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Results: 51-74/74
HYPOKALEMIC PERIODIC PARALYSIS AND THE DIHYDROPYRIDINE RECEPTOR (CACNLIA3) - GENOTYPE-PHENOTYPE CORRELATIONS FOR 2 PREDOMINANT MUTATIONS AND EVIDENCE FOR THE ABSENCE OF A FOUNDER EFFECT IN 16 CAUCASIAN FAMILIES
Authors: ELBAZ A VALESANTOS J JURKATROTT K LAPIE P OPHOFF RA BADY B LINKS TP PIUSSAN C VILA A MONNIER N PADBERG GW ABE K FEINGOLD N GUIMARAES J WINTZEN AR VANDERHOEVEN JH SAUDUBRAY JM GRUNFELD JP LENOIR G NIVET H ECHENNE B FRANTS RR FARDEAU M LEHMANNHORN F FONTAINE B
Citation: A. Elbaz et al., HYPOKALEMIC PERIODIC PARALYSIS AND THE DIHYDROPYRIDINE RECEPTOR (CACNLIA3) - GENOTYPE-PHENOTYPE CORRELATIONS FOR 2 PREDOMINANT MUTATIONS AND EVIDENCE FOR THE ABSENCE OF A FOUNDER EFFECT IN 16 CAUCASIAN FAMILIES, American journal of human genetics, 56(2), 1995, pp. 374-380
AN EVALUATION OF GENETIC-HETEROGENEITY IN 145 BREAST-CANCER OVARIAN-CANCER FAMILIES
Authors: NAROD SA FORD D DEVILEE P BARKARDOTTIR RB LYNCH HT SMITH SA PONDER BAJ WEBER BL GARBER JE BIRCH JM CORNELIS RS KELSELL DP SPURR NK SMYTH E HAITES N SOBOL H BIGNON YJ CHANGCLAUDE J HAMANN U LINDBLOM A BORG A PIVER MS GALLION HH STRUEWING JP WHITTEMORE A TONIN P GOLDGAR DE EASTON DF MILNER B ALLAN L SIMARD J ROMMENS J MCGILLIVRAY B GREEN R IVES E BOYD N ROSEN B COLE D MORGAN K MOSLEHI R PONDER B PETO J SMITH S STRATTON M DICIOCCIO RA GALLION H SANTIBANEZKOREF MS TEARE MD EVANS DG STOPPALYONNET D LALLE P BONAITI C ESSIOUX L GIRODET C MAUGARDLOUBOUTIN C NICOLLEAU G LONGY M TOULOUSE C HORSTEIN I BIRNBAUM D EISINGER F KARENGUEVEN F NOGUCHI T HARDOUIN A RIO P MACHELARDROUMAGNAC M NOGUES C COHENHAGUENAUER O LORTHOLARY A BAY JO ARASON A BARKDARDOTTIR RB EGILSSON V BISHOP DT KELSELL D MURDAY VA SOLOMON E SPURR N TURNER G LENOIR G FEUNTEUN J LYNCH H LYNCH J WATSON P CONWAY T BONNARDEL C SEROVA O TORCHARD D LARSSON C VASEN H VANLEEUWEN I CORNELISSE CJ STEEL M PORTER D COHEN BB CAROTHERS A CANNONALBRIGHT LA GOLDGAR D SKOLNICK M BECHER H JOHANNSSON O WEBER B COLLINS F BOEHNKE M GARBER J LI F
Citation: Sa. Narod et al., AN EVALUATION OF GENETIC-HETEROGENEITY IN 145 BREAST-CANCER OVARIAN-CANCER FAMILIES, American journal of human genetics, 56(1), 1995, pp. 254-264
IDENTIFICATION OF A NEW FRAMESHIFT MUTATION (3724 DELG) IN EXON-19 OFTHE CFTR GENE
Authors: BIENVENU T LENOIR G FONKNECHTEN N DESCLAUXARRAMOND F KAPLAN JC BELDJORD C
Citation: T. Bienvenu et al., IDENTIFICATION OF A NEW FRAMESHIFT MUTATION (3724 DELG) IN EXON-19 OFTHE CFTR GENE, Human mutation, 3(1), 1994, pp. 69-70
