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Genesis (New York, N.Y. : 2000)
|
May 3, 2006
Transgenic mice expressing tamoxifen-inducible Cre for somatic gene modification in renal epithelial cells
Irma S Lantinga-van Leeuwen, Wouter N Leonhard, Annemieke van de Wal, et al.
Kidney International
|
March 8, 2013
Cyst expansion and regression in a mouse model of polycystic kidney disease
Hester Happé, Annemieke M van der Wal, Daniela C F Salvatori, et al.
Human Molecular Genetics
|
January 5, 2002
Distinct subcellular expression of endogenous polycystin-2 in the plasma membrane and Golgi apparatus of MDCK cells
Martijn S Scheffers, Hang Le, Paola van der Bent, et al.
American Journal of Physiology. Renal Physiology
|
February 25, 2011
Curcumin inhibits cystogenesis by simultaneous interference of multiple signaling pathways: in vivo evidence from a Pkd1-deletion model
Wouter N Leonhard, Annemieke van der Wal, Zlata Novalic, et al.
European Journal of Human Genetics : EJHG
|
April 19, 2007
A t(4;6)(q12;p23) translocation disrupts a membrane-associated O-acetyl transferase gene (MBOAT1) in a patient with a novel brachydactyly-syndactyly syndrome
Johannes G Dauwerse, Bert B A de Vries, Cokkie H Wouters, et al.
Human Molecular Genetics
|
February 5, 2003
Loss of CBP acetyltransferase activity by PHD finger mutations in Rubinstein-Taybi syndrome
Eric Kalkhoven, Jeroen H Roelfsema, Hans Teunissen, et al.
American Journal of Medical Genetics. Part A
|
September 24, 2004
Feeling at risk: how women interpret their familial breast cancer risk
Sandra van Dijk, Wilma Otten, Christi J van Asperen, et al.
Journal of the American Society of Nephrology : JASN
|
February 21, 2012
Dose-dependent effects of sirolimus on mTOR signaling and polycystic kidney disease
Zlata Novalic, Annemieke M van der Wal, Wouter N Leonhard, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2007
Diagnosis of genetic abnormalities in developmentally delayed patients: a new strategy combining MLPA and array-CGH
Marjolein Kriek, Jeroen Knijnenburg, Stefan J White, et al.
American Journal of Human Genetics
|
August 16, 2006
Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase
Saskia A J Lesnik Oberstein, Marjolein Kriek, Stefan J White, et al.
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Search research articles
Search
Showing results (41-50 of 112) with videos related to
Sort By:
Page
of 12
Genesis (New York, N.Y. : 2000)
|
May 3, 2006
Transgenic mice expressing tamoxifen-inducible Cre for somatic gene modification in renal epithelial cells
Irma S Lantinga-van Leeuwen, Wouter N Leonhard, Annemieke van de Wal, et al.
Kidney International
|
March 8, 2013
Cyst expansion and regression in a mouse model of polycystic kidney disease
Hester Happé, Annemieke M van der Wal, Daniela C F Salvatori, et al.
Human Molecular Genetics
|
January 5, 2002
Distinct subcellular expression of endogenous polycystin-2 in the plasma membrane and Golgi apparatus of MDCK cells
Martijn S Scheffers, Hang Le, Paola van der Bent, et al.
American Journal of Physiology. Renal Physiology
|
February 25, 2011
Curcumin inhibits cystogenesis by simultaneous interference of multiple signaling pathways: in vivo evidence from a Pkd1-deletion model
Wouter N Leonhard, Annemieke van der Wal, Zlata Novalic, et al.
European Journal of Human Genetics : EJHG
|
April 19, 2007
A t(4;6)(q12;p23) translocation disrupts a membrane-associated O-acetyl transferase gene (MBOAT1) in a patient with a novel brachydactyly-syndactyly syndrome
Johannes G Dauwerse, Bert B A de Vries, Cokkie H Wouters, et al.
Human Molecular Genetics
|
February 5, 2003
Loss of CBP acetyltransferase activity by PHD finger mutations in Rubinstein-Taybi syndrome
Eric Kalkhoven, Jeroen H Roelfsema, Hans Teunissen, et al.
American Journal of Medical Genetics. Part A
|
September 24, 2004
Feeling at risk: how women interpret their familial breast cancer risk
Sandra van Dijk, Wilma Otten, Christi J van Asperen, et al.
Journal of the American Society of Nephrology : JASN
|
February 21, 2012
Dose-dependent effects of sirolimus on mTOR signaling and polycystic kidney disease
Zlata Novalic, Annemieke M van der Wal, Wouter N Leonhard, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2007
Diagnosis of genetic abnormalities in developmentally delayed patients: a new strategy combining MLPA and array-CGH
Marjolein Kriek, Jeroen Knijnenburg, Stefan J White, et al.
American Journal of Human Genetics
|
August 16, 2006
Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase
Saskia A J Lesnik Oberstein, Marjolein Kriek, Stefan J White, et al.
Page
of 12