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Veronica van Heyningen

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Chemicals & Drugs

Disorders

Living Beings

Mice

Anatomy

Chromosomes, Human, Pair 11

Physiology

Concepts & Ideas

Molecular Sequence Data

Procedures

Genes & Molecular Sequences

Wilms Tumor Genes

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Publications

TOP 3
Sansom Stephen N; Griffiths Dean S; Faedo Andrea; Kleinjan Dirk-Jan; Ruan Youlin; Smith James; van Heyningen Veronica; Rubenstein John L; Livesey Frederick J
The level of the transcription factor Pax6 is essential for controlling the balance between neural stem cell self-renewal and neurogenesis.
Hingorani Melanie; Williamson Kathleen A; Moore Anthony T; van Heyningen Veronica
Detailed ophthalmologic evaluation of 43 individuals with PAX6 mutations.
Chen Yu; Doughman Yong-qiu; Gu Shi; Jarrell Andrew; Aota Shin-ichi; Cvekl Ales; Watanabe Michiko; Dunwoodie Sally L; Johnson Randall S; van Heyningen Veronica; Kleinjan Dirk A; Beebe David C; Yang Yu-Chung
Cited2 is required for the proper formation of the hyaloid vasculature and for lens morphogenesis.

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All Publications

2009: Sansom Stephen N; Griffiths Dean S; Faedo Andrea; Kleinjan Dirk-Jan; Ruan Youlin; Smith James; van Heyningen Veronica; Rubenstein John L; Livesey Frederick J
The level of the transcription factor Pax6 is essential for controlling the balance between neural stem cell self-renewal and neurogenesis.
PLoS genetics 2009;5(6):e1000511.
2009: Hingorani Melanie; Williamson Kathleen A; Moore Anthony T; van Heyningen Veronica
Detailed ophthalmologic evaluation of 43 individuals with PAX6 mutations.
Investigative ophthalmology & visual science 2009;50(6):2581-90.
2008: Chen Yu; Doughman Yong-qiu; Gu Shi; Jarrell Andrew; Aota Shin-ichi; Cvekl Ales; Watanabe Michiko; Dunwoodie Sally L; Johnson Randall S; van Heyningen Veronica; Kleinjan Dirk A; Beebe David C; Yang Yu-Chung
Cited2 is required for the proper formation of the hyaloid vasculature and for lens morphogenesis.
Development (Cambridge, England) 2008;135(17):2939-48.
2008: Yeyati Patricia L; van Heyningen Veronica
Incapacitating the evolutionary capacitor: Hsp90 modulation of disease.
Current opinion in genetics & development 2008;18(3):264-72.
2008: Robinson David O; Howarth Rachel J; Williamson Kathleen A; van Heyningen Veronica; Beal Sarah J; Crolla John A
Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia.
American journal of medical genetics. Part A 2008;146A(5):558-69.
2008: Kleinjan Dirk A; Bancewicz Ruth M; Gautier Philippe; Dahm Ralf; Schonthaler Helia B; Damante Giuseppe; Seawright Anne; Hever Ann M; Yeyati Patricia L; van Heyningen Veronica; Coutinho Pedro
Subfunctionalization of duplicated zebrafish pax6 genes by cis-regulatory divergence.
PLoS genetics 2008;4(2):e29.
2007: van Heyningen Veronica; Hoovers Jan M N; de Kraker Jan; Crolla John A
Raised risk of Wilms tumour in patients with aniridia and submicroscopic WT1 deletion.
Journal of medical genetics 2007;44(12):787-90.
2007: Hewitt Alex W; Kearns Lisa S; Jamieson Robyn V; Williamson Kathy A; van Heyningen Veronica; Mackey David A
PAX6 mutations may be associated with high myopia.
Ophthalmic genetics 2007;28(3):179-82.
2007: Henderson R Alex; Williamson Kathy; Cumming Sally; Clarke Michael P; Lynch Sally Ann; Hanson Isabel M; FitzPatrick David R; Sisodiya Sanjay; van Heyningen Veronica
Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia.
European journal of human genetics : EJHG 2007;15(8):898-901.
