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Results: 1-25 | 26-33
Results: 1-25/33
RET LIGANDS (GDNF, NEURTURIN) MUTATIONS IN COMBINATION WITH RET MUTATIONS - A MODEL OF MULTIGENIC INHERITANCE IN HIRSCHSPRUNG-DISEASE
Authors: SALOMON R DORAY B AMIEL J PELET A ATTIE T BACHY B MUNNICH A LYONNET S
Citation: R. Salomon et al., RET LIGANDS (GDNF, NEURTURIN) MUTATIONS IN COMBINATION WITH RET MUTATIONS - A MODEL OF MULTIGENIC INHERITANCE IN HIRSCHSPRUNG-DISEASE, European journal of human genetics, 6, 1998, pp. 4049-4049
MUTATION OF THE RET LIGAND, NEURTURIN, SUPPORTS MULTIGENIC INHERITANCE IN HIRSCHSPRUNG-DISEASE
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
MUTATION OF THE RET LIGAND, NEURTURIN, SUPPORTS MULTIGENIC INHERITANCE IN HIRSCHSPRUNG-DISEASE (VOL 7, PG 1449, 1998)
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 (VOL 7, PG 1449, 1998), Human molecular genetics (Print), 7(11), 1998, pp. 1831-1831
VARIOUS MECHANISMS CAUSE RET-MEDIATED SIGNALING DEFECTS IN HIRSCHSPRUNGS-DISEASE
Authors: PELET A GENESTE O EDERY P PASINI A CHAPPUIS S ATTIE T MUNNICH A LENOIR G LYONNET S BILLAUD M
Citation: A. Pelet et al., VARIOUS MECHANISMS CAUSE RET-MEDIATED SIGNALING DEFECTS IN HIRSCHSPRUNGS-DISEASE, The Journal of clinical investigation, 101(6), 1998, pp. 1415-1423
MUTATIONS OF THE RET-GDNF SIGNALING PATHWAY IN ONDINES-CURSE
Authors: AMIEL J SALOMON R ATTIE T PELET A TRANG H MOKHTARI M GAULTIER C MUNNICH A LYONNET S
Citation: J. Amiel et al., MUTATIONS OF THE RET-GDNF SIGNALING PATHWAY IN ONDINES-CURSE, American journal of human genetics, 62(3), 1998, pp. 715-717
ENDOTHELIN-3 GENE-MUTATIONS IN ISOLATED AND SYNDROMIC HIRSCHSPRUNG-DISEASE
Authors: BIDAUD C SALOMON R VANCAMP G PELET A ATTIE T ENG C BONDUELLE M AMIEL J NIHOULFEKETE C WILLEMS PJ MUNNICH A LYONNET S
Citation: C. Bidaud et al., ENDOTHELIN-3 GENE-MUTATIONS IN ISOLATED AND SYNDROMIC HIRSCHSPRUNG-DISEASE, European journal of human genetics, 5(4), 1997, pp. 247-251
MUTATIONS OF THE EDN3 GENE IN ISOLATED AND SYNDROMIC HIRSCHSPRUNGS-DISEASE
Authors: BIDAUD C SALOMON R EDERY P VANCAMP G PELET A BONDUELLE M NIHOULFEKETE C WILLEMS PJ MUNNICH A LYONNET S
Citation: C. Bidaud et al., MUTATIONS OF THE EDN3 GENE IN ISOLATED AND SYNDROMIC HIRSCHSPRUNGS-DISEASE, Gastroenterologie clinique et biologique, 21(8-9), 1997, pp. 548-554
MOLECULAR-BASIS OF HIRSCHSPRUNGS-DISEASE
Authors: AMIEL J ATTIE T SALOMON R EDERY P PELET A NIHOULFEKETE C MUNNICH A LYONNET S
Citation: J. Amiel et al., MOLECULAR-BASIS OF HIRSCHSPRUNGS-DISEASE, Gut, 41, 1997, pp. 11-12
MULTIGENIC INHERITANCE OF HIRSCHSPRUNG-DISEASE
Authors: BOLK S PELET A HOFSTRA RMW SALOMON B ANGRIST M BUYS CHCM LYONNET S CHAKRAVARTI A
