R Kucherlapati - JoVE Visualize

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American Journal of Medical Genetics|September 20, 1996

Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndromeH M Lachman, B Morrow, R Shprintzen, et al.

Genomics|January 15, 1994

Twenty-one polymorphic markers from human chromosome 12 for integration of genetic and physical mapsJ M LeBlanc-Straceski, K T Montgomery, H Kissel, et al.

Human Molecular Genetics|May 1, 1996

Isolation of a new clathrin heavy chain gene with muscle-specific expression from the region commonly deleted in velo-cardio-facial syndromeH Sirotkin, B Morrow, R DasGupta, et al.

Genomics|June 1, 1997

Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndromeH Sirotkin, B Morrow, B Saint-Jore, et al.

Cancer Research|August 17, 2001

p21(WAF1/cip1) is an important determinant of intestinal cell response to sulindac in vitro and in vivoW Yang, A Velcich, J Mariadason, et al.

Cancer Research|November 3, 2001

The distinct spectra of tumor-associated Apc mutations in mismatch repair-deficient Apc1638N mice define the roles of MSH3 and MSH6 in DNA repair and intestinal tumorigenesisM Kuraguchi, K Yang, E Wong, et al.

Medinfo. MEDINFO|January 1, 1995

Network-based informatics support of research collaborations in the Human Genome Project and the Human Brain ProjectP L Miller, P M Nadkarni, R Kucherlapati, et al.

Genomics|August 1, 1994

Mapping of the 12q12-q22 region with respect to tumor translocation breakpointsF Pedeutour, S Merscher, E Durieux, et al.

Genes, Chromosomes & Cancer|September 19, 2000

Somatic Apc mutations are selected upon their capacity to inactivate the beta-catenin downregulating activityR Smits, N Hofland, W Edelmann, et al.

Genome Research|October 24, 2000

High-resolution transcript map of the region spanning D12S1629 and D12S312 at chromosome 12q13: triple A syndrome-linked regionH Lee, E Choi, Y Seomun, et al.

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Showing results (71-80 of 115) with videos related to

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Pageof 12

American Journal of Medical Genetics|September 20, 1996

Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndromeH M Lachman, B Morrow, R Shprintzen, et al.

Genomics|January 15, 1994

Twenty-one polymorphic markers from human chromosome 12 for integration of genetic and physical mapsJ M LeBlanc-Straceski, K T Montgomery, H Kissel, et al.

Human Molecular Genetics|May 1, 1996

Isolation of a new clathrin heavy chain gene with muscle-specific expression from the region commonly deleted in velo-cardio-facial syndromeH Sirotkin, B Morrow, R DasGupta, et al.

Genomics|June 1, 1997

Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndromeH Sirotkin, B Morrow, B Saint-Jore, et al.

Cancer Research|August 17, 2001

p21(WAF1/cip1) is an important determinant of intestinal cell response to sulindac in vitro and in vivoW Yang, A Velcich, J Mariadason, et al.

Cancer Research|November 3, 2001

The distinct spectra of tumor-associated Apc mutations in mismatch repair-deficient Apc1638N mice define the roles of MSH3 and MSH6 in DNA repair and intestinal tumorigenesisM Kuraguchi, K Yang, E Wong, et al.

Medinfo. MEDINFO|January 1, 1995

Network-based informatics support of research collaborations in the Human Genome Project and the Human Brain ProjectP L Miller, P M Nadkarni, R Kucherlapati, et al.

Genomics|August 1, 1994

Mapping of the 12q12-q22 region with respect to tumor translocation breakpointsF Pedeutour, S Merscher, E Durieux, et al.

Genes, Chromosomes & Cancer|September 19, 2000

Somatic Apc mutations are selected upon their capacity to inactivate the beta-catenin downregulating activityR Smits, N Hofland, W Edelmann, et al.

Genome Research|October 24, 2000

High-resolution transcript map of the region spanning D12S1629 and D12S312 at chromosome 12q13: triple A syndrome-linked regionH Lee, E Choi, Y Seomun, et al.

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