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Results: 1-19 |
Results: 19
THE MOUSE MID1 GENE - IMPLICATIONS FOR THE PATHOGENESIS OF OPITZ-SYNDROME AND THE EVOLUTION OF THE MAMMALIAN PSEUDOAUTOSOMAL REGION
Authors: DALZOTTO L QUADERI NA ELLIOTT R LINGERFELTER PA CARREL L VALSECCHI V MONTINI E YEN CH CHAPMAN V KALCHEVA I ARRIGO G ZUFFARDI O THOMAS S WILLARD HF BALLABIO A DISTECHE CM RUGARLI EI
Citation: L. Dalzotto et al., THE MOUSE MID1 GENE - IMPLICATIONS FOR THE PATHOGENESIS OF OPITZ-SYNDROME AND THE EVOLUTION OF THE MAMMALIAN PSEUDOAUTOSOMAL REGION, Human molecular genetics, 7(3), 1998, pp. 489-499
OPITZ G BBB SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NEW RING FINGER GENE ON XP22/
Authors: QUADERI NA SCHWEIGER S GAUDENZ K FRANCO B RUGARLI EI BERGER W FELDMAN GJ VOLTA M ANDOLFI G GILGENKRANTZ S MARION RW HENNEKAM RCM OPITZ JM MUENKE M ROPERS HH BALLABIO A
Citation: Na. Quaderi et al., OPITZ G BBB SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NEW RING FINGER GENE ON XP22/, Nature genetics, 17(3), 1997, pp. 285-291
A NOVEL HUMAN SERINE-THREONINE PHOSPHATASE RELATED TO THE DROSOPHILA RETINAL-DEGENERATION-C (RDGC) GENE IS SELECTIVELY EXPRESSED IN SENSORYNEURONS OF NEURAL CREST ORIGIN
Authors: MONTINI E RUGARLI EI VANDEVOSSE E ANDOLFI G MARIANI M PUCA AA CONSALEZ GG DENDUNNEN JT BALLABIO A FRANCO B
Citation: E. Montini et al., A NOVEL HUMAN SERINE-THREONINE PHOSPHATASE RELATED TO THE DROSOPHILA RETINAL-DEGENERATION-C (RDGC) GENE IS SELECTIVELY EXPRESSED IN SENSORYNEURONS OF NEURAL CREST ORIGIN, Human molecular genetics, 6(7), 1997, pp. 1137-1145
JAGGED2 - A PUTATIVE NOTCH LIGAND EXPRESSED IN THE APICAL ECTODERMAL RIDGE AND IN SITES OF EPITHELIAL-MESENCHYMAL INTERACTIONS
Authors: VALSECCHI V GHEZZI C BALLABIO A RUGARLI EI
Citation: V. Valsecchi et al., JAGGED2 - A PUTATIVE NOTCH LIGAND EXPRESSED IN THE APICAL ECTODERMAL RIDGE AND IN SITES OF EPITHELIAL-MESENCHYMAL INTERACTIONS, Mechanisms of development, 69(1-2), 1997, pp. 203-207
EVIDENCE OF EVOLUTIONARY UP-REGULATION OF THE SINGLE ACTIVE X-CHROMOSOME IN MAMMALS BASED ON CLC4 EXPRESSION LEVELS IN MUS-SPRETUS AND MUS MUSCULUS
Authors: ADLER DA RUGARLI EI LINGENFELTER PA TSUCHIYA K POSLINSKI D LIGGITT HD CHAPMAN VM ELLIOTT RW BALLABIO A DISTECHE CM
Citation: Da. Adler et al., EVIDENCE OF EVOLUTIONARY UP-REGULATION OF THE SINGLE ACTIVE X-CHROMOSOME IN MAMMALS BASED ON CLC4 EXPRESSION LEVELS IN MUS-SPRETUS AND MUS MUSCULUS, Proceedings of the National Academy of Sciences of the United Statesof America, 94(17), 1997, pp. 9244-9248
