R P Woychik|K Alagramam - JoVE Visualize

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Mutation Research|August 1, 1998

Functional genomics in the post-genome eraR P Woychik, M L Klebig, M J Justice, et al.

The Journal of Clinical Investigation|April 16, 1998

Epidermal growth factor receptor activity mediates renal cyst formation in polycystic kidney diseaseW G Richards, W E Sweeney, B K Yoder, et al.

Growth Factors (Chur, Switzerland)|March 20, 1998

Characterization of growth factor responsiveness and alterations in growth factor homeostasis involved in the tumorigenic conversion of mouse oval cellsR J Isfort, D B Cody, W G Richards, et al.

Genes & Development|February 15, 1994

Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (a(t)) and white-bellied agouti (Aw) reveals alternative forms of agouti transcriptsS J Bultman, M L Klebig, E J Michaud, et al.

Genomics|June 1, 1990

Location of the gene involving the small eye mutation on mouse chromosome 2 suggests homology with human aniridia 2 (AN2)R van der Meer-de Jong, M E Dickinson, R P Woychik, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 21, 1999

An agouti mutation lacking the basic domain induces yellow pigmentation but not obesity in transgenic miceR J Miltenberger, R L Mynatt, B D Bruce, et al.

Development (Cambridge, England)|May 11, 2000

The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determinationN S Murcia, W G Richards, B K Yoder, et al.

Nature Genetics|January 4, 2001

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin geneK N Alagramam, C L Murcia, H Y Kwon, et al.

Molecular and Cellular Biology|October 1, 1985

Synthesis of bovine growth hormone in primates by using a herpesvirus vectorR C Desrosiers, J Kamine, A Bakker, et al.

Genes & Development|June 15, 1994

Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineageE J Michaud, M J van Vugt, S J Bultman, et al.

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Showing results (31-40 of 68) with videos related to

Sort By:

Pageof 7

Mutation Research|August 1, 1998

Functional genomics in the post-genome eraR P Woychik, M L Klebig, M J Justice, et al.

The Journal of Clinical Investigation|April 16, 1998

Epidermal growth factor receptor activity mediates renal cyst formation in polycystic kidney diseaseW G Richards, W E Sweeney, B K Yoder, et al.

Growth Factors (Chur, Switzerland)|March 20, 1998

Characterization of growth factor responsiveness and alterations in growth factor homeostasis involved in the tumorigenic conversion of mouse oval cellsR J Isfort, D B Cody, W G Richards, et al.

Genes & Development|February 15, 1994

Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (a(t)) and white-bellied agouti (Aw) reveals alternative forms of agouti transcriptsS J Bultman, M L Klebig, E J Michaud, et al.

Genomics|June 1, 1990

Location of the gene involving the small eye mutation on mouse chromosome 2 suggests homology with human aniridia 2 (AN2)R van der Meer-de Jong, M E Dickinson, R P Woychik, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 21, 1999

An agouti mutation lacking the basic domain induces yellow pigmentation but not obesity in transgenic miceR J Miltenberger, R L Mynatt, B D Bruce, et al.

Development (Cambridge, England)|May 11, 2000

The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determinationN S Murcia, W G Richards, B K Yoder, et al.

Nature Genetics|January 4, 2001

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin geneK N Alagramam, C L Murcia, H Y Kwon, et al.

Molecular and Cellular Biology|October 1, 1985

Synthesis of bovine growth hormone in primates by using a herpesvirus vectorR C Desrosiers, J Kamine, A Bakker, et al.

Genes & Development|June 15, 1994

Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineageE J Michaud, M J van Vugt, S J Bultman, et al.

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