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Table of contents of journal: *Human molecular genetics (Print)

Results: 1-25/275

Authors: ROUQUIER S FRIEDMAN C DELETTRE C VANDENENGH G BLANCHER A CROUAUROY B TRASK BJ GIORGI D
Citation: S. Rouquier et al., A GENE RECENTLY INACTIVATED IN HUMAN DEFINES A NEW OLFACTORY RECEPTORFAMILY IN MAMMALS, Human molecular genetics (Print), 7(9), 1998, pp. 1337-1345

Authors: DU H DUANMU M WITTE D GRABOWSKI GA
Citation: H. Du et al., TARGETED DISRUPTION OF THE MOUSE LYSOSOMAL ACID LIPASE GENE - LONG-TERM SURVIVAL WITH MASSIVE CHOLESTERYL ESTER AND TRIGLYCERIDE STORAGE, Human molecular genetics (Print), 7(9), 1998, pp. 1347-1354

Authors: LUNKES A MANDEL JL
Citation: A. Lunkes et Jl. Mandel, A CELLULAR-MODEL THAT RECAPITULATES MAJOR PATHOGENIC STEPS OF HUNTINGTONS-DISEASE, Human molecular genetics (Print), 7(9), 1998, pp. 1355-1361

Authors: YUAN ZR KOHSAKA T IKEGAYA T SUZUKI T OKANO S ABE J KOBAYASHI N YAMADA M
Citation: Zr. Yuan et al., MUTATIONAL ANALYSIS OF THE JAGGED-1 GENE IN ALAGILLE-SYNDROME FAMILIES, Human molecular genetics (Print), 7(9), 1998, pp. 1363-1369

Authors: AGULNIK AI ZHARKIKH A BOETTGERTONG H BOURGERON T MCELREAVEY K BISHOP CE
Citation: Ai. Agulnik et al., EVOLUTION OF THE DAZ GENE FAMILY SUGGESTS THAT Y-LINKED DAZ PLAYS LITTLE, OR A LIMITED, ROLE IN SPERMATOGENESIS BUT UNDERLINES A RECENT AFRICAN ORIGIN FOR HUMAN-POPULATIONS, Human molecular genetics (Print), 7(9), 1998, pp. 1371-1377

Authors: KRUSHKAL J XIONG MM FERRELL R SING CF TURNER ST BOERWINKLE E
Citation: J. Krushkal et al., LINKAGE AND ASSOCIATION OF ADRENERGIC AND DOPAMINE-RECEPTOR GENES IN THE DISTAL PORTION OF THE LONG ARM OF CHROMOSOME-5 WITH SYSTOLIC BLOOD-PRESSURE VARIATION, Human molecular genetics (Print), 7(9), 1998, pp. 1379-1383

Authors: HOWARD PL DALLY GY WONG MH HO A WELEBER RG PILLERS DM RAY PN
Citation: Pl. Howard et al., LOCALIZATION OF DYSTROPHIN ISOFORM DP71 TO THE INNER LIMITING MEMBRANE OF THE RETINA SUGGESTS A UNIQUE FUNCTIONAL CONTRIBUTION OF DP71 IN THE RETINA, Human molecular genetics (Print), 7(9), 1998, pp. 1385-1391

Authors: OBER C COX NJ ABNEY M DIRIENZO A LANDER ES CHANGYALEKET B GIDLEY H KURTZ B LEE J NANCE M PETTERSSON A PRESCOTT J RICHARDSON A SCHLENKER E SUMMERHILL E WILLADSEN S PARRY R
Citation: C. Ober et al., GENOME-WIDE SEARCH FOR ASTHMA SUSCEPTIBILITY LOCI IN A FOUNDER POPULATION, Human molecular genetics (Print), 7(9), 1998, pp. 1393-1398