2007: Bamiou Doris-Eva; Free Samantha L; Sisodiya Sanjay M; Chong Wui K; Musiek Frank; Williamson Kathleen A; van Heyningen Veronica; Moore Anthony T; Gadian David; Luxon Linda M
Auditory interhemispheric transfer deficits, hearing difficulties, and brain magnetic resonance imaging abnormalities in children with congenital aniridia due to PAX6 mutations.
Archives of pediatrics & adolescent medicine 2007;161(5):463-9.
2007: Bamiou Doris-Eva; Campbell Nicole G; Musiek Frank E; Taylor Rachael; Chong W K; Moore Anthony; van Heyningen Veronica; Free Samantha; Sisodiya Sanjay; Luxon Linda M
Auditory and verbal working memory deficits in a child with congenital aniridia due to a PAX6 mutation.
International journal of audiology 2007;46(4):196-202.
2007: Yeyati Patricia L; Bancewicz Ruth M; Maule John; van Heyningen Veronica
Hsp90 selectively modulates phenotype in vertebrate development.
PLoS genetics 2007;3(3):e43.
2007: Manuel Martine; Georgala Petrina A; Carr Catherine B; Chanas Simon; Kleinjan Dirk A; Martynoga Ben; Mason John O; Molinek Michael; Pinson Jeni; Pratt Thomas; Quinn Jane C; Simpson T Ian; Tyas David A; van Heyningen Veronica; West John D; Price David J
Controlled overexpression of Pax6 in vivo negatively autoregulates the Pax6 locus, causing cell-autonomous defects of late cortical progenitor proliferation with little effect on cortical arealization.
Development (Cambridge, England) 2007;134(3):545-55.
2006: Kleinjan Dirk A; Seawright Anne; Mella Sebastien; Carr Catherine B; Tyas David A; Simpson T Ian; Mason John O; Price David J; van Heyningen Veronica
Long-range downstream enhancers are essential for Pax6 expression.
Developmental biology 2006;299(2):563-81.
2006: Hever A M; Williamson K A; van Heyningen V
Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2.
Clinical genetics 2006;69(6):459-70.
2006: Williamson Kathleen A; Hever Ann M; Rainger Joe; Rogers R Curtis; Magee Alex; Fiedler Zdenek; Keng Wee Teik; Sharkey Freddie H; McGill Niolette; Hill Clare J; Schneider Adele; Messina Mario; Turnpenny Peter D; Fantes Judy A; van Heyningen Veronica; FitzPatrick David R
Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome.
Human molecular genetics 2006;15(9):1413-22.
2006: Sisodiya Sanjay M; Ragge Nicola K; Cavalleri Gianpiero L; Hever Ann; Lorenz Birgit; Schneider Adele; Williamson Kathleen A; Stevens John M; Free Samantha L; Thompson Pamela J; van Heyningen Veronica; Fitzpatrick David R
Role of SOX2 mutations in human hippocampal malformations and epilepsy.
Epilepsia 2006;47(3):534-42.
2006: Faivre Laurence; Williamson Kathleen A; Faber Valérie; Laurent Nicole; Grimaldi Marianne; Thauvin-Robinet Christel; Durand Christine; Mugneret Francine; Gouyon Jean-Bernard; Bron Alain; Huet Frédéric; Hayward Caroline; Heyningen Veronica van; Fitzpatrick David R
Recurrence of SOX2 anophthalmia syndrome with gonosomal mosaicism in a phenotypically normal mother.
American journal of medical genetics. Part A 2006;140(6):636-9.
2006: Tyas David A; Simpson T Ian; Carr Catherine B; Kleinjan Dirk A; van Heyningen Veronica; Mason John O; Price David J
Functional conservation of Pax6 regulatory elements in humans and mice demonstrated with a novel transgenic reporter mouse.
BMC developmental biology 2006;6():21.
2005: Aijaz Saima; Allen Jennifer; Tregidgo Robert; van Heyningen Veronica; Hanson Isabel; Clark Brian J
Expression analysis of SIX3 and SIX6 in human tissues reveals differences in expression and a novel correlation between the expression of SIX3 and the genes encoding isocitrate dehyhrogenase and cadherin 18.
Genomics 2005;86(1):86-99.
2005: Fitzpatrick David R; van Heyningen Veronica
Developmental eye disorders.
Current opinion in genetics & development 2005;15(3):348-53.
