  • type
  • partner_function
  • manager
  • contact
  • status
  • grant
  • research
  • event
  • study
  • language
  • program
  • funders

Filters

To filter for exact value matches:

?<fieldname>=<value>

Possible exact filters:

  • organization
  • category
  • manager
  • contact
  • status
  • grant
  • research
  • study
  • language
  • funders
  • program

For advanced filtering use lookups:

?<fieldname>__<lookup>=<value>

All fields with advanced lookups can also be used for exact value matches as described above.

Possible advanced lookups:

  • begin_planned: gt, gte, lt, lte
  • begin_effective: gt, gte, lt, lte
  • end_planned: gt, gte, lt, lte
  • end_effective: gt, gte, lt, lte
GET /v1/research/project/?format=api&offset=360&ordering=end_effective
HTTP 200 OK
  Allow: GET, HEAD, OPTIONS
  Content-Type: application/json
  Vary: Accept
  
  {
    "count": 2244,
    "next": "https://api-test.medunigraz.at/v1/research/project/?format=api&limit=20&offset=380&ordering=end_effective",
    "previous": "https://api-test.medunigraz.at/v1/research/project/?format=api&limit=20&offset=340&ordering=end_effective",
    "results": [
        {
            "id": 2607,
            "title": {
                "de": "Die Rolle der Phospholipid-Scramblase 1 (PLSCR1) in der Differenzierung und Fusion von humanen Trophoblasten ",
                "en": "The role of Phospholipid-Scramblase 1 (PLSCR1) in human trophoblast differentiation and fusion"
            },
            "short": null,
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2011-05-13T02:00:00+02:00",
            "begin_effective": "2011-05-13T02:00:00+02:00",
            "end_planned": "2011-11-30T01:00:00+01:00",
            "end_effective": "2011-11-30T01:00:00+01:00",
            "assignment": "2011-10-05T11:53:24+02:00",
            "program": null,
            "subprogram": null,
            "organization": 14017,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": 53232,
            "contact": null,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                530
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "2607-53232-10"
            ]
        },
        {
            "id": 1725,
            "title": {
                "de": "Role of T regulatory cells in polymorphic light eruption",
                "en": "Role of T regulatory cells in polymorphic light eruption"
            },
            "short": "polymorphic light eruption",
            "url": null,
            "abstract": {
                "de": "Die polymorphe Lichtdermatose (PLD- \"Sonnenallergie\"), deren Prävalenz (mit bis zu 20%) vor allem bei jungen Frauen außerordentlich hoch ist, ist durch an sonnenexponierten Körperstellen auftretende, stark juckende Hautveränderungen gekennzeichnet. Die Ätiopathogenese der PLD ist unbekannt, eine Störung der UV-induzierten Immunsuppression mit Immunreaktionen gegen Photoneoantigene der Haut wird vermutet. Bei der Immunsuppression nach UV-EInwirkung kommt den regulatorischen T-Zellen (CD4+CD25+FoxP3+) (Tregs), einer Subpoulation der T-Helfer Zellen, eine bedeutende Rolle zu.\r\nIm vorliegenden Projekt soll die Hypothese geprüft werden, dass Tregs von PLD-Patienten pathogenetisch bedeutsam im Jahresverlauf abnormal fluktuierende Spiegel und Funktionen aufweisen, welche möglicherweise durch Photohardening (UV-Abhärtung) normalisierbar sind. Aus einem besseren Verständnis der Pathogenese der PLD könnten möglicherweise Ansätze für neue therapeutische Strategien resultieren.",
                "en": "Die polymorphe Lichtdermatose (PLD- \"Sonnenallergie\"), deren Prävalenz (mit bis zu 20%) vor allem bei jungen Frauen außerordentlich hoch ist, ist durch an sonnenexponierten Körperstellen auftretende, stark juckende Hautveränderungen gekennzeichnet. Die Ätiopathogenese der PLD ist unbekannt, eine Störung der UV-induzierten Immunsuppression mit Immunreaktionen gegen Photoneoantigene der Haut wird vermutet. Bei der Immunsuppression nach UV-EInwirkung kommt den regulatorischen T-Zellen (CD4+CD25+FoxP3+) (Tregs), einer Subpoulation der T-Helfer Zellen, eine bedeutende Rolle zu.\r\nIm vorliegenden Projekt soll die Hypothese geprüft werden, dass Tregs von PLD-Patienten pathogenetisch bedeutsam im Jahresverlauf abnormal fluktuierende Spiegel und Funktionen aufweisen, welche möglicherweise durch Photohardening (UV-Abhärtung) normalisierbar sind. Aus einem besseren Verständnis der Pathogenese der PLD könnten möglicherweise Ansätze für neue therapeutische Strategien resultieren."
