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Showing results (271-280 of 391) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1990
Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16pJ G Dauwerse, T Kievits, G C Beverstock, 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.
International Journal of Cancer|March 3, 1995
Mechanisms of MRP over-expression in four human lung-cancer cell lines and analysis of the MRP ampliconE W Eijdems, M De Haas, J M Coco-Martin, et al.
American Journal of Human Genetics|March 1, 1995
Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypesH M Mitchison, A M O'Rawe, P E Taschner, 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.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 28, 2004
Risk estimation for healthy women from breast cancer families: new insights and new strategiesChristi J van Asperen, M A Jonker, C E Jacobi, 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.
Molecular Genetics and Metabolism|April 7, 1999
A murine model for juvenile NCL: gene targeting of mouse Cln3N D Greene, D L Bernard, P E Taschner, et al.
NPJ Digital Medicine|May 22, 2026
A multilevel meta-analysis of passive smartphone sensing of adolescent mental healthMerel M L Leijse, Aaliyah Hansen, Imara K Semeijn, et al.
Pageof 40

Showing results (271-280 of 391) with videos related to

Sort By:
Pageof 40
Cytogenetics and Cell Genetics|January 1, 1990
Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16pJ G Dauwerse, T Kievits, G C Beverstock, 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.
International Journal of Cancer|March 3, 1995
Mechanisms of MRP over-expression in four human lung-cancer cell lines and analysis of the MRP ampliconE W Eijdems, M De Haas, J M Coco-Martin, et al.
American Journal of Human Genetics|March 1, 1995
Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypesH M Mitchison, A M O'Rawe, P E Taschner, 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.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 28, 2004
Risk estimation for healthy women from breast cancer families: new insights and new strategiesChristi J van Asperen, M A Jonker, C E Jacobi, 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.
Molecular Genetics and Metabolism|April 7, 1999
A murine model for juvenile NCL: gene targeting of mouse Cln3N D Greene, D L Bernard, P E Taschner, et al.
NPJ Digital Medicine|May 22, 2026
A multilevel meta-analysis of passive smartphone sensing of adolescent mental healthMerel M L Leijse, Aaliyah Hansen, Imara K Semeijn, et al.
Pageof 40