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Results:
1-11
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Results: 11
Authors:
TIMPL P
SPANAGEL R
SILLABER I
KRESSE A
REUL JMHM
STALLA GK
BLANQUET V
STECKLER T
HOLSBOER F
WURST W
Citation: P. Timpl et al., IMPAIRED STRESS-RESPONSE AND REDUCED ANXIETY IN MICE LACKING A FUNCTIONAL CORTICOTROPIN-RELEASING HORMONE-RECEPTOR 1, Nature genetics, 19(2), 1998, pp. 162-166
Authors:
MINIOU P
JEANPIERRE M
BOURCHIS D
BARBOSA ACC
BLANQUET V
VIEGASPEQUIGNOT E
Citation: P. Miniou et al., ALPHA-SATELLITE DNA METHYLATION IN NORMAL INDIVIDUALS AND IN ICF PATIENTS - HETEROGENEOUS METHYLATION OF CONSTITUTIVE HETEROCHROMATIN IN ADULT AND FETAL TISSUES, Human genetics, 99(6), 1997, pp. 738-745
Authors:
BLANQUET V
WURST W
Citation: V. Blanquet et W. Wurst, GENETIC NETWORK CONTROLLING MID-HINDBRAIN DEVELOPMENT, Developmental biology, 186(2), 1997, pp. 139-139
Authors:
DOZ F
PETER M
SCHLEIERMACHER G
VIELH P
VALIDIRE P
PUTTERMAN M
BLANQUET V
DESJARDINS L
DUFIER JL
ZUCKER JM
MOSSERI V
THOMAS G
MAGDELENAT H
DELATTRE O
Citation: F. Doz et al., N-MYC AMPLIFICATION LOSS OF HETEROZYGOSITY ON THE SHORT ARM OF CHROMOSOME-I AND DNA-PLOIDY IN RETINOBLASTOMA, European journal of cancer, 32A(4), 1996, pp. 645-649
Authors:
FAVOR J
SANDULACHE R
NEUHAUSERKLAUS A
PRETSCH W
CHATTERJEE B
SENFT E
WURST W
BLANQUET V
GRIMES P
SPORLE R
SCHUGHART K
Citation: J. Favor et al., THE MOUSE PAX2(1NEU) MUTATION IS IDENTICAL TO A HUMAN PAX2 MUTATION IN A FAMILY WITH RENAL-COLOBOMA SYNDROME AND RESULTS IN DEVELOPMENTAL DEFECTS OF THE BRAIN, EAR, EYE, AND KIDNEY, Proceedings of the National Academy of Sciences of the United Statesof America, 93(24), 1996, pp. 13870-13875
Authors:
BLANQUET V
TURLEAU C
GROSSMORAND MS
BEAUFORT CS
DOZ F
BESMOND C
Citation: V. Blanquet et al., SPECTRUM OF GERMLINE MUTATIONS IN THE RB1 GENE - A STUDY OF 232 PATIENTS WITH HEREDITARY AND NON HEREDITARY RETINOBLASTOMA, Human molecular genetics, 4(3), 1995, pp. 383-388
Authors:
DELMER A
SENAMAUDBEAUFORT C
BLANQUET V
PATERLINI P
BRECHOT C
Citation: A. Delmer et al., CYCLIN-DEPENDENT KINASE-4 INHIBITORS (P16(INK4A) MTS1 AND P15(INK4B)/MTS2) GENES STRUCTURE AND EXPRESSION IN HEPATOCELLULAR CARCINOMAS (HCC)/, Hepatology, 22(4), 1995, pp. 1205-1205
Authors:
BLANQUET V
GROSS MS
TURLEAU C
SENAMAUDBEAUFORT C
DOZ F
BESMOND C
Citation: V. Blanquet et al., 3 NOVEL GERMLINE MUTATIONS IN EXON-8 AND EXON-18 OF THE RETINOBLASTOMA GENE, Human molecular genetics, 3(7), 1994, pp. 1185-1186
Authors:
MINIOU P
JEANPIERRE M
BLANQUET V
SIBELLA V
BONNEAU D
HERBELIN C
FISCHER A
NIVELEAU A
VIEGASPEQUIGNOT E
Citation: P. Miniou et al., ABNORMAL METHYLATION PATTERN IN CONSTITUTIVE AND FACULTATIVE (X-INACTIVE CHROMOSOME) HETEROCHROMATIN OF ICF PATIENTS, Human molecular genetics, 3(12), 1994, pp. 2093-2102
Authors:
DESBOIS C
MAGRE J
BLANQUET V
CAPEAU J
GOOSSENS M
BESMOND C
Citation: C. Desbois et al., DETECTION OF SEQUENCE VARIATIONS IN THE HUMAN INSULIN-RECEPTOR GENE BY PARALLEL DENATURING GRADIENT GEL-ELECTROPHORESIS, Human mutation, 2(5), 1993, pp. 395-403
Authors:
BLANQUET V
TURLEAU C
GROSS MS
GOOSSENS M
BESMOND C
Citation: V. Blanquet et al., IDENTIFICATION OF GERMLINE MUTATIONS IN THE RB1 GENE BY DENATURANT GRADIENT GEL-ELECTROPHORESIS AND POLYMERASE CHAIN-REACTION DIRECT SEQUENCING, Human molecular genetics, 2(7), 1993, pp. 975-979
Risultati:
1-11
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