Citation: S. Bolk et al., MULTIGENIC INHERITANCE OF HIRSCHSPRUNG-DISEASE, American journal of human genetics, 61(4), 1997, pp. 215-215
VARIOUS MECHANISMS CAUSE RET-MEDIATED SIGNALING DEFECTS IN HIRSCHSPRUNG-DISEASE
Authors: PELET A GENESTE O EDERY P CHAPPUIS S PASINI A ATTIE T MUNNICH A LENOIR G LYONNET S BILLAUD M
Citation: A. Pelet et al., VARIOUS MECHANISMS CAUSE RET-MEDIATED SIGNALING DEFECTS IN HIRSCHSPRUNG-DISEASE, American journal of human genetics, 61(4), 1997, pp. 2006-2006
EXCLUSION OF ENDOTHELIN-1 AS A CANDIDATE GENE IN MAJOR BRANCHIAL ARCHANOMALY SYNDROMES IN HUMAN
Authors: DORAY B SALOMAN R PELET A AMIEL J MUNNICH A LYONNET S
Citation: B. Doray et al., EXCLUSION OF ENDOTHELIN-1 AS A CANDIDATE GENE IN MAJOR BRANCHIAL ARCHANOMALY SYNDROMES IN HUMAN, American journal of human genetics, 61(4), 1997, pp. 2398-2398
GERMLINE MUTATIONS OF THE RET LIGAND GDNF ARE NOT SUFFICIENT TO CAUSEHIRSCHSPRUNG DISEASE
Authors: SALOMON R ATTIE T PELET A BIDAUD C ENG C AMIEL J SARNACKI S GOULET O RICOUR C NIHOULFEKETE C MUNNICH A LYONNET S
Citation: R. Salomon et al., GERMLINE MUTATIONS OF THE RET LIGAND GDNF ARE NOT SUFFICIENT TO CAUSEHIRSCHSPRUNG DISEASE, Nature genetics, 14(3), 1996, pp. 345-347
MUTATION OF THE ENDOTHELIN-3 GENE IN THE WAARDENBURG-HIRSCHSPRUNG DISEASE (SHAH-WAARDENBURG SYNDROME)
Authors: EDERY P ATTIE T AMIEL J PELET A ENG C HOFSTRA RMW MARTELLI H BIDAUD C MUNNICH A LYONNET S
Citation: P. Edery et al., MUTATION OF THE ENDOTHELIN-3 GENE IN THE WAARDENBURG-HIRSCHSPRUNG DISEASE (SHAH-WAARDENBURG SYNDROME), Nature genetics, 12(4), 1996, pp. 442-444
HETEROZYGOUS ENDOTHELIN RECEPTOR-B (EDNRB) MUTATIONS IN ISOLATED HIRSCHSPRUNG DISEASE
Authors: AMIEL J ATTIE T JAN D PELET A EDERY P BIDAUD C LACOMBE D TAM P SIMEONI J FLORI E NIHOULFEKETE C MUNNICH A LYONNET S
Citation: J. Amiel et al., HETEROZYGOUS ENDOTHELIN RECEPTOR-B (EDNRB) MUTATIONS IN ISOLATED HIRSCHSPRUNG DISEASE, Human molecular genetics, 5(3), 1996, pp. 355-357
MUTATIONS OF THE FIBROBLAST GROWTH-FACTOR RECEPTOR-3 GENE IN ACHONDROPLASIA
Authors: ROUSSEAU F BONAVENTURE J LEGEAIMALLET L PELET A ROZET JM MAROTEAUX P LEMERRER M MUNNICH A
Citation: F. Rousseau et al., MUTATIONS OF THE FIBROBLAST GROWTH-FACTOR RECEPTOR-3 GENE IN ACHONDROPLASIA, Hormone research, 45(1-2), 1996, pp. 108-110
GENETICS OF HIRSCHSPRUNGS-DISEASE
Authors: ATTIE T AMIEL J JAN D EDERY P PELET A SALOMON R MUNNICH A LYONNET S NIHOULFEKETE C
Citation: T. Attie et al., GENETICS OF HIRSCHSPRUNGS-DISEASE, Annales de chirurgie, 50(7), 1996, pp. 538-541
DIVERSITY OF RET PROTOONCOGENE MUTATIONS IN FAMILIAL AND SPORADIC HIRSCHSPRUNG DISEASE
Authors: ATTIE T PELET A EDERY P ENG C MULLIGAN LM AMIEL J BOUTRAND L BELDJORD C NIHOULFEKETE C MUNNICH A PONDER BAJ LYONNET S