Authors: OKUMOTO K ITOH R SHIMOZAWA N SUZUKI Y TAMURA S KONDO N FUJIKI Y
Citation: K. Okumoto et al., MUTATIONS IN PEX10 IS THE CAUSE OF ZELLWEGER PEROXISOME DEFICIENCY SYNDROME OF COMPLEMENTATION GROUP-B, Human molecular genetics (Print), 7(9), 1998, pp. 1399-1405

Authors: HEANEY C SHALEV H ELBEDOUR K CARMI R STAACK JB SHEFFIELD VC BEIER DR
Citation: C. Heaney et al., HUMAN AUTOSOMAL RECESSIVE OSTEOPETROSIS MAPS TO 11Q13, A POSITION PREDICTED BY COMPARATIVE MAPPING OF THE MURINE OSTEOSCLEROSIS (OC) MUTATION, Human molecular genetics (Print), 7(9), 1998, pp. 1407-1410

Authors: GERAGHTY MT VAUGHN D NICHOLSON AJ LIN WW JIMENEZSANCHEZ G OBIE C FLYNN MP VALLE D HU CAA
Citation: Mt. Geraghty et al., MUTATIONS IN THE DELTA(1)-PYRROLINE 5-CARBOXYLATE DEHYDROGENASE GENE CAUSE TYPE-II HYPERPROLINEMIA, Human molecular genetics (Print), 7(9), 1998, pp. 1411-1415

Authors: NINKINA NN ALIMOVAKOST MV PATERSON JWE DELANEY L COHEN BB IMREH S GNUCHEV NV DAVIES AM BUCHMAN VL
Citation: Nn. Ninkina et al., ORGANIZATION, EXPRESSION AND POLYMORPHISM OF THE HUMAN PERSYN GENE, Human molecular genetics (Print), 7(9), 1998, pp. 1417-1424

Authors: COOPER G RUBINSZTEIN DC AMOS W
Citation: G. Cooper et al., ASCERTAINMENT BIAS CANNOT ENTIRELY ACCOUNT FOR HUMAN MICROSATELLITES BEING LONGER THAN THEIR CHIMPANZEE HOMOLOGS, Human molecular genetics (Print), 7(9), 1998, pp. 1425-1429

Authors: WALDER K NORMAN RA HANSON RL SCHRAUWEN P NEVEROVA M JENKINSON CP EASLICK J WARDEN CH PECQUEUR C RAIMBAULT S RICQUIER D HARPER M SILVER K SHULDINER AR SOLANES G LOWELL BB CHUNG WK LEIBEL RL PRATLEY R RAVUSSIN E
Citation: K. Walder et al., ASSOCIATION BETWEEN UNCOUPLING PROTEIN POLYMORPHISMS (UCP2-UCP3) AND ENERGY-METABOLISM OBESITY IN PIMA-INDIANS, Human molecular genetics (Print), 7(9), 1998, pp. 1431-1435

Authors: SAHLY I GOGAT K KOBETZ A MARCHANT D MENASCHE M CASTEL IN REVAH F DUFIER JL GUERREMILLO M ABITBOL MM
Citation: I. Sahly et al., PROMINENT NEURONAL-SPECIFIC TUB GENE-EXPRESSION IN CELLULAR TARGETS OF TUBBY MICE MUTATION, Human molecular genetics (Print), 7(9), 1998, pp. 1437-1447

Authors: DORAY B SALOMON R AMIEL J PELET A TOURAINE R BILLAUD M ATTIE T BACHY B MUNNICH A LYONNET S
Citation: B. Doray et al., MUTATION OF THE RET LIGAND, NEURTURIN, SUPPORTS MULTIGENIC INHERITANCE IN HIRSCHSPRUNG-DISEASE, Human molecular genetics (Print), 7(9), 1998, pp. 1449-1452

