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

Results: 1-25/301

Authors: LAMB NE FEINGOLD E SAVAGE A AVRAMOPOULOS D FREEMAN S GU Y HALLBERG A HERSEY J KARADIMA G PETTAY D SAKER D SHEN J TAFT L MIKKELSEN M PETERSEN MB HASSOLD T SHERMAN SL
Citation: Ne. Lamb et al., CHARACTERIZATION OF SUSCEPTIBLE CHIASMA CONFIGURATIONS THAT INCREASE THE RISK FOR MATERNAL NONDISJUNCTION OF CHROMOSOME-21, Human molecular genetics, 6(9), 1997, pp. 1391-1399

Authors: ZOUALI H HANI EH PHILIPPI A VIONNET N BECKMANN JS DEMENAIS F FROGUEL P
Citation: H. Zouali et al., A SUSCEPTIBILITY LOCUS FOR EARLY-ONSET NON-INSULIN-DEPENDENT (TYPE-2)DIABETES-MELLITUS MAPS TO CHROMOSOME 20Q, PROXIMAL TO THE PHOSPHOENOLPYRUVATE CARBOXYKINASE GENE, Human molecular genetics, 6(9), 1997, pp. 1401-1408

Authors: VANBAKEL I SEPP T WARD S YATES JRW GREEN AJ
Citation: I. Vanbakel et al., MUTATIONS IN THE TSC2 GENE - ANALYSIS OF THE COMPLETE CODING SEQUENCEUSING THE PROTEIN TRUNCATION TEST (PTT), Human molecular genetics, 6(9), 1997, pp. 1409-1414

Authors: MILLINGTONWARD S ONEILL B TUOHY G ALJANDAL N KIANG AS KENNA PF PALFI A HAYDEN P MANSERGH F KENNAN A HUMPHRIES P FARRAR GJ
Citation: S. Millingtonward et al., STRATEGEMS IN-VITRO FOR GENE THERAPIES DIRECTED TO DOMINANT MUTATIONS, Human molecular genetics, 6(9), 1997, pp. 1415-1426

Authors: FOUCAULT F VAURY C BARAKAT A THIBOUT D PLANCHON P JAULIN C PRAZ F AMORGUERET M
Citation: F. Foucault et al., CHARACTERIZATION OF A NEW BLM MUTATION ASSOCIATED WITH A TOPOISOMERASE II-ALPHA DEFECT IN A PATIENT WITH BLOOMS SYNDROME, Human molecular genetics, 6(9), 1997, pp. 1427-1434

Authors: DANKO I WILLIAMS P HERWEIJER H ZHANG G LATENDRESSE JS BOCK I WOLFF JA
Citation: I. Danko et al., HIGH EXPRESSION OF NAKED PLASMID DNA IN MUSCLES OF YOUNG RODENTS, Human molecular genetics, 6(9), 1997, pp. 1435-1443

Authors: PALLAVICINI A ZIMBELLO R TISO N MURARO T RAMPOLDI L BORTOLUZZI S VALLE G LANFRANCHI G DANIELI GA
Citation: A. Pallavicini et al., THE PRELIMINARY TRANSCRIPT MAP OF A HUMAN SKELETAL-MUSCLE, Human molecular genetics, 6(9), 1997, pp. 1445-1450

Authors: KELLY CL RHEAD WJ KUTSCHKE WK BRIX AE HAMM DA PINKERT CA LINDSEY JR WOOD PA
Citation: Cl. Kelly et al., FUNCTIONAL CORRECTION OF SHORT-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY IN TRANSGENIC MICE - IMPLICATIONS FOR GENE-THERAPY OF HUMAN MITOCHONDRIAL ENZYME DEFICIENCIES, Human molecular genetics, 6(9), 1997, pp. 1451-1455

