Gianfrancesco F - Search Results

1

The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone.

Scotto di Carlo F, Pazzaglia L, Esposito T, Gianfrancesco F. Scotto di Carlo F, et al. Among authors: gianfrancesco f. J Bone Miner Res. 2020 Aug;35(8):1387-1398. doi: 10.1002/jbmr.3964. Epub 2020 Feb 19. J Bone Miner Res. 2020. PMID: 31991009 Free article.

2

A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation.

D'Esposito M, Ciccodicola A, Gianfrancesco F, Esposito T, Flagiello L, Mazzarella R, Schlessinger D, D'Urso M. D'Esposito M, et al. Among authors: gianfrancesco f. Nat Genet. 1996 Jun;13(2):227-9. doi: 10.1038/ng0696-227. Nat Genet. 1996. PMID: 8640232

3

Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome.

Gianfrancesco F, Esposito T, Ruini L, Houlgatte R, Nagaraja R, D'Esposito M, Rocchi M, Auffray C, Schlessinger D, D'Urso M, Forabosco A. Gianfrancesco F, et al. Gene. 1997 Mar 18;187(2):179-84. doi: 10.1016/s0378-1119(96)00743-3. Gene. 1997. PMID: 9099878

4

Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene.

Gianfrancesco F, Esposito T, Ciccodicola A, D'Esposito M, Mazzarella R, D'Urso M, Forabosco A. Gianfrancesco F, et al. Cytogenet Cell Genet. 1999;84(3-4):164-6. doi: 10.1159/000015247. Cytogenet Cell Genet. 1999. PMID: 10393420 No abstract available.

5

Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region.

Ciccodicola A, D'Esposito M, Esposito T, Gianfrancesco F, Migliaccio C, Miano MG, Matarazzo MR, Vacca M, Franzè A, Cuccurese M, Cocchia M, Curci A, Terracciano A, Torino A, Cocchia S, Mercadante G, Pannone E, Archidiacono N, Rocchi M, Schlessinger D, D'Urso M. Ciccodicola A, et al. Among authors: gianfrancesco f. Hum Mol Genet. 2000 Feb 12;9(3):395-401. doi: 10.1093/hmg/9.3.395. Hum Mol Genet. 2000. PMID: 10655549

6

Characterization of the murine orthologue of a novel human subtelomeric multigene family.

Gianfrancesco F, Falco G, Esposito T, Rocchi M, D'Urso M. Gianfrancesco F, et al. Cytogenet Cell Genet. 2001;94(1-2):98-100. doi: 10.1159/000048796. Cytogenet Cell Genet. 2001. PMID: 11701968 No abstract available.

7

Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution.

Gianfrancesco F, Sanges R, Esposito T, Tempesta S, Rao E, Rappold G, Archidiacono N, Graves JA, Forabosco A, D'Urso M. Gianfrancesco F, et al. Genome Res. 2001 Dec;11(12):2095-100. doi: 10.1101/gr.197001. Genome Res. 2001. PMID: 11731500 Free PMC article.

8

Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate.

Gianfrancesco F, Esposito T, Ombra MN, Forabosco P, Maninchedda G, Fattorini M, Casula S, Vaccargiu S, Casu G, Cardia F, Deiana I, Melis P, Falchi M, Pirastu M. Gianfrancesco F, et al. Am J Hum Genet. 2003 Jun;72(6):1479-91. doi: 10.1086/375628. Epub 2003 May 9. Am J Hum Genet. 2003. PMID: 12740763 Free PMC article.

9

Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage.

Gianfrancesco F, Esposito T, Casu G, Maninchedda G, Roberto R, Pirastu M. Gianfrancesco F, et al. Gene. 2004 Sep 15;339:131-8. doi: 10.1016/j.gene.2004.06.030. Gene. 2004. PMID: 15363853

10

[Multifactorial disorder: molecular and evolutionary insights of uric acid nephrolithiasis].

Gianfrancesco F, Esposito T. Gianfrancesco F, et al. Minerva Med. 2005 Dec;96(6):409-16. Minerva Med. 2005. PMID: 16518303 Review. Italian.

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