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Immunology Letters
|
January 16, 2003
Divalent cation transport and susceptibility to infectious and autoimmune disease: continuation of the Ity/Lsh/Bcg/Nramp1/Slc11a1 gene story
Jenefer M Blackwell, Susan Searle, Hiba Mohamed, et al.
Wiley Interdisciplinary Reviews. Systems Biology and Medicine
|
August 18, 2012
Large-scale mouse knockouts and phenotypes
Ramiro Ramírez-Solis, Edward Ryder, Richard Houghton, et al.
Genetics
|
December 10, 2016
Improving the Identification of Phenotypic Abnormalities and Sexual Dimorphism in Mice When Studying Rare Event Categorical Characteristics
Natasha A Karp, Ruth Heller, Shay Yaacoby, et al.
Genome Biology
|
July 5, 2011
The mouse genetics toolkit: revealing function and mechanism
Louise van der Weyden, Jacqueline K White, David J Adams, et al.
The Biochemical Journal
|
June 19, 2004
Incomplete glycosylation and defective intracellular targeting of mutant solute carrier family 11 member 1 (Slc11a1)
Jacqueline K White, Abigail Stewart, Jean-Francois Popoff, et al.
Infection and Immunity
|
July 11, 2007
Slc11a1, formerly Nramp1, is expressed in dendritic cells and influences major histocompatibility complex class II expression and antigen-presenting cell function
Carmel B Stober, Sven Brode, Jacqueline K White, et al.
DNA and Cell Biology
|
February 18, 2004
Comparative analysis of two slc11 (Nramp) loci in Takifugu rubripes
Dean Sibthorpe, Anne-Marie Baker, Brian J Gilmartin, et al.
Journal of Biomedical Semantics
|
February 12, 2016
Reporting phenotypes in mouse models when considering body size as a potential confounder
Anika Oellrich, Terrence F Meehan, Helen Parkinson, et al.
Journal of Leukocyte Biology
|
December 17, 2004
Slc11a1-mediated resistance to Salmonella enterica serovar Typhimurium and Leishmania donovani infections does not require functional inducible nitric oxide synthase or phagocyte oxidase activity
Jacqueline K White, Pietro Mastroeni, Jean-François Popoff, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
November 20, 2012
Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1
Erika A Bosman, Jeanne Estabel, Ozama Ismail, et al.
Page
of 9
Search research articles
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Showing results (1-10 of 87) with videos related to
Sort By:
Page
of 9
Immunology Letters
|
January 16, 2003
Divalent cation transport and susceptibility to infectious and autoimmune disease: continuation of the Ity/Lsh/Bcg/Nramp1/Slc11a1 gene story
Jenefer M Blackwell, Susan Searle, Hiba Mohamed, et al.
Wiley Interdisciplinary Reviews. Systems Biology and Medicine
|
August 18, 2012
Large-scale mouse knockouts and phenotypes
Ramiro Ramírez-Solis, Edward Ryder, Richard Houghton, et al.
Genetics
|
December 10, 2016
Improving the Identification of Phenotypic Abnormalities and Sexual Dimorphism in Mice When Studying Rare Event Categorical Characteristics
Natasha A Karp, Ruth Heller, Shay Yaacoby, et al.
Genome Biology
|
July 5, 2011
The mouse genetics toolkit: revealing function and mechanism
Louise van der Weyden, Jacqueline K White, David J Adams, et al.
The Biochemical Journal
|
June 19, 2004
Incomplete glycosylation and defective intracellular targeting of mutant solute carrier family 11 member 1 (Slc11a1)
Jacqueline K White, Abigail Stewart, Jean-Francois Popoff, et al.
Infection and Immunity
|
July 11, 2007
Slc11a1, formerly Nramp1, is expressed in dendritic cells and influences major histocompatibility complex class II expression and antigen-presenting cell function
Carmel B Stober, Sven Brode, Jacqueline K White, et al.
DNA and Cell Biology
|
February 18, 2004
Comparative analysis of two slc11 (Nramp) loci in Takifugu rubripes
Dean Sibthorpe, Anne-Marie Baker, Brian J Gilmartin, et al.
Journal of Biomedical Semantics
|
February 12, 2016
Reporting phenotypes in mouse models when considering body size as a potential confounder
Anika Oellrich, Terrence F Meehan, Helen Parkinson, et al.
Journal of Leukocyte Biology
|
December 17, 2004
Slc11a1-mediated resistance to Salmonella enterica serovar Typhimurium and Leishmania donovani infections does not require functional inducible nitric oxide synthase or phagocyte oxidase activity
Jacqueline K White, Pietro Mastroeni, Jean-François Popoff, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
November 20, 2012
Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1
Erika A Bosman, Jeanne Estabel, Ozama Ismail, et al.
Page
of 9