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Results: 1-25 | 26-27
Results: 1-25/27
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
IDENTIFICATION OF A NOVEL TRANSCRIPT PRODUCED BY THE GENE RESPONSIBLEFOR THE HERMANSKY-PUDLAK-SYNDROME IN PUERTO-RICO
Authors: WILDENBERG SC FRYER JP GARDNER JM OETTING WS BRILLIANT MH KING RA
Citation: Sc. Wildenberg et al., IDENTIFICATION OF A NOVEL TRANSCRIPT PRODUCED BY THE GENE RESPONSIBLEFOR THE HERMANSKY-PUDLAK-SYNDROME IN PUERTO-RICO, Journal of investigative dermatology, 110(5), 1998, pp. 777-781
MOUSE-CHROMOSOME-7
Authors: BRILLIANT MH WILLIAMS RW HOLDENER BC ANGEL JM STERN M HUNTER K
Citation: Mh. Brilliant et al., MOUSE-CHROMOSOME-7, Mammalian genome, 7, 1997, pp. 121-142
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
MICE DEVOID OF GAMMA-AMINOBUTYRATE TYPE-A RECEPTOR BETA-3 SUBUNIT HAVE EPILEPSY, CLEFT-PALATE, AND HYPERSENSITIVE BEHAVIOR
Authors: HOMANICS GE DELOREY TM FIRESTONE LL QUINLAN JJ HANDFORTH A HARRISON NL KRASOWSKI MD RICK CEM KORPI ER MAKELA R BRILLIANT MH HAGIWARA N FERGUSON C SNYDER K OLSEN RW
Citation: Ge. Homanics et al., MICE DEVOID OF GAMMA-AMINOBUTYRATE TYPE-A RECEPTOR BETA-3 SUBUNIT HAVE EPILEPSY, CLEFT-PALATE, AND HYPERSENSITIVE BEHAVIOR, Proceedings of the National Academy of Sciences of the United Statesof America, 94(8), 1997, pp. 4143-4148
THE MOUSE PALE EAR (EP) MUTATION IS THE HOMOLOG OF HUMAN HERMANSKY-PUDLAK-SYNDROME
Authors: GARDNER JM WILDENBERG SC KEIPER NM NOVAK EK RUSINIAK ME SWANK RT PURI N FINGER JN HAGIWARA N LEHMAN AL GALES TL BAYER ME KING RA BRILLIANT MH
Citation: Jm. Gardner et al., THE MOUSE PALE EAR (EP) MUTATION IS THE HOMOLOG OF HUMAN HERMANSKY-PUDLAK-SYNDROME, Proceedings of the National Academy of Sciences of the United Statesof America, 94(17), 1997, pp. 9238-9243
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
EXPRESSION OF PACE4 IN CHEMICALLY-INDUCED CARCINOMAS IS ASSOCIATED WITH SPINDLE-CELL TUMOR CONVERSION AND INCREASED INVASIVE ABILITY
Authors: HUBBARD FC GOODROW TL LIU SC BRILLIANT MH BASSET P MAINS RE KLEINSZANTO AJP
Citation: Fc. Hubbard et al., EXPRESSION OF PACE4 IN CHEMICALLY-INDUCED CARCINOMAS IS ASSOCIATED WITH SPINDLE-CELL TUMOR CONVERSION AND INCREASED INVASIVE ABILITY, Cancer research, 57(23), 1997, pp. 5226-5231
IDENTIFICATION OF A NOVEL CDNA ASSOCIATED WITH THE HERMANSKY-PUDLAK-SYNDROME (HPS)
Authors: WILDENBERG SC FRYER JP GARDNER JM OETTING WS SWANK RT BRILLIANT MH KING RA
Citation: Sc. Wildenberg et al., IDENTIFICATION OF A NOVEL CDNA ASSOCIATED WITH THE HERMANSKY-PUDLAK-SYNDROME (HPS), American journal of human genetics, 61(4), 1997, pp. 1974-1974
THE CLINICAL SPECTRUM OF ALBINISM IN HUMANS
Authors: OETTING WS BRILLIANT MH KING RA
Citation: Ws. Oetting et al., THE CLINICAL SPECTRUM OF ALBINISM IN HUMANS, Molecular medicine today, 2(8), 1996, pp. 330-335
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
MOLECULAR ANALYSIS OF THE CDNAS ENCODED BY THE P(UN) AND P(J) ALLELESOF THE PINK-EYED DILUTION LOCUS
Authors: OAKEY RJ KEIPER NM CHING AS BRILLIANT MH
Citation: Rj. Oakey et al., MOLECULAR ANALYSIS OF THE CDNAS ENCODED BY THE P(UN) AND P(J) ALLELESOF THE PINK-EYED DILUTION LOCUS, Mammalian genome, 7(4), 1996, pp. 315-316