            },
            "begin_planned": "2009-01-01T01:00:00+01:00",
            "begin_effective": "2009-01-01T01:00:00+01:00",
            "end_planned": "2010-12-31T01:00:00+01:00",
            "end_effective": "2011-11-30T01:00:00+01:00",
            "assignment": "2009-01-16T14:41:21+01:00",
            "program": 79,
            "subprogram": null,
            "organization": 14047,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": 51618,
            "contact": 51618,
            "status": 2,
            "research": 2,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                12
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "1725-54011-12",
                "1725-51618-10"
            ]
        },
        {
            "id": 825,
            "title": {
                "de": "MPO-modifiziertes High-Density Lipoprotein und Rezeptoren",
                "en": "MPO-modified high-density lipoprotein and receptors"
            },
            "short": "MPO-mod. HD LDL",
            "url": null,
            "abstract": {
                "de": "The vascular endothelium is a wide spread organ responsible for the regulation of hemodynamics, angiogenic vascular remodeling, metabolic, synthetic, antiinflammatory, and antithrombogenic processes. Diminished nitric oxide (NO) availability has been linked to vascular disease and a heightened state of inflammation is characterized, in part, by an increase in vascular myeloperoxidase and proteins in vivo modified by its principal oxidant, hypochlourous acid/hypochlorous acid/hypochlorite (HOCI/OCI). Modification of high-density lipoprotein (HDL) by HOCI generates a proatherogenic and proinflammatory lipoprotein particle. HOCI-HDL, present in human lesions material and on endothelial cells, attenuates the expression and activity of vasuloprotective endothelial NO synthase (eNOS). Therefore, one part of this application is to clarify the mechanisms that governs interaction of HODI-HDL and its lipid (plasmalogen)-derived oxidant 2-chlorohexadecanal with eNOS, to focus whether caveolae-located proteins are involved, to profile alterations in endothelial gene expression patterns, and to investigate endothelium-dependent vascular relaxation in aortic rings and perfused vessels. As endothelial dysfunction may be induced by receptor-ligand interaction, the other part of this application will focus on interaction of HOCI-HDL with candidate receptors mediating (patho)physiologically relevant cellualar responses, i.e. activation of transcription factors, kinases and production of cytokines, leadng to the perpetuation of the inflammatory response and endothelial dysfunction. To answer these questions cell lines overexpressing candidate receptors will be used before adapting the cellular signaling cascade patterns to a specific endothelial cell line. We propose that myeloperoxidase-modified HDL- a unique and clinically significant marker for atherosclerosis - mediates endothelial dysfunction by specific receptor-evoked intracellular signaling pathways. ",
                "en": "The vascular endothelium is a wide spread organ responsible for the regulation of hemodynamics, angiogenic vascular remodeling, metabolic, synthetic, antiinflammatory, and antithrombogenic processes. Diminished nitric oxide (NO) availability has been linked to vascular disease and a heightened state of inflammation is characterized, in part, by an increase in vascular myeloperoxidase and proteins in vivo modified by its principal oxidant, hypochlourous acid/hypochlorous acid/hypochlorite (HOCI/OCI). Modification of high-density lipoprotein (HDL) by HOCI generates a proatherogenic and proinflammatory lipoprotein particle. HOCI-HDL, present in human lesions material and on endothelial cells, attenuates the expression and activity of vasuloprotective endothelial NO synthase (eNOS). Therefore, one part of this application is to clarify the mechanisms that governs interaction of HODI-HDL and its lipid (plasmalogen)-derived oxidant 2-chlorohexadecanal with eNOS, to focus whether caveolae-located proteins are involved, to profile alterations in endothelial gene expression patterns, and to investigate endothelium-dependent vascular relaxation in aortic rings and perfused vessels. As endothelial dysfunction may be induced by receptor-ligand interaction, the other part of this application will focus on interaction of HOCI-HDL with candidate receptors mediating (patho)physiologically relevant cellualar responses, i.e. activation of transcription factors, kinases and production of cytokines, leadng to the perpetuation of the inflammatory response and endothelial dysfunction. To answer these questions cell lines overexpressing candidate receptors will be used before adapting the cellular signaling cascade patterns to a specific endothelial cell line. We propose that myeloperoxidase-modified HDL- a unique and clinically significant marker for atherosclerosis - mediates endothelial dysfunction by specific receptor-evoked intracellular signaling pathways. "
