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Boris Utsch

Showing results (11-20 of 32) with videos related to

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Kidney & Blood Pressure Research|February 19, 2003
Novel NCCT gene mutations as a cause of Gitelman's syndrome and a systematic review of mutant and polymorphic NCCT allelesAnnette Reissinger, Michael Ludwig, Boris Utsch, et al.
Pediatric Nephrology (Berlin, Germany)|October 22, 2005
Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndromeBoris Utsch, John A Sayer, Massimo Attanasio, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndromeBoris Utsch, Colleen D McCabe, Kenneth Galbraith, et al.
Frontiers in Endocrinology|March 11, 2020
Estimated Glomerular Filtration Rates Calculated by New and Old Equations in Children and Adolescents With Type 1 Diabetes-What to Do With the Results?Claudia Boettcher, Boris Utsch, Angela Galler, et al.
European Journal of Medical Genetics|August 28, 2007
Delayed transport of tissue-nonspecific alkaline phosphatase with missense mutations causing hypophosphatasiaIsabelle Brun-Heath, Anne-Sophie Lia-Baldini, Stéphane Maillard, 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.
Clinical Kidney Journal|February 10, 2021
Transvascular kidney biopsy in adolescent patients-safe alternative to open proceduresBoris Utsch, Hanno Hoppe, Katalin Dittrich, et al.
Human Mutation|March 19, 2005
Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisisJulia Hoefele, Ralf Sudbrak, Richard Reinhardt, et al.
Human Molecular Genetics|September 24, 2004
Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse modelJeffrey W Innis, Douglas Mortlock, Zhi Chen, et al.
American Journal of Medical Genetics. Part A|September 14, 2006
Bladder exstrophy and Epstein type congenital macrothrombocytopenia: evidence for a common cause?Boris Utsch, Analisa DiFeo, Annegret Kujat, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Kidney & Blood Pressure Research|February 19, 2003
Novel NCCT gene mutations as a cause of Gitelman's syndrome and a systematic review of mutant and polymorphic NCCT allelesAnnette Reissinger, Michael Ludwig, Boris Utsch, et al.
Pediatric Nephrology (Berlin, Germany)|October 22, 2005
Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndromeBoris Utsch, John A Sayer, Massimo Attanasio, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndromeBoris Utsch, Colleen D McCabe, Kenneth Galbraith, et al.
Frontiers in Endocrinology|March 11, 2020
Estimated Glomerular Filtration Rates Calculated by New and Old Equations in Children and Adolescents With Type 1 Diabetes-What to Do With the Results?Claudia Boettcher, Boris Utsch, Angela Galler, et al.
European Journal of Medical Genetics|August 28, 2007
Delayed transport of tissue-nonspecific alkaline phosphatase with missense mutations causing hypophosphatasiaIsabelle Brun-Heath, Anne-Sophie Lia-Baldini, Stéphane Maillard, 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.
Clinical Kidney Journal|February 10, 2021
Transvascular kidney biopsy in adolescent patients-safe alternative to open proceduresBoris Utsch, Hanno Hoppe, Katalin Dittrich, et al.
Human Mutation|March 19, 2005
Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisisJulia Hoefele, Ralf Sudbrak, Richard Reinhardt, et al.
Human Molecular Genetics|September 24, 2004
Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse modelJeffrey W Innis, Douglas Mortlock, Zhi Chen, et al.
American Journal of Medical Genetics. Part A|September 14, 2006
Bladder exstrophy and Epstein type congenital macrothrombocytopenia: evidence for a common cause?Boris Utsch, Analisa DiFeo, Annegret Kujat, et al.
Pageof 4