Literature DB >> 6678340

Hereditary erythroblastic anaemia in the laboratory mouse.

K Shimizu, H Keino, N Ogasawara, K Esaki.   

Abstract

Hereditary erythroblastic anaemia was found in a homozygous mutant (hea/hea) of an inbred strain CFO, which originated from noninbred CF#1 mice from Carworth Inc. This newly-described anaemia is inherited as an autosomal recessive and is lethal at 15-25 days of age. Erythrocytes of anaemic mice show striking polychromasia, anisocytosis, and poikilocytosis. One of the most marked features of this anaemia is the presence of large numbers of nucleated cells, mainly orthochromatophilic erythroblasts and myeloid cells, in the circulation. They also include immature erythroid and myeloid cells. Many naked nuclei appear on smears from circulating blood of anaemic infants. Erythrocytes, haematocrit percentage, and haemoglobin content of older anaemic infants were only about 50% of those of the normal. Formation of erythroid, myeloid cells, and megakaryocytes in the bone marrow seems to be progressively affected by mutant alleles in the anaemic infants.

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Year:  1983        PMID: 6678340     DOI: 10.1258/002367783781070678

Source DB:  PubMed          Journal:  Lab Anim        ISSN: 0023-6772            Impact factor:   2.471


  3 in total

1.  Novel roles for erythroid Ankyrin-1 revealed through an ENU-induced null mouse mutant.

Authors:  Gerhard Rank; Rosemary Sutton; Vikki Marshall; Rachel J Lundie; Jacinta Caddy; Tony Romeo; Kate Fernandez; Matthew P McCormack; Brian M Cooke; Simon J Foote; Brendan S Crabb; David J Curtis; Douglas J Hilton; Benjamin T Kile; Stephen M Jane
Journal:  Blood       Date:  2009-01-28       Impact factor: 22.113

2.  Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias.

Authors:  Rui Chen; Silvia Giliani; Gaetana Lanzi; George I Mias; Silvia Lonardi; Kerry Dobbs; John Manis; Hogune Im; Jennifer E Gallagher; Douglas H Phanstiel; Ghia Euskirchen; Philippe Lacroute; Keith Bettinger; Daniele Moratto; Katja Weinacht; Davide Montin; Eleonora Gallo; Giovanna Mangili; Fulvio Porta; Lucia D Notarangelo; Stefania Pedretti; Waleed Al-Herz; Wasmi Alfahdli; Anne Marie Comeau; Russell S Traister; Sung-Yun Pai; Graziella Carella; Fabio Facchetti; Kari C Nadeau; Michael Snyder; Luigi D Notarangelo
Journal:  J Allergy Clin Immunol       Date:  2013-07-04       Impact factor: 14.290

3.  Multiple intestinal atresia with combined immune deficiency related to TTC7A defect is a multiorgan pathology: study of a French-Canadian-based cohort.

Authors:  Isabel Fernandez; Natalie Patey; Valérie Marchand; Mirela Birlea; Bruno Maranda; Elie Haddad; Hélène Decaluwe; Françoise Le Deist
Journal:  Medicine (Baltimore)       Date:  2014-12       Impact factor: 1.889

  3 in total

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