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Matthias T F Wolf

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 24, 2004
Medullary cystic kidney disease type 1 in a large Native-American kindredRaymond L Kiser, Matthias T F Wolf, Jeffrey L Martin, et al.
Pediatric Nephrology (Berlin, Germany)|October 11, 2008
Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)Matthias T F Wolf, Bethan E Hoskins, Bodo B Beck, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 10, 2011
Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKDBodo B Beck, Howard Trachtman, Michael Gitman, et al.
Journal of the American Society of Nephrology : JASN|September 15, 2007
Evidence of oligogenic inheritance in nephronophthisisJulia Hoefele, Matthias T F Wolf, John F O'Toole, et al.
Journal of the American Society of Nephrology : JASN|April 3, 2016
Mucin-1 Increases Renal TRPV5 Activity In Vitro, and Urinary Level Associates with Calcium Nephrolithiasis in PatientsMingzhu Nie, Manjot S Bal, Zhufeng Yang, et al.
Frontiers in Physiology|April 19, 2024
Ghrelin enhances tubular magnesium absorption in the kidneyMingzhu Nie, Jing Zhang, Manjot Bal, et al.
Human Mutation|December 14, 2007
Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencingEdgar A Otto, Juliana Helou, Susan J Allen, et al.
Kidney International|August 13, 2003
Refinement of the critical region for MCKD1 by detection of transcontinental haplotype sharingMatthias T F Wolf, Stephanie M Karle, Stella Schwarz, et al.
Human Genetics|June 2, 2006
Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharingMatthias T F Wolf, Bettina E Mucha, Hans C Hennies, et al.
Kidney International|July 16, 2004
Telomeric refinement of the MCKD1 locus on chromosome 1q21Matthias T F Wolf, Bruno van Vlem, Hans C Hennies, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 24, 2004
Medullary cystic kidney disease type 1 in a large Native-American kindredRaymond L Kiser, Matthias T F Wolf, Jeffrey L Martin, et al.
Pediatric Nephrology (Berlin, Germany)|October 11, 2008
Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)Matthias T F Wolf, Bethan E Hoskins, Bodo B Beck, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 10, 2011
Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKDBodo B Beck, Howard Trachtman, Michael Gitman, et al.
Journal of the American Society of Nephrology : JASN|September 15, 2007
Evidence of oligogenic inheritance in nephronophthisisJulia Hoefele, Matthias T F Wolf, John F O'Toole, et al.
Journal of the American Society of Nephrology : JASN|April 3, 2016
Mucin-1 Increases Renal TRPV5 Activity In Vitro, and Urinary Level Associates with Calcium Nephrolithiasis in PatientsMingzhu Nie, Manjot S Bal, Zhufeng Yang, et al.
Frontiers in Physiology|April 19, 2024
Ghrelin enhances tubular magnesium absorption in the kidneyMingzhu Nie, Jing Zhang, Manjot Bal, et al.
Human Mutation|December 14, 2007
Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencingEdgar A Otto, Juliana Helou, Susan J Allen, et al.
Kidney International|August 13, 2003
Refinement of the critical region for MCKD1 by detection of transcontinental haplotype sharingMatthias T F Wolf, Stephanie M Karle, Stella Schwarz, et al.
Human Genetics|June 2, 2006
Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharingMatthias T F Wolf, Bettina E Mucha, Hans C Hennies, et al.
Kidney International|July 16, 2004
Telomeric refinement of the MCKD1 locus on chromosome 1q21Matthias T F Wolf, Bruno van Vlem, Hans C Hennies, et al.
Pageof 5