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Institution
Boston Children's Hospital
Division of Nephrology
Address
300 Longwood Avenue
Boston MA 02115
USA
Boston MA 02115
Projects
Research Grants
Completed projects
Elucidating Nephrocystin Function by Targeted Disruption of the NPHP1 Gene
(Applicant
Hildebrandt, Friedhelm
)
Fibronektin-Glomerulopathie: Identifizierung und molekulare Charakterisierung des verantwortlichen Gens
(Applicant
Hildebrandt, Friedhelm
)
Gen-Identifizierung und -Funktionsanalyse bei autosomal-dominanter "Medullary Cystic Kidney Disease (MCKD)
(Applicant
Fuchshuber, Arno
)
Heisenberg Fellowships
Completed projects
Pädiatrie
(Applicant
Hildebrandt, Friedhelm
)
WBP Fellowship
Current projects
Identification and functional characterization of novel monogenic causes for spina bifida
(Applicant
Kolvenbach, Caroline
)
Oligonucleotide-based therapy for UMOD-associated autosomal dominant tubulointerstitial kidney disease (ADTKD-UMOD) by allele-specific siRNA knockdown
(Applicant
Riedhammer, Korbinian
)
Completed projects
Disease mechanisms of ZMYM2 mutations, a new monogenic cause for congenital anomalies of the kidney and urinary tract
(Applicant
Seltzsam, Steve
)
Steroid resistant nephrotic syndrome (SRNS) – Discover and functionally characterize full-penetrance causes of SRNS
(Applicant
Lemberg, Katharina
)
The effect on the small GTPase CDC42 by NOS1AP SRNS mutations
(Applicant
Merz, Lea
)
Collaborative Research Centres
Completed projects
Elucidating novel mechanisms of focal adhesion signaling by targeted disruption of the mouse nephrocystin gene (Kurztitel: Nephrocystin signaling)
(Project Head
Hildebrandt, Friedhelm
)
Research Fellowships
Completed projects
Characterization of novel single gene causes of nephrotic syndrome in Drosophila
(Applicant
Hermle, Tobias
)
Discovery and functional characterization of full-penetrance single-gene causes of steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis
(Applicant
Buerger, Florian
)
Effect of Rho GTPase-regulating protein DLC1 on podocytes
(Applicant
Klämbt, Verena
)
Identification of CAKUT-associated genes using a worldwide patient-cohort and high-throughput methods for genetic analysis
(Applicant
van der Ven, Amelie
)
Molecular genetic causes of renal ciliopathies - a candidate gene approach including the survivin signaling pathways
(Applicant
Jobst-Schwan, Tilman
)
Additional Information
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