Mohandas N - Search Results

1

Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis.

Wandersee NJ, Roesch AN, Hamblen NR, de Moes J, van der Valk MA, Bronson RT, Gimm JA, Mohandas N, Demant P, Barker JE. Wandersee NJ, et al. Among authors: mohandas n. Blood. 2001 Jan 15;97(2):543-50. doi: 10.1182/blood.v97.2.543. Blood. 2001. PMID: 11154235 Free article.

2

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.

3

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.

4

Evaluation of biochemical changes during in vivo erythrocyte senescence in the dog.

Rettig MP, Low PS, Gimm JA, Mohandas N, Wang J, Christian JA. Rettig MP, et al. Among authors: mohandas n. Blood. 1999 Jan 1;93(1):376-84. Blood. 1999. PMID: 9864184 Free article.

5

Natural history of hereditary spherocytosis during the first year of life.

Delhommeau F, Cynober T, Schischmanoff PO, Rohrlich P, Delaunay J, Mohandas N, Tchernia G. Delhommeau F, et al. Among authors: mohandas n. Blood. 2000 Jan 15;95(2):393-7. Blood. 2000. PMID: 10627440 Free article.

6

Lutheran blood group glycoprotein and its newly characterized mouse homologue specifically bind alpha5 chain-containing human laminin with high affinity.

Parsons SF, Lee G, Spring FA, Willig TN, Peters LL, Gimm JA, Tanner MJ, Mohandas N, Anstee DJ, Chasis JA. Parsons SF, et al. Among authors: mohandas n. Blood. 2001 Jan 1;97(1):312-20. doi: 10.1182/blood.v97.1.312. Blood. 2001. PMID: 11133776 Free article.

7

Murine recessive hereditary spherocytosis, sph/sph, is caused by a mutation in the erythroid alpha-spectrin gene.

Wandersee NJ, Birkenmeier CS, Gifford EJ, Mohandas N, Barker JE. Wandersee NJ, et al. Among authors: mohandas n. Hematol J. 2000;1(4):235-42. doi: 10.1038/sj.thj.6200030. Hematol J. 2000. PMID: 11920196

8

Functional characterization of spectrin-actin-binding domains in 4.1 family of proteins.

Gimm JA, An X, Nunomura W, Mohandas N. Gimm JA, et al. Among authors: mohandas n. Biochemistry. 2002 Jun 11;41(23):7275-82. doi: 10.1021/bi0256330. Biochemistry. 2002. PMID: 12044158

9

Mutations in the murine erythroid alpha-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton.

Wandersee NJ, Birkenmeier CS, Bodine DM, Mohandas N, Barker JE. Wandersee NJ, et al. Among authors: mohandas n. Blood. 2003 Jan 1;101(1):325-30. doi: 10.1182/blood-2002-01-0113. Epub 2002 Aug 8. Blood. 2003. PMID: 12393645 Free article.

10

Mechanism of protein sorting during erythroblast enucleation: role of cytoskeletal connectivity.

Lee JC, Gimm JA, Lo AJ, Koury MJ, Krauss SW, Mohandas N, Chasis JA. Lee JC, et al. Among authors: mohandas n. Blood. 2004 Mar 1;103(5):1912-9. doi: 10.1182/blood-2003-03-0928. Epub 2003 Oct 16. Blood. 2004. PMID: 14563645 Free article.

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