Authors: PASTINEN T PEROLA M NIINI P TERWILLIGER J SALOMAA V VARTIAINEN E PELTONEN L SYVANEN AC
Citation: T. Pastinen et al., ARRAY-BASED MULTIPLEX ANALYSIS OF CANDIDATE GENES REVEALS 2 INDEPENDENT AND ADDITIVE GENETIC RISK-FACTORS FOR MYOCARDIAL-INFARCTION IN THE FINNISH POPULATION, Human molecular genetics (Print), 7(9), 1998, pp. 1453-1462

Authors: FABER PW BARNES GT SRINIDHI J CHEN JM GUSELLA JF MACDONALD ME
Citation: Pw. Faber et al., HUNTINGTIN INTERACTS WITH A FAMILY OF WW DOMAIN PROTEINS, Human molecular genetics (Print), 7(9), 1998, pp. 1463-1474

Authors: ANDERSON J BURNS HD ENRIQUEZHARRIS P WILKIE AOM HEATH JK
Citation: J. Anderson et al., APERT SYNDROME MUTATIONS IN FIBROBLAST-GROWTH-FACTOR RECEPTOR-2 EXHIBIT INCREASED AFFINITY FOR FGF LIGAND, Human molecular genetics (Print), 7(9), 1998, pp. 1475-1483

Authors: KOUTNIKOVA H CAMPUZANO V KOENIG M
Citation: H. Koutnikova et al., MATURATION OF WILD-TYPE AND MUTATED FRATAXIN BY THE MITOCHONDRIAL PROCESSING PEPTIDASE, Human molecular genetics (Print), 7(9), 1998, pp. 1485-1489

Authors: MCCARTHY EMS PHILLIPS JA
Citation: Ems. Mccarthy et Ja. Phillips, CHARACTERIZATION OF AN INTRON SPLICE ENHANCER THAT REGULATES ALTERNATIVE SPLICING OF HUMAN GH PRE-MESSENGER-RNA, Human molecular genetics (Print), 7(9), 1998, pp. 1491-1496

Authors: GOTTLIEB S HANES SD GOLDEN JA OAKEY RJ BUDARF ML
Citation: S. Gottlieb et al., GOOSECOID-LIKE, A GENE DELETED IN DIGEORGE AND VELOCARDIOFACIAL SYNDROMES, RECOGNIZES DNA WITH A BICOID-LIKE SPECIFICITY AND IS EXPRESSED IN THE DEVELOPING MOUSE-BRAIN, Human molecular genetics (Print), 7(9), 1998, pp. 1497-1505

Authors: HOLMES C ARRANZ MJ POWELL JF COLLIER DA LOVESTONE S
Citation: C. Holmes et al., 5-HT2A AND 5-HT2C RECEPTOR POLYMORPHISMS AND PSYCHOPATHOLOGY IN LATE-ONSET ALZHEIMERS-DISEASE, Human molecular genetics (Print), 7(9), 1998, pp. 1507-1509

Authors: LAMBERT JC BERR C PASQUIER F DELACOURTE A FRIGARD B COTTEL D PEREZTUR J MOUROUX V MOHR M CECYRE D GALASKO D LENDON C POIRIER J HARDY J MANN D AMOUYEL P CHARTIERHARLIN MC
Citation: Jc. Lambert et al., PRONOUNCED IMPACT OF TH1 E47CS MUTATION COMPARED WITH -491 AT MUTATION ON NEURAL APOE GENE-EXPRESSION AND RISK OF DEVELOPING ALZHEIMERS-DISEASE/, Human molecular genetics (Print), 7(9), 1998, pp. 1511-1516

Authors: MARQUARDT A STOHR H PASSMORE LA KRAMER F RIVERA A WEBER BHF
Citation: A. Marquardt et al., MUTATIONS IN A NOVEL GENE, VMD2, ENCODING A PROTEIN OF UNKNOWN PROPERTIES CAUSE JUVENILE-ONSET VITELLIFORM MACULAR DYSTROPHY (BESTS-DISEASE), Human molecular genetics (Print), 7(9), 1998, pp. 1517-1525
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