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Institution
Uniklinik Köln
Institut für Humangenetik
Address
Kerpener Straße 34
50931 Köln
Deutschland
GERiT
This institution in GERiT
50931 Köln
Projects
Research Grants
Current projects
Elucidate the regulatory cascade controlling mitochondrial fission in mitosis and its impact on mitotic progression and chromosome segregation
(Applicant
Piano, Ph.D., Valentina
)
Isoform specific mediation of TAU toxicity and differential neuronal vulnerability
(Applicant
Zempel, Hans
)
Completed projects
Analysis of the influence of histone deacetylase inhibitors on the SMN2 histone code and the pathogenesis of spinal muscular atrophy
(Applicant
Wirth, Brunhilde
)
Aufklärung der Funktion des TFNR-Proteins und Beteiligung an der Gehirnentwicklung
(Applicant
Wirth, Brunhilde
)
Gene identification and functional analyses of genetically unsolved patients with neuromuscular disorders
(Applicant
Wirth, Brunhilde
)
Genetische und funktionelle Analysen von LRP5 und seinem Pseudogen bei einem Osteoporosis Pseudoglioma-Syndrom-ähnlichem Phänotyp und bei Osteoporose
(Applicant
Netzer, Christian
)
Genomic profiling in bilateral renal agenesis, the most severe end of the CAKUT spectrum
(Applicants
Beck, Bodo
;
Höfele, Julia
)
Genomic profiling in (recurrent) steroid-resistant nephrotic syndrome
(Applicants
Altmüller, Janine
;
Beck, Bodo
)
Molecular genetic, histologic, immunhistochemical and functional characterization of adipose tissue from patients with Multiple Symmetric Lipomatosis
(Applicants
Schreml, Stephan
;
Schreml, Julia
)
Molekulare und funktionelle Analyse von modifizierenden Genen bei spinaler Muskelatrophie
(Applicant
Wirth, Brunhilde
)
Plastin 3: Unravelling a novel pathomechanism for osteoporosis
(Applicant
Wirth, Brunhilde
)
Spinal muscular atrophy: Analysis of pathomechanistic impact of protective genetic modifiers in mouse models
(Applicant
Wirth, Brunhilde
)
The power of protective modifier NCALD to develop an efficient combinatorial therapy for spinal muscular atrophy
(Applicant
Wirth, Brunhilde
)
The role of miRNA biogenesis and decay in spinal muscular atrophy
(Applicant
Wirth, Brunhilde
)
Understanding primary hyperoxaluria type 1 towards the development of innovative therapeutic strategies
(Applicant
Beck, Bodo
)
Collaborative Research Centres
Current projects
Understanding plastin 3 and its interactors in motor neuron function and plasticity in health and disease
(Project Heads
Kloppenburg, Peter
;
Wirth, Brunhilde
)
Completed projects
Analyse der molekularen Ursachen der spinalen Muskelatrophie als Grundlage einer Therapie
(Project Head
Wirth, Brunhilde
)
Research Units
Current projects
FOR 2722: Novel molecular determinants for musculoskeletal extracellular matrix homeostasis – a systemic approach (M2)
(Spokesperson
Brachvogel, Bent
)
Unravelling of pathomechanisms for plastin 3 associated bone and cartilage diseases
(Applicants
Niehoff, Anja
;
Wirth, Brunhilde
)
Clinical Research Units
Current projects
KFO 329: Disease pathways in podocyte injury – from molecular mechanisms to individualized treatment options
(Spokesperson
Benzing, Thomas
)
Sequencing-based innovative approaches to study FSGS
(Applicants
Altmüller, Janine
;
Antczak, Ph.D., Philipp
;
Beck, Bodo
)
Research Training Groups
Completed projects
GRK 246: Pathogenesis of Diseases of the Central Nervous System
(Spokesperson
Propping, Peter
)
GRK 1960: Neural Circuit Analysis on the Cellular and Subcellular Level
(Spokesperson
Büschges, Ansgar
)
Additional Information
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