            },
            "begin_planned": "2006-07-01T02:00:00+02:00",
            "begin_effective": "2006-12-16T01:00:00+01:00",
            "end_planned": "2009-06-30T02:00:00+02:00",
            "end_effective": "2011-12-15T01:00:00+01:00",
            "assignment": "2006-05-16T17:47:52+02:00",
            "program": 72,
            "subprogram": null,
            "organization": 14013,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": 51833,
            "contact": 51833,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                9
            ],
            "funder_projectcode": "P19074",
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "825-51833-10"
            ]
        },
        {
            "id": 2460,
            "title": {
                "de": "Etablierung organtypischer Zellkultur für Herzgewebe",
                "en": "Establishing of organotypic cell culture for heart tissue"
            },
            "short": "ORGANOTYPIC CELL CULTURE HEART TISSUE",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2011-03-01T01:00:00+01:00",
            "begin_effective": "2011-05-01T02:00:00+02:00",
            "end_planned": "2011-08-31T02:00:00+02:00",
            "end_effective": "2011-12-30T01:00:00+01:00",
            "assignment": "2011-04-07T13:19:02+02:00",
            "program": null,
            "subprogram": null,
            "organization": 14073,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": null,
            "contact": null,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                135
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": []
        },
        {
            "id": 2451,
            "title": {
                "de": "Ein US28/GNA Fusionsprotein zur Induktion der Apoptose beim Melanom",
                "en": "A US28/GNA Fusion Protein to Induce Apoptosis in Melanoma "
            },
            "short": "US28/GNA and Melanoma",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2011-03-01T01:00:00+01:00",
            "begin_effective": "2011-04-01T02:00:00+02:00",
            "end_planned": "2011-05-31T02:00:00+02:00",
            "end_effective": "2011-12-30T01:00:00+01:00",
            "assignment": "2011-03-23T11:47:48+01:00",
            "program": null,
            "subprogram": null,
            "organization": 14047,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": 53662,
            "contact": 53662,
            "status": 2,
            "research": 3,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                135
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "2451-53662-10"
            ]
        },
        {
            "id": 2406,
            "title": {
                "de": "Adipokine Visfatin und Chemerin im Kindes- und Jugendalter",
                "en": "The adipokines visfatin and chemerin in childhood and adolescence"
            },
            "short": "ADIPOKINE VISFATIN CHEMERIN",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2010-10-01T02:00:00+02:00",
            "begin_effective": "2011-03-01T01:00:00+01:00",
            "end_planned": "2011-10-01T02:00:00+02:00",
            "end_effective": "2011-12-30T01:00:00+01:00",
            "assignment": "2011-02-15T12:46:08+01:00",
            "program": null,
            "subprogram": null,
            "organization": 14091,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": null,
            "contact": null,
            "status": 2,
            "research": 4,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                135
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": []
        },
        {
            "id": 2457,
            "title": {
                "de": "INTEROCEPTION AND ARTERIAL STIFFNESS",
                "en": "INTEROCEPTION AND ARTERIAL STIFFNESS"
            },
            "short": "STRESS HYPOXIC CONDITIONS",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2011-04-01T02:00:00+02:00",
            "begin_effective": "2011-03-28T02:00:00+02:00",
            "end_planned": "2011-12-30T01:00:00+01:00",
            "end_effective": "2011-12-30T01:00:00+01:00",
            "assignment": "2011-03-29T11:56:04+02:00",
            "program": null,
            "subprogram": null,
            "organization": 29447,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": null,
            "contact": null,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                135
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": []
        },
        {
            "id": 2031,
            "title": {
                "de": "Genetic variants in the RAD51, BRCA1 and BRCA2 genes as predictors of radiation response and toxicity in prostate cancer patients",