CYTOGENETIC AND MOLECULAR ANALYSIS OF 6Q-DELETIONS IN BURKITTS-LYMPHOMA CELL-LINES
Authors: PARSA NZ GAIDANO G MUKHERJEE AB HAUPTSCHEIN RS LENOIR G DALLAFAVERA R CHAGANTI RSK
Citation: Nz. Parsa et al., CYTOGENETIC AND MOLECULAR ANALYSIS OF 6Q-DELETIONS IN BURKITTS-LYMPHOMA CELL-LINES, Genes, chromosomes & cancer, 9(1), 1994, pp. 13-18
THE GENE FOR HEREDITARY BREAST-OVARIAN CANCER, BRCA1, MAPS DISTAL TO EDH17B2 IN CHROMOSOME REGION 17Q12-Q21
Authors: TONIN P SEROVA O SIMARD J LENOIR G FEUNTEUN J MORGAN K LYNCH H NAROD S
Citation: P. Tonin et al., THE GENE FOR HEREDITARY BREAST-OVARIAN CANCER, BRCA1, MAPS DISTAL TO EDH17B2 IN CHROMOSOME REGION 17Q12-Q21, Human molecular genetics, 3(9), 1994, pp. 1679-1682
GERM-LINE EXCLUSION OF A SINGLE P53 ALLELE BY PREMATURE TERMINATION OF TRANSLATION IN A LI-FRAUMENI SYNDROME FAMILY
Authors: STOLZENBERG MC BRUGIERES L GARDES M DESSARPSFREICHEY F CHOMPRET A BRESSAC B LENOIR G BONAITIPELLIE C LEMERLE J FEUNTEUN J
Citation: Mc. Stolzenberg et al., GERM-LINE EXCLUSION OF A SINGLE P53 ALLELE BY PREMATURE TERMINATION OF TRANSLATION IN A LI-FRAUMENI SYNDROME FAMILY, Oncogene, 9(10), 1994, pp. 2799-2804
BREAST-CANCER IN MALE AND MUTATION OF AND ROGENS RECEPTOR
Authors: LOBACCARO JM LUMBROSO S POUJOL N BELON C NAMER M PUJOL H CUTULI BF SOBOL H HANS D LESIMPLE T AYME Y LENOIR G HERON JF STOPPALYONNET D BIGNON Y SULTAN C
Citation: Jm. Lobaccaro et al., BREAST-CANCER IN MALE AND MUTATION OF AND ROGENS RECEPTOR, Pathologie et biologie, 42(10), 1994, pp. 1053-1054
GENETICS OF NEM2
Authors: SCHUFFENECKER I ROSSEL M CHAMBE B GINET N BILLAUD M LENOIR G
Citation: I. Schuffenecker et al., GENETICS OF NEM2, Pathologie et biologie, 42(10), 1994, pp. 1061-1061
HEREDITARY BREAST-CANCER AND FAMILY CANCER SYNDROMES
Authors: LYNCH HT LYNCH J CONWAY T WATSON P FEUNTEUN J LENOIR G NAROD S FITZGIBBONS R
Citation: Ht. Lynch et al., HEREDITARY BREAST-CANCER AND FAMILY CANCER SYNDROMES, World journal of surgery, 18(1), 1994, pp. 21-31
HISTOLOGY OF BRCA1-ASSOCIATED OVARIAN-TUMORS
Authors: NAROD S TONIN P LYNCH H WATSON P FEUNTEUN J LENOIR G
Citation: S. Narod et al., HISTOLOGY OF BRCA1-ASSOCIATED OVARIAN-TUMORS, Lancet, 343(8891), 1994, pp. 236-236
INSULIN RESPONSES TO INTRAVENOUS GLUCOSE AND THE HYPERGLYCEMIC CLAMP IN CYSTIC-FIBROSIS PATIENTS WITH DIFFERENT DEGREES OF GLUCOSE-TOLERANCE
Authors: RAKOTOAMBININA B DELAISI B LABORDE K SILLY C DEBLIC J LENOIR G ROBERT JJ
