Red blood cell membrane - Is it a mirror for systemic non-hematological genetic disorders?

Indian Journal of Human Genetics

Volumn 10, Issue 2, 2004, Pages 39-40

  Mohanty, Dipika ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN; ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ADENOSINE TRIPHOSPHATE; CYTOSKELETON PROTEIN; GLUCOSE TRANSPORTER; MEMBRANE PROTEIN;

ANION EXCHANGE; BINDING SITE; CELL STRUCTURE; CONFORMATIONAL TRANSITION; EDITORIAL; ENVIRONMENTAL FACTOR; ENZYME SUBUNIT; ERYTHROCYTE; ERYTHROCYTE MEMBRANE; ESSENTIAL HYPERTENSION; GENETIC DISORDER; GENETIC SUSCEPTIBILITY; HEMATOLOGY; HUMAN; MOLECULAR GENETICS; MOLECULAR WEIGHT; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION;

EID: 12344300819     PISSN: 09716866     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Editorial

References (4)

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2. + binding and phospholipid composition in erythrocyte membranes of white hypertensive and normasive indivisuals. Hypertencion 1996;27;456-64.
3. Duhm J. Pathways of lithium transport across the human erythrocyte membrane. In: Thelier M, Wisldocq J-C, editors Lithium Kinetics. Carnforth, uk: Marius press 1992, 27-53.
4. Sharma P, Fatibenne J, Ferraro FJ, Monteith S, Brown, et al. A genome-wide search for suspectibility loci to hypertension 2000:35:1291-6.