CLC4 EXPRESSION LEVELS IN MUS-SPRETUS AND MUS MUSCULUS CONSISTENT WITH UP-REGULATION OF THE SINGLE ACTIVE X-CHROMOSOME IN MAMMALS
Authors: DISTECHE CM ADLER DA RUGARLI EI LINGENFELTER PA TSUCHIYA K POSLINSKI D LIGGITT HD CHAPMAN VM ELLIOTT RW BALLABIO A
Citation: Cm. Disteche et al., CLC4 EXPRESSION LEVELS IN MUS-SPRETUS AND MUS MUSCULUS CONSISTENT WITH UP-REGULATION OF THE SINGLE ACTIVE X-CHROMOSOME IN MAMMALS, American journal of human genetics, 61(4), 1997, pp. 127-127
THE KALLMANN-SYNDROME GENE-PRODUCT EXPRESSED IN COS CELLS IS CLEAVED ON THE CELL-SURFACE TO YIELD A DIFFUSIBLE COMPONENT
Authors: RUGARLI EI GHEZZI C VALSECCHI V BALLABIO A
Citation: Ei. Rugarli et al., THE KALLMANN-SYNDROME GENE-PRODUCT EXPRESSED IN COS CELLS IS CLEAVED ON THE CELL-SURFACE TO YIELD A DIFFUSIBLE COMPONENT, Human molecular genetics, 5(8), 1996, pp. 1109-1115
A NEW REGION OF CONSERVATION IS DEFINED BETWEEN HUMAN AND MOUSE X-CHROMOSOMES
Authors: DINULOS MB BASSI MT RUGARLI EI CHAPMAN V BALLABIO A DISTECHE CM
Citation: Mb. Dinulos et al., A NEW REGION OF CONSERVATION IS DEFINED BETWEEN HUMAN AND MOUSE X-CHROMOSOMES, Genomics, 35(1), 1996, pp. 244-247
DIFFERENT CHROMOSOMAL LOCALIZATION OF THE CLCN4 GENE IN MUS-SPRETUS AND C57BL 6J MICE/
Authors: RUGARLI EI ADLER DA BORSANI G TSUCHIYA K FRANCO B HAUGE X DISTECHE C CHAPMAN V BALLABIO A
Citation: Ei. Rugarli et al., DIFFERENT CHROMOSOMAL LOCALIZATION OF THE CLCN4 GENE IN MUS-SPRETUS AND C57BL 6J MICE/, Nature genetics, 10(4), 1995, pp. 466-471
CLONING OF A HUMAN HOMOLOG OF THE XENOPUS-LAEVIS APX GENE FROM THE OCULAR ALBINISM TYPE-1 CRITICAL REGION
Authors: SCHIAFFINO MV BASSI MT RUGARLI EI RENIERI A GALLI L BALLABIO A
Citation: Mv. Schiaffino et al., CLONING OF A HUMAN HOMOLOG OF THE XENOPUS-LAEVIS APX GENE FROM THE OCULAR ALBINISM TYPE-1 CRITICAL REGION, Human molecular genetics, 4(3), 1995, pp. 373-382
CHARACTERIZATION OF A HUMAN AND MURINE GENE (CLCN3) SHARING SIMILARITIES TO VOLTAGE-GATED CHLORIDE CHANNELS AND TO A YEAST INTEGRAL MEMBRANE-PROTEIN
Authors: BORSANI G RUGARLI EI TAGLIALATELA M WONG C BALLABIO A
Citation: G. Borsani et al., CHARACTERIZATION OF A HUMAN AND MURINE GENE (CLCN3) SHARING SIMILARITIES TO VOLTAGE-GATED CHLORIDE CHANNELS AND TO A YEAST INTEGRAL MEMBRANE-PROTEIN, Genomics, 27(1), 1995, pp. 131-141
REELIN - A NOVEL EXTRACELLULAR-MATRIX PROTEIN INVOLVED IN BRAIN LAMINATION
Authors: RUGARLI EI BALLABIO A