Citation: T. Attie et al., DIVERSITY OF RET PROTOONCOGENE MUTATIONS IN FAMILIAL AND SPORADIC HIRSCHSPRUNG DISEASE, Human molecular genetics, 4(8), 1995, pp. 1381-1386
MUTATION OF THE ENDOTHELIN-RECEPTOR-B GENE IN WAARDENBURG-HIRSCHSPRUNG-DISEASE
Authors: ATTIE T TILL M PELET A AMIEL J EDERY P BOUTRAND L MUNNICH A LYONNET S
Citation: T. Attie et al., MUTATION OF THE ENDOTHELIN-RECEPTOR-B GENE IN WAARDENBURG-HIRSCHSPRUNG-DISEASE, Human molecular genetics, 4(12), 1995, pp. 2407-2409
EXCLUSION OF RET AND PAX-3 LOCI IN WAARDENBURG-HIRSCHSPRUNG-DISEASE
Authors: ATTIE T TILL M PELET A EDERY P BONNET JP MUNNICH A LYONNET S
Citation: T. Attie et al., EXCLUSION OF RET AND PAX-3 LOCI IN WAARDENBURG-HIRSCHSPRUNG-DISEASE, Journal of Medical Genetics, 32(4), 1995, pp. 312-313
ENDOTHELIN RECEPTOR-B GENE MUTATION IN A CONSANGUINEOUS FAMILY WITH WAARDENBURG-HIRSCHSPRUNGS DISEASE
Authors: ATTIE T TILL M AMIEL J EDERY P PELET A MUNNICH A LYONNET S
Citation: T. Attie et al., ENDOTHELIN RECEPTOR-B GENE MUTATION IN A CONSANGUINEOUS FAMILY WITH WAARDENBURG-HIRSCHSPRUNGS DISEASE, American journal of human genetics, 57(4), 1995, pp. 21-21
A GENE FOR HOLT-GRAM SYNDROME MAPS TO THE DISTAL LONG ARM OF CHROMOSOME-12
Authors: BONNET D PELET A LEGEAIMALLET L SIDI D MATHIEU M PARENT P PLAUCHU H SERVILLE F SCHINZEL A WEISSENBACH J KACHANER J MUNNICH A LYONNET S
Citation: D. Bonnet et al., A GENE FOR HOLT-GRAM SYNDROME MAPS TO THE DISTAL LONG ARM OF CHROMOSOME-12, Nature genetics, 6(4), 1994, pp. 405-408
A GENE FOR ACHONDROPLASIA-HYPOCHONDROPLASIA MAPS TO CHROMOSOME 4P
Authors: LEMERRER M ROUSSEAU F LEGEAIMALLET L LANDAIS JC PELET A BONAVENTURE J SANAK M WEISSENBACH J STOLL C MUNNICH A MAROTEAUX P
Citation: M. Lemerrer et al., A GENE FOR ACHONDROPLASIA-HYPOCHONDROPLASIA MAPS TO CHROMOSOME 4P, Nature genetics, 6(3), 1994, pp. 318-321
A 7 BP DELETION OF THE RET PROTOONCOGENE IN FAMILIAL HIRSCHSPRUNGS-DISEASE
Authors: ATTIE T PELET A SARDA P ENG C EDERY P MULLIGAN LM PONDER BAJ MUNNICH A LYONNET S
Citation: T. Attie et al., A 7 BP DELETION OF THE RET PROTOONCOGENE IN FAMILIAL HIRSCHSPRUNGS-DISEASE, Human molecular genetics, 3(8), 1994, pp. 1439-1440
MUTATIONS OF THE RET PROTOONCOGENE IN HIR SCHSPRUNGS-DISEASE
Authors: LYONNET S EDERY P MULLIGAN LM PELET A DOW E ABEL L HOLDER S NIHOULFEKETE C PONDER BAJ MUNNICH A
Citation: S. Lyonnet et al., MUTATIONS OF THE RET PROTOONCOGENE IN HIR SCHSPRUNGS-DISEASE, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 317(4), 1994, pp. 358-362
A NOVEL POLYMORPHISM IN THE CODING SEQUENCE OF THE HUMAN RET PROTOONCOGENE
Authors: EDERY P ATTIE T MULLIGAN LM PELET A ENG C PONDER BAJ MUNNICH A LYONNET S
Citation: P. Edery et al., A NOVEL POLYMORPHISM IN THE CODING SEQUENCE OF THE HUMAN RET PROTOONCOGENE, Human genetics, 94(5), 1994, pp. 579-580
Risultati: 1-25 | 26-33