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Results: 1-25 | 26-37
Results: 1-25/37
EVIDENCE AGAINST LINKAGE OF FAMILIAL COMBINED HYPERLIPIDEMIA TO THE APOLIPOPROTEIN AI-CIII-AIV GENE-COMPLEX
Authors: WIJSMAN EM BRUNZELL JD JARVIK GP AUSTIN MA MOTULSKY AG DEEB SS
Citation: Em. Wijsman et al., EVIDENCE AGAINST LINKAGE OF FAMILIAL COMBINED HYPERLIPIDEMIA TO THE APOLIPOPROTEIN AI-CIII-AIV GENE-COMPLEX, Arteriosclerosis, thrombosis, and vascular biology, 18(2), 1998, pp. 215-226
HEREDITARY HEMOCHROMATOSIS - GENE DISCOVERY AND ITS IMPLICATIONS FOR POPULATION-BASED SCREENING
Authors: BURKE W THOMSON E KHOURY MJ MCDONNELL SM PRESS N ADAMS PC BARTON JC BEUTLER E BRITTENHAM G BUCHANAN A CLAYTON EW COGSWELL ME MESLIN EM MOTULSKY AG POWELL LW SIGAL E WILFOND BS COLLINS FS
Citation: W. Burke et al., HEREDITARY HEMOCHROMATOSIS - GENE DISCOVERY AND ITS IMPLICATIONS FOR POPULATION-BASED SCREENING, JAMA, the journal of the American Medical Association, 280(2), 1998, pp. 172-178
SEVERITY OF COLOR-VISION DEFECTS - ELECTRORETINOGRAPHIC (ERG), MOLECULAR AND BEHAVIORAL-STUDIES
Authors: CROGNALE MA TELLER DY MOTULSKY AG DEEB SS
Citation: Ma. Crognale et al., SEVERITY OF COLOR-VISION DEFECTS - ELECTRORETINOGRAPHIC (ERG), MOLECULAR AND BEHAVIORAL-STUDIES, Vision research (Oxford), 38(21), 1998, pp. 3377-3385
PREVENTING CORONARY HEART-DISEASE - VITAMIN-B AND HOMOCYSTEINE
Authors: OMENN GS BERESFORD SAA MOTULSKY AG
Citation: Gs. Omenn et al., PREVENTING CORONARY HEART-DISEASE - VITAMIN-B AND HOMOCYSTEINE, Circulation, 97(5), 1998, pp. 421-424
VISUAL PIGMENT GENE STRUCTURE AND EXPRESSION IN HUMAN RETINAE
Authors: YAMAGUCHI T MOTULSKY AG DEEB SS
Citation: T. Yamaguchi et al., VISUAL PIGMENT GENE STRUCTURE AND EXPRESSION IN HUMAN RETINAE, Human molecular genetics, 6(7), 1997, pp. 981-990
HOT PAPERS - NUTRITION GENETICS - A QUANTITATIVE ASSESSMENT OF PLASMAHOMOCYSTEINE AS A RISK FACTOR FOR VASCULAR-DISEASE BY BOUSHEY,C.J., BERESFORD,S.A.A., OMENN,G.S., MOTULSKY,A.G. - COMMENTS/
Authors: MOTULSKY AG
Citation: Ag. Motulsky, HOT PAPERS - NUTRITION GENETICS - A QUANTITATIVE ASSESSMENT OF PLASMAHOMOCYSTEINE AS A RISK FACTOR FOR VASCULAR-DISEASE BY BOUSHEY,C.J., BERESFORD,S.A.A., OMENN,G.S., MOTULSKY,A.G. - COMMENTS/, The Scientist, 11(18), 1997, pp. 12-12
GENETIC SCREENING OF ADOLESCENTS - REPLY
Authors: MOTULSKY AG
Citation: Ag. Motulsky, GENETIC SCREENING OF ADOLESCENTS - REPLY, The New England journal of medicine, 337(9), 1997, pp. 640-640
SCREENING FOR GENETIC-DISEASES
Authors: MOTULSKY AG
Citation: Ag. Motulsky, SCREENING FOR GENETIC-DISEASES, The New England journal of medicine, 336(18), 1997, pp. 1314-1316
EVIDENCE FOR MAJOR GENE INFLUENCES ON TRIGLYCERIDE (TG) LEVELS IN HYPERTRIGLYCERIDEMIC FAMILIES
