17 results for author:"Camerino G." in Literature citations
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| Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination. Pearlman A., Loke J., Le Caignec C., White S., Chin L., Friedman A., Warr N., Willan J., Brauer D., Farmer C. et al. Am. J. Hum. Genet. 87:898-904(2010) · UniProtKB (1) · Mapped (3) |
| Statins and fenofibrate affect skeletal muscle chloride conductance in rats by differently impairing ClC-1 channel regulation and expression. Pierno S., Camerino G.M., Cippone V., Rolland J.F., Desaphy J.F., De Luca A., Liantonio A., Bianco G., Kunic J.D., George A.L. Jr. et al. Br. J. Pharmacol. 156:1206-1215(2009) · Mapped (2) |
| Activation of beta-catenin signaling by Rspo1 controls differentiation of the mammalian ovary. Chassot A.A., Ranc F., Gregoire E.P., Roepers-Gajadien H.L., Taketo M.M., Camerino G., de Rooij D.G., Schedl A., Chaboissier M.C. Hum. Mol. Genet. 17:1264-1277(2008) · Mapped (85) |
| CXorf6 is a causative gene for hypospadias. Fukami M., Wada Y., Miyabayashi K., Nishino I., Hasegawa T., Camerino G., Kretz C., Buj-Bello A., Laporte J., Yamada G. et al. Nat. Genet. 38:1369-1371(2006) · UniProtKB (1) · Mapped (12) |
| R-spondin1 is essential in sex determination, skin differentiation and malignancy. Parma P., Radi O., Vidal V., Chaboissier M.C., Dellambra E., Valentini S., Guerra L., Schedl A., Camerino G. Nat. Genet. 38:1304-1309(2006) · UniProtKB (2) |
| A new submicroscopic deletion that refines the 9p region for sex reversal. Calvari V., Bertini V., De Grandi A., Peverali G., Zuffardi O., Ferguson-Smith M., Knudtzon J., Camerino G., Borsani G., Guioli S. Genomics 65:203-212(2000) · UniProtKB (6) |
| The expression pattern of a mouse doublesex-related gene is consistent with a role in gonadal differentiation. De Grandi A., Calvari V., Bertini V., Bulfone A., Peverali G., Camerino G., Borsani G., Guioli S. Mech. Dev. 90:323-326(2000) · UniProtKB (1) |
| DAX-1, an 'antitestis' gene. Goodfellow P.N., Camerino G. Cell. Mol. Life Sci. 55:857-863(1999) · Mapped (2) |
| Dax1 antagonizes Sry action in mammalian sex determination. Swain A., Narvaez V., Burgoyne P., Camerino G., Lovell-Badge R. |
| The candidate sex-reversing DAX1 gene is autosomal in marsupials: implications for the evolution of sex determination in mammals. Pask A., Toder R., Wilcox S.A., Camerino G., Graves J.A. Genomics 41:422-426(1997) · Mapped (2) |
| Steroidogenic factor 1 and Dax-1 colocalize in multiple cell lineages: potential links in endocrine development. Ikeda Y., Swain A., Weber T.J., Hentges K.E., Zanaria E., Lalli E., Tamai K.T., Sassone-Corsi P., Lovell-Badge R., Camerino G. et al. Mol. Endocrinol. 10:1261-1272(1996) · Mapped (6) |
| Mouse Dax1 expression is consistent with a role in sex determination as well as in adrenal and hypothalamus function. Swain A., Zanaria E., Hacker A., Lovell-Badge R., Camerino G. Nat. Genet. 12:404-409(1996) · Mapped (6) |
| A family of rapidly evolving genes from the sex reversal critical region in Xp21. Dabovic B., Zanaria E., Bardoni B., Lisa A., Bordignon C., Russo V., Matessi C., Traversari C., Camerino G. Mamm. Genome 6:571-580(1995) · UniProtKB (2) |
| Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Muscatelli F., Strom T.M., Walker A.P., Zanaria E., Recan D., Meindl A., Bardoni B., Guioli S., Zehetner G., Rabl W. et al. Nature 372:672-676(1994) · UniProtKB (1) |
| An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita. Zanaria E., Muscatelli F., Bardoni B., Strom T.M., Guioli S., Guo W., Lalli E., Moser C., Walker A.P., McCabe E.R.B. et al. Nature 372:635-641(1994) · UniProtKB (1) |
| Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequences. Mandel J.L., Arveiler B., Camerino G., Hanauer A., Heilig R., Koenig M., Oberle I. Cold Spring Harb. Symp. Quant. Biol. 51:195-203(1986) · UniProtKB (1) · Mapped (14) |
| A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Franco B., Guioli S., Pragliola A., Inceri B., Bardoni B., Tonlorenzi R., Carrozo R., Maestrini E., Pieretti M., Taillon-Miller P. et al. Nature 353:529-536(1991) · UniProtKB (1) |