MOUSE CHROMOSOME-7
Authors: BRILLIANT MH WILLIAMS RW HOLDENER BC ANGEL JM
Citation: Mh. Brilliant et al., MOUSE CHROMOSOME-7, Mammalian genome, 6, 1996, pp. 135-150
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
THE GAMMA-AMINOBUTYRIC-ACID RECEPTOR GAMMA-3 SUBUNIT GENE (GABRG3) ISTIGHTLY LINKED TO THE ALPHA-5 SUBUNIT GENE (GABRA5) ON HUMAN-CHROMOSOME 15Q11-Q13 AND IS TRANSCRIBED IN THE SAME ORIENTATION
Authors: GREGER V KNOLL JHM WOOLF E GLATT K TYNDALE RF DELOREY TM OLSEN RW TOBIN AJ SIKELA JM NAKATSU Y BRILLIANT MH WHITING PJ LALANDE M
Citation: V. Greger et al., THE GAMMA-AMINOBUTYRIC-ACID RECEPTOR GAMMA-3 SUBUNIT GENE (GABRG3) ISTIGHTLY LINKED TO THE ALPHA-5 SUBUNIT GENE (GABRA5) ON HUMAN-CHROMOSOME 15Q11-Q13 AND IS TRANSCRIBED IN THE SAME ORIENTATION, Genomics, 26(2), 1995, pp. 258-264
ONE-DIMENSIONAL GENOME SCANNING - IDENTIFICATION OF THE BASIS OF A MOUSE MUTATION AND IDENTIFICATION OF GENOMIC CHANGES IN OVARIAN-CARCINOMA
Authors: BRILLIANT MH GONDO Y MAGLIOCCO A
Citation: Mh. Brilliant et al., ONE-DIMENSIONAL GENOME SCANNING - IDENTIFICATION OF THE BASIS OF A MOUSE MUTATION AND IDENTIFICATION OF GENOMIC CHANGES IN OVARIAN-CARCINOMA, Electrophoresis, 16(2), 1995, pp. 163-167
THEORETICAL BASIS OF ONE-DIMENSIONAL GENOME SCANNING - A DIRECT METHOD TO IDENTIFY THE SITE OF A MUTATION
Authors: GONDO Y BRILLIANT MH
Citation: Y. Gondo et Mh. Brilliant, THEORETICAL BASIS OF ONE-DIMENSIONAL GENOME SCANNING - A DIRECT METHOD TO IDENTIFY THE SITE OF A MUTATION, Electrophoresis, 16(2), 1995, pp. 174-178
MUTATIONS AND POLYMORPHISMS OF THE HUMAN P-GENE ASSOCIATED WITH P-RELATED OCULOCUTANEOUS ALBINISM (OCA2)
Authors: OETTING WS BRILLIANT MH GARDINER JM FRYER JP KING RA
Citation: Ws. Oetting et al., MUTATIONS AND POLYMORPHISMS OF THE HUMAN P-GENE ASSOCIATED WITH P-RELATED OCULOCUTANEOUS ALBINISM (OCA2), American journal of human genetics, 57(4), 1995, pp. 1432-1432
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
GENOME SCANNING DETECTS GENETIC ALTERATIONS IN HUMAN OVARIAN-CARCINOMA
Authors: MAGLIOCCO AM BRILLIANT MH
Citation: Am. Magliocco et Mh. Brilliant, GENOME SCANNING DETECTS GENETIC ALTERATIONS IN HUMAN OVARIAN-CARCINOMA, Human mutation, 4(2), 1994, pp. 141-149
MOUSE CHROMOSOME-7
Authors: BRILLIANT MH WILLIAMS RW CONTI CJ ANGEL JM OAKEY RJ HOLDENER BC
Citation: Mh. Brilliant et al., MOUSE CHROMOSOME-7, Mammalian genome, 5, 1994, pp. 104-123
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
A TRIBUTE TO RUSSELL,TIBBY
Authors: BRILLIANT MH
Citation: Mh. Brilliant, A TRIBUTE TO RUSSELL,TIBBY, Pigment cell research, 7(3), 1994, pp. 129-130
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
THE ORIGINAL PINK-EYED DILUTION MUTATION-(P) AROSE IN ASIATIC MICE - IMPLICATIONS FOR THE H4 MINOR HISTOCOMPATIBILITY ANTIGEN, MYOD1 REGULATION AND THE ORIGIN OF INBRED STRAINS
Authors: BRILLIANT MH CHING A NAKATSU Y EICHER EM
Citation: Mh. Brilliant et al., THE ORIGINAL PINK-EYED DILUTION MUTATION-(P) AROSE IN ASIATIC MICE - IMPLICATIONS FOR THE H4 MINOR HISTOCOMPATIBILITY ANTIGEN, MYOD1 REGULATION AND THE ORIGIN OF INBRED STRAINS, Genetics, 138(1), 1994, pp. 203-211
Risultati: 1-25 | 26-27