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Results: 1-10 |
Results: 10
A VERY LARGE PROTEIN WITH DIVERSE FUNCTIONAL MOTIFS IS DEFICIENT IN RJS (RUNTY, JERKY, STERILE) MICE
Authors: LEHMAN AL NAKATSU Y CHING A BRONSON RT OAKEY RJ KEIPERHRYNKO N FINGER JN DURHAMPIERRE D HORTON DB NEWTON JM LYON MF BRILLIANT MH
Citation: Al. Lehman et al., A VERY LARGE PROTEIN WITH DIVERSE FUNCTIONAL MOTIFS IS DEFICIENT IN RJS (RUNTY, JERKY, STERILE) MICE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(16), 1998, pp. 9436-9441
TYPE-2 OCULOCUTANEOUS ALBINISM (OCA2) IN ZIMBABWE AND CAMEROON - DISTRIBUTION OF THE 2.7-KB DELETION ALLELE OF THE P GENE
Authors: PURI N DURHAMPIERRE D AQUARON R LUND PM KING RA BRILLIANT MH
Citation: N. Puri et al., TYPE-2 OCULOCUTANEOUS ALBINISM (OCA2) IN ZIMBABWE AND CAMEROON - DISTRIBUTION OF THE 2.7-KB DELETION ALLELE OF THE P GENE, Human genetics, 100(5-6), 1997, pp. 651-656
OCULOCUTANEOUS ALBINISM IN AN ISOLATED TONGA COMMUNITY IN ZIMBABWE
Authors: LUND PM PURI N DURHAMPIERRE D KING RA BRILLIANT MH
Citation: Pm. Lund et al., OCULOCUTANEOUS ALBINISM IN AN ISOLATED TONGA COMMUNITY IN ZIMBABWE, Journal of Medical Genetics, 34(9), 1997, pp. 733-735
ESTIMATION OF CARRIER FREQUENCY OF A 2.7 KB DELETION ALLELE OF THE P GENE ASSOCIATED WITH OCA2 IN AFRICAN-AMERICANS
Authors: DURHAMPIERRE D KING RA NABER JM LAKEN S BRILLIANT MH
Citation: D. Durhampierre et al., ESTIMATION OF CARRIER FREQUENCY OF A 2.7 KB DELETION ALLELE OF THE P GENE ASSOCIATED WITH OCA2 IN AFRICAN-AMERICANS, Human mutation, 7(4), 1996, pp. 370-373
MELANOSOMAL TYROSINE TRANSPORT IN NORMAL AND PINK-EYED DILUTION MURINE MELANOCYTES
Authors: GAHL WA POTTERF B DURHAMPIERRE D BRILLIANT MH HEARING VJ
Citation: Wa. Gahl et al., MELANOSOMAL TYROSINE TRANSPORT IN NORMAL AND PINK-EYED DILUTION MURINE MELANOCYTES, Pigment cell research, 8(5), 1995, pp. 229-233
AFRICAN ORIGIN OF AN INTRAGENIC DELETION OF THE HUMAN-P GENE IN TYROSINASE POSITIVE OCULOCUTANEOUS ALBINISM
Authors: DURHAMPIERRE D GARDNER JM NAKATSU Y KING RA FRANCKE U CHING A AQUARON R DELMARMOL V BRILLIANT MH
Citation: D. Durhampierre et al., AFRICAN ORIGIN OF AN INTRAGENIC DELETION OF THE HUMAN-P GENE IN TYROSINASE POSITIVE OCULOCUTANEOUS ALBINISM, Nature genetics, 7(2), 1994, pp. 176-179
THE MOUSE PINK-EYED DILUTION GENE - ASSOCIATION WITH HYPOPIGMENTATIONIN PRADER-WILLI AND ANGELMAN SYNDROMES AND WITH HUMAN OCA2
Authors: BRILLIANT MH KING R FRANCKE U SCHUFFENHAUER S MEITINGER T GARDNER JM DURHAMPIERRE D NAKATSU Y
Citation: Mh. Brilliant et al., THE MOUSE PINK-EYED DILUTION GENE - ASSOCIATION WITH HYPOPIGMENTATIONIN PRADER-WILLI AND ANGELMAN SYNDROMES AND WITH HUMAN OCA2, Pigment cell research, 7(6), 1994, pp. 398-402
IDENTIFICATION OF A MELANOSOMAL MEMBRANE-PROTEIN ENCODED BY THE PINK-EYED DILUTION (TYPE-II OCULOCUTANEOUS ALBINISM) GENE
Authors: ROSEMBLAT S DURHAMPIERRE D GARDNER JM NAKATSU Y BRILLIANT MH ORLOW SJ
Citation: S. Rosemblat et al., IDENTIFICATION OF A MELANOSOMAL MEMBRANE-PROTEIN ENCODED BY THE PINK-EYED DILUTION (TYPE-II OCULOCUTANEOUS ALBINISM) GENE, Proceedings of the National Academy of Sciences of the United Statesof America, 91(25), 1994, pp. 12071-12075
A CLUSTER OF 3 GABA(A) RECEPTOR SUBUNIT GENES IS DELETED IN A NEUROLOGICAL MUTANT OF THE MOUSE P-LOCUS
Authors: NAKATSU Y TYNDALE RF DELOREY TM DURHAMPIERRE D GARDNER JM MCDANEL HJ NGUYEN Q WAGSTAFF J LALANDE M SIKELA JM OLSEN RW TOBIN AJ BRILLIANT MH
Citation: Y. Nakatsu et al., A CLUSTER OF 3 GABA(A) RECEPTOR SUBUNIT GENES IS DELETED IN A NEUROLOGICAL MUTANT OF THE MOUSE P-LOCUS, Nature, 364(6436), 1993, pp. 448-450
THE MOUSE PINK-EYED DILUTION GENE - ASSOCIATION WITH HUMAN TYROSINASE-POSITIVE OCULOCUTANEOUS ALBINISM (OCA2), AND HYPOPIGMENTATION IN PRADER-WILLI-SYNDROME AND ANGELMAN SYNDROME
Authors: BRILLIANT MH GARDNER JM DURHAMPIERRE D NAKATSU Y KING RA
Citation: Mh. Brilliant et al., THE MOUSE PINK-EYED DILUTION GENE - ASSOCIATION WITH HUMAN TYROSINASE-POSITIVE OCULOCUTANEOUS ALBINISM (OCA2), AND HYPOPIGMENTATION IN PRADER-WILLI-SYNDROME AND ANGELMAN SYNDROME, American journal of human genetics, 53(3), 1993, pp. 161-161
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