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Results: 1-25/57
Authors:
MIYAGAWA K
KENT J
MOORE A
CHARLIEU JP
LITTLE MH
WILLIAMSON KA
KELSEY A
BROWN KW
HASSAM S
BRINER J
HAYASHI Y
HIRAI H
YAZAKI Y
VANHEYNINGEN V
HASTIE ND
Citation: K. Miyagawa et al., LOSS OF WT1 FUNCTION LEADS TO ECTOPIC MYOGENESIS IN WILMS-TUMOR, Nature genetics, 18(1), 1998, pp. 15-17
Authors:
LOVE J
AXTON R
CHURCHILL A
VANHEYNINGEN V
HANSON I
Citation: J. Love et al., A NEW SET OF PRIMERS FOR MUTATION ANALYSIS OF THE HUMAN PAX6 GENE, Human mutation, 12(2), 1998, pp. 128-134
Authors:
PROSSER J
VANHEYNINGEN V
Citation: J. Prosser et V. Vanheyningen, PAX6 MUTATIONS REVIEWED, Human mutation, 11(2), 1998, pp. 93-108
Authors:
KLEINJAN DJ
VANHEYNINGEN V
Citation: Dj. Kleinjan et V. Vanheyningen, POSITION EFFECT IN HUMAN GENETIC-DISEASE, Human molecular genetics (Print), 7(10), 1998, pp. 1611-1618
Authors:
MAALOUF EF
FERGUSON J
VANHEYNINGEN V
MODI N
Citation: Ef. Maalouf et al., IN-UTERO NEPHROPATHY, DENYS-DRASH-SYNDROME AND POTTER PHENOTYPE, Pediatric nephrology, 12(6), 1998, pp. 449-451
Authors:
BROWN A
MCKIE M
VANHEYNINGEN V
PROSSER J
Citation: A. Brown et al., THE HUMAN-PAX6-MUTATION-DATABASE, Nucleic acids research, 26(1), 1998, pp. 259-264
Authors:
MILES C
ELGAR G
COLES E
KLEINJAN DJ
VANHEYNINGEN V
HASTIE N
Citation: C. Miles et al., COMPLETE SEQUENCING OF THE FUGU WAGR REGION FROM WT1 TO PAX6 - DRAMATIC COMPACTION AND CONSERVATION OF SYNTENY WITH HUMAN-CHROMOSOME 11P13, Proceedings of the National Academy of Sciences of the United Statesof America, 95(22), 1998, pp. 13068-13072
Authors:
VANHEYNINGEN V
Citation: V. Vanheyningen, DEVELOPMENTAL EYE DISEASE - A GENOME ERA PARADIGM, Clinical genetics, 54(4), 1998, pp. 272-282
Authors:
VANHEYNINGEN V
Citation: V. Vanheyningen, MODEL ORGANISMS ILLUMINATE HUMAN-GENETICS AND DISEASE, Molecular medicine, 3(4), 1997, pp. 231-237
Authors:
VANHEYNINGEN V
Citation: V. Vanheyningen, SUGAR AND SPICE AND ALL THINGS SPLICE, Nature genetics, 17(4), 1997, pp. 367-368
Authors:
AXTON RA
HANSON IM
LOVE J
SEAWRIGHT A
PROSSER J
VANHEYNINGEN V
Citation: Ra. Axton et al., COMBINED SSCP HETERODUPLEX ANALYSIS IN THE SCREENING FOR PAX6 MUTATIONS/, Molecular and cellular probes, 11(4), 1997, pp. 287-292
Authors:
KENT J
LEE M
SCHEDL A
BOYLE S
FANTES J
POWELL M
RUSHMERE N
ABBOTT C
VANHEYNINGEN V
BICKMORE WA
Citation: J. Kent et al., THE RETICULOCALBIN GENE MAPS TO THE WAGR REGION IN HUMAN AND TO THE SMALL EYE HARWELL DELETION IN MOUSE, Genomics, 42(2), 1997, pp. 260-267
Authors:
AALFS CM
FANTES JA
WENNIGERPRICK LJJM
SLUIJTER S
HENNEKAM RCM
VANHEYNINGEN V
HOOVERS JMN
Citation: Cm. Aalfs et al., TANDEM DUPLICATION OF 11P12-P13 IN A CHILD WITH BORDERLINE DEVELOPMENT DELAY AND EYE ABNORMALITIES - DOSE-EFFECT OF THE PAX6 GENE-PRODUCT, American journal of medical genetics, 73(3), 1997, pp. 267-271
Authors:
ERICSON J
RASHBASS P
SCHEDL A
BRENNERMORTON S
KAWAKAMI A
VANHEYNINGEN V
JESSELL TM
BRISCOE J
Citation: J. Ericson et al., PAX6 CONTROLS PROGENITOR-CELL IDENTITY AND NEURONAL FATE IN RESPONSE TO GRADED SHH SIGNALING, Cell, 90(1), 1997, pp. 169-180
