Forabosco A - Search Results

1

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome.

Pilia G, Hughes-Benzie RM, MacKenzie A, Baybayan P, Chen EY, Huber R, Neri G, Cao A, Forabosco A, Schlessinger D. Pilia G, et al. Among authors: forabosco a. Nat Genet. 1996 Mar;12(3):241-7. doi: 10.1038/ng0396-241. Nat Genet. 1996. PMID: 8589713

2

Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmel syndrome.

Pellegrini M, Pilia G, Pantano S, Lucchini F, Uda M, Fumi M, Cao A, Schlessinger D, Forabosco A. Pellegrini M, et al. Among authors: forabosco a. Dev Dyn. 1998 Dec;213(4):431-9. doi: 10.1002/(SICI)1097-0177(199812)213:4<431::AID-AJA8>3.0.CO;2-7. Dev Dyn. 1998. PMID: 9853964 Free article.

3

Genes and translocations involved in POF.

Schlessinger D, Herrera L, Crisponi L, Mumm S, Percesepe A, Pellegrini M, Pilia G, Forabosco A. Schlessinger D, et al. Among authors: forabosco a. Am J Med Genet. 2002 Aug 15;111(3):328-33. doi: 10.1002/ajmg.10565. Am J Med Genet. 2002. PMID: 12210333 Review.

4

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development.

Uda M, Ottolenghi C, Crisponi L, Garcia JE, Deiana M, Kimber W, Forabosco A, Cao A, Schlessinger D, Pilia G. Uda M, et al. Among authors: forabosco a. Hum Mol Genet. 2004 Jun 1;13(11):1171-81. doi: 10.1093/hmg/ddh124. Epub 2004 Mar 31. Hum Mol Genet. 2004. PMID: 15056605

5

PLAC1, an Xq26 gene with placenta-specific expression.

Cocchia M, Huber R, Pantano S, Chen EY, Ma P, Forabosco A, Ko MS, Schlessinger D. Cocchia M, et al. Among authors: forabosco a. Genomics. 2000 Sep 15;68(3):305-12. doi: 10.1006/geno.2000.6302. Genomics. 2000. PMID: 10995572

6

X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes.

Mumm S, Herrera L, Waeltz PW, Scardovi A, Nagaraja R, Esposito T, Schlessinger D, Rocchi M, Forabosco A. Mumm S, et al. Among authors: forabosco a. Genomics. 2001 Aug;76(1-3):30-6. doi: 10.1006/geno.2001.6611. Genomics. 2001. PMID: 11560122

7

Foxl2 is required for commitment to ovary differentiation.

Ottolenghi C, Omari S, Garcia-Ortiz JE, Uda M, Crisponi L, Forabosco A, Pilia G, Schlessinger D. Ottolenghi C, et al. Among authors: forabosco a. Hum Mol Genet. 2005 Jul 15;14(14):2053-62. doi: 10.1093/hmg/ddi210. Epub 2005 Jun 8. Hum Mol Genet. 2005. PMID: 15944199

8

Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cells.

Ottolenghi C, Pelosi E, Tran J, Colombino M, Douglass E, Nedorezov T, Cao A, Forabosco A, Schlessinger D. Ottolenghi C, et al. Among authors: forabosco a. Hum Mol Genet. 2007 Dec 1;16(23):2795-804. doi: 10.1093/hmg/ddm235. Epub 2007 Aug 29. Hum Mol Genet. 2007. PMID: 17728319

9

Determination and stability of sex.

Ottolenghi C, Uda M, Crisponi L, Omari S, Cao A, Forabosco A, Schlessinger D. Ottolenghi C, et al. Among authors: forabosco a. Bioessays. 2007 Jan;29(1):15-25. doi: 10.1002/bies.20515. Bioessays. 2007. PMID: 17187356 Review.

10

Transcriptional control of ovarian development in somatic cells.

Ottolenghi C, Colombino M, Crisponi L, Cao A, Forabosco A, Schlessinger D, Uda M. Ottolenghi C, et al. Among authors: forabosco a. Semin Reprod Med. 2007 Jul;25(4):252-63. doi: 10.1055/s-2007-980219. Semin Reprod Med. 2007. PMID: 17594606 Review.

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