GGP09126/TI_/Telethon/Italy[Grants and Funding] - Search Results

Year	Number of Results
2010	1
2011	2
2012	1
2013	3
2014	3
2024	0

1

Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome.

Castronovo C, Rossetti R, Rusconi D, Recalcati MP, Cacciatore C, Beccaria E, Calcaterra V, Invernizzi P, Larizza D, Finelli P, Persani L. Castronovo C, et al. Hum Reprod. 2014 Feb;29(2):368-79. doi: 10.1093/humrep/det436. Epub 2013 Dec 8. Hum Reprod. 2014. PMID: 24324027 Free PMC article.

2

A clinical research integration special program (CRISP) for young women with primary ovarian insufficiency.

Falorni A, Minarelli V, Eads CM, Joachim CM, Persani L, Rossetti R, Yurttas Beim P, Pellegrini VA, Schnatz PF, Rafique S, Kissell K, Calis KA, Popat V, Nelson LM. Falorni A, et al. Panminerva Med. 2014;56(4):245-61. Epub 2014 Oct 7. Panminerva Med. 2014. PMID: 25288327 Free PMC article. Review.

3

The fundamental role of bone morphogenetic protein 15 in ovarian function and its involvement in female fertility disorders.

Persani L, Rossetti R, Di Pasquale E, Cacciatore C, Fabre S. Persani L, et al. Hum Reprod Update. 2014 Nov-Dec;20(6):869-83. doi: 10.1093/humupd/dmu036. Epub 2014 Jun 30. Hum Reprod Update. 2014. PMID: 24980253 Review.

4

Genes involved in human premature ovarian failure.

Persani L, Rossetti R, Cacciatore C. Persani L, et al. J Mol Endocrinol. 2010 Nov;45(5):257-79. doi: 10.1677/JME-10-0070. Epub 2010 Jul 28. J Mol Endocrinol. 2010. PMID: 20668067 Review.

5

Genetic defects of ovarian TGF-β-like factors and premature ovarian failure.

Persani L, Rossetti R, Cacciatore C, Fabre S. Persani L, et al. J Endocrinol Invest. 2011 Mar;34(3):244-51. doi: 10.1007/BF03347073. Epub 2011 Feb 4. J Endocrinol Invest. 2011. PMID: 21297384 Review.

6

Blood cell mitochondrial DNA content and premature ovarian aging.

Bonomi M, Somigliana E, Cacciatore C, Busnelli M, Rossetti R, Bonetti S, Paffoni A, Mari D, Ragni G, Persani L; Italian Network for the study of Ovarian Dysfunctions. Bonomi M, et al. PLoS One. 2012;7(8):e42423. doi: 10.1371/journal.pone.0042423. Epub 2012 Aug 3. PLoS One. 2012. PMID: 22879975 Free PMC article.

7

Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheep.

Demars J, Fabre S, Sarry J, Rossetti R, Gilbert H, Persani L, Tosser-Klopp G, Mulsant P, Nowak Z, Drobik W, Martyniuk E, Bodin L. Demars J, et al. PLoS Genet. 2013 Apr;9(4):e1003482. doi: 10.1371/journal.pgen.1003482. Epub 2013 Apr 25. PLoS Genet. 2013. PMID: 23637641 Free PMC article.

8

Cytogenetics of premature ovarian failure: an investigation on 269 affected women.

Baronchelli S, Conconi D, Panzeri E, Bentivegna A, Redaelli S, Lissoni S, Saccheri F, Villa N, Crosti F, Sala E, Martinoli E, Volontè M, Marozzi A, Dalprà L. Baronchelli S, et al. J Biomed Biotechnol. 2011;2011:370195. doi: 10.1155/2011/370195. Epub 2011 Jan 17. J Biomed Biotechnol. 2011. PMID: 21318170 Free PMC article.

9

Positive selection in bone morphogenetic protein 15 targets a natural mutation associated with primary ovarian insufficiency in human.

Auclair S, Rossetti R, Meslin C, Monestier O, Di Pasquale E, Pascal G, Persani L, Fabre S. Auclair S, et al. PLoS One. 2013 Oct 16;8(10):e78199. doi: 10.1371/journal.pone.0078199. eCollection 2013. PLoS One. 2013. PMID: 24147118 Free PMC article.

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