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Results: 1-17 |
Results: 17
RPA2, A GENE FOR THE 32 KDA SUBUNIT OF REPLICATION PROTEIN-A ON CHROMOSOME 1P35-36, IS NOT MUTATED IN PATIENTS WITH FAMILIAL MELANOMA LINKED TO CHROMOSOME 1P36
Authors: PING YJ NAKATSU Y GOLDSTEIN AM TUCKER MA KRAEMER KH TANAKA K
Citation: Yj. Ping et al., RPA2, A GENE FOR THE 32 KDA SUBUNIT OF REPLICATION PROTEIN-A ON CHROMOSOME 1P35-36, IS NOT MUTATED IN PATIENTS WITH FAMILIAL MELANOMA LINKED TO CHROMOSOME 1P36, Melanoma research, 8(1), 1998, pp. 47-52
MUTATIONAL ANALYSIS OF A FUNCTION OF XERODERMA-PIGMENTOSUM GROUP-A (XPA) PROTEIN IN STRAND-SPECIFIC DNA-REPAIR
Authors: KOBAYASHI T TAKEUCHI S SAIJO M NAKATSU Y MORIOKA H OTSUKA E WAKASUGI M NIKAIDO O TANAKA K
Citation: T. Kobayashi et al., MUTATIONAL ANALYSIS OF A FUNCTION OF XERODERMA-PIGMENTOSUM GROUP-A (XPA) PROTEIN IN STRAND-SPECIFIC DNA-REPAIR, Nucleic acids research, 26(20), 1998, pp. 4662-4668
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
STRAND SPECIFICITY AND ABSENCE OF HOT-SPOTS FOR P53 MUTATIONS IN ULTRAVIOLET B-INDUCED SKIN TUMORS OF XPA-DEFICIENT MICE
Authors: TAKEUCHI S NAKATSU Y NAKANE H MURAI H HIROTA S KITAMURA Y OKUYAMA A TANAKA K
Citation: S. Takeuchi et al., STRAND SPECIFICITY AND ABSENCE OF HOT-SPOTS FOR P53 MUTATIONS IN ULTRAVIOLET B-INDUCED SKIN TUMORS OF XPA-DEFICIENT MICE, Cancer research, 58(4), 1998, pp. 641-646
MUTATIONS IN THE XPD GENE LEADING TO XERODERMA-PIGMENTOSUM SYMPTOMS
Authors: KOBAYASHI T KURAOKA I SAIJO M NAKATSU Y TANAKA A SOMEDA Y FUKURO S TANAKA K
Citation: T. Kobayashi et al., MUTATIONS IN THE XPD GENE LEADING TO XERODERMA-PIGMENTOSUM SYMPTOMS, Human mutation, 9(4), 1997, pp. 322-331
LOSS OF THE XERODERMA-PIGMENTOSUM GROUP-A GENE (XPA) ENHANCES APOPTOSIS OF CULTURED CEREBELLAR NEURONS INDUCED BY UV BUT NOT BY LOW-K+ MEDIUM
Authors: ENOKIDO Y INAMURA N ARAKI T SATOH T NAKANE H YOSHINO M NAKATSU Y TANAKA K HATANAKA H
Citation: Y. Enokido et al., LOSS OF THE XERODERMA-PIGMENTOSUM GROUP-A GENE (XPA) ENHANCES APOPTOSIS OF CULTURED CEREBELLAR NEURONS INDUCED BY UV BUT NOT BY LOW-K+ MEDIUM, Journal of neurochemistry, 69(1), 1997, pp. 246-251
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
NUCLEOTIDE EXCISION-REPAIR DEFECT AND CARCINOGENESIS IN XPA-KNOCKED OUT MICE
Authors: TANAKA K NAKATSU Y SAIJO M KURAOKA I MATSUDA T KOBAYASHI T MURAI H NAKANE H
Citation: K. Tanaka et al., NUCLEOTIDE EXCISION-REPAIR DEFECT AND CARCINOGENESIS IN XPA-KNOCKED OUT MICE, Journal of cellular biochemistry, 1995, pp. 272-272
HIGH-INCIDENCE OF ULTRAVIOLET-B-INDUCED OR CHEMICAL-CARCINOGEN-INDUCED SKIN TUMORS IN MICE LACKING THE XERODERMA-PIGMENTOSUM GROUP-A GENE
Authors: NAKANE H TAKEUCHI S YUBA S SAIJO M NAKATSU Y MURAI H NAKATSURU Y ISHIKAWA T HIROTA S KITAMURA Y KATO Y TSUNODA Y MIYAUCHI H HORIO T TOKUNAGA T MATSUNAGA T NIKAIDO O NISHIMUNE Y OKADA Y TANAKA K
Citation: H. Nakane et al., HIGH-INCIDENCE OF ULTRAVIOLET-B-INDUCED OR CHEMICAL-CARCINOGEN-INDUCED SKIN TUMORS IN MICE LACKING THE XERODERMA-PIGMENTOSUM GROUP-A GENE, Nature, 377(6545), 1995, pp. 165-168
DNA-REPAIR PROTEIN XPA BINDS REPLICATION PROTEIN-A (RPA)
Authors: MATSUDA T SAIJO M KURAOKA I KOBAYASHI T NAKATSU Y NAGAI A ENJOJI T MASUTANI C SUGASAWA K HANAOKA F YASUI A TANAKA K
Citation: T. Matsuda et al., DNA-REPAIR PROTEIN XPA BINDS REPLICATION PROTEIN-A (RPA), The Journal of biological chemistry, 270(8), 1995, pp. 4152-4157
ENHANCEMENT OF DAMAGE-SPECIFIC DNA-BINDING OF XPA BY INTERACTION WITHTHE ERCC1 DNA-REPAIR PROTEIN
Authors: NAGAI A SAIJO M KURAOKA I MATSUDA T KODO N NAKATSU Y MIMAKI T MINO M BIGGERSTAFF M WOOD RD SIJBERS A HOEIJMAKERS JHJ TANAKA K
Citation: A. Nagai et al., ENHANCEMENT OF DAMAGE-SPECIFIC DNA-BINDING OF XPA BY INTERACTION WITHTHE ERCC1 DNA-REPAIR PROTEIN, Biochemical and biophysical research communications, 211(3), 1995, pp. 960-966
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
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
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
Risultati: 1-17 |