Literature DB >> 5988206

Hemoglobin J Cape Town-alpha-2 92 arginine replaced by glutamine beta-2.

M C Botha, D Beale, W A Isaacs, H Lehmann.   

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Year:  1966        PMID: 5988206     DOI: 10.1038/212792a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


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  10 in total

1.  Structure-function relations of human hemoglobins.

Authors:  Alain J Marengo-Rowe
Journal:  Proc (Bayl Univ Med Cent)       Date:  2006-07

2.  Haemoglobin Rahere (beta Lys-Thr): A new high affinity haemoglobin associated with decreased 2, 3-diphosphoglycerate binding and relative polycythaemia.

Authors:  P A Lorkin; A D Stephens; M E Beard; P F Wrigley; L Adams; H Lehmann
Journal:  Br Med J       Date:  1975-10-25

3.  Inherited haemoglobin variants in a South African population.

Authors:  A R Bird; P Ellis; K Wood; C Mathew; C Karabus
Journal:  J Med Genet       Date:  1987-04       Impact factor: 6.318

4.  Hemoglobin Malmö Beta-97 (FG-4) histidine--glutamine: a cause of polycythemia.

Authors:  S H Boyer; S Charache; V F Fairbanks; J E Maldonado; A Noyes; E E Gayle
Journal:  J Clin Invest       Date:  1972-03       Impact factor: 14.808

5.  Hemoglobin Yoshizuka (G10(108)beta asparagine--aspartic acid): a new variant with a reduced oxygen affinity from a Japanese family.

Authors:  T Imamura; S Fujita; Y Ohta; M Hanada; T Yanase
Journal:  J Clin Invest       Date:  1969-12       Impact factor: 14.808

6.  Hb Cemenelum [alpha 92 (FG4) Arg-->Trp]: a hemoglobin variant of the alpha 1/beta 2 interface that displays a moderate increase in oxygen affinity.

Authors:  H Wajcman; J Kister; A M'Rad; A M Soummer; F Galacteros
Journal:  Ann Hematol       Date:  1994-02       Impact factor: 3.673

7.  Familial polycythaemia caused by a new haemoglobin variant: Hb Heathrow, beta 103 (G5) phenylalanine leads to leucine.

Authors:  J M White; L Szur; I D Gillies; P A Lorkin; H Lehmann
Journal:  Br Med J       Date:  1973-09-29

8.  Oxygen equilibrium of hemoglobin J Cape Town.

Authors:  S Charache; T Jenkins
Journal:  J Clin Invest       Date:  1971-07       Impact factor: 14.808

Review 9.  Thalassemic hemoglobinopathies.

Authors:  M H Steinberg; J G Adams
Journal:  Am J Pathol       Date:  1983-12       Impact factor: 4.307

10.  An "acquired" hemoglobin J variant in a sickle cell disease patient.

Authors:  Nawwar Swedan; Kathleen Nicol; Phylis Moder; Samir Kahwash
Journal:  Ther Clin Risk Manag       Date:  2008-06       Impact factor: 2.423

  10 in total

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