Citation: B. Rakotoambinina et al., INSULIN RESPONSES TO INTRAVENOUS GLUCOSE AND THE HYPERGLYCEMIC CLAMP IN CYSTIC-FIBROSIS PATIENTS WITH DIFFERENT DEGREES OF GLUCOSE-TOLERANCE, Pediatric research, 36(5), 1994, pp. 667-671
ALL-RACE ELECTIONS IN SOUTH-AFRICA - POWER TO THE PEOPLE
Authors: LENOIR G
Citation: G. Lenoir, ALL-RACE ELECTIONS IN SOUTH-AFRICA - POWER TO THE PEOPLE, The Black scholar, 24(3), 1994, pp. 11
CHRONOLOGY OF SOUTH-AFRICAN HISTORY
Authors: MARRENGANE N LENOIR G
Citation: N. Marrengane et G. Lenoir, CHRONOLOGY OF SOUTH-AFRICAN HISTORY, The Black scholar, 24(3), 1994, pp. 40-43
GENETIC-MAPPING OF THE BREAST-OVARIAN CANCER SYNDROME TO A SMALL INTERVAL ON CHROMOSOME-17Q12-21 - EXCLUSION OF CANDIDATE GENES EDH17B2 ANDRARA
Authors: SIMARD J FEUNTEUN J LENOIR G TONIN P NORMAND T THE VL VIVIER A LASKO D MORGAN K ROULEAU GA LYNCH H LABRIE F NAROD SA
Citation: J. Simard et al., GENETIC-MAPPING OF THE BREAST-OVARIAN CANCER SYNDROME TO A SMALL INTERVAL ON CHROMOSOME-17Q12-21 - EXCLUSION OF CANDIDATE GENES EDH17B2 ANDRARA, Human molecular genetics, 2(8), 1993, pp. 1193-1199
GERMLINE DELETION IN A NEUROFIBROMATOSIS TYPE-2 KINDRED INACTIVATES THE NF2 GENE AND A CANDIDATE MENINGIOMA LOCUS
Authors: SANSON M MARINEAU C DESMAZE C LUTCHMAN M RUTTLEDGE M BARON C NAROD S DELATTRE O LENOIR G THOMAS G AURIAS A ROULEAU GA
Citation: M. Sanson et al., GERMLINE DELETION IN A NEUROFIBROMATOSIS TYPE-2 KINDRED INACTIVATES THE NF2 GENE AND A CANDIDATE MENINGIOMA LOCUS, Human molecular genetics, 2(8), 1993, pp. 1215-1220
THE HUMAN INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-4 GENE MAPS TO CHROMOSOME REGION 17Q12-Q21.1 AND IS CLOSE TO THE GENE FOR HEREDITARY BREAST OVARIAN-CANCER
Authors: TONIN P EHRENBORG E LENOIR G FEUNTEUN J LYNCH H MORGAN K ZAZZI H VIVIER A POLLAK M HUYNH H LUTHMAN H LARSSON C NAROD S
Citation: P. Tonin et al., THE HUMAN INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-4 GENE MAPS TO CHROMOSOME REGION 17Q12-Q21.1 AND IS CLOSE TO THE GENE FOR HEREDITARY BREAST OVARIAN-CANCER, Genomics, 18(2), 1993, pp. 414-417
COMBINATORIAL GENERATION OF VARIABLE FUSION PROTEINS IN THE EWING FAMILY OF TUMORS
Authors: ZUCMAN J MELOT T DESMAZE C GHYSDAEL J PLOUGASTEL B PETER M ZUCKER JM TRICHE TJ SHEER D TURCCAREL C AMBROS P COMBARET V LENOIR G AURIAS A THOMAS G DELATTRE O
Citation: J. Zucman et al., COMBINATORIAL GENERATION OF VARIABLE FUSION PROTEINS IN THE EWING FAMILY OF TUMORS, EMBO journal, 12(12), 1993, pp. 4481-4487
INCREASING INCIDENCE OF BREAST-CANCER IN FAMILY WITH BRCA1 MUTATION
