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American Journal of Human Genetics|December 5, 1998
The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene clusterM Vollmer, M Jung, F Rüschendorf, et al.
Human Mutation|September 12, 2000
A deletion distinct from the classical homologous recombination of juvenile nephronophthisis type 1 (NPH1) allows exact molecular definition of deletion breakpointsE Otto, R Betz, C Rensing, et al.
The American Journal of Physiology|November 1, 1992
Induction and intracellular localization of HSP-72 after renal ischemiaS K Van Why, F Hildebrandt, T Ardito, et al.
Nature Genetics|November 5, 1997
A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1F Hildebrandt, E Otto, C Rensing, et al.
Kidney International|February 13, 2001
Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisisF Hildebrandt, C Rensing, R Betz, et al.
Kidney International. Supplement|July 1, 1991
Molecular biology of renal Na(+)-H+ exchangersP Igarashi, R F Reilly, F Hildebrandt, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 1, 1997
Late occurrence of cysts in autosomal dominant medullary cystic kidney diseaseH P Neumann, I Zäuner, B Strahm, et al.
AJNR. American Journal of Neuroradiology|August 29, 2020
MRI Spectrum of Brain Involvement in Sphingosine-1-Phosphate Lyase Insufficiency SyndromeK W Martin, N Weaver, K Alhasan, et al.
Genomics|August 31, 2000
Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genesM Vollmer, M Kremer, R Ruf, et al.
Molecular and Cellular Probes|February 20, 2002
Novel NPR1 polymorphic variants and its exclusion as a candidate gene for medullary cystic kidney disease (ADMCKD) type 1M Koptides, R Mean, C Stavrou, et al.
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