Authors:
ERICSON J
BRISCOE J
RASHBASS P
VANHEYNINGEN V
JESSELL TM
Citation: J. Ericson et al., GRADED SONIC HEDGEHOG SIGNALING AND THE SPECIFICATION OF CELL FATE INTHE VENTRAL NEURAL-TUBE, Cold Spring Harbor Symposia on Quantitative Biology, 62, 1997, pp. 451-466
Authors:
AXTON R
HANSON I
DANES S
SELLAR G
VANHEYNINGEN V
PROSSER J
Citation: R. Axton et al., THE INCIDENCE OF PAX6 MUTATION IN PATIENTS WITH SIMPLE ANIRIDIA - AN EVALUATION OF MUTATION DETECTION IN 12 CASES, Journal of Medical Genetics, 34(4), 1997, pp. 279-286
Authors:
CROLLA JA
CAWDERY JE
OLEY CA
YOUNG ID
GRAY J
FANTES J
VANHEYNINGEN V
Citation: Ja. Crolla et al., A FISH APPROACH TO DEFINING THE EXTENT AND POSSIBLE CLINICAL-SIGNIFICANCE OF DELETIONS AT THE WAGR LOCUS, Journal of Medical Genetics, 34(3), 1997, pp. 207-212
Authors:
VANHEYNINGEN V
Citation: V. Vanheyningen, CHANGING TACK ON THE MAP, Nature genetics, 13(2), 1996, pp. 134
Authors:
ENGELKAMP D
VANHEYNINGEN V
Citation: D. Engelkamp et V. Vanheyningen, TRANSCRIPTION FACTORS IN DISEASE, Current opinion in genetics & development, 6(3), 1996, pp. 334-342
Authors:
MACKAY M
FANTES J
SCHERER S
BOYLE S
WEST K
TSUI LC
BELLONI E
LUTZ E
VANHEYNINGEN V
HARMAR AJ
Citation: M. Mackay et al., CHROMOSOMAL LOCALIZATION IN MOUSE AND HUMAN OF THE VASOACTIVE-INTESTINAL-PEPTIDE RECEPTOR-TYPE-2 GENE - A POSSIBLE CONTRIBUTOR TO THE HOLOPROSENCEPHALY-3 PHENOTYPE, Genomics, 37(3), 1996, pp. 345-353
Authors:
POOK MA
THAKRAR R
POTTINGER B
HARDING B
PORTEOUS D
VANHEYNINGEN V
COWELL J
JONES C
POVEY S
DAVIES KE
THAKKER RV
Citation: Ma. Pook et al., EAGI AND NOTI LINKING CLONES FROM HUMAN-CHROMOSOME-11 AND HUMAN-CHROMOSOME-XP, Human genetics, 97(6), 1996, pp. 742-749
Authors:
SHOWS TB
ALDERS M
BENNETT S
BURBEE D
CARTWRIGHT P
CHANDRASEKHARAPPA S
COOPER P
COURSEAUX A
DAVIES C
DEVIGNES MD
DEVILEE P
ELLIOTT R
EVANS G
FANTES J
GARNER H
GAUDRAY P
GERHARD DS
GESSLER M
HIGGINS M
HUMMERICH H
JAMES M
LAGERCRANTZ J
LITT M
LITTLE P
MANNENS M
MUNROE D
NOWAK N
OBRIEN S
PARKER N
PERLIN M
REID L
RICHARD C
SAWICKI M
SWALLOW D
THAKKER R
VANHEYNINGEN V
VANSCHOTHORST E
VORECHOVSKY I
WADELIUS C
WEBER B
ZABEL B
Citation: Tb. Shows et al., REPORT OF THE 5TH INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-11 MAPPING (1996), Cytogenetics and cell genetics, 74(1-2), 1996, pp. 2-52
Authors:
SCHEDL A
ROSS A
LEE M
ENGELKAMP D
RASHBASS P
VANHEYNINGEN V
HASTIE ND
Citation: A. Schedl et al., INFLUENCE OF PAX6 GENE DOSAGE ON DEVELOPMENT - OVEREXPRESSION CAUSES SEVERE EYE ABNORMALITIES, Cell, 86(1), 1996, pp. 71-82
Authors:
EVANS KL
VANHEYNINGEN V
PORTEOUS DJ
Citation: Kl. Evans et al., PLACEMENT AND REFINED MAPPING OF ESTABLISHED AND NEW MARKERS ON HUMAN-CHROMOSOME 11Q USING A SMALL PANEL OF SOMATIC-CELL HYBRIDS, European journal of human genetics, 3(1), 1995, pp. 42-48
Authors:
LITTLE M
HOLMES G
BICKMORE W
VANHEYNINGEN V
HASTIE N
WAINWRIGHT B
Citation: M. Little et al., DNA-BINDING CAPACITY OF THE WT1 PROTEIN IS ABOLISHED BY DENYS-DRASH SYNDROME WT1 POINT MUTATIONS, Human molecular genetics, 4(3), 1995, pp. 351-358