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American Journal of Human Genetics
|
December 1, 1988
Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7
J J O'Donnell, K Vannas-Sulonen, T B Shows, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1988
Cloning and chromosomal assignment of a human cDNA encoding a T cell- and natural killer cell-specific trypsin-like serine protease
H K Gershenfeld, R J Hershberger, T B Shows, et al.
Cytogenetics and Cell Genetics
|
January 1, 1991
Epidermal type I transglutaminase (TGM1) is assigned to human chromosome 14
R R Polakowska, R L Eddy, T B Shows, et al.
Cytogenetics and Cell Genetics
|
January 1, 1985
Chromosome mapping of genes on the short arm of human chromosome 11: parathyroid hormone gene is at 11p15 together with the genes for insulin, c-Harvey-ras 1, and beta-hemoglobin
B U Zabel, H M Kronenberg, G I Bell, et al.
Genomics
|
February 1, 1993
Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1
L H Philipson, R L Eddy, T B Shows, et al.
Biochimica Et Biophysica Acta
|
April 10, 1996
Characterization of the human AMPD3 gene reveals that 5' exon useage is subject to transcriptional control by three tandem promoters and alternative splicing
D K Mahnke-Zizelman, R Eddy, T B Shows, et al.
Birth Defects Original Article Series
|
January 1, 1975
Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridization
M C Rattazzi, J A Brown, R G Davidson, et al.
Experimental Cell Research
|
October 1, 1982
Assignment of a fibronection gene to human chromosome 2 using monoclonal antibodies
G A Koch, R C Schoen, R J Klebe, et al.
American Journal of Human Genetics
|
March 1, 1976
Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis
M C Rattazzi, J A Brown, R G Davidson, et al.
Genomics
|
April 1, 1990
Structure and chromosomal localization of the human thrombospondin gene
F W Wolf, R L Eddy, T B Shows, et al.
Page
of 39
Search research articles
Search
Showing results (121-130 of 381) with videos related to
Sort By:
Page
of 39
American Journal of Human Genetics
|
December 1, 1988
Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7
J J O'Donnell, K Vannas-Sulonen, T B Shows, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1988
Cloning and chromosomal assignment of a human cDNA encoding a T cell- and natural killer cell-specific trypsin-like serine protease
H K Gershenfeld, R J Hershberger, T B Shows, et al.
Cytogenetics and Cell Genetics
|
January 1, 1991
Epidermal type I transglutaminase (TGM1) is assigned to human chromosome 14
R R Polakowska, R L Eddy, T B Shows, et al.
Cytogenetics and Cell Genetics
|
January 1, 1985
Chromosome mapping of genes on the short arm of human chromosome 11: parathyroid hormone gene is at 11p15 together with the genes for insulin, c-Harvey-ras 1, and beta-hemoglobin
B U Zabel, H M Kronenberg, G I Bell, et al.
Genomics
|
February 1, 1993
Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1
L H Philipson, R L Eddy, T B Shows, et al.
Biochimica Et Biophysica Acta
|
April 10, 1996
Characterization of the human AMPD3 gene reveals that 5' exon useage is subject to transcriptional control by three tandem promoters and alternative splicing
D K Mahnke-Zizelman, R Eddy, T B Shows, et al.
Birth Defects Original Article Series
|
January 1, 1975
Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridization
M C Rattazzi, J A Brown, R G Davidson, et al.
Experimental Cell Research
|
October 1, 1982
Assignment of a fibronection gene to human chromosome 2 using monoclonal antibodies
G A Koch, R C Schoen, R J Klebe, et al.
American Journal of Human Genetics
|
March 1, 1976
Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis
M C Rattazzi, J A Brown, R G Davidson, et al.
Genomics
|
April 1, 1990
Structure and chromosomal localization of the human thrombospondin gene
F W Wolf, R L Eddy, T B Shows, et al.
Page
of 39