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Martin Zenker

Showing results (21-30 of 338) with videos related to

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Przeglad Lekarski|August 11, 2006
[LAMB2 gene mutation as a cause of congenital nephrotic syndrome with distinct eye abnormalities and hypotonia]Aleksandra Zurowska, Iga Załuska-Leśniewska, Martin Zenker
Gastroenterology|January 30, 2007
Pancreatic development and diseaseDavid A Cano, Matthias Hebrok, Martin Zenker
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|February 29, 2020
Long-term Culture of EBV-induced Human Lymphoblastoid Cell Lines Reveals Chromosomal InstabilityMarianne Volleth, Martin Zenker, Ivana Joksic, et al.
Human Mutation|September 8, 2007
Recurrent inversion with concomitant deletion and insertion events in the coagulation factor VIII gene suggests a new mechanism for X-chromosomal rearrangements causing hemophilia AChristiane Mühle, Martin Zenker, Nadia Chuzhanova, et al.
American Journal of Medical Genetics. Part A|August 13, 2005
Demonstration of two novel LAMB2 mutations in the original Pierson syndrome family reported 42 years agoMartin Zenker, Michel Pierson, Philippe Jonveaux, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Fraser syndrome due to homozygosity for a splice site mutation of FREM2Yousef Shafeghati, Andrea Kniepert, Ghazal Vakili, et al.
Journal of Molecular Medicine (Berlin, Germany)|January 11, 2007
An unexpected new role of mutant Ras: perturbation of human embryonic developmentChristian P Kratz, Charlotte M Niemeyer, Martin Zenker
European Journal of Pediatrics|June 18, 2010
Eponym: Johanson-Blizzard syndromeNima Rezaei, Mozhgan Sabbaghian, Zhifeng Liu, et al.
Indian Journal of Pediatrics|December 7, 2011
Infantile nephrotic syndrome with microcephaly and global developmental delay: the Galloway Mowat SyndromeSriram Krishnamurthy, N G Rajesh, Ananthakrishnan Ramesh, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 22, 2006
A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2Verena Matejas, Lihadh Al-Gazali, Iradj Amirlak, et al.
Pageof 34

Showing results (21-30 of 338) with videos related to

Sort By:
Pageof 34
Przeglad Lekarski|August 11, 2006
[LAMB2 gene mutation as a cause of congenital nephrotic syndrome with distinct eye abnormalities and hypotonia]Aleksandra Zurowska, Iga Załuska-Leśniewska, Martin Zenker
Gastroenterology|January 30, 2007
Pancreatic development and diseaseDavid A Cano, Matthias Hebrok, Martin Zenker
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|February 29, 2020
Long-term Culture of EBV-induced Human Lymphoblastoid Cell Lines Reveals Chromosomal InstabilityMarianne Volleth, Martin Zenker, Ivana Joksic, et al.
Human Mutation|September 8, 2007
Recurrent inversion with concomitant deletion and insertion events in the coagulation factor VIII gene suggests a new mechanism for X-chromosomal rearrangements causing hemophilia AChristiane Mühle, Martin Zenker, Nadia Chuzhanova, et al.
American Journal of Medical Genetics. Part A|August 13, 2005
Demonstration of two novel LAMB2 mutations in the original Pierson syndrome family reported 42 years agoMartin Zenker, Michel Pierson, Philippe Jonveaux, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Fraser syndrome due to homozygosity for a splice site mutation of FREM2Yousef Shafeghati, Andrea Kniepert, Ghazal Vakili, et al.
Journal of Molecular Medicine (Berlin, Germany)|January 11, 2007
An unexpected new role of mutant Ras: perturbation of human embryonic developmentChristian P Kratz, Charlotte M Niemeyer, Martin Zenker
European Journal of Pediatrics|June 18, 2010
Eponym: Johanson-Blizzard syndromeNima Rezaei, Mozhgan Sabbaghian, Zhifeng Liu, et al.
Indian Journal of Pediatrics|December 7, 2011
Infantile nephrotic syndrome with microcephaly and global developmental delay: the Galloway Mowat SyndromeSriram Krishnamurthy, N G Rajesh, Ananthakrishnan Ramesh, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 22, 2006
A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2Verena Matejas, Lihadh Al-Gazali, Iradj Amirlak, et al.
Pageof 34