Authors: EDWARDS KL BRUNZELL JD MOTULSKY AG AUSTIN MA
Citation: Kl. Edwards et al., EVIDENCE FOR MAJOR GENE INFLUENCES ON TRIGLYCERIDE (TG) LEVELS IN HYPERTRIGLYCERIDEMIC FAMILIES, Circulation, 96(8), 1997, pp. 1873-1873
20-YEAR CARDIOVASCULAR-DISEASE (CVD) MORTALITY IN FAMILIAL COMBINED HYPERLIPIDEMIA AND FAMILIAL HYPERTRIGLYCERIDEMIA - AN HISTORICAL COHORTSTUDY
Authors: AUSTIN MA MCKNIGHT B EDWARDS KL WALLACE KJ BRADLEY CM MCNEELY MJ BRUNZELL JD MOTULSKY AG
Citation: Ma. Austin et al., 20-YEAR CARDIOVASCULAR-DISEASE (CVD) MORTALITY IN FAMILIAL COMBINED HYPERLIPIDEMIA AND FAMILIAL HYPERTRIGLYCERIDEMIA - AN HISTORICAL COHORTSTUDY, Circulation, 96(8), 1997, pp. 2304-2304
LOW-FREQUENCY OF SKEWED X-INACTIVATION IN IDENTICAL FEMALE TWINS
Authors: JARVIK GP MOTULSKY AG
Citation: Gp. Jarvik et Ag. Motulsky, LOW-FREQUENCY OF SKEWED X-INACTIVATION IN IDENTICAL FEMALE TWINS, American journal of human genetics, 61(4), 1997, pp. 572-572
THE ADVENT OF THE UNPATIENTS
Authors: JONSEN AR DURFY SJ BURKE W MOTULSKY AG
Citation: Ar. Jonsen et al., THE ADVENT OF THE UNPATIENTS, Nature medicine, 2(6), 1996, pp. 622-624
UPDATE ON NOMENCLATURE FOR HUMAN GENE-MUTATIONS
Authors: BEAUDET AL ANTONARAKIS SE BEUTLER E COTTON RGH DESNICK RJ KAZAZIAN HH MCALPINE PJ MCKUSICK A MOTULSKY AG SCRIVER CR SHOWS TB TSUI LC VALLE D
Citation: Al. Beaudet et al., UPDATE ON NOMENCLATURE FOR HUMAN GENE-MUTATIONS, Human mutation, 8(3), 1996, pp. 197-202
MUTATION NOMENCLATURE - NICKNAMES, SYSTEMATIC NAMES, AND UNIQUE IDENTIFIERS
Authors: BEUTLER E MCKUSICK VA MOTULSKY AG SCRIVER CR HUTCHINSON F
Citation: E. Beutler et al., MUTATION NOMENCLATURE - NICKNAMES, SYSTEMATIC NAMES, AND UNIQUE IDENTIFIERS, Human mutation, 8(3), 1996, pp. 203-206
GENE-THERAPY IN THE UNITED-STATES - A 5-YEAR STATUS-REPORT
Authors: ROSS G ERICKSON R KNORR D MOTULSKY AG PARKMAN R SAMULSKI J STRAUS SE SMITH BR
Citation: G. Ross et al., GENE-THERAPY IN THE UNITED-STATES - A 5-YEAR STATUS-REPORT, Human gene therapy, 7(14), 1996, pp. 1781-1790
WERNER SYNDROME - ENTERING THE HELICASE ERA
Authors: EPSTEIN CJ MOTULSKY AG
Citation: Cj. Epstein et Ag. Motulsky, WERNER SYNDROME - ENTERING THE HELICASE ERA, BioEssays, 18(12), 1996, pp. 1025-1027
RELATIONSHIP BETWEEN STRUCTURE OF THE X-CHROMOSOME LINKED COLOR-VISION GENES AND THEIR LEVELS OF EXPRESSION IN HUMAN RETINAE
Authors: YAMAGUCHI T MOTULSKY AG DEEB SS
Citation: T. Yamaguchi et al., RELATIONSHIP BETWEEN STRUCTURE OF THE X-CHROMOSOME LINKED COLOR-VISION GENES AND THEIR LEVELS OF EXPRESSION IN HUMAN RETINAE, Investigative ophthalmology & visual science, 37(3), 1996, pp. 1544-1544
FOLIC-ACID FORTIFICATION OF FOOD - REPLY
Authors: BERESFORD SAA MOTULSKY AG OMENN GS BOUSHEY CJ
