Familial and hereditary renal cancer syndromes (Q37320995)

19 August 2017

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title

Familial and hereditary renal cancer syndromes (English)

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19 August 2017

Jonathan A Coleman

1

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publication date

1 November 2008

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Urologic Clinics of North America

19 August 2017

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19 August 2017

35

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19 August 2017

4

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19 August 2017

563-72; v

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Familial Renal Carcinoma: Clinical Evaluation, Clinical Subtypes and Risk of Renal Carcinoma Development

19 August 2017

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https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

von Hippel-Lindau disease

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Ethical and legal aspects of cancer genetic testing

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

HIF overexpression correlates with biallelic loss of fumarate hydratase in renal cancer: novel role of fumarate in regulation of HIF stability

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

The von Hippel-Lindau tumor-suppressor gene product forms a stable complex with human CUL-2, a member of the Cdc53 family of proteins

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Regulation of hypoxia-inducible mRNAs by the von Hippel-Lindau tumor suppressor protein requires binding to complexes containing elongins B/C and Cul2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Pseudohypoxic pathways in renal cell carcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Genetic basis of cancer of the kidney: disease-specific approaches to therapy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

The von Hippel-Lindau tumor suppressor protein and clear cell renal carcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Genotype-phenotype correlations in von Hippel-Lindau disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Genotype-phenotype correlation in von Hippel-Lindau disease with retinal angiomatosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Solid renal tumor severity in von Hippel Lindau disease is related to germline deletion length and location.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Clinical characterization of retinal capillary hemangioblastomas in a large population of patients with von Hippel-Lindau disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

The relationship between renal tumor size and metastases in patients with von Hippel-Lindau disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Salvage partial nephrectomy for hereditary renal cancer: feasibility and outcomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Radio frequency ablation of small renal tumors:: intermediate results

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Radiofrequency-assisted laparoscopic partial nephrectomy: clinical and histologic results

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Robotic partial nephrectomy for complex renal tumors: surgical technique

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: a role for laparoscopic and cortical-sparing surgery

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Partial adrenalectomy: the National Cancer Institute experience

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Laparoscopic adrenal surgery for recurrent tumours in patients with hereditary phaeochromocytoma.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Hereditary papillary renal carcinoma type I

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

MET expression in sporadic renal cell carcinomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Duplication and overexpression of the mutant allele of the MET proto-oncogene in multiple hereditary papillary renal cell tumours

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Original Articles: Kidney Cancer: Hereditary Papillary Renal Cell Carcinoma: Clinical Studies in 10 Families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Perifollicular fibromatosis cutis with polyps of the colon?a cutaneo-intestinal syndrome sui generis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Hereditary Multiple Fibrofolliculomas With Trichodiscomas and Acrochordons

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Novel mutations in the BHD gene and absence of loss of heterozygosity in fibrofolliculomas of Birt-Hogg-Dubé patients.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Localized Birt-Hogg-Dubé syndrome with prominent perivascular fibromas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Acrochordons are not a component of the Birt-Hogg-Dubé syndrome: does this syndrome exist? Case reports and review of the literature

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Evaluation and management of renal tumors in the Birt-Hogg-Dubé syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Lung cysts, spontaneous pneumothorax, and genetic associations in 89 families with Birt-Hogg-Dubé syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Birt-Hogg-Dubé syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Expression of Birt-Hogg-Dubé gene mRNA in normal and neoplastic human tissues

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Birt-Hogg-Dubé syndrome: A review of the literature and the differential diagnosis of firm facial papules

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reports

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Renal Tumors in the Birt-Hogg-Dubé Syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Clinical and genetic studies of Birt-Hogg-Dubé syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Birt-Hogg-Dubé syndrome: clinical and genetic studies of 20 families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Hereditary leiomyomatosis and renal cell cancer (HLRCC).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

The morphologic spectrum of kidney tumors in hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Missense mutations in fumarate hydratase in multiple cutaneous and uterine leiomyomatosis and renal cell cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

No evidence for epigenetic inactivation of fumarate hydratase in leiomyomas and leiomyosarcomas

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Genetic heterogeneity among uterine leiomyomata: insights into malignant progression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Accumulation of Krebs cycle intermediates and over-expression of HIF1alpha in tumours which result from germline FH and SDH mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Targeted inactivation of fh1 causes proliferative renal cyst development and activation of the hypoxia pathway

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Conventional renal cancer in a patient with fumarate hydratase mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

HIF and fumarate hydratase in renal cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Inherited susceptibility to uterine leiomyomas and renal cell cancer

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Hereditary leiomyomatosis and renal cell cancer: an unusual and aggressive form of hereditary renal carcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Hereditary leiomyomatosis and renal cell cancer: a syndrome associated with an aggressive form of inherited renal cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Mechanisms of disease: hereditary leiomyomatosis and renal cell cancer--a distinct form of hereditary kidney cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Malignant tumors of the kidney, brain, and soft tissues in children and young adults with the tuberous sclerosis complex.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Functional characterisation of the TSC1-TSC2 complex to assess multiple TSC2 variants identified in single families affected by tuberous sclerosis complex

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Physical mapping within the tuberous sclerosis linkage group in region 9q32-q34.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Two loci for tuberous sclerosis: one on 9q34 and one on 16p13.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Refined localization of TSC1 by combined analysis of 9q34 and 16p13 data in 14 tuberous sclerosis families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype--phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Renal manifestations of tuberous sclerosis complex: Incidence, prognosis, and predictive factors