Authors: JANATA J KOGEKAR N FENTON WA
Citation: J. Janata et al., EXPRESSION AND KINETIC CHARACTERIZATION OF METHYLMALONYL-COA MUTASE FROM PATIENTS WITH THE MUT- PHENOTYPE - EVIDENCE FOR NATURALLY-OCCURRING INTERALLELIC COMPLEMENTATION, Human molecular genetics, 6(9), 1997, pp. 1457-1464

Authors: CORBIN F BOUILLON M FORTIN A MORIN S ROUSSEAU F KHANDJIAN EW
Citation: F. Corbin et al., THE FRAGILE-X MENTAL-RETARDATION PROTEIN IS ASSOCIATED WITH POLY(A)(-RNA IN ACTIVELY TRANSLATING POLYRIBOSOMES() MESSENGER), Human molecular genetics, 6(9), 1997, pp. 1465-1472

Authors: WATNICK TJ PIONTEK KB CORDAL TM WEBER H GANDOLPH MA QIAN F LENS XM NEUMANN HPH GERMINO GG
Citation: Tj. Watnick et al., AN UNUSUAL PATTERN OF MUTATION IN THE DUPLICATED PORTION OF PKD1 IS REVEALED BY USE OF A NOVEL STRATEGY FOR MUTATION DETECTION, Human molecular genetics, 6(9), 1997, pp. 1473-1481

Authors: SANDFORD R SGOTTO B APARICIO S BRENNER S VAUDIN M WILSON RK CHISSOE S PEPIN K BATEMAN A CHOTHIA C HUGHES J HARRIS P
Citation: R. Sandford et al., COMPARATIVE-ANALYSIS OF THE POLYCYSTIC KIDNEY-DISEASE-1 (PKD1) GENE REVEALS AN INTEGRAL MEMBRANE GLYCOPROTEIN WITH MULTIPLE EVOLUTIONARY CONSERVED DOMAINS, Human molecular genetics, 6(9), 1997, pp. 1483-1489

Authors: WALDER RY SHALEV H BRENNAN TMH CARMI R ELBEDOUR K SCOTT DA HANAUER A MARK AL PATIL S STONE EM SHEFFIELD VC
Citation: Ry. Walder et al., FAMILIAL HYPOMAGNESEMIA MAPS TO CHROMOSOME 9Q, NOT TO THE X-CHROMOSOME - GENETIC-LINKAGE MAPPING AND ANALYSIS OF A BALANCED TRANSLOCATION BREAKPOINT, Human molecular genetics, 6(9), 1997, pp. 1491-1497

Authors: DEGOUYON BM ZHAO W LAPORTE J MANDEL JL METZENBERG A HERMAN GE
Citation: Bm. Degouyon et al., CHARACTERIZATION OF MUTATIONS IN THE MYOTUBULARIN GENE IN 26 PATIENTSWITH X-LINKED MYOTUBULAR MYOPATHY, Human molecular genetics, 6(9), 1997, pp. 1499-1504

Authors: LAPORTE J GUIRAUDCHAUMEIL C VINCENT MC MANDEL JL TANNER SM LIECHTIGALLATI S WALLGRENPETTERSSON C DAHL N KRESS W BOLHUIS PA FARDEAU M SAMSON F BERTINI E
Citation: J. Laporte et al., MUTATIONS IN THE MTM1 GENE IMPLICATED IN X-LINKED MYOTUBULAR MYOPATHY, Human molecular genetics, 6(9), 1997, pp. 1505-1511

Authors: SWENSEN J HOFFMAN M SKOLNICK MH NEUHAUSEN SL
Citation: J. Swensen et al., IDENTIFICATION OF A 14 KB DELETION INVOLVING THE PROMOTER REGION OF BRCA1 IN A BREAST-CANCER FAMILY, Human molecular genetics, 6(9), 1997, pp. 1513-1517