2005: Ragge Nicola K; Brown Alison G; Poloschek Charlotte M; Lorenz Birgit; Henderson R Alex; Clarke Michael P; Russell-Eggitt Isabelle; Fielder Alistair; Gerrelli Dianne; Martinez-Barbera Juan Pedro; Ruddle Piers; Hurst Jane; Collin J Richard O; Salt Alison; Cooper Simon T; Thompson Pamela J; Sisodiya Sanjay M; Williamson Kathleen A; Fitzpatrick David R; van Heyningen Veronica; Hanson Isabel M
Heterozygous mutations of OTX2 cause severe ocular malformations.
American journal of human genetics 2005;76(6):1008-22.
2005: Ragge Nicola K; Lorenz Birgit; Schneider Adele; Bushby Kate; de Sanctis Luisa; de Sanctis Ugo; Salt Alison; Collin J Richard O; Vivian Anthony J; Free Samantha L; Thompson Pamela; Williamson Kathleen A; Sisodiya Sanjay M; van Heyningen Veronica; Fitzpatrick David R
SOX2 anophthalmia syndrome.
American journal of medical genetics. Part A 2005;135(1):1-7; discussion 8.
2005: Kleinjan Dirk A; van Heyningen Veronica
Long-range control of gene expression: emerging mechanisms and disruption in disease.
American journal of human genetics 2005;76(1):8-32.
2004: Aijaz Saima; Clark Brian J; Williamson Kathleen; van Heyningen Veronica; Morrison Danny; Fitzpatrick David; Collin Richard; Ragge Nicola; Christoforou Andrea; Brown Alison; Hanson Isabel
Absence of SIX6 mutations in microphthalmia, anophthalmia, and coloboma.
Investigative ophthalmology & visual science 2004;45(11):3871-6.
2004: Bamiou Doris-Eva; Musiek Frank E; Sisodiya Sanjay M; Free Samantha L; Davies Rosalyn A; Moore Anthony; van Heyningen Veronica; Luxon Linda M
Deficient auditory interhemispheric transfer in patients with PAX6 mutations.
Annals of neurology 2004;56(4):503-9.
2004: Van Heyningen Veronica; Yeyati Patricia L
Mechanisms of non-Mendelian inheritance in genetic disease.
Human molecular genetics 2004;13 Spec No 2():R225-33.
2004: Thompson P J; Mitchell T N; Free S L; Williamson K A; Hanson I M; van Heyningen V; Moore A T; Sisodiya S M
Cognitive functioning in humans with mutations of the PAX6 gene.
Neurology 2004;62(7):1216-8.
2004: Kleinjan Dirk A; Seawright Anne; Childs Andrew J; van Heyningen Veronica
Conserved elements in Pax6 intron 7 involved in (auto)regulation and alternative transcription.
Developmental biology 2004;265(2):462-77.
2003: Free Samantha L; Mitchell Tejal N; Williamson Kathleen A; Churchill Amanda J; Shorvon Simon D; Moore Anthony T; van Heyningen Veronica; Sisodiya Sanjay M
Quantitative MR image analysis in subjects with defects in the PAX6 gene.
NeuroImage 2003;20(4):2281-90.
2003: Kleinjan Dirk A; van Heyningen Veronica
Turned off by RNA.
Nature genetics 2003;34(2):125-6.
2003: Mitchell Tejal N; Free Samantha L; Williamson Kathleen A; Stevens John M; Churchill Amanda J; Hanson Isabel M; Shorvon Simon D; Moore Anthony T; van Heyningen Veronica; Sisodiya Sanjay M
Polymicrogyria and absence of pineal gland due to PAX6 mutation.
Annals of neurology 2003;53(5):658-63.
2003: Fantes Judy; Ragge Nicola K; Lynch Sally-Ann; McGill Niolette I; Collin J Richard O; Howard-Peebles Patricia N; Hayward Caroline; Vivian Anthony J; Williamson Kathy; van Heyningen Veronica; FitzPatrick David R
Mutations in SOX2 cause anophthalmia.
Nature genetics 2003;33(4):461-3.
2002: Crolla John A; van Heyningen Veronica
Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia.
American journal of human genetics 2002;71(5):1138-49.
2002: van Heyningen Veronica; Cox David R
Advice to governments: scientific give and take.
Nature reviews. Genetics 2002;3(8):631-6.
2002: van Heyningen Veronica; Williamson Kathleen A
PAX6 in sensory development.
Human molecular genetics 2002;11(10):1161-7.
2002: Griffin Caroline; Kleinjan Dirk A; Doe Brendan; van Heyningen Veronica
