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Human Molecular Genetics
|
July 1, 1997
Mutations in the Chediak-Higashi syndrome gene (CHS1) indicate requirement for the complete 3801 amino acid CHS protein
M A Karim, D L Nagle, H H Kandil, et al.
Cell
|
July 30, 1993
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
C A Hodgkinson, K J Moore, A Nakayama, et al.
Journal of Dairy Science
|
June 1, 1997
Relationships between in situ protein degradability and grass developmental morphology
R B Mitchell, D D Redfearn, L E Moser, et al.
Epilepsia
|
January 1, 1994
Family history of seizures in posttraumatic and alcohol-associated seizure disorders
B A Schaumann, J F Annegers, S B Johnson, et al.
Nature Genetics
|
November 14, 1997
Theoretical and empirical issues for marker-assisted breeding of congenic mouse strains
P Markel, P Shu, C Ebeling, et al.
The Journal of Biological Chemistry
|
May 1, 2001
ATP-binding cassette transporter A1 contains an NH2-terminal signal anchor sequence that translocates the protein's first hydrophilic domain to the exoplasmic space
M L Fitzgerald, A J Mendez, K J Moore, et al.
Nature Genetics
|
February 1, 1993
Anchored reference loci for comparative genome mapping in mammals
S J O'Brien, J E Womack, L A Lyons, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1988
Dilute suppressor dsu acts semidominantly to suppress the coat color phenotype of a deletion mutation, dl20J, of the murine dilute locus
K J Moore, P K Seperack, M C Strobel, et al.
Genetical Research
|
December 1, 1991
The liver/erythrocyte pyruvate kinase gene complex [Pk-1] in the mouse: regulatory gene mutations
L A Fitton, M Davidson, K J Moore, et al.
American Journal of Human Genetics
|
September 1, 1996
Homozygosity mapping of the gene for Chediak-Higashi syndrome to chromosome 1q42-q44 in a segment of conserved synteny that includes the mouse beige locus (bg)
K Fukai, J Oh, M A Karim, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 116) with videos related to
Sort By:
Page
of 12
Human Molecular Genetics
|
July 1, 1997
Mutations in the Chediak-Higashi syndrome gene (CHS1) indicate requirement for the complete 3801 amino acid CHS protein
M A Karim, D L Nagle, H H Kandil, et al.
Cell
|
July 30, 1993
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
C A Hodgkinson, K J Moore, A Nakayama, et al.
Journal of Dairy Science
|
June 1, 1997
Relationships between in situ protein degradability and grass developmental morphology
R B Mitchell, D D Redfearn, L E Moser, et al.
Epilepsia
|
January 1, 1994
Family history of seizures in posttraumatic and alcohol-associated seizure disorders
B A Schaumann, J F Annegers, S B Johnson, et al.
Nature Genetics
|
November 14, 1997
Theoretical and empirical issues for marker-assisted breeding of congenic mouse strains
P Markel, P Shu, C Ebeling, et al.
The Journal of Biological Chemistry
|
May 1, 2001
ATP-binding cassette transporter A1 contains an NH2-terminal signal anchor sequence that translocates the protein's first hydrophilic domain to the exoplasmic space
M L Fitzgerald, A J Mendez, K J Moore, et al.
Nature Genetics
|
February 1, 1993
Anchored reference loci for comparative genome mapping in mammals
S J O'Brien, J E Womack, L A Lyons, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1988
Dilute suppressor dsu acts semidominantly to suppress the coat color phenotype of a deletion mutation, dl20J, of the murine dilute locus
K J Moore, P K Seperack, M C Strobel, et al.
Genetical Research
|
December 1, 1991
The liver/erythrocyte pyruvate kinase gene complex [Pk-1] in the mouse: regulatory gene mutations
L A Fitton, M Davidson, K J Moore, et al.
American Journal of Human Genetics
|
September 1, 1996
Homozygosity mapping of the gene for Chediak-Higashi syndrome to chromosome 1q42-q44 in a segment of conserved synteny that includes the mouse beige locus (bg)
K Fukai, J Oh, M A Karim, et al.
Page
of 12