Literature DB >> 10477710

Identification of the molecular genetic defect of patients with methemoglobin M-Kankakee (M-Iwate), alpha87 (F8) His --> Tyr: evidence for an electrostatic model of alphaM hemoglobin assembly.

A Ameri1, V F Fairbanks, G A Yanik, F Mahdi, S N Thibodeau, D J McCormick, L A Boxer, K T McDonagh.   

Abstract

We determined that the molecular defect of 2 patients with hemoglobin (Hb) M-Kankakee [Hb M-Iwate, alpha87 (F8) His --> Tyr] resides in the alpha1-globin gene. The proportion of Hb M observed is higher than that predicted for an alpha1-globin variant. Our evidence suggests that the greater-than-expected proportion of Hb M-Kankakee results from preferential association of the electronegative beta-globin chains with the alpha(M)-globin chains that are more electropositive than normal alpha-globin chains.

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Year:  1999        PMID: 10477710

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  3 in total

Review 1.  Hemoglobin variants: biochemical properties and clinical correlates.

Authors:  Christopher S Thom; Claire F Dickson; David A Gell; Mitchell J Weiss
Journal:  Cold Spring Harb Perspect Med       Date:  2013-03-01       Impact factor: 6.915

2.  Familial congenital cyanosis caused by Hb-M(Yantai)(α-76 GAC → TAC, Asp → Tyr).

Authors:  Yanbo Sun; Pingyu Wang; Youjie Li; Fei Jiao; Zunling Li; Ying Ma; Wei Li; Shuyang Xie
Journal:  Genet Mol Biol       Date:  2010-09-01       Impact factor: 1.771

3.  De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobin M Iwate and symptomatic methemoglobinemia since birth.

Authors:  Marcos Borato Viana; André Rolim Belisário
Journal:  Rev Bras Hematol Hemoter       Date:  2014-03-29
  3 in total

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