New 3' elements control Pax6 expression in the developing pretectum, neural retina and olfactory region.
Mechanisms of development 2002;112(1-2):89-100.
2002: Kleinjan Dirk A; Seawright Anne; Elgar Greg; van Heyningen Veronica
Characterization of a novel gene adjacent to PAX6, revealing synteny conservation with functional significance.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(2):102-7.
2002: Morrison D; FitzPatrick D; Hanson I; Williamson K; van Heyningen V; Fleck B; Jones I; Chalmers J; Campbell H
National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology.
Journal of medical genetics 2002;39(1):16-22.
2002: Estivill-Torrus Guillermo; Pearson Helen; van Heyningen Veronica; Price David J; Rashbass Penny
Pax6 is required to regulate the cell cycle and the rate of progression from symmetrical to asymmetrical division in mammalian cortical progenitors.
Development (Cambridge, England) 2002;129(2):455-66.
2002: Jamieson Robyn V; Perveen Rahat; Kerr Bronwyn; Carette Martin; Yardley Jill; Heon Elise; Wirth M Gabriela; van Heyningen Veronica; Donnai Di; Munier Francis; Black Graeme C M
Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma.
Human molecular genetics 2002;11(1):33-42.
2001: Kleinjan D A; Seawright A; Schedl A; Quinlan R A; Danes S; van Heyningen V
Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6.
Human molecular genetics 2001;10(19):2049-59.
2001: Malandrini A; Mari F; Palmeri S; Gambelli S; Berti G; Bruttini M; Bardelli A M; Williamson K; van Heyningen V; Renieri A
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation.
Clinical genetics 2001;60(2):151-4.
2001: Sisodiya S M; Free S L; Williamson K A; Mitchell T N; Willis C; Stevens J M; Kendall B E; Shorvon S D; Hanson I M; Moore A T; van Heyningen V
PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humans.
Nature genetics 2001;28(3):214-6.
2000: Sherbotie J R; van Heyningen V; Axton R; Williamson K; Finn L S; Kaplan B S
Hemolytic uremic syndrome associated with Denys-Drash syndrome.
Pediatric nephrology (Berlin, Germany) 2000;14(12):1092-7.
2000: Perveen R; Lloyd I C; Clayton-Smith J; Churchill A; van Heyningen V; Hanson I; Taylor D; McKeown C; Super M; Kerr B; Winter R; Black G C
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations.
Investigative ophthalmology & visual science 2000;41(9):2456-60.
1999: Engelkamp D; Rashbass P; Seawright A; van Heyningen V
Role of Pax6 in development of the cerebellar system.
Development (Cambridge, England) 1999;126(16):3585-96.
1999: Heyman I; Frampton I; van Heyningen V; Hanson I; Teague P; Taylor A; Simonoff E
Psychiatric disorder and cognitive function in a family with an inherited novel mutation of the developmental control gene PAX6.
Psychiatric genetics 1999;9(2):85-90.
1999: Davies R; Moore A; Schedl A; Bratt E; Miyahawa K; Ladomery M; Miles C; Menke A; van Heyningen V; Hastie N
Multiple roles for the Wilms' tumor suppressor, WT1.
Cancer research 1999;59(7 Suppl):1747s-1750s; discussion 1751s.
1999: Hanson I; Churchill A; Love J; Axton R; Moore T; Clarke M; Meire F; van Heyningen V
Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations.
Human molecular genetics 1999;8(2):165-72.
1999: Borsani G; DeGrandi A; Ballabio A; Bulfone A; Bernard L; Banfi S; Gattuso C; Mariani M; Dixon M; Donnai D; Metcalfe K; Winter R; Robertson M; Axton R; Brown A; van Heyningen V; Hanson I
EYA4, a novel vertebrate gene related to Drosophila eyes absent.
Human molecular genetics 1999;8(1):11-23.
1998: van Heyningen V
Developmental eye disease--a genome era paradigm.
Clinical genetics 1998;54(4):272-82.
1998: Miles C; Elgar G; Coles E; Kleinjan D J; van Heyningen V; Hastie N
