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Human Mutation
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January 1, 1992
Missense mutations causing mild hemophilia A in Iceland detected by denaturing gradient gel electrophoresis
S Jonsdottir, C Diamond, B Levinson, et al.
Science (New York, N.Y.)
|
January 14, 1972
Cellular site of glucocorticoid-receptor complex formation
B B Levinson, J D Baxter, G G Rousseau, et al.
American Journal of Human Genetics
|
March 1, 1995
Similar splicing mutations of the Menkes/mottled copper-transporting ATPase gene in occipital horn syndrome and the blotchy mouse
S Das, B Levinson, C Vulpe, et al.
Nature Genetics
|
January 1, 1993
Are X-linked cutis laxa and Menkes disease allelic?
B Levinson, J Gitschier, C Vulpe, et al.
Genomics
|
July 11, 1992
Sequence of the human factor VIII-associated gene is conserved in mouse
B Levinson, J R Bermingham, A Metzenberg, et al.
The Journal of Biological Chemistry
|
June 10, 1985
Cloned mouse ribonucleotide reductase subunit M1 cDNA reveals amino acid sequence homology with Escherichia coli and herpesvirus ribonucleotide reductases
I W Caras, B B Levinson, M Fabry, et al.
Nature Genetics
|
April 1, 1994
The mottled gene is the mouse homologue of the Menkes disease gene
B Levinson, C Vulpe, B Elder, et al.
Melanoma Research
|
February 6, 2003
Concurrent interferon-alpha and radiation for head and neck melanoma
N P Nguyen, B Levinson, S Dutta, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 29, 2007
Neural correlates of attentional expertise in long-term meditation practitioners
J A Brefczynski-Lewis, A Lutz, H S Schaefer, et al.
Nature Genetics
|
August 2, 2001
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome
B Zhou, S K Westaway, B Levinson, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 74) with videos related to
Sort By:
Page
of 8
Human Mutation
|
January 1, 1992
Missense mutations causing mild hemophilia A in Iceland detected by denaturing gradient gel electrophoresis
S Jonsdottir, C Diamond, B Levinson, et al.
Science (New York, N.Y.)
|
January 14, 1972
Cellular site of glucocorticoid-receptor complex formation
B B Levinson, J D Baxter, G G Rousseau, et al.
American Journal of Human Genetics
|
March 1, 1995
Similar splicing mutations of the Menkes/mottled copper-transporting ATPase gene in occipital horn syndrome and the blotchy mouse
S Das, B Levinson, C Vulpe, et al.
Nature Genetics
|
January 1, 1993
Are X-linked cutis laxa and Menkes disease allelic?
B Levinson, J Gitschier, C Vulpe, et al.
Genomics
|
July 11, 1992
Sequence of the human factor VIII-associated gene is conserved in mouse
B Levinson, J R Bermingham, A Metzenberg, et al.
The Journal of Biological Chemistry
|
June 10, 1985
Cloned mouse ribonucleotide reductase subunit M1 cDNA reveals amino acid sequence homology with Escherichia coli and herpesvirus ribonucleotide reductases
I W Caras, B B Levinson, M Fabry, et al.
Nature Genetics
|
April 1, 1994
The mottled gene is the mouse homologue of the Menkes disease gene
B Levinson, C Vulpe, B Elder, et al.
Melanoma Research
|
February 6, 2003
Concurrent interferon-alpha and radiation for head and neck melanoma
N P Nguyen, B Levinson, S Dutta, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 29, 2007
Neural correlates of attentional expertise in long-term meditation practitioners
J A Brefczynski-Lewis, A Lutz, H S Schaefer, et al.
Nature Genetics
|
August 2, 2001
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome
B Zhou, S K Westaway, B Levinson, et al.
Page
of 8