Bassères DS - Search Results

1

Human leukocyte formin: a novel protein expressed in lymphoid malignancies and associated with Akt.

Favaro PM, de Souza Medina S, Traina F, Bassères DS, Costa FF, Saad ST. Favaro PM, et al. Among authors: basseres ds. Biochem Biophys Res Commun. 2003 Nov 14;311(2):365-71. doi: 10.1016/j.bbrc.2003.10.012. Biochem Biophys Res Commun. 2003. PMID: 14592423

2

ARHGAP10, a novel human gene coding for a potentially cytoskeletal Rho-GTPase activating protein.

Bassères DS, Tizzei EV, Duarte AA, Costa FF, Saad ST. Bassères DS, et al. Biochem Biophys Res Commun. 2002 Jun 14;294(3):579-85. doi: 10.1016/S0006-291X(02)00514-4. Biochem Biophys Res Commun. 2002. PMID: 12056806

3

Characterisation of a new splice variant of MASK-BP3(ARF) and MASK human genes, and their expression patterns during haematopoietic cell differentiation.

Santos Duarte Ada S, Traina F, Favaro PM, Bassères DS, de Carvalho IC, Medina Sde S, Costa FF, Saad ST. Santos Duarte Ada S, et al. Among authors: basseres ds. Gene. 2005 Dec 19;363:113-22. doi: 10.1016/j.gene.2005.08.002. Epub 2005 Nov 16. Gene. 2005. PMID: 16297570

4

Beta-spectrin Campinas: a novel shortened beta-chain variant associated with skipping of exon 30 and hereditary elliptocytosis.

Basserès DS, Pranke PH, Sales TS, Costa FF, Saad ST. Basserès DS, et al. Br J Haematol. 1997 Jun;97(3):579-85. doi: 10.1046/j.1365-2141.1997.932906.x. Br J Haematol. 1997. PMID: 9207403 Free article.

5

Expression of spectrin alpha I/65 hereditary elliptocytosis in patients from Brazil.

Pranke PH, Basseres DS, Costa FF, Saad ST. Pranke PH, et al. Among authors: basseres ds. Br J Haematol. 1996 Sep;94(3):470-5. Br J Haematol. 1996. PMID: 8790144

6

Presence of allele alphaLELY in an Amazonian Indian population.

Bassères DS, Salles TS, Costa FF, Saad ST. Bassères DS, et al. Am J Hematol. 1998 Mar;57(3):212-4. doi: 10.1002/(sici)1096-8652(199803)57:3<212::aid-ajh5>3.0.co;2-y. Am J Hematol. 1998. PMID: 9495371 Free article.

7

beta-Spectrin S(ta) Bárbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicism.

Bassères DS, Duarte AS, Hassoun H, Costa FF, Saad ST. Bassères DS, et al. Br J Haematol. 2001 Nov;115(2):347-53. doi: 10.1046/j.1365-2141.2001.03103.x. Br J Haematol. 2001. PMID: 11703334 Free article.

8

Expression of spectrin alphaI/50 hereditary elliptocytosis and its association with the alphaLELY allele.

Bassères DS, Pranke PH, Vicentim D, Costa FF, Saad ST. Bassères DS, et al. Acta Haematol. 1998;100(1):32-8. doi: 10.1159/000040860. Acta Haematol. 1998. PMID: 9691144

9

Association of the alpha-spectrin R28H mutation with allele alphaLELY and with alphaI/alphaII domain haplotypes in three Brazilian families.

Bassères DS, Bordin S, Costa FF, Saad ST. Bassères DS, et al. Eur J Haematol. 2000 Jan;64(1):53-8. doi: 10.1034/j.1600-0609.2000.80217.x. Eur J Haematol. 2000. PMID: 10680706

10

beta-Spectrin São PauloII, a novel frameshift mutation of the beta-spectrin gene associated with hereditary spherocytosis and instability of the mutant mRNA.

Bassères DS, Tavares AC, Costa FF, Saad ST. Bassères DS, et al. Braz J Med Biol Res. 2002 Aug;35(8):921-5. doi: 10.1590/s0100-879x2002000800009. Braz J Med Biol Res. 2002. PMID: 12185384 Free article.

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