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 States of America 1998;95(22):13068-72.
1998: Miyagawa K; Kent J; Moore A; Charlieu J P; Little M H; Williamson K A; Kelsey A; Brown K W; Hassam S; Briner J; Hayashi Y; Hirai H; Yazaki Y; van Heyningen V; Hastie N D
Loss of WT1 function leads to ectopic myogenesis in Wilms' tumour.
Nature genetics 1998;18(1):15-7.
1998: Brown A; McKie M; van Heyningen V; Prosser J
The Human PAX6 Mutation Database.
Nucleic acids research 1998;26(1):259-64.
1998: Kleinjan D J; van Heyningen V
Position effect in human genetic disease.
Human molecular genetics 1998;7(10):1611-8.
1998: Love J; Axton R; Churchill A; van Heyningen V; Hanson I
A new set of primers for mutation analysis of the human PAX6 gene.
Human mutation 1998;12(2):128-34.
1998: Prosser J; van Heyningen V
PAX6 mutations reviewed.
Human mutation 1998;11(2):93-108.
1997: Aalfs C M; Fantes J A; Wenniger-Prick L J; Sluijter S; Hennekam R C; van Heyningen V; Hoovers J M
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 1997;73(3):267-71.
1997: Axton R A; Hanson I M; Love J; Seawright A; Prosser J; van Heyningen V
Combined SSCP/heteroduplex analysis in the screening for PAX6 mutations.
Molecular and cellular probes 1997;11(4):287-92.
1997: Ericson J; Rashbass P; Schedl A; Brenner-Morton S; Kawakami A; van Heyningen V; Jessell T M; Briscoe J
Pax6 controls progenitor cell identity and neuronal fate in response to graded Shh signaling.
Cell 1997;90(1):169-80.
1997: Kent J; Lee M; Schedl A; Boyle S; Fantes J; Powell M; Rushmere N; Abbott C; van Heyningen V; Bickmore W A
The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouse.
Genomics 1997;42(2):260-7.
1997: Axton R; Hanson I; Danes S; Sellar G; van Heyningen V; Prosser J
The incidence of PAX6 mutation in patients with simple aniridia: an evaluation of mutation detection in 12 cases.
Journal of medical genetics 1997;34(4):279-86.
1997: van Heyningen V
Model organisms illuminate human genetics and disease.
Molecular medicine (Cambridge, Mass.) 1997;3(4):231-7.
1997: Crolla J A; Cawdery J E; Oley C A; Young I D; Gray J; Fantes J; van Heyningen V
A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
Journal of medical genetics 1997;34(3):207-12.
1997: Ericson J; Briscoe J; Rashbass P; van Heyningen V; Jessell T M
Graded sonic hedgehog signaling and the specification of cell fate in the ventral neural tube.
Cold Spring Harbor symposia on quantitative biology 1997;62():451-66.
1996: Mackay M; Fantes J; Scherer S; Boyle S; West K; Tsui L C; Belloni E; Lutz E; Van Heyningen V; Harmar A J
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotype.
Genomics 1996;37(3):345-53.
1996: Schedl A; Ross A; Lee M; Engelkamp D; Rashbass P; van Heyningen V; Hastie N D
Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalities.
Cell 1996;86(1):71-82.
1996: Engelkamp D; van Heyningen V
Transcription factors in disease.
Current opinion in genetics & development 1996;6(3):334-42.
1995: Kent J; Coriat A M; Sharpe P T; Hastie N D; van Heyningen V
The evolution of WT1 sequence and expression pattern in the vertebrates.
Oncogene 1995;11(9):1781-92.
1995: Hanson I; Van Heyningen V
Pax6: more than meets the eye.
Trends in genetics : TIG 1995;11(7):268-72.
1995: Hanson I; Brown A; van Heyningen V
A new PAX6 mutation in familial aniridia.
Journal of medical genetics 1995;32(6):488-9.
1995: Larsson S H; Charlieu J P; Miyagawa K; Engelkamp D; Rassoulzadegan M; Ross A; Cuzin F; van Heyningen V; Hastie N D
Subnuclear localization of WT1 in splicing or transcription factor domains is regulated by alternative splicing.
Cell 1995;81(3):391-401.
1995: Charlieu J P; Larsson S; Miyagawa K; van Heyningen V; Hastie N D
