Mohandas N - Search Results

1

Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia.

Da Costa L, Mohandas N, Sorette M, Grange MJ, Tchernia G, Cynober T. Da Costa L, et al. Among authors: mohandas n. Blood. 2001 Nov 15;98(10):2894-9. doi: 10.1182/blood.v98.10.2894. Blood. 2001. PMID: 11698268 Free article.

2

Human reticulocyte maturation and its relevance to erythropoietic stress.

Coulombel L, Tchernia G, Mohandas N. Coulombel L, et al. Among authors: mohandas n. J Lab Clin Med. 1979 Sep;94(3):467-74. J Lab Clin Med. 1979. PMID: 572850

3

Hereditary elliptocytosis due to both qualitative and quantitative defects in membrane skeletal protein 4.1.

Conboy JG, Shitamoto R, Parra M, Winardi R, Kabra A, Smith J, Mohandas N. Conboy JG, et al. Among authors: mohandas n. Blood. 1991 Nov 1;78(9):2438-43. Blood. 1991. PMID: 1932756 Free article.

4

Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis.

Warkentin TE, Barr RD, Ali MA, Mohandas N. Warkentin TE, et al. Among authors: mohandas n. Blood. 1990 Jan 1;75(1):266-70. Blood. 1990. PMID: 2294990 Free article.

5

Glycophorin C content of human erythrocyte membrane is regulated by protein 4.1.

Reid ME, Takakuwa Y, Conboy J, Tchernia G, Mohandas N. Reid ME, et al. Among authors: mohandas n. Blood. 1990 Jun 1;75(11):2229-34. Blood. 1990. PMID: 2346783 Free article.

6

Functional role for glycophorin C and its interaction with the human red cell membrane skeletal component, protein 4.1.

Reid ME, Takakuwa Y, Tchernia G, Jensen RH, Chasis JA, Mohandas N. Reid ME, et al. Among authors: mohandas n. Prog Clin Biol Res. 1989;319:553-71; discussion 572-3. Prog Clin Biol Res. 1989. PMID: 2622928 No abstract available.

7

Membrane assembly and remodeling during reticulocyte maturation.

Chasis JA, Prenant M, Leung A, Mohandas N. Chasis JA, et al. Among authors: mohandas n. Blood. 1989 Aug 15;74(3):1112-20. Blood. 1989. PMID: 2752157 Free article.

8

Hereditary poikilocytic anemia associated with the co-inheritance of two alpha spectrin abnormalities.

Iarocci TA, Wagner GM, Mohandas N, Lane PA, Mentzer WC. Iarocci TA, et al. Among authors: mohandas n. Blood. 1988 May;71(5):1390-6. Blood. 1988. PMID: 3359047 Free article.

9

Restoration of normal membrane stability to unstable protein 4.1-deficient erythrocyte membranes by incorporation of purified protein 4.1.

Takakuwa Y, Tchernia G, Rossi M, Benabadji M, Mohandas N. Takakuwa Y, et al. Among authors: mohandas n. J Clin Invest. 1986 Jul;78(1):80-5. doi: 10.1172/JCI112577. J Clin Invest. 1986. PMID: 3722387 Free PMC article.

10

Molecular basis of hereditary elliptocytosis due to protein 4.1 deficiency.

Conboy J, Mohandas N, Tchernia G, Kan YW. Conboy J, et al. Among authors: mohandas n. N Engl J Med. 1986 Sep 11;315(11):680-5. doi: 10.1056/NEJM198609113151105. N Engl J Med. 1986. PMID: 3755799

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