                "en": "Genetic variants in the RAD51, BRCA1 and BRCA2 genes as predictors of radiation response and toxicity in prostate cancer patients"
            },
            "short": "GENETIC_PROSTATE_CANCER_OeNB",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2010-01-01T01:00:00+01:00",
            "begin_effective": "2010-01-01T01:00:00+01:00",
            "end_planned": "2011-12-31T01:00:00+01:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2010-01-11T15:12:11+01:00",
            "program": 79,
            "subprogram": null,
            "organization": 14060,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": 50495,
            "contact": null,
            "status": 2,
            "research": 2,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                12
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "2031-50495-10",
                "2031-50910-12"
            ]
        },
        {
            "id": 1510,
            "title": {
                "de": "EuroSTEC: Soft tissue engineering for congenital birth defects in children: from \"biomatrix - cell interaction - model system\" to clinical trials",
                "en": "EuroSTEC: Soft tissue engineering for congenital birth defects in children: from \"biomatrix - cell interaction - model system\" to clinical trials"
            },
            "short": "IMPPACT",
            "url": null,
            "abstract": {
                "de": "IMPPACT will develop an intervention planning and monitoring application for Radiofrequency Ablation (RFA) of malignant liver tumours. RFA is a minimally invasive form to treat cancer without open surgery, by placing a needle inside the malignancy and destroying it through intensive heating. Though the advantages of this approach ale obvious, the intervention is currently hard to plan, almost impossible to monitor or assess, and therefore is not the first choice for treatment. IMPPACT will develop a physiological model of the liver and simulate the intervention's result, accounting for patient specific physiological factors. Gaps in the understanding of particular aspects of the RFA treatment will be closed by multi-scale studies on cells and animals. New findings will be evaluated microscopically and transformed into macroscopic equations. The long-established bio-heat equation will be extended to incorporate multiple scales. Validation will be performed at multiple levels. Images from ongoing patient treatment will be used to cross check validity for human physiology. Final validation will be performed at macroscopic level through visual comparison of simulation and treatment results gathered in animal studies and during patient treatment. This extensive validation together with a user-centered software design approach will guarantee suitability of the solution for clinical practice. The consortium consists of two Hospitals, three Universities, one Research Institute and one industrial SME. The final project deliverables will be the patient specific intervention planning system and an augmented reality training simulator for the RFA intervention.",
                "en": "IMPPACT will develop an intervention planning and monitoring application for Radiofrequency Ablation (RFA) of malignant liver tumours. RFA is a minimally invasive form to treat cancer without open surgery, by placing a needle inside the malignancy and destroying it through intensive heating. Though the advantages of this approach ale obvious, the intervention is currently hard to plan, almost impossible to monitor or assess, and therefore is not the first choice for treatment. IMPPACT will develop a physiological model of the liver and simulate the intervention's result, accounting for patient specific physiological factors. Gaps in the understanding of particular aspects of the RFA treatment will be closed by multi-scale studies on cells and animals. New findings will be evaluated microscopically and transformed into macroscopic equations. The long-established bio-heat equation will be extended to incorporate multiple scales. Validation will be performed at multiple levels. Images from ongoing patient treatment will be used to cross check validity for human physiology. Final validation will be performed at macroscopic level through visual comparison of simulation and treatment results gathered in animal studies and during patient treatment. This extensive validation together with a user-centered software design approach will guarantee suitability of the solution for clinical practice. The consortium consists of two Hospitals, three Universities, one Research Institute and one industrial SME. The final project deliverables will be the patient specific intervention planning system and an augmented reality training simulator for the RFA intervention."