Does the Wilms' tumour suppressor gene, WT1, play roles in both splicing and transcription?
Journal of cell science. Supplement 1995;19():95-9.
1995: Evans K L; van Heyningen V; Porteous D J
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 : EJHG 1995;3(1):42-8.
1994: Williamson K A; Van Heyningen V
Towards an understanding of Wilms' tumour.
International journal of experimental pathology 1994;75(3):147-55.
1994: Hanson I M; Fletcher J M; Jordan T; Brown A; Taylor D; Adams R J; Punnett H H; van Heyningen V
Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly.
Nature genetics 1994;6(2):168-73.
1994: van Heyningen V
Immortalized cell lines. Their creation and use in gene mapping.
Methods in molecular biology (Clifton, N.J.) 1994;29():303-22.
1994: Miyagawa K; Kent J; Schedl A; van Heyningen V; Hastie N D
Wilms' tumour--a case of disrupted development.
Journal of cell science. Supplement 1994;18():1-5.
1993: Hanson I M; Seawright A; Hardman K; Hodgson S; Zaletayev D; Fekete G; van Heyningen V
PAX6 mutations in aniridia.
Human molecular genetics 1993;2(7):915-20.
1993: Bickmore W A; Longbottom D; Oghene K; Fletcher J M; van Heyningen V
Colocalization of the human CD59 gene to 11p13 with the MIC11 cell surface antigen.
Genomics 1993;17(1):129-35.
1993: Armstrong J F; Kaufman M H; van Heyningen V; Bard J B
Embryonic kidney rudiments grown in adult mice fail to mimic the Wilms' phenotype, but show strain-specific morphogenesis.
Experimental nephrology 1993;1(3):168-74.
1993: Little M H; Williamson K A; Mannens M; Kelsey A; Gosden C; Hastie N D; van Heyningen V
Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion.
Human molecular genetics 1993;2(3):259-64.
1993: Evans K L; Fantes J; Simpson C; Arveiler B; Muir W; Fletcher J; van Heyningen V; Steel K P; Brown K A; Brown S D
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I.
Human molecular genetics 1993;2(2):115-8.
1992: Fantes J A; Bickmore W A; Fletcher J M; Ballesta F; Hanson I M; van Heyningen V
Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.
American journal of human genetics 1992;51(6):1286-94.
1992: Hanson I M; Seawright A; van Heyningen V
The human BDNF gene maps between FSHB and HVBS1 at the boundary of 11p13-p14.
Genomics 1992;13(4):1331-3.
1992: Jordan T; Hanson I; Zaletayev D; Hodgson S; Prosser J; Seawright A; Hastie N; van Heyningen V
The human PAX6 gene is mutated in two patients with aniridia.
Nature genetics 1992;1(5):328-32.
1992: Bickmore W A; Oghene K; Little M H; Seawright A; van Heyningen V; Hastie N D
Modulation of DNA binding specificity by alternative splicing of the Wilms tumor wt1 gene transcript.
Science (New York, N.Y.) 1992;257(5067):235-7.
1992: Little M H; Prosser J; Condie A; Smith P J; Van Heyningen V; Hastie N D
Zinc finger point mutations within the WT1 gene in Wilms tumor patients.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(11):4791-5.
1992: Hill R; Van Heyningen V
Mouse mutations and human disorders are paired.
Trends in genetics : TIG 1992;8(4):119-20.
1992: Longbottom D; Sallenave J M; van Heyningen V
Subunit structure of calgranulins A and B obtained from sputum, plasma, granulocytes and cultured epithelial cells.
Biochimica et biophysica acta 1992;1120(2):215-22.
1992: Little M H; Dunn R; Byrne J A; Seawright A; Smith P J; Pritchard-Jones K; van Heyningen V; Hastie N D
Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours.
Oncogene 1992;7(4):635-41.
1992: Hill R E; Favor J; Hogan B L; Ton C C; Saunders G F; Hanson I M; Prosser J; Jordan T; Hastie N D; van Heyningen V
Mouse Small eye results from mutations in a paired-like homeobox-containing gene.
Nature 1992;355(6362):750.
1992: Van Heyningen V; Hastie N D
