K. J. Moore

发表

Identification and expression cloning of a leptin receptor, OB-R

Rene Devos, L. Tartaglia, R. Devos, 1995, Cell.

Endotoxin-tolerant Mice Have Mutations in Toll-like Receptor 4 (Tlr4)

L. Larivière, D. Malo, P. Gros, 1999, The Journal of experimental medicine.

Identification and Characterization of the Mouse Obesity Gene tubby: A Member of a Novel Gene Family

C. Ebeling, G. Carlson, T. Brody, 1996, Cell.

Anchored reference loci for comparative genome mapping in mammals

Nancy A. Jenkins, Neal G. Copeland, Stephen J. O'Brien, 1993, Nature Genetics.

Theoretical and empirical issues for marker-assisted breeding of congenic mouse strains

C. Ebeling, G. Carlson, J. Smutko, 1997, Nature Genetics.

Mouse chromosome 6

R. Elliott, K. J. Moore, R. W. Elliott, 2009, Mammalian Genome.

Chromosomal localization of three pulmonary surfactant protein genes in the mouse.

N. Copeland, N. Jenkins, J. Whitsett, 1992, Genomics.

The physical and genetic map surrounding the Lyst gene on mouse chromosome 13.

C. Ebeling, G. Carlson, G. Duyk, 1997, Genomics.

Dilute suppressor dsu acts semidominantly to suppress the coat color phenotype of a deletion mutation, dl20J, of the murine dilute locus.

N. Copeland, N. Jenkins, K. J. Moore, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Spontaneous germ-line ecotropic murine leukemia virus infection: implications for retroviral insertional mutagenesis and germ-line gene transfer.

N. Copeland, D. Gilbert, N. Jenkins, 1989, Progress in nucleic acid research and molecular biology.

Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences

A. Ferré-D’Amaré, S. Burley, N. Copeland, 1994, Nature Genetics.

Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein

N. Jenkins, E. Steingrímsson, K. J. Moore, 1993, Cell.

Insight into the microphthalmia gene.

K. J. Moore, 1995, Trends in genetics : TIG.

Identification and mutation analysis of the complete gene for Chediak–Higashi syndrome

P. Bork, R. Spritz, G. Duyk, 1996, Nature Genetics.

Apparent genotype-phenotype correlation in childhood, adolescent, and adult Chediak-Higashi syndrome.

R. Spritz, Koji Suzuki, H. Miyajima, 2002, American journal of medical genetics.

A phenotype-sensitizing Apoe-deficient genetic background reveals novel atherosclerosis predisposition loci in the mouse.

G. Duyk, Jonathan D. Smith, J. Breslow, 2002, Genetics.

Genetic background determines the extent of atherosclerosis in ApoE-deficient mice.

S. Heath, J. Breslow, K. J. Moore, 1999, Arteriosclerosis, thrombosis, and vascular biology.

Analysis of the Pax-3 gene in the mouse mutant splotch.

K. Steel, J. Nadeau, M. Goulding, 1993, Genomics.

Missense polymorphism in the human carboxypeptidase E gene alters enzymatic activity

M. Permutt, S. Jawahar, A. Parker, 2001, Human mutation.

Interaction of the murine dilute suppressor gene (dsu) with fourteen coat color mutations.

N. Copeland, N. Jenkins, K. J. Moore, 1990, Genetics.

Mouse Chromosome 6

R. Elliott, K. J. Moore, R. W. Elliott, 2004, Mammalian Genome.

A retroviral insertion in the dilute (d) locus provides molecular access to this region of mouse chromosome 9.

N. Copeland, N. Jenkins, D. Kingsley, 1989, Progress in nucleic acid research and molecular biology.

Identification of the murine beige gene by YAC complementation and positional cloning

M. Justice, T. Brody, G. Duyk, 1996, Nature Genetics.

The mahogany protein is a receptor involved in suppression of obesity

P. Bork, C. Ebeling, G. Carlson, 1999, Nature.

Chromosomal localization and genomic characterization of the mouse melastatin gene (Mlsn1).

J. Hunter, J. Smutko, K. J. Moore, 1998, Genomics.

Multiple mouse chromosomal loci for dynein-based motility.

C. Echeverri, R. Vallee, N. Copeland, 1996, Genomics.

Identification, chromosomal location, and genome organization of mammalian G-protein-coupled receptors.

M. Simon, N. Copeland, D. Gilbert, 1993, Genomics.

In Silico Quantitative Trait Locus Map for Atherosclerosis Susceptibility in Apolipoprotein E–Deficient Mice

K. Wittkowski, Jonathan D. Smith, J. Breslow, 2003, Arteriosclerosis, thrombosis, and vascular biology.

The murine dilute suppressor gene dsu suppresses the coat-color phenotype of three pigment mutations that alter melanocyte morphology, d, ash and ln.

N. Copeland, N. Jenkins, K. J. Moore, 1988, Genetics.

The murine dilute suppressor gene encodes a cell autonomous suppressor.

N. Copeland, N. Jenkins, K. J. Moore, 1994, Genetics.

An allele (Pk-1b) from wild-caught mice that affects the activity and kinetics of erythrocyte and liver pyruvate kinase

K. J. Moore, G. Bulfield, 1981, Biochemical Genetics.

Cloning and regional assignment of the human myosin heavy chain 12 (MYH12) gene to chromosome band 15q21.

U. Francke, N. Copeland, N. Jenkins, 1995, Cytogenetics and cell genetics.

Mouse chromosome 6

R. Elliott, K. J. Moore, 2004, Mammalian Genome.