            },
            "begin_planned": "2008-06-01T02:00:00+02:00",
            "begin_effective": "2008-09-01T02:00:00+02:00",
            "end_planned": "2011-05-31T02:00:00+02:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2008-04-09T17:00:52+02:00",
            "program": 24,
            "subprogram": null,
            "organization": 14073,
            "category": 10,
            "type": 10,
            "partner_function": 2,
            "manager": 50874,
            "contact": 50874,
            "status": 2,
            "research": 3,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                10
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "1510-50874-10",
                "1510-62118-12",
                "1510-51955-12",
                "1510-51983-12"
            ]
        },
        {
            "id": 2023,
            "title": {
                "de": "Induction of immunological changes by endoluminal photodynamic therapy (PDT) for esophageal carcinoma",
                "en": "Induction of immunological changes by endoluminal photodynamic therapy (PDT) for esophageal carcinoma"
            },
            "short": "PDT_ESOPHAGEAL_CARCINOMA",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2010-01-01T01:00:00+01:00",
            "begin_effective": "2010-01-01T01:00:00+01:00",
            "end_planned": "2011-12-31T01:00:00+01:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2009-12-18T12:29:42+01:00",
            "program": 79,
            "subprogram": null,
            "organization": 14077,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": 51615,
            "contact": 51615,
            "status": 2,
            "research": 2,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                12
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "2023-62056-12",
                "2023-51615-10",
                "2023-51618-12"
            ]
        },
        {
            "id": 1771,
            "title": {
                "de": "Rett Disorder: The Pre-Regression Period",
                "en": "Rett Disorder: The Pre-Regression Period"
            },
            "short": "RETT DISORDER",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": null,
            "begin_effective": "2007-01-01T01:00:00+01:00",
            "end_planned": null,
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2009-03-30T17:24:34+02:00",
            "program": null,
            "subprogram": null,
            "organization": 14010,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": null,
            "contact": null,
            "status": 2,
            "research": 2,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                530
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": []
        },
        {
            "id": 1329,
            "title": {
                "de": "Mapping of the bound proton fraction in the elderly brain",
                "en": "Mapping of the bound proton fraction in the elderly brain"
            },
            "short": "BOUND_PROTON_ELDERLY_BRAIN_FWF07",
            "url": null,
            "abstract": {
                "de": "The aim of this proposal is to investigate whether the bound pool fraction as a new and quantitative MR measure allows more insight into age related brain tissue changes than other quantitative MR measures. The specific aims are:\r\n\r\n*Develop a MR pulse sequence that allows to map the bound proton fraction on high field systems (>=3T) within a clinically reasonable measurement time (<15min). The sequence should offer whole brain coverage and should overcome current limitations such as the susceptibility for motion and B1 effects.\r\n\r\n*Measure the BPF in brain tissue of a large cohort of the Ausitria Stroke Prevention Study (ASPS). This gives us the opportunity to study a representative and homogeneous group of normal elderly people without a history or signs of neuropsychiatric diseases. By using a younger control cohort, we want to investigate how the BPF changes as a function of age, sex and anatonic region including cortical structures. In addition, we want to find out how the BPF varies within WMH with different severity and how it relates to the BPF in normal appearing brain tissue and to the neurocognitive performance.\r\n\r\n*Compare the sensitivity and specificity of bound proton fraction mapping to more established measures of brain tissue changes including atrophy, diffusion weighted imaging, and magnetization transfer imaging.",
