Literature DB >> 13949483

Familial hypohaptoglobinemia. A genetically determined trait segragating from glucose-6-phosphate dehydrogenase deficiency.

A GOTTLIEB, N WISCH, J ROSS.   

Abstract

Entities:  

Keywords:  BLOOD PROTEIN DISORDERS; GLUCOSEPHOSPHATE DEHYDROGENASE; HAPTOGLOBINS

Mesh：

Substances：

Year:  1963        PMID： 13949483

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


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  4 in total

1.  THE FORMATION OF DUMPY VORTICES IN MOSAICS OF DROSOPHILA MELANOGASTER.

Authors:  J L KING
Journal:  Genetics       Date:  1964-03       Impact factor: 4.562

2.  Quantitative variations of haptoglobins in Caucasian family.

Authors:  G I Higashi; H A Lubs
Journal:  J Med Genet       Date:  1966-12       Impact factor: 6.318

3.  Low plasma haptoglobin in march haemoglobinuria.

Authors:  R B Payne
Journal:  J Clin Pathol       Date:  1966-03       Impact factor: 3.411

4.  Increase in GLUT1 in smooth muscle alters vascular contractility and increases inflammation in response to vascular injury.

Authors:  Neeta Adhikari; David L Basi; Marjorie Carlson; Ami Mariash; Zhigang Hong; Ute Lehman; Sureni Mullegama; Edward K Weir; Jennifer L Hall
Journal:  Arterioscler Thromb Vasc Biol       Date:  2010-10-14       Impact factor: 8.311
  4 in total

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