Literature DB >> 14449719

On the recombination of canine and human haemoglobins.

E R HUEHNS, E M SHOOTER, G H BEAVEN.   

Abstract

Entities:  

Keywords:  DOGS/blood; HEMOGLOBIN/chemistry

Mesh:

Substances:

Year:  1962        PMID: 14449719     DOI: 10.1016/s0022-2836(62)80012-6

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


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  25 in total

1.  Haemoglobin Hasharon in a north Italian community.

Authors:  R Alberti; G M Mariuzzi; M Marinucci; E Bruni; L Tenteri
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

2.  A Swiss family with hemoglobin P Galveston beta117His leads to Arg, including two patients with hb P/beta thalassemia.

Authors:  E E Di Iorio; K H Winterhalter; K Wilson; A Rosenmund; H R Marti
Journal:  Blut       Date:  1975-08

3.  HEREDITARY HEINZ-BODY ANAEMIA, THROMBOCYTOPENIA, AND HAEMOGLOBINOPATHY (HB KOELN) IN A GLASGOW FAMILY.

Authors:  H E HUTCHISON; P H PINKERTON; P WATERS; H LEHMANN; D BEALE; A S DOUGLAS
Journal:  Br Med J       Date:  1964-10-31

4.  DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.

Authors:  E R HUEHNS; F HECHT; J V KEIL; A G MOTULSKY
Journal:  Proc Natl Acad Sci U S A       Date:  1964-01       Impact factor: 11.205

5.  HOMOZYGOUS SICKLE-CELL ANAEMIA ARISING FROM TWO DIFFERENT HAEMOGLOBINS S. INTERACTION OF HAEMOGLOBINS S AND STANLEYVILLE-II.

Authors:  M HALL-CRAGGS; P D MARSDEN; A B RAPER; H LEHMANN; D BEALE
Journal:  Br Med J       Date:  1964-07-11

6.  A NEW HAEMOGLOBIN IN A THAI FAMILY. A CASE OF HAEMOGLOBIN SIRIRAJ-BETA THALASSAEMIA.

Authors:  S TUCHINDA; D BEALE; H LEHMANN
Journal:  Br Med J       Date:  1965-06-19

Review 7.  HUMAN HAEMOGLOBINS.

Authors:  E R HUEHNS; E M SHOOTER
Journal:  J Med Genet       Date:  1965-03       Impact factor: 6.318

8.  The abnormal haemoglobins in haemoglobin-H disease.

Authors:  N DANCE; E R HUEHNS; G H BEAVEN
Journal:  Biochem J       Date:  1963-05       Impact factor: 3.857

9.  The properties and reactions of haemoglobin F(1) and their bearing on the dissociation equilibrium of haemoglobin.

Authors:  E R Huehns
Journal:  Biochem J       Date:  1966-12       Impact factor: 3.857

10.  Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndrome.

Authors:  R M Goodman; M B Katznelson; M Hertz; A Katznelson
Journal:  J Med Genet       Date:  1976-04       Impact factor: 6.318

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