                "en": "The aim of this proposal is to investigate whether the bound pool fraction as a new and quantitative MR measure allows more insight into age related brain tissue changes than other quantitative MR measures. The specific aims are:\r\n\r\n*Develop a MR pulse sequence that allows to map the bound proton fraction on high field systems (>=3T) within a clinically reasonable measurement time (<15min). The sequence should offer whole brain coverage and should overcome current limitations such as the susceptibility for motion and B1 effects.\r\n\r\n*Measure the BPF in brain tissue of a large cohort of the Ausitria Stroke Prevention Study (ASPS). This gives us the opportunity to study a representative and homogeneous group of normal elderly people without a history or signs of neuropsychiatric diseases. By using a younger control cohort, we want to investigate how the BPF changes as a function of age, sex and anatonic region including cortical structures. In addition, we want to find out how the BPF varies within WMH with different severity and how it relates to the BPF in normal appearing brain tissue and to the neurocognitive performance.\r\n\r\n*Compare the sensitivity and specificity of bound proton fraction mapping to more established measures of brain tissue changes including atrophy, diffusion weighted imaging, and magnetization transfer imaging."
            },
            "begin_planned": "2007-08-01T02:00:00+02:00",
            "begin_effective": "2008-01-01T01:00:00+01:00",
            "end_planned": "2010-07-31T02:00:00+02:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2007-07-10T14:42:36+02:00",
            "program": 72,
            "subprogram": null,
            "organization": 14051,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": 51279,
            "contact": 51279,
            "status": 2,
            "research": 3,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                9
            ],
            "funder_projectcode": "P20103",
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "1329-51279-10"
            ]
        },
        {
            "id": 2498,
            "title": {
                "de": "Die Rolle von Metalloproteasen und Endothelin im ersten Schwangerschaftstrimester",
                "en": "The role of metalloproteinases and endothelin in the first trimester of pregnancy"
            },
            "short": "METALLPROTEINASES_ENDOTHELIN_PREGNANCY",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2011-07-01T02:00:00+02:00",
            "begin_effective": "2011-07-01T02:00:00+02:00",
            "end_planned": "2011-12-31T01:00:00+01:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2011-06-16T12:49:53+02:00",
            "program": null,
            "subprogram": null,
            "organization": 14038,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": null,
            "contact": null,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                457
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": []
        },
        {
            "id": 1868,
            "title": {
                "de": "Computer-based analysis of heart rate variability (HRV) during different methods of acupuncture",
                "en": "Computer-based analysis of heart rate variability (HRV) during different methods of acupuncture"
            },
            "short": "HRV during acupuncture",
            "url": null,
            "abstract": {
                "de": "Die Herzratenvariabilität stellt die prozentuelle Änderung aufeinander folgender Kammerkomplexe im EKG dar. Der Parameter HRV wird durch das Blutdruckkontrollsystem, Einflüsse vom Hypothalamus und vor allem durch den vagalen Teil des Kreislaufzentrums im unteren Hirnstamm vermittelt. Eine computergestützte Analyse der HRV soll während unterschiedlicher Methoden der Akupunktur und anderer Stimulationsmethoden im gegenständlichen Projekt zum Einsatz kommen. Für die Untersuchungen soll ein Medilog AR 12 verwendet werden. Insgesamt sollen 80 Probanden (im Alter 20-50 Jahren) während unterschiedlicher Akupunktursitzungen (Nadel- und Laserakupunktur) untersucht werden. Dabei werden die folgenden Akupunkturpunkte verwendet: Neiguan (Pe.6), Shenmen (He.7) und Hegu (Di.4). Innerhalb dieses Projektes soll die HRV auch während Stimulationen des Punktes Yintang (Ex.1) näher untersucht werden. Das Projekt könnte dazu beitragen, die Beziehungen zwischen westlicher und östlicher Medizin zu vertiefen.",
