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Canonical WNT signalling determines lineage specificity in Wilms tumour

Oncogene, 2009-02, Vol.28 (8), p.1063-1075

2009

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Reduced expression of a gene proliferation signature is associated with enhanced malignancy in colon cancer

British journal of cancer, 2008-09, Vol.99 (6), p.966-973

2008

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Genome wide expression profiling identifies genes associated with colorectal liver metastasis

Oncology reports, 2007-06, Vol.17 (6), p.1541-1549

2007

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Imprinting, expression, and localisation of DLK1 in Wilms tumours

Journal of clinical pathology, 2005-02, Vol.58 (2), p.145-150

2005

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Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?

Journal of medical genetics, 1998-01, Vol.35 (1), p.45-48

1998

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A necropsy case of Denys-Drash syndrome with a WT1 mutation in exon 7

Journal of medical genetics, 2002-08, Vol.39 (8), p.e48-48

2002

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Long-term peritoneal dialysis is a risk factor of sclerosing encapsulating peritonitis for children

Peritoneal dialysis international, 2000-07, Vol.20 (4), p.445-451

2000

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WTX mutations can occur both early and late in the pathogenesis of Wilms tumour

Journal of medical genetics, 2010-11, Vol.47 (11), p.791-794

2010

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Constitutional WT1 mutations correlate with clinical features in children with progressive nephropathy

Journal of medical genetics, 2000-09, Vol.37 (9), p.698-701

2000

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A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors

Journal of biochemistry (Tokyo), 2000-11, Vol.128 (5), p.847-853

2000

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Epigenetic differences between Wilms' tumours in white and east-Asian children

The Lancet (British edition), 2004-02, Vol.363 (9407), p.446-451

2004

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Translation and Validation of the Mongolian Version of the Childbirth Experience Questionnaire

Journal of patient experience, 2021-11, Vol.8, p.237437352110606-23743735211060636

2021

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Wilms' tumors and malformation complexes

Nihon rinshō, 2000-07, Vol.58 (7), p.1419

2000

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Acinic cell carcinoma in an African pygmy hedgehog (Atelerix albiventris)

Veterinary clinical pathology, 2004-03, Vol.33 (1), p.39-42

2004

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In Situ Synthesis of Field-responsive Nanocrystalline BaTiO3 Particles Modified with Functional Organics

Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology, 2005-12, Vol.7 (6), p.633-640

2005

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Expression of mitogen-activated protein kinases in human renal dysplasia

Kidney international, 2002-03, Vol.61 (3), p.899-906

2002

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Myogenesis in Wilms' tumors is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathway

Pediatric and developmental pathology, 2004-03, Vol.7 (2), p.125-137

2004

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Novel electro-rheological nanocrystalline dielectric particles modified with or embedded in organics

Journal of the European Ceramic Society, 2004, Vol.24 (6), p.1911-1917

2004

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High frequency of inactivation of the imprinted H19 gene in “sporadic” hepatoblastoma

International journal of cancer, 1999-08, Vol.82 (4), p.490-497

1999

Volltextzugriff (PDF)

Embryonal hyperplasia of Bowman's capsular epithelium in patients with WT1 mutations

Pediatric nephrology (Berlin, West), 2003, Vol.18 (1), p.9-13

2003

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Beckwith-Wiedemann syndrome-associated hepatoblastoma: wnt signal activation occurs later in tumorigenesis in patients with 11p15.5 uniparental disomy

Pediatric and developmental pathology, 2003-07, Vol.6 (4), p.299-306

2003

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Correct usage of "loss of imprinting"

American journal of medical genetics. Part A, 2005-11, Vol.138A (4), p.412-412

2005

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Insulin-like growth factor-II imprinting in cancer

The Lancet (British edition), 2002-06, Vol.359 (9323), p.2050-2051

2002

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A novel WT1 gene mutation associated with wilms' tumor and congenital male genitourinary malformation

Pediatric research, 2001-09, Vol.50 (3), p.337-344

2001

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Myogenesis in Wilms' tumor is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathway

Pediatric and developmental pathology, 2004-11, Vol.7 (5), p.549

2004

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Canonical WNT signalling determines lineage specificity in Wilms tumour

Reduced expression of a gene proliferation signature is associated with enhanced malignancy in colon cancer

Genome wide expression profiling identifies genes associated with colorectal liver metastasis

Imprinting, expression, and localisation of DLK1 in Wilms tumours

Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?

A necropsy case of Denys-Drash syndrome with a WT1 mutation in exon 7

Long-term peritoneal dialysis is a risk factor of sclerosing encapsulating peritonitis for children

WTX mutations can occur both early and late in the pathogenesis of Wilms tumour

Constitutional WT1 mutations correlate with clinical features in children with progressive nephropathy

A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors

Epigenetic differences between Wilms' tumours in white and east-Asian children

Translation and Validation of the Mongolian Version of the Childbirth Experience Questionnaire

Wilms' tumors and malformation complexes

Acinic cell carcinoma in an African pygmy hedgehog (Atelerix albiventris)

In Situ Synthesis of Field-responsive Nanocrystalline BaTiO3 Particles Modified with Functional Organics

Expression of mitogen-activated protein kinases in human renal dysplasia

Myogenesis in Wilms' tumors is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathway

Novel electro-rheological nanocrystalline dielectric particles modified with or embedded in organics

High frequency of inactivation of the imprinted H19 gene in “sporadic” hepatoblastoma

Embryonal hyperplasia of Bowman's capsular epithelium in patients with WT1 mutations

Beckwith-Wiedemann syndrome-associated hepatoblastoma: wnt signal activation occurs later in tumorigenesis in patients with 11p15.5 uniparental disomy

Correct usage of "loss of imprinting"

Insulin-like growth factor-II imprinting in cancer

A novel WT1 gene mutation associated with wilms' tumor and congenital male genitourinary malformation

Myogenesis in Wilms' tumor is associated with mutations of the WT1 gene and activation of Bcl-2 and the Wnt signaling pathway

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