Citation: Saa. Beresford et al., FOLIC-ACID FORTIFICATION OF FOOD - REPLY, JAMA, the journal of the American Medical Association, 275(9), 1996, pp. 682-683
TOWARD LOCALIZATION OF THE WERNER SYNDROME GENE BY LINKAGE DISEQUILIBRIUM AND ANCESTRAL HAPLOTYPING - LESSONS LEARNED FROM ANALYSIS OF 35 CHROMOSOME 8P11.1-21.1 MARKERS
Authors: GODDARD KAB YU CE OSHIMA J MIKI T NAKURA J PIUSSAN C MARTIN GM SCHELLENBERG GD WIJSMAN EM BROWN WT BURG G CERIMELE D COTTINI F EPSTEIN CJ FISCHER W FRACCARO M FUJIWARA Y FUKUCHI KI HIWADA K HOEHN H HOSOKAWA Y HURLIMANN AF ISHAWATA H KAMINO K KIHARA K KISO S LIN Y MAEDA T MATTHEWS J MATSUMURA T MCKAY JE MELARAGNO MI MITSUDA M MOTULSKY AG MURAKAMI T MURANO S NIIKAWA N POOT M OGIHARA T RIZZO M SAIDA T SCAPPATICCI S TANNOK TCA TAMAKI S UTSU N UYENO B WAKAYAMA A YANAGAWA M YEVICH II YOSHIDA S ZIGRANG W
Citation: Kab. Goddard et al., TOWARD LOCALIZATION OF THE WERNER SYNDROME GENE BY LINKAGE DISEQUILIBRIUM AND ANCESTRAL HAPLOTYPING - LESSONS LEARNED FROM ANALYSIS OF 35 CHROMOSOME 8P11.1-21.1 MARKERS, American journal of human genetics, 58(6), 1996, pp. 1286-1302
NUTRITIONAL ECOGENETICS - HOMOCYSTEINE-RELATED ARTERIOSCLEROTIC VASCULAR-DISEASE, NEURAL-TUBE DEFECTS, AND FOLIC-ACID
Authors: MOTULSKY AG
Citation: Ag. Motulsky, NUTRITIONAL ECOGENETICS - HOMOCYSTEINE-RELATED ARTERIOSCLEROTIC VASCULAR-DISEASE, NEURAL-TUBE DEFECTS, AND FOLIC-ACID, American journal of human genetics, 58(1), 1996, pp. 17-20
MOLECULAR-GENETICS OF HUMAN COLOR-VISION
Authors: DEEB SS MOTULSKY AG
Citation: Ss. Deeb et Ag. Motulsky, MOLECULAR-GENETICS OF HUMAN COLOR-VISION, Behavior genetics, 26(3), 1996, pp. 195-207
JEWISH DISEASES AND ORIGINS
Authors: MOTULSKY AG
Citation: Ag. Motulsky, JEWISH DISEASES AND ORIGINS, Nature genetics, 9(2), 1995, pp. 99-101
MOLECULAR-PATTERNS AND SEQUENCE POLYMORPHISMS IN THE RED AND GREEN VISUAL PIGMENT GENES OF JAPANESE MEN
Authors: DEEB SS ALVAREZ A MALKKI M MOTULSKY AG
Citation: Ss. Deeb et al., MOLECULAR-PATTERNS AND SEQUENCE POLYMORPHISMS IN THE RED AND GREEN VISUAL PIGMENT GENES OF JAPANESE MEN, Human genetics, 95(5), 1995, pp. 501-506
LARGE-FIELD RAYLEIGH MATCHES MODELED FROM L M OPSIN GENE ARRAY AND PHOTOPIGMENT OPTICAL DENSITIES/
Authors: SANOCKI E TELLER DY MOTULSKY AG DEEB SS
Citation: E. Sanocki et al., LARGE-FIELD RAYLEIGH MATCHES MODELED FROM L M OPSIN GENE ARRAY AND PHOTOPIGMENT OPTICAL DENSITIES/, Investigative ophthalmology & visual science, 36(4), 1995, pp. 209-209
EXPRESSION OF HUMAN CONE PIGMENT GENES IN THE RETINA
Authors: YAMAGUCHI T MOTULSKY AG DEEB SS
Citation: T. Yamaguchi et al., EXPRESSION OF HUMAN CONE PIGMENT GENES IN THE RETINA, Investigative ophthalmology & visual science, 36(4), 1995, pp. 1054-1054
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