Franco B - Search Results

1

IL1RAPL2 maps to Xq22 and is specifically expressed in the central nervous system.

Ferrante MI, Ghiani M, Bulfone A, Franco B. Ferrante MI, et al. Among authors: franco b. Gene. 2001 Sep 19;275(2):217-21. doi: 10.1016/s0378-1119(01)00659-x. Gene. 2001. PMID: 11587848

2

A novel human serine-threonine phosphatase related to the Drosophila retinal degeneration C (rdgC) gene is selectively expressed in sensory neurons of neural crest origin.

Montini E, Rugarli EI, Van de Vosse E, Andolfi G, Mariani M, Puca AA, Consalez GG, den Dunnen JT, Ballabio A, Franco B. Montini E, et al. Among authors: franco b. Hum Mol Genet. 1997 Jul;6(7):1137-45. doi: 10.1093/hmg/6.7.1137. Hum Mol Genet. 1997. PMID: 9215685

3

Identification and characterization of CDS2, a mammalian homolog of the Drosophila CDP-diacylglycerol synthase gene.

Volta M, Bulfone A, Gattuso C, Rossi E, Mariani M, Consalez GG, Zuffardi O, Ballabio A, Banfi S, Franco B. Volta M, et al. Among authors: franco b. Genomics. 1999 Jan 1;55(1):68-77. doi: 10.1006/geno.1998.5610. Genomics. 1999. PMID: 9889000

4

Identification of SCML2, a second human gene homologous to the Drosophila sex comb on midleg (Scm): A new gene cluster on Xp22.

Montini E, Buchner G, Spalluto C, Andolfi G, Caruso A, den Dunnen JT, Trump D, Rocchi M, Ballabio A, Franco B. Montini E, et al. Among authors: franco b. Genomics. 1999 May 15;58(1):65-72. doi: 10.1006/geno.1999.5755. Genomics. 1999. PMID: 10331946

5

Identification and characterization of AFG3L2, a novel paraplegin-related gene.

Banfi S, Bassi MT, Andolfi G, Marchitiello A, Zanotta S, Ballabio A, Casari G, Franco B. Banfi S, et al. Among authors: franco b. Genomics. 1999 Jul 1;59(1):51-8. doi: 10.1006/geno.1999.5818. Genomics. 1999. PMID: 10395799

6

MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development.

Buchner G, Montini E, Andolfi G, Quaderi N, Cainarca S, Messali S, Bassi MT, Ballabio A, Meroni G, Franco B. Buchner G, et al. Among authors: franco b. Hum Mol Genet. 1999 Aug;8(8):1397-407. doi: 10.1093/hmg/8.8.1397. Hum Mol Genet. 1999. PMID: 10400986

7

Identification of a new EGF-repeat-containing gene from human Xp22: a candidate for developmental disorders.

Buchner G, Orfanelli U, Quaderi N, Bassi MT, Andolfi G, Ballabio A, Franco B. Buchner G, et al. Among authors: franco b. Genomics. 2000 Apr 1;65(1):16-23. doi: 10.1006/geno.2000.6146. Genomics. 2000. PMID: 10777661

8

MAEG, an EGF-repeat containing gene, is a new marker associated with dermatome specification and morphogenesis of its derivatives.

Buchner G, Broccoli V, Bulfone A, Orfanelli U, Gattuso C, Ballabio A, Franco B. Buchner G, et al. Among authors: franco b. Mech Dev. 2000 Nov;98(1-2):179-82. doi: 10.1016/s0925-4773(00)00462-7. Mech Dev. 2000. PMID: 11044626 Free article.

9

Identification of the gene for oral-facial-digital type I syndrome.

Ferrante MI, Giorgio G, Feather SA, Bulfone A, Wright V, Ghiani M, Selicorni A, Gammaro L, Scolari F, Woolf AS, Sylvie O, Bernard L, Malcolm S, Winter R, Ballabio A, Franco B. Ferrante MI, et al. Among authors: franco b. Am J Hum Genet. 2001 Mar;68(3):569-76. doi: 10.1086/318802. Epub 2001 Feb 13. Am J Hum Genet. 2001. PMID: 11179005 Free PMC article.

10

Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes.

Toutain A, Dessay B, Ronce N, Ferrante MI, Tranchemontagne J, Newbury-Ecob R, Wallgren-Pettersson C, Burn J, Kaplan J, Rossi A, Russo S, Walpole I, Hartsfield JK, Oyen N, Nemeth A, Bitoun P, Trump D, Moraine C, Franco B. Toutain A, et al. Among authors: franco b. Eur J Hum Genet. 2002 Sep;10(9):516-20. doi: 10.1038/sj.ejhg.5200846. Eur J Hum Genet. 2002. PMID: 12173028

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