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G M Landes

Showing results (11-20 of 33) with videos related to

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The Journal of Biological Chemistry|June 23, 1995
Isolation and characterization of human casein kinase I epsilon (CKI), a novel member of the CKI gene familyK J Fish, A Cegielska, M E Getman, et al.
Functional & Integrative Genomics|January 17, 2002
A modified two-step phage display selection for isolation of polycystin-1 ligandsN O Bukanov, A L Meek, K W Klinger, et al.
Human Molecular Genetics|March 11, 1999
Two novel genes in the center of the 11p15 imprinted domain escape genomic imprintingM P Lee, S Brandenburg, G M Landes, et al.
Genomics|October 15, 1996
A novel ribosomal protein L3-like gene (RPL3L) maps to the autosomal dominant polycystic kidney disease gene regionT J Van Raay, T D Connors, K W Klinger, et al.
Biotechniques|June 1, 1997
Evaluation of DNA sequencing ambiguities using tetramethylammonium chloride hybridization conditionsT D Connors, T C Burn, T VanRaay, et al.
American Journal of Human Genetics|May 1, 1993
Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1M J Dixon, J Dixon, T Houseal, et al.
Human Molecular Genetics|June 22, 2000
Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1O Ibraghimov-Beskrovnaya, N O Bukanov, L C Donohue, et al.
Human Molecular Genetics|July 1, 1992
Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2M J Dixon, J Dixon, D Raskova, et al.
Cytogenetics and Cell Genetics|December 22, 1998
Comparative genomic hybridization and its application to Wilms' tumorigenesisM E Getman, T W Houseal, G A Miller, et al.
Genomics|April 15, 1997
The NTN2L gene encoding a novel human netrin maps to the autosomal dominant polycystic kidney disease region on chromosome 16p13.3T J Van Raay, S M Foskett, T D Connors, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
The Journal of Biological Chemistry|June 23, 1995
Isolation and characterization of human casein kinase I epsilon (CKI), a novel member of the CKI gene familyK J Fish, A Cegielska, M E Getman, et al.
Functional & Integrative Genomics|January 17, 2002
A modified two-step phage display selection for isolation of polycystin-1 ligandsN O Bukanov, A L Meek, K W Klinger, et al.
Human Molecular Genetics|March 11, 1999
Two novel genes in the center of the 11p15 imprinted domain escape genomic imprintingM P Lee, S Brandenburg, G M Landes, et al.
Genomics|October 15, 1996
A novel ribosomal protein L3-like gene (RPL3L) maps to the autosomal dominant polycystic kidney disease gene regionT J Van Raay, T D Connors, K W Klinger, et al.
Biotechniques|June 1, 1997
Evaluation of DNA sequencing ambiguities using tetramethylammonium chloride hybridization conditionsT D Connors, T C Burn, T VanRaay, et al.
American Journal of Human Genetics|May 1, 1993
Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1M J Dixon, J Dixon, T Houseal, et al.
Human Molecular Genetics|June 22, 2000
Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1O Ibraghimov-Beskrovnaya, N O Bukanov, L C Donohue, et al.
Human Molecular Genetics|July 1, 1992
Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2M J Dixon, J Dixon, D Raskova, et al.
Cytogenetics and Cell Genetics|December 22, 1998
Comparative genomic hybridization and its application to Wilms' tumorigenesisM E Getman, T W Houseal, G A Miller, et al.
Genomics|April 15, 1997
The NTN2L gene encoding a novel human netrin maps to the autosomal dominant polycystic kidney disease region on chromosome 16p13.3T J Van Raay, S M Foskett, T D Connors, et al.
Pageof 4