                "en": "Die Herzratenvariabilität stellt die prozentuelle Änderung aufeinander folgender Kammerkomplexe im EKG dar. Der Parameter HRV wird durch das Blutdruckkontrollsystem, Einflüsse vom Hypothalamus und vor allem durch den vagalen Teil des Kreislaufzentrums im unteren Hirnstamm vermittelt. Eine computergestützte Analyse der HRV soll während unterschiedlicher Methoden der Akupunktur und anderer Stimulationsmethoden im gegenständlichen Projekt zum Einsatz kommen. Für die Untersuchungen soll ein Medilog AR 12 verwendet werden. Insgesamt sollen 80 Probanden (im Alter 20-50 Jahren) während unterschiedlicher Akupunktursitzungen (Nadel- und Laserakupunktur) untersucht werden. Dabei werden die folgenden Akupunkturpunkte verwendet: Neiguan (Pe.6), Shenmen (He.7) und Hegu (Di.4). Innerhalb dieses Projektes soll die HRV auch während Stimulationen des Punktes Yintang (Ex.1) näher untersucht werden. Das Projekt könnte dazu beitragen, die Beziehungen zwischen westlicher und östlicher Medizin zu vertiefen."
            },
            "begin_planned": "2009-10-01T02:00:00+02:00",
            "begin_effective": "2010-01-01T01:00:00+01:00",
            "end_planned": "2011-09-30T02:00:00+02:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2009-07-13T18:54:46+02:00",
            "program": 79,
            "subprogram": null,
            "organization": 14044,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": null,
            "contact": null,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                12
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "1868-54121-12"
            ]
        },
        {
            "id": 1002,
            "title": {
                "de": "EuroSTEC: Soft tissue engineering for congenital birth defects in children: from \"biomatrix - cell interaction - model system\" to clinical trials",
                "en": "EuroSTEC: Soft tissue engineering for congenital birth defects in children: from \"biomatrix - cell interaction - model system\" to clinical trials"
            },
            "short": "EuroSTEC",
            "url": null,
            "abstract": {
                "de": "The aim of this project is to use modern tissue engineering approaches to treat children with structural disorders present at birth, such as spina bifida, urogenital defects or abdominal wall defects and surrounding anomalies. The project strives to elucidate underlying mechanisms and take a translational route through in vitro and animal experiments.\r\nThis project will give more insight in the opportunities for advanced technical possibilities with tissue engineering techniques and new treatment strategies for severe and major structural congenital birth defects in children. \r\n",
                "en": "The aim of this project is to use modern tissue engineering approaches to treat children with structural disorders present at birth, such as spina bifida, urogenital defects or abdominal wall defects and surrounding anomalies. The project strives to elucidate underlying mechanisms and take a translational route through in vitro and animal experiments.\r\nThis project will give more insight in the opportunities for advanced technical possibilities with tissue engineering techniques and new treatment strategies for severe and major structural congenital birth defects in children. \r\n"
            },
            "begin_planned": "2006-11-01T01:00:00+01:00",
            "begin_effective": "2007-01-01T01:00:00+01:00",
            "end_planned": "2011-10-31T01:00:00+01:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2007-01-15T14:22:41+01:00",
            "program": 21,
            "subprogram": null,
            "organization": 14049,
            "category": 10,
            "type": 10,
            "partner_function": 2,
            "manager": null,
            "contact": null,
            "status": 2,
            "research": 2,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                10
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": []
        },
        {
            "id": 2341,
            "title": {
                "de": "Einzelzellanalyse in der forensischen Medizin",
                "en": "Single cell analysis in forensic medicine"
            },
            "short": "Single cell analysis",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2010-05-01T02:00:00+02:00",
            "begin_effective": "2010-12-01T01:00:00+01:00",
            "end_planned": "2011-04-30T02:00:00+02:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2010-11-17T11:21:30+01:00",
            "program": null,
            "subprogram": null,
            "organization": 14017,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": 54171,
            "contact": 54171,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                135
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "2341-54171-10"
            ]
        },
        {
            "id": 2130,
            "title": {
                "de": "Kinder erzählen: Text- und Erzählkompetenz im Vorschulalter: eine Voraussetzung für den schulischen Erfolg.",
                "en": "Narratives in first language acquisition."