Authors: NAROD S LYNCH H CONWAY T WATSON P FEUNTEUN J LENOIR G
Citation: S. Narod et al., INCREASING INCIDENCE OF BREAST-CANCER IN FAMILY WITH BRCA1 MUTATION, Lancet, 341(8852), 1993, pp. 1101-1102
ALTERATION IN A NEW GENE ENCODING A PUTATIVE MEMBRANE-ORGANIZING PROTEIN CAUSES NEUROFIBROMATOSIS TYPE-2
Authors: ROULEAU GA MEREL P LUTCHMAN M SANSON M ZUCMAN J MARINEAU C HOANGXUAN K DEMCZUK S DESMAZE C PLOUGASTEL B PULST SM LENOIR G BIJLSMA E FASHOLD R DUMANSKI J DEJONG P PARRY D ELDRIGE R AURIAS A DELATTRE O THOMAS G
Citation: Ga. Rouleau et al., ALTERATION IN A NEW GENE ENCODING A PUTATIVE MEMBRANE-ORGANIZING PROTEIN CAUSES NEUROFIBROMATOSIS TYPE-2, Nature, 363(6429), 1993, pp. 515-521
SEVERE CYSTIC-FIBROSIS IN A CHILD HOMOZYGOUS FOR THE G542 NONSENSE MUTATION IN THE CFTR GENE
Authors: BIENVENU T BELDJORD C FONKNECHTEN N KAPLAN JC LENOIR G
Citation: T. Bienvenu et al., SEVERE CYSTIC-FIBROSIS IN A CHILD HOMOZYGOUS FOR THE G542 NONSENSE MUTATION IN THE CFTR GENE, Journal of Medical Genetics, 30(7), 1993, pp. 621-622
SERUM INTERLEUKIN-10 IN NON-HODGKINS-LYMPHOMA - A PROGNOSTIC FACTOR
Authors: BLAY JY BURDIN N ROUSSET F LENOIR G BIRON P PHILIP T BANCHEREAU J FAVROT MC
Citation: Jy. Blay et al., SERUM INTERLEUKIN-10 IN NON-HODGKINS-LYMPHOMA - A PROGNOSTIC FACTOR, Blood, 82(7), 1993, pp. 2169-2174
DNA SCREENING FOR BREAST OVARIAN-CANCER SUSCEPTIBILITY BASED ON LINKED MARKERS - A FAMILY STUDY
Authors: LYNCH HT WATSON P CONWAY TA LYNCH JF SLOMINSKICASTER SM NAROD SA FEUNTEUN J LENOIR G
Citation: Ht. Lynch et al., DNA SCREENING FOR BREAST OVARIAN-CANCER SUSCEPTIBILITY BASED ON LINKED MARKERS - A FAMILY STUDY, Archives of internal medicine, 153(17), 1993, pp. 1979-1987
ROUTINE PROSTAGLANDIN ASSAY BY GC-MS IN MULTIWELL TISSUE-CULTURE PLATES - APPLICATION TO HUMAN SYNOVIOCYTES AND CHONDROCYTES
Authors: KNOTT I RAES M DIEU M LENOIR G BURTON M REMACLE J
Citation: I. Knott et al., ROUTINE PROSTAGLANDIN ASSAY BY GC-MS IN MULTIWELL TISSUE-CULTURE PLATES - APPLICATION TO HUMAN SYNOVIOCYTES AND CHONDROCYTES, Analytical biochemistry, 210(2), 1993, pp. 360-365
ACUTE AND CHRONIC EFFECTS OF AEROSOLIZED AMILORIDE ON THE RESPIRATORYMECHANICS OF CYSTIC-FIBROSIS INFANTS
Authors: TRANG TTH SILLY C LENOIR G GAULTIER C
Citation: Tth. Trang et al., ACUTE AND CHRONIC EFFECTS OF AEROSOLIZED AMILORIDE ON THE RESPIRATORYMECHANICS OF CYSTIC-FIBROSIS INFANTS, The American review of respiratory disease, 147(4), 1993, pp. 580-580
Risultati: 1-25 | 26-50 | 51-74 |