Citation: Ei. Rugarli et A. Ballabio, REELIN - A NOVEL EXTRACELLULAR-MATRIX PROTEIN INVOLVED IN BRAIN LAMINATION, BioEssays, 17(10), 1995, pp. 832-834
THE DISTAL END OF THE X-CHROMOSOME DIFFERS BETWEEN 2 CLOSELY-RELATED MOUSE-SPECIES
Authors: TSUCHIYA K RUGARLI EI DINULOS MB ADLER DA CHAPMAN VM DISTECHE CM BALLABIO A
Citation: K. Tsuchiya et al., THE DISTAL END OF THE X-CHROMOSOME DIFFERS BETWEEN 2 CLOSELY-RELATED MOUSE-SPECIES, American journal of human genetics, 57(4), 1995, pp. 1581-1581
A GENE FROM THE XP22.3 REGION SHARES HOMOLOGY WITH VOLTAGE-GATED CHLORIDE CHANNELS
Authors: VANSLEGTENHORST MA BASSI MT BORSANI G WAPENAAR MC FERRERO GB DECONCILIIS L RUGARLI EI GRILLO A FRANCO B ZOGHBI HY BALLABIO A
Citation: Ma. Vanslegtenhorst et al., A GENE FROM THE XP22.3 REGION SHARES HOMOLOGY WITH VOLTAGE-GATED CHLORIDE CHANNELS, Human molecular genetics, 3(4), 1994, pp. 547-552
EXPRESSION OF THE KALLMANN-SYNDROME GENE IN HUMAN FETAL BRAIN AND IN THE MANIPULATED CHICK-EMBRYO
Authors: LUTZ B KURATANI S RUGARLI EI WAWERSIK S WONG C BIEBER FR BALLABIO A EICHELE G
Citation: B. Lutz et al., EXPRESSION OF THE KALLMANN-SYNDROME GENE IN HUMAN FETAL BRAIN AND IN THE MANIPULATED CHICK-EMBRYO, Human molecular genetics, 3(10), 1994, pp. 1717-1723
ROLE OF THE KALLMANN SYNDROME GENE IN OLFACTORY SYSTEM-DEVELOPMENT
Authors: RUGARLI EI LUTZ B KURATANI S EICHELE G BALLABIO A
Citation: Ei. Rugarli et al., ROLE OF THE KALLMANN SYNDROME GENE IN OLFACTORY SYSTEM-DEVELOPMENT, The FASEB journal, 8(4), 1994, pp. 10000258-10000258
EXPRESSION PATTERN OF THE KALLMANN SYNDROME GENE IN THE OLFACTORY SYSTEM SUGGESTS A ROLE IN NEURONAL TARGETING
Authors: RUGARLI EI LUTZ B KURATANI SC WAWERSIK S BORSANI G BALLABIO A EICHELE G
Citation: Ei. Rugarli et al., EXPRESSION PATTERN OF THE KALLMANN SYNDROME GENE IN THE OLFACTORY SYSTEM SUGGESTS A ROLE IN NEURONAL TARGETING, Nature genetics, 4(1), 1993, pp. 19-26
KALLMANN SYNDROME - FROM GENETICS TO NEUROBIOLOGY
Authors: RUGARLI EI BALLABIO A
Citation: Ei. Rugarli et A. Ballabio, KALLMANN SYNDROME - FROM GENETICS TO NEUROBIOLOGY, JAMA, the journal of the American Medical Association, 270(22), 1993, pp. 2713-2716
X-LINKED KALLMANN SYNDROME - A NEURONAL TARGETING DEFECT IN THE OLFACTORY SYSTEM
Authors: LUTZ B RUGARLI EI EICHELE G BALLABIO A
Citation: B. Lutz et al., X-LINKED KALLMANN SYNDROME - A NEURONAL TARGETING DEFECT IN THE OLFACTORY SYSTEM, FEBS letters, 325(1-2), 1993, pp. 128-134
Risultati: 1-19 |