            },
            "short": "TEXT- UND ERZÄHLKOMPETENZ",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2010-03-01T01:00:00+01:00",
            "begin_effective": "2010-03-01T01:00:00+01:00",
            "end_planned": "2011-12-31T01:00:00+01:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2010-02-24T10:55:39+01:00",
            "program": null,
            "subprogram": null,
            "organization": 14010,
            "category": 10,
            "type": 10,
            "partner_function": 2,
            "manager": 58883,
            "contact": 58883,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                135
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "2130-58883-10"
            ]
        },
        {
            "id": 2550,
            "title": {
                "de": "Endothelin und Matrixmetalloproteinasen im ersten Schwangerschaftstrimester",
                "en": "Endothelin and matrix metalloproteinases in the first trimester of pregnancy"
            },
            "short": "EndothelMatrix",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2011-08-01T02:00:00+02:00",
            "begin_effective": "2011-08-01T02:00:00+02:00",
            "end_planned": "2011-12-31T01:00:00+01:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2011-08-02T14:12:12+02:00",
            "program": null,
            "subprogram": null,
            "organization": 14038,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": null,
            "contact": null,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                135
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": []
        },
        {
            "id": 2092,
            "title": {
                "de": "Analysis of germline polymorphisms in the VEGF/VEGFR pathway to predict colorectal cancer outcome",
                "en": "Analysis of germline polymorphisms in the VEGF/VEGFR pathway to predict colorectal cancer outcome"
            },
            "short": "GERMLINE POLYMORPH VEGF/VEGFR",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2010-01-01T01:00:00+01:00",
            "begin_effective": "2010-01-01T01:00:00+01:00",
            "end_planned": "2010-12-31T01:00:00+01:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2010-02-09T11:47:57+01:00",
            "program": null,
            "subprogram": null,
            "organization": 14085,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": null,
            "contact": null,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                894
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": [
                "2092-58814-12"
            ]
        },
        {
            "id": 2097,
            "title": {
                "de": "Role of SPN in PP1-mediated RyR2 regulation and intracellular Ca2+ handling",
                "en": "Role of SPN in PP1-mediated RyR2 regulation and intracellular Ca2+ handling"
            },
            "short": "ROLE OF SPN ",
            "url": null,
            "abstract": {
                "de": null,
                "en": null
            },
            "begin_planned": "2010-01-01T01:00:00+01:00",
            "begin_effective": "2010-01-01T01:00:00+01:00",
            "end_planned": "2011-12-31T01:00:00+01:00",
            "end_effective": "2011-12-31T01:00:00+01:00",
            "assignment": "2010-02-09T12:56:38+01:00",
            "program": null,
            "subprogram": null,
            "organization": 14083,
            "category": 10,
            "type": 10,
            "partner_function": 4,
            "manager": null,
            "contact": null,
            "status": 2,
            "research": 1,
            "grant": 10,
            "event": null,
            "study": null,
            "language": null,
            "funders": [
                894
            ],
            "funder_projectcode": null,
            "ethics_committee": null,
            "edudract_number": null,
            "persons": []
        }
    ]
}