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K J Moore

Showing results (81-90 of 116) with videos related to

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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 proteinM 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 proteinC 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 morphologyR B Mitchell, D D Redfearn, L E Moser, et al.
Epilepsia|January 1, 1994
Family history of seizures in posttraumatic and alcohol-associated seizure disordersB 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 strainsP 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 spaceM L Fitzgerald, A J Mendez, K J Moore, et al.
Nature Genetics|February 1, 1993
Anchored reference loci for comparative genome mapping in mammalsS 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 locusK 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 mutationsL 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.
Pageof 12

Showing results (81-90 of 116) with videos related to

Sort By:
Pageof 12
Human Molecular Genetics|July 1, 1997
Mutations in the Chediak-Higashi syndrome gene (CHS1) indicate requirement for the complete 3801 amino acid CHS proteinM 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 proteinC 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 morphologyR B Mitchell, D D Redfearn, L E Moser, et al.
Epilepsia|January 1, 1994
Family history of seizures in posttraumatic and alcohol-associated seizure disordersB 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 strainsP 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 spaceM L Fitzgerald, A J Mendez, K J Moore, et al.
Nature Genetics|February 1, 1993
Anchored reference loci for comparative genome mapping in mammalsS 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 locusK 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 mutationsL 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.
Pageof 12