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Results: 1-16 |
Results: 16
THE HUMAN NECDIN GENE, NDN, IS MATERNALLY IMPRINTED AND LOCATED IN THE PRADER-WILLI-SYNDROME CHROMOSOMAL REGION
Authors: JAY P ROUGEULLE C MASSACRIER A MONCLA A MATTEI MG MALZAC P ROECKEL N TAVIAUX S LEFRANC JLB CAU P BERTA P LALANDE M MUSCATELLI F
Citation: P. Jay et al., THE HUMAN NECDIN GENE, NDN, IS MATERNALLY IMPRINTED AND LOCATED IN THE PRADER-WILLI-SYNDROME CHROMOSOMAL REGION, Nature genetics, 17(3), 1997, pp. 357-361
THE MOUSE NECDIN GENE IS EXPRESSED FROM THE PATERNAL ALLELE ONLY AND LIES IN THE 7C REGION OF THE MOUSE-CHROMOSOME-7, A REGION OF CONSERVEDSYNTENY TO THE HUMAN PRADER-WILLI-SYNDROME REGION
Authors: WATRIN F ROECKEL N LACROIX L MIGNON C MATTEI MG DISTECHE C MUSCATELLI F
Citation: F. Watrin et al., THE MOUSE NECDIN GENE IS EXPRESSED FROM THE PATERNAL ALLELE ONLY AND LIES IN THE 7C REGION OF THE MOUSE-CHROMOSOME-7, A REGION OF CONSERVEDSYNTENY TO THE HUMAN PRADER-WILLI-SYNDROME REGION, European journal of human genetics, 5(5), 1997, pp. 324-332
2 MEMBERS OF THE HUMAN MAGEB GENE FAMILY LOCATED IN XP21.3 ARE EXPRESSED IN TUMORS OF VARIOUS HISTOLOGICAL ORIGINS
Authors: LURQUIN C DESMET C BRASSEUR F MUSCATELLI F MARTELANGE V DEPLAEN E BRASSEUR R MONACO AP BOON T
Citation: C. Lurquin et al., 2 MEMBERS OF THE HUMAN MAGEB GENE FAMILY LOCATED IN XP21.3 ARE EXPRESSED IN TUMORS OF VARIOUS HISTOLOGICAL ORIGINS, Genomics, 46(3), 1997, pp. 397-408
MUTATIONS AND PHENOTYPE IN ISOLATED GLYCEROL KINASE-DEFICIENCY
Authors: WALKER AP MUSCATELLI F STAFFORD AN CHELLY J DAHL N BLOMQUIST HK DELANGHE J WILLEMS PJ STEINMANN B MONACO AP
Citation: Ap. Walker et al., MUTATIONS AND PHENOTYPE IN ISOLATED GLYCEROL KINASE-DEFICIENCY, American journal of human genetics, 58(6), 1996, pp. 1205-1211
ISOLATION AND CHARACTERIZATION OF A MAGE GENE FAMILY IN THE XP21.3 REGION
Authors: MUSCATELLI F WALKER AP DEPLAEN E STAFFORD AN MONACO AP
Citation: F. Muscatelli et al., ISOLATION AND CHARACTERIZATION OF A MAGE GENE FAMILY IN THE XP21.3 REGION, Proceedings of the National Academy of Sciences of the United Statesof America, 92(11), 1995, pp. 4987-4991
BMX, A NOVEL NONRECEPTOR TYROSINE KINASE GENE OF THE BTK ITK/TEC/TXK FAMILY LOCATED IN CHROMOSOME XP22.2/
Authors: TAMAGNONE L LAHTINEN I MUSTONEN T VIRTANEVA K FRANCIS F MUSCATELLI F ALITALO R SMITH CIE LARSSON C ALITALO K
Citation: L. Tamagnone et al., BMX, A NOVEL NONRECEPTOR TYROSINE KINASE GENE OF THE BTK ITK/TEC/TXK FAMILY LOCATED IN CHROMOSOME XP22.2/, Oncogene, 9(12), 1994, pp. 3683-3688
GENE DELETION CAUSING ADRENAL HYPOPLASIA CONGENITA AND HYPOGONADOTROPIC HYPOGONADISM
Authors: MATFIN G SHEAVES R MUSCATELLI F WALKER A MONACO A GRANT D NWOSE O WASS JAH
Citation: G. Matfin et al., GENE DELETION CAUSING ADRENAL HYPOPLASIA CONGENITA AND HYPOGONADOTROPIC HYPOGONADISM, Clinical endocrinology, 40(6), 1994, pp. 807-808
AN UNUSUAL MEMBER OF THE NUCLEAR HORMONE-RECEPTOR SUPERFAMILY RESPONSIBLE FOR X-LINKED ADRENAL HYPOPLASIA CONGENITA
Authors: ZANARIA E MUSCATELLI F BARDONI B STROM TM GUIOLI S GUO WW LALLI E MOSER C WALKER AP MCCABE ERB MEITINGER T MONACO AP SASSONECORSI P CAMERINO G
