Perera EM - Search Results

1

Structural and functional characterization of the mouse tescalcin promoter.

Perera EM, Bao Y, Kos L, Berkovitz G. Perera EM, et al. Gene. 2010 Sep 15;464(1-2):50-62. doi: 10.1016/j.gene.2010.06.002. Epub 2010 Jun 9. Gene. 2010. PMID: 20540995

2

Expression and evolutionary conservation of the tescalcin gene during development.

Bao Y, Hudson QJ, Perera EM, Akan L, Tobet SA, Smith CA, Sinclair AH, Berkovitz GD. Bao Y, et al. Among authors: perera em. Gene Expr Patterns. 2009 Jun;9(5):273-81. doi: 10.1016/j.gep.2009.03.004. Epub 2009 Apr 2. Gene Expr Patterns. 2009. PMID: 19345287

3

Megakaryocyte development is normal in mice with targeted disruption of Tescalcin.

Ukarapong S, Bao Y, Perera EM, Berkovitz GD. Ukarapong S, et al. Among authors: perera em. Exp Cell Res. 2012 Mar 10;318(5):662-9. doi: 10.1016/j.yexcr.2012.01.009. Epub 2012 Jan 18. Exp Cell Res. 2012. PMID: 22285131

4

Tescalcin, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, Col9a3, and renin are expressed in the mouse testis during the early stages of gonadal differentiation.

Perera EM, Martin H, Seeherunvong T, Kos L, Hughes IA, Hawkins JR, Berkovitz GD. Perera EM, et al. Endocrinology. 2001 Jan;142(1):455-63. doi: 10.1210/endo.142.1.7882. Endocrinology. 2001. PMID: 11145610

5

Characterization of tescalcin, a novel EF-hand protein with a single Ca2+-binding site: metal-binding properties, localization in tissues and cells, and effect on calcineurin.

Gutierrez-Ford C, Levay K, Gomes AV, Perera EM, Som T, Kim YM, Benovic JL, Berkovitz GD, Slepak VZ. Gutierrez-Ford C, et al. Among authors: perera em. Biochemistry. 2003 Dec 16;42(49):14553-65. doi: 10.1021/bi034870f. Biochemistry. 2003. PMID: 14661968

6

46,XX sex reversal with partial duplication of chromosome arm 22q.

Seeherunvong T, Perera EM, Bao Y, Benke PJ, Benigno A, Donahue RP, Berkovitz GD. Seeherunvong T, et al. Among authors: perera em. Am J Med Genet A. 2004 Jun 1;127A(2):149-51. doi: 10.1002/ajmg.a.20630. Am J Med Genet A. 2004. PMID: 15108202

7

Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD.

Seeherunvong T, Ukarapong S, McElreavey K, Berkovitz GD, Perera EM. Seeherunvong T, et al. Among authors: perera em. J Pediatr Endocrinol Metab. 2012;25(1-2):121-3. doi: 10.1515/jpem.2011.370. J Pediatr Endocrinol Metab. 2012. PMID: 22570960

8

Madelung-like deformity in pseudohypoparathyroidism type 1b.

Sanchez J, Perera E, Jan de Beur S, Ding C, Dang A, Berkovitz GD, Levine MA. Sanchez J, et al. J Clin Endocrinol Metab. 2011 Sep;96(9):E1507-11. doi: 10.1210/jc.2011-1411. Epub 2011 Jul 13. J Clin Endocrinol Metab. 2011. PMID: 21752878 Free PMC article.

9

The transcription factors Ets1 and Sox10 interact during murine melanocyte development.

Saldana-Caboverde A, Perera EM, Watkins-Chow DE, Hansen NF, Vemulapalli M, Mullikin JC; NISC Comparative Sequencing Program; Pavan WJ, Kos L. Saldana-Caboverde A, et al. Among authors: perera em. Dev Biol. 2015 Nov 15;407(2):300-12. doi: 10.1016/j.ydbio.2015.04.012. Epub 2015 Apr 23. Dev Biol. 2015. PMID: 25912689 Free PMC article.

10

Clinical, biochemical, and molecular investigations of a genetic isolate of growth hormone insensitivity (Laron's syndrome).

Baumbach L, Schiavi A, Bartlett R, Perera E, Day J, Brown MR, Stein S, Eidson M, Parks JS, Cleveland W. Baumbach L, et al. J Clin Endocrinol Metab. 1997 Feb;82(2):444-51. doi: 10.1210/jcem.82.2.3784. J Clin Endocrinol Metab. 1997. PMID: 9024234

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