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Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes

The Journal of pathology, 2008-08, Vol.215 (4), p.377-387

2008

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Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux

Nature genetics, 1995-04, Vol.9 (4), p.358-364

1995

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Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

Nature (London), 1993-04, Vol.362 (6422), p.749-751

1993

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Mutation of PAX2 in two siblings with renal-coloboma syndrome

Human molecular genetics, 1995-11, Vol.4 (11), p.2183-2184

1995

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The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomalies

Journal of medical genetics, 1998-10, Vol.35 (10), p.806-812

1998

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Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations

American journal of human genetics, 1997-04, Vol.60 (4), p.869-878

1997

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Human insulin-like growth factor type I and type II receptors are not imprinted

Human molecular genetics, 1993-12, Vol.2 (12), p.2163-2165

1993

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Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux

Journal of medical genetics, 1998-04, Vol.35 (4), p.338-339

1998

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Genomic structure of the human PAX2 gene

Genomics (San Diego, Calif.), 1996-07, Vol.35 (1), p.258-261

1996

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Dinucleotide repeat polymorphism at the D11S860 locus

Nucleic acids research, 1992-03, Vol.20 (5), p.1161-1161

1992

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Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologies

Clinical genetics, 1997-05, Vol.51 (5), p.331-337

1997

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Mutation of the gene in a family with optic nerve colobomas, renal anomolies and vesicoureteral reflux

Nature genetics, 1996-05, Vol.13 (1), p.129-129

1996

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Analyzing tumor heterogeneity and driver genes in single myeloid leukemia cells with SBCapSeq

Nature biotechnology, 2016-09, Vol.34 (9), p.962-972

2016

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Gene and protein expression signature of endometrial glandular and stromal compartments during the window of implantation

Fertility and sterility, 2012-06, Vol.97 (6), p.1365-1373.e2

2012

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The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissues

PloS one, 2012-06, Vol.7 (6), p.e39574-e39574

2012

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Slow proliferation as a biological feature of colorectal cancer metastasis

British journal of cancer, 2009-09, Vol.101 (5), p.822-828

2009

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SunSmart Accreditation and Use of a Professional Policy Drafting Service: Both Positively and Independently Associated with High Sun Protective Hat Scores Derived from Primary School Policies

Journal of skin cancer, 2020, Vol.2020 (2020), p.1-7

2020

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Changes in awareness of cancer risk factors among adult New Zealanders (CAANZ): 2001 to 2015

Health education research, 2017-04, Vol.32 (2), p.153-162

2017

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133p53 isoform promotes tumour invasion and metastasis via interleukin-6 activation of JAK-STAT and RhoA-ROCK signalling

Nature communications, 2018-01, Vol.9 (1), p.254-13, Article 254

2018

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Characterization of the cyanobacteria and associated bacterial community from an ephemeral wetland in New Zealand

Journal of phycology, 2016-10, Vol.52 (5), p.761-773

2016

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Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice

Human molecular genetics, 2000-01, Vol.9 (1), p.1-11

2000

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Familial fibronectin glomerulopathy: analysis of chromosome 1q32 and uteroglobin gene loci in a large New Zealand family

Nephrology (Carlton, Vic.), 2001-10, Vol.6 (5), p.191-197

2001

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Primary renal hypoplasia in humans and mice with PAX2 mutations : evidence of increased apoptosis in fetal kidneys of Pax21Neu +/-mutant mice

Human molecular genetics, 2000, Vol.9 (1), p.1-11

2000

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Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescent

Clinical dysmorphology, 1999-10, Vol.8 (4), p.269-276

1999

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Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2 super(1Neu) +/- mutant mice

Human molecular genetics, 2000-01, Vol.9 (1), p.1-11

2000

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Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

Mutation of PAX2 in two siblings with renal-coloboma syndrome

The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomalies

Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations

Human insulin-like growth factor type I and type II receptors are not imprinted

Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux

Genomic structure of the human PAX2 gene

Dinucleotide repeat polymorphism at the D11S860 locus

Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologies

Mutation of the gene in a family with optic nerve colobomas, renal anomolies and vesicoureteral reflux

Analyzing tumor heterogeneity and driver genes in single myeloid leukemia cells with SBCapSeq

Gene and protein expression signature of endometrial glandular and stromal compartments during the window of implantation

The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissues

Slow proliferation as a biological feature of colorectal cancer metastasis

SunSmart Accreditation and Use of a Professional Policy Drafting Service: Both Positively and Independently Associated with High Sun Protective Hat Scores Derived from Primary School Policies

Changes in awareness of cancer risk factors among adult New Zealanders (CAANZ): 2001 to 2015

133p53 isoform promotes tumour invasion and metastasis via interleukin-6 activation of JAK-STAT and RhoA-ROCK signalling

Characterization of the cyanobacteria and associated bacterial community from an ephemeral wetland in New Zealand

Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice

Familial fibronectin glomerulopathy: analysis of chromosome 1q32 and uteroglobin gene loci in a large New Zealand family

Primary renal hypoplasia in humans and mice with PAX2 mutations : evidence of increased apoptosis in fetal kidneys of Pax21Neu +/-mutant mice

Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescent

Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2 super(1Neu) +/- mutant mice

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