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Martijn H Breuning

Showing results (51-60 of 112) with videos related to

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Medicine|July 16, 2003
Myocardial infarction in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)Saskia A J Lesnik Oberstein, J Wouter Jukema, Sjoerd G Van Duinen, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 28, 2007
Pathogenic sequence for dissecting aneurysm formation in a hypomorphic polycystic kidney disease 1 mouse modelSabrine Hassane, Nanna Claij, Irma S Lantinga-van Leeuwen, et al.
Human Molecular Genetics|April 30, 2009
Toxic tubular injury in kidneys from Pkd1-deletion mice accelerates cystogenesis accompanied by dysregulated planar cell polarity and canonical Wnt signaling pathwaysHester Happé, Wouter N Leonhard, Annemieke van der Wal, et al.
American Journal of Human Genetics|July 12, 2002
Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridizationStefan White, Margot Kalf, Qiang Liu, et al.
Human Genetics|March 23, 2007
Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3Mark B Consugar, Vickie J Kubly, Donna J Lager, et al.
European Journal of Human Genetics : EJHG|June 7, 2012
An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophyApollonia T J M Helderman-van den Enden, Kamlesh Madan, Martijn H Breuning, et al.
The Journal of Pathology|June 16, 2010
Elevated TGFbeta-Smad signalling in experimental Pkd1 models and human patients with polycystic kidney diseaseSabrine Hassane, Wouter N Leonhard, Annemieke van der Wal, et al.
Journal of the American Society of Nephrology : JASN|July 29, 2005
Increased activity of activator protein-1 transcription factor components ATF2, c-Jun, and c-Fos in human and mouse autosomal dominant polycystic kidney diseaseNgoc Hang Le, Annemieke van der Wal, Paola van der Bent, et al.
CA: a Cancer Journal for Clinicians|July 28, 2006
Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinoma): a guide for cliniciansYvonne M C Hendriks, Andrea E de Jong, Hans Morreau, et al.
Hepatology (Baltimore, Md.)|April 2, 2004
Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver diseaseJoost P H Drenth, Esa Tahvanainen, Rene H M te Morsche, et al.
Pageof 12

Showing results (51-60 of 112) with videos related to

Sort By:
Pageof 12
Medicine|July 16, 2003
Myocardial infarction in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)Saskia A J Lesnik Oberstein, J Wouter Jukema, Sjoerd G Van Duinen, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 28, 2007
Pathogenic sequence for dissecting aneurysm formation in a hypomorphic polycystic kidney disease 1 mouse modelSabrine Hassane, Nanna Claij, Irma S Lantinga-van Leeuwen, et al.
Human Molecular Genetics|April 30, 2009
Toxic tubular injury in kidneys from Pkd1-deletion mice accelerates cystogenesis accompanied by dysregulated planar cell polarity and canonical Wnt signaling pathwaysHester Happé, Wouter N Leonhard, Annemieke van der Wal, et al.
American Journal of Human Genetics|July 12, 2002
Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridizationStefan White, Margot Kalf, Qiang Liu, et al.
Human Genetics|March 23, 2007
Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3Mark B Consugar, Vickie J Kubly, Donna J Lager, et al.
European Journal of Human Genetics : EJHG|June 7, 2012
An urgent need for a change in policy revealed by a study on prenatal testing for Duchenne muscular dystrophyApollonia T J M Helderman-van den Enden, Kamlesh Madan, Martijn H Breuning, et al.
The Journal of Pathology|June 16, 2010
Elevated TGFbeta-Smad signalling in experimental Pkd1 models and human patients with polycystic kidney diseaseSabrine Hassane, Wouter N Leonhard, Annemieke van der Wal, et al.
Journal of the American Society of Nephrology : JASN|July 29, 2005
Increased activity of activator protein-1 transcription factor components ATF2, c-Jun, and c-Fos in human and mouse autosomal dominant polycystic kidney diseaseNgoc Hang Le, Annemieke van der Wal, Paola van der Bent, et al.
CA: a Cancer Journal for Clinicians|July 28, 2006
Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinoma): a guide for cliniciansYvonne M C Hendriks, Andrea E de Jong, Hans Morreau, et al.
Hepatology (Baltimore, Md.)|April 2, 2004
Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver diseaseJoost P H Drenth, Esa Tahvanainen, Rene H M te Morsche, et al.
Pageof 12