ArticleMammalian genome : official journal of the International Mammalian Genome Society1994
Molecular map of chromosome 19 including three genes affecting bleeding time: ep, ru, and bm.
Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
14 citing papers in PubMed.
- A single nucleotide mutation in Nppc is associated with a long bone abnormality in lbab mice.BMC genetics · 2007Article
- The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation.Proceedings of the National Academy of Sciences of the United States of America · 2003Article
- Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity.American journal of human genetics · 1998Article
- rim2 (recombination-induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak syndrome (HPS): genetic and physical mapping.Mammalian genome : official journal of the International Mammalian Genome Society · 1998Article
- Lung disease in mice with cystic fibrosis.The Journal of clinical investigation · 1997Article
- The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome.Proceedings of the National Academy of Sciences of the United States of America · 1997Article
- Mart1 is located on mouse chromosome 19 and is excluded as a candidate for ep and ru.Mammalian genome : official journal of the International Mammalian Genome Society · 1997Article
- A fusion pore phenotype in mast cells of the ruby-eye mouse.Proceedings of the National Academy of Sciences of the United States of America · 1996Article
- PCR-analyzed microsatellites for the inbred mouse strain 129/Sv, the strain most commonly used in gene knockout technology.Mammalian genome : official journal of the International Mammalian Genome Society · 1996Article
- High-resolution genetic mapping of the gunmetal gene which regulates platelet production.Mammalian genome : official journal of the International Mammalian Genome Society · 1996Article
- Molecular markers near the mouse brachymorphic (bm) gene, which affects connective tissues and bleeding time.Mammalian genome : official journal of the International Mammalian Genome Society · 1996Article
- A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2.American journal of human genetics · 1995Article
- Pigmentation, pleiotropy, and genetic pathways in humans and mice.American journal of human genetics · 1995Article
- Molecular markers near two mouse chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD).Mammalian genome : official journal of the International Mammalian Genome Society · 1995Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
The mouse ruby eye (ru) and pale ear (ep) pigment dilution genes cause platelet storage pool deficiency (SPD) and prolonged bleeding times. The brachymorphic (bm) gene, in addition to causing skeletal abnormalities, is also associated with prolonged bleeding times. All three hemorrhagic genes are found within 10 cM on Chromosome (Chr) 19. In this study, 15 microsatellite markers and five cDNAs, spanning 21 cM of Chr 19, were mapped in relation to the bm, ep, and ru genes in 457 progeny of an interspecific backcross utilizing the highly inbred strain PWK derived from the Mus musculus musculus species. Several markers were found to be closely linked to the three genes and should be useful as entry points in their eventual molecular identification.
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