Berkovitz G - Search Results

1

Structural and functional characterization of the mouse tescalcin promoter.

Perera EM, Bao Y, Kos L, Berkovitz G. Perera EM, et al. Among authors: berkovitz g. 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: berkovitz gd. 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: berkovitz gd. 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. Among authors: berkovitz gd. 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. 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. 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: berkovitz gd. 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. Among authors: berkovitz gd. 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

Early recognition of gonadal dysgenesis in congenital nephrotic syndrome .

Ukarapong S, Berkovitz G, McElreavey K, Bashamboo A, Bao Y. Ukarapong S, et al. Among authors: berkovitz g. Clin Nephrol. 2016 Dec;86 (2016)(12):341-344. doi: 10.5414/CN108925. Clin Nephrol. 2016. PMID: 27719739

10

Genetic mechanisms that regulate testis determination.

Carrillo AA, Berkovitz GD. Carrillo AA, et al. Rev Endocr Metab Disord. 2004 Mar;5(1):77-82. doi: 10.1023/B:REMD.0000016126.57801.c0. Rev Endocr Metab Disord. 2004. PMID: 14966391 Review. No abstract available.

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