Wilms' tumour: reconciling genetics and biology.
Trends in genetics : TIG 1992;8(1):16-21.
1991: Ton C C; Hirvonen H; Miwa H; Weil M M; Monaghan P; Jordan T; van Heyningen V; Hastie N D; Meijers-Heijboer H; Drechsler M
Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region.
Cell 1991;67(6):1059-74.
1991: Hill R E; Favor J; Hogan B L; Ton C C; Saunders G F; Hanson I M; Prosser J; Jordan T; Hastie N D; van Heyningen V
Mouse small eye results from mutations in a paired-like homeobox-containing gene.
Nature 1991;354(6354):522-5.
1990: Dorin J R; Emslie E; van Heyningen V
Related calcium-binding proteins map to the same subregion of chromosome 1q and to an extended region of synteny on mouse chromosome 3.
Genomics 1990;8(3):420-6.
1990: van Heyningen V; Bickmore W A; Seawright A; Fletcher J M; Maule J; Fekete G; Gessler M; Bruns G A; Huerre-Jeanpierre C; Junien C
Role for the Wilms tumor gene in genital development?
Proceedings of the National Academy of Sciences of the United States of America 1990;87(14):5383-6.
1990: Porteous D J; Dorin J R; Wilkinson M M; Fletcher J M; Emslie E; van Heyningen V
SV40-mediated tumor selection and chromosome transfer to enrich for cystic fibrosis region.
Somatic cell and molecular genetics 1990;16(1):29-38.
1990: van Heyningen V; Dorin J
Possible role for two calcium-binding proteins of the S-100 family, co-expressed in granulocytes and certain epithelia.
Advances in experimental medicine and biology 1990;269():139-43.
1989: Porteous D J; Wilkinson M M; Fletcher J M; van Heyningen V
Human-mouse hybrids carrying fragments of single human chromosomes selected by tumor growth.
Genomics 1989;5(4):680-4.
1989: Bickmore W A; Porteous D J; Christie S; Seawright A; Fletcher J M; Maule J C; Couillin P; Junien C; Hastie N D; van Heyningen V
CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridia.
Genomics 1989;5(4):685-93.
1989: Bickmore W A; Maule J C; van Heyningen V; Porteous D J
Long-range structure of H-ras 1-selected transgenomes.
Somatic cell and molecular genetics 1989;15(3):229-35.
1989: Hastie N D; Bickmore W; Pritchard-Jones K; Porteous D J; van Heyningen V
Wilms tumour: a developmental anomaly.
Princess Takamatsu symposia 1989;20():145-50.
1988: Wilkinson M M; Busuttil A; Hayward C; Brock D J; Dorin J R; Van Heyningen V
Expression pattern of two related cystic fibrosis-associated calcium-binding proteins in normal and abnormal tissues.
Journal of cell science 1988;91 ( Pt 2)():221-30.
1988: Spurr N K; Gough A C; Gosden J; Rout D; Porteous D J; van Heyningen V; Docherty A J
Restriction fragment length polymorphism analysis and assignment of the metalloproteinases stromelysin and collagenase to the long arm of chromosome 11.
Genomics 1988;2(2):119-27.
1988: Seawright A; Fletcher J M; Fantes J A; Morrison H; Porteous D J; Li S S; Hastie N D; Van Heyningen V
Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids.
Somatic cell and molecular genetics 1988;14(1):21-30.
1988: Bickmore W; Christie S; van Heyningen V; Hastie N D; Porteous D J
Hitch-hiking from HRAS1 to the WAGR locus with CMGT markers.
Nucleic acids research 1988;16(1):51-60.
1988: Meehan R R; Gosden J R; Rout D; Hastie N D; Friedberg T; Adesnik M; Buckland R; van Heyningen V; Fletcher J; Spurr N K
Human cytochrome P-450 PB-1: a multigene family involved in mephenytoin and steroid oxidations that maps to chromosome 10.
American journal of human genetics 1988;42(1):26-37.
1988: Hastie N D; Porteous D J; Bickmore W; Maule J; van Heyningen V
Molecular analysis of the aniridia--Wilms' tumor syndrome.
Current topics in microbiology and immunology 1988;137():41-6.

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