Citation: E. Zanaria et al., AN UNUSUAL MEMBER OF THE NUCLEAR HORMONE-RECEPTOR SUPERFAMILY RESPONSIBLE FOR X-LINKED ADRENAL HYPOPLASIA CONGENITA, Nature, 372(6507), 1994, pp. 635-641
MUTATIONS IN THE DAX-1 GENE GIVE RISE TO BOTH X-LINKED ADRENAL HYPOPLASIA CONGENITA AND HYPOGONADOTROPIC HYPOGONADISM
Authors: MUSCATELLI F STROM TM WALKER AP ZANARIA E RECAN D MEINDL A BARDONI B GUIOLI S ZEHETNER G RABL W SCHWARZ HP KAPLAN JC CAMERINO G MEITINGER T MONACO AP
Citation: F. Muscatelli et al., MUTATIONS IN THE DAX-1 GENE GIVE RISE TO BOTH X-LINKED ADRENAL HYPOPLASIA CONGENITA AND HYPOGONADOTROPIC HYPOGONADISM, Nature, 372(6507), 1994, pp. 672-676
A NOVEL PUTATIVE RECEPTOR PROTEIN TYROSINE KINASE OF THE MET FAMILY
Authors: RONSIN C MUSCATELLI F MATTEI MG BREATHNACH R
Citation: C. Ronsin et al., A NOVEL PUTATIVE RECEPTOR PROTEIN TYROSINE KINASE OF THE MET FAMILY, Oncogene, 8(5), 1993, pp. 1195-1202
PHYSICAL MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XP21
Authors: WALKER AP HO MF MUSCATELLI F CHELLY J CLARKE E ISHIKAWABRUSH Y MONACO AP
Citation: Ap. Walker et al., PHYSICAL MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XP21, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 182-182
PHYSICAL AND GENETIC-MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XCEN-]Q21
Authors: CHELLY J RIDER S FAIRWEATHER N ISHIKAWABRUSH Y MUSCATELLI F MONACO AP
Citation: J. Chelly et al., PHYSICAL AND GENETIC-MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XCEN-]Q21, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 182-182
THE OLFR1 GENE ENCODING THE HGMP07E PUTATIVE OLFACTORY RECEPTOR MAPS TO THE 17P13-]P12 REGION OF THE HUMAN GENOME AND REVEALS AN MSPI RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM
Authors: SCHURMANS S MUSCATELLI F MIOT F MATTEI MG VASSART G PARMENTIER M
Citation: S. Schurmans et al., THE OLFR1 GENE ENCODING THE HGMP07E PUTATIVE OLFACTORY RECEPTOR MAPS TO THE 17P13-]P12 REGION OF THE HUMAN GENOME AND REVEALS AN MSPI RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM, Cytogenetics and cell genetics, 63(3), 1993, pp. 200-204
ISOLATION AND CHARACTERIZATION OF A REPETITIVE DNA-SEQUENCE FROM LEISHMANIA-INFANTUM - DEVELOPMENT OF A VISCERAL LEISHMANIASIS POLYMERASE CHAIN-REACTION
Authors: PIARROUX R AZAIEZ R LOSSI AM REYNIER P MUSCATELLI F GAMBARELLI F FONTES M DUMON H QUILICI M
Citation: R. Piarroux et al., ISOLATION AND CHARACTERIZATION OF A REPETITIVE DNA-SEQUENCE FROM LEISHMANIA-INFANTUM - DEVELOPMENT OF A VISCERAL LEISHMANIASIS POLYMERASE CHAIN-REACTION, The American journal of tropical medicine and hygiene, 49(3), 1993, pp. 364-369
ISOLATION OF CANDIDATE GENE(S) FOR ADRENOCORTICAL HYPOPLASIA-CONGENITA AND (OR) HYPOGONADOTROPIC HYPOGONADISM X-LINKED DISEASES
Authors: MUSCATELLI F WALKER AP MEITINGER T MONACO AP
Citation: F. Muscatelli et al., ISOLATION OF CANDIDATE GENE(S) FOR ADRENOCORTICAL HYPOPLASIA-CONGENITA AND (OR) HYPOGONADOTROPIC HYPOGONADISM X-LINKED DISEASES, American journal of human genetics, 53(3), 1993, pp. 931-931
PHYSICAL MAPPING OF AN XQ-PROXIMAL INTERSTITIAL DUPLICATION IN A MALE
Authors: MUSCATELLI F VERNA JM PHILIP N MONCLA A MATTEI MG MATTEI JF FONTES M
Citation: F. Muscatelli et al., PHYSICAL MAPPING OF AN XQ-PROXIMAL INTERSTITIAL DUPLICATION IN A MALE, Human genetics, 88(6), 1992, pp. 691-694
Risultati: 1-16 |