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Laurence Heidet

Showing results (11-20 of 99) with videos related to

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Prenatal Diagnosis|August 21, 2012
Prognosis and outcome of pregnancies exposed to renin-angiotensin system blockersEmmanuel Spaggiari, Laurence Heidet, Gilles Grange, et al.
Molecular and Cellular Biology|January 1, 2004
Early glomerular filtration defect and severe renal disease in podocin-deficient miceSéverine Roselli, Laurence Heidet, Mireille Sich, et al.
Pediatric Nephrology (Berlin, Germany)|March 22, 2020
Bi-allelic mutations in renin-angiotensin system genes, associated with renal tubular dysgenesis, can also present as a progressive chronic kidney diseaseMarc Fila, Vincent Morinière, Philippe Eckart, et al.
Kidney International|August 26, 2004
In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutationShao-Yu Zhang, Arnaud Marlier, Olivier Gribouval, et al.
Journal of the American Society of Nephrology : JASN|December 26, 2001
Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromesChristelle Arrondel, Nicolas Vodovar, Bertrand Knebelmann, et al.
Pediatric Nephrology (Berlin, Germany)|March 31, 2012
Clinical practice recommendations for the treatment of Alport syndrome: a statement of the Alport Syndrome Research CollaborativeClifford E Kashtan, Jie Ding, Martin Gregory, et al.
Nucleic Acids Research|May 28, 2016
Human mutations affect the epigenetic/bookmarking function of HNF1BJonathan Lerner, Alessia Bagattin, Francisco Verdeguer, et al.
The Journal of Biological Chemistry|February 13, 2007
The alloantigenic sites of alpha3alpha4alpha5(IV) collagen: pathogenic X-linked alport alloantibodies target two accessible conformational epitopes in the alpha5NC1 domainJeong Suk Kang, Clifford E Kashtan, A Neil Turner, et al.
The Journal of Clinical Investigation|April 17, 2002
The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytesClaudia Rohr, Jürgen Prestel, Laurence Heidet, et al.
BMC Pediatrics|August 13, 2014
Fanconi syndrome and severe polyuria: an uncommon clinicobiological presentation of a Gitelman syndromeKarim Bouchireb, Olivia Boyer, Lamisse Mansour-Hendili, et al.
Pageof 10

Showing results (11-20 of 99) with videos related to

Sort By:
Pageof 10
Prenatal Diagnosis|August 21, 2012
Prognosis and outcome of pregnancies exposed to renin-angiotensin system blockersEmmanuel Spaggiari, Laurence Heidet, Gilles Grange, et al.
Molecular and Cellular Biology|January 1, 2004
Early glomerular filtration defect and severe renal disease in podocin-deficient miceSéverine Roselli, Laurence Heidet, Mireille Sich, et al.
Pediatric Nephrology (Berlin, Germany)|March 22, 2020
Bi-allelic mutations in renin-angiotensin system genes, associated with renal tubular dysgenesis, can also present as a progressive chronic kidney diseaseMarc Fila, Vincent Morinière, Philippe Eckart, et al.
Kidney International|August 26, 2004
In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutationShao-Yu Zhang, Arnaud Marlier, Olivier Gribouval, et al.
Journal of the American Society of Nephrology : JASN|December 26, 2001
Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromesChristelle Arrondel, Nicolas Vodovar, Bertrand Knebelmann, et al.
Pediatric Nephrology (Berlin, Germany)|March 31, 2012
Clinical practice recommendations for the treatment of Alport syndrome: a statement of the Alport Syndrome Research CollaborativeClifford E Kashtan, Jie Ding, Martin Gregory, et al.
Nucleic Acids Research|May 28, 2016
Human mutations affect the epigenetic/bookmarking function of HNF1BJonathan Lerner, Alessia Bagattin, Francisco Verdeguer, et al.
The Journal of Biological Chemistry|February 13, 2007
The alloantigenic sites of alpha3alpha4alpha5(IV) collagen: pathogenic X-linked alport alloantibodies target two accessible conformational epitopes in the alpha5NC1 domainJeong Suk Kang, Clifford E Kashtan, A Neil Turner, et al.
The Journal of Clinical Investigation|April 17, 2002
The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytesClaudia Rohr, Jürgen Prestel, Laurence Heidet, et al.
BMC Pediatrics|August 13, 2014
Fanconi syndrome and severe polyuria: an uncommon clinicobiological presentation of a Gitelman syndromeKarim Bouchireb, Olivia Boyer, Lamisse Mansour-Hendili, et al.
Pageof 10