Authors: COLOMER V ENGELENDER S SHARP AH DUAN K COOPER JK LANAHAN A LYFORD G WORLEY P ROSS CA
Citation: V. Colomer et al., HUNTINGTIN-ASSOCIATED PROTEIN-1 (HAP1) BINDS TO A TRIO-LIKE POLYPEPTIDE, WITH A RAD GUANINE-NUCLEOTIDE EXCHANGE FACTOR DOMAIN, Human molecular genetics, 6(9), 1997, pp. 1519-1525

Authors: KNOLL A SCHUNKERT H REICHWALD K DANSER AHJ BAUER D PLATZER M STEIN G ROSENTHAL A
Citation: A. Knoll et al., HUMAN RENIN BINDING-PROTEIN - COMPLETE GENOMIC SEQUENCE AND ASSOCIATION OF AN INTRONIC T C POLYMORPHISM WITH THE PRORENIN LEVEL IN MALES/, Human molecular genetics, 6(9), 1997, pp. 1527-1534

Authors: LAMB BT CALL LM SLUNT HH BARDEL KA LAWLER AM ECKMAN CB YOUNKIN SG HOLTZ G WAGNER SL PRICE DL SISODIA SS GEARHART JD
Citation: Bt. Lamb et al., ALTERED METABOLISM OF FAMILIAL ALZHEIMERS-DISEASE-LINKED AMYLOID PRECURSOR PROTEIN VARIANTS IN YEAST ARTIFICIAL CHROMOSOME TRANSGENIC MICE, Human molecular genetics, 6(9), 1997, pp. 1535-1541

Authors: JOYCE JA LAM WK CATCHPOOLE DJ JENKS P REIK W MAHER ER SCHOFIELD PN
Citation: Ja. Joyce et al., IMPRINTING OF IGF2 AND H19 - LACK OF RECIPROCITY IN SPORADIC BECKWITH-WIEDEMANN-SYNDROME, Human molecular genetics, 6(9), 1997, pp. 1543-1548

Authors: DOSSANTOS NR DEBRUIJN DRH BALEMANS M JANSSEN B GARTNER F LOPES JM DELEEUW B VANKESSEL AG
Citation: Nr. Dossantos et al., NUCLEAR-LOCALIZATION OF SYT, SSX AND THE SYNOVIAL SARCOMA-ASSOCIATED SYT-SSX FUSION PROTEINS, Human molecular genetics, 6(9), 1997, pp. 1549-1558

Authors: BRETT D WHITEHOUSE S ANTONSON P SHIPLEY J COOPER C GOODWIN G
Citation: D. Brett et al., THE SYT PROTEIN INVOLVED IN THE T(X-18) SYNOVIAL SARCOMA TRANSLOCATION IS A TRANSCRIPTIONAL ACTIVATOR LOCALIZED IN NUCLEAR-BODIES, Human molecular genetics, 6(9), 1997, pp. 1559-1564

Authors: BOIS P COLLICK A BROWN J JEFFREYS AJ
Citation: P. Bois et al., HUMAN MINISATELLITE MS32 (D1S8) DISPLAYS SOMATIC BUT NOT GERMLINE INSTABILITY IN TRANSGENIC MICE, Human molecular genetics, 6(9), 1997, pp. 1565-1571

Authors: WEBER B GUO XH WRAITH JE COOPER A KLEIJER WJ BUNGE S HOPWOOD JJ
Citation: B. Weber et al., NOVEL MUTATIONS IN SANFILIPPO-A-SYNDROME - IMPLICATIONS FOR ENZYME FUNCTION, Human molecular genetics, 6(9), 1997, pp. 1573-1579

Authors: EZER S SCHLESSINGER D SRIVASTAVA A KERE J
Citation: S. Ezer et al., ANHIDROTIC ECTODERMAL DYSPLASIA (EDA) PROTEIN EXPRESSED IN MCF-7 CELLS ASSOCIATES WITH CELL-MEMBRANE AND INDUCES ROUNDING, Human molecular genetics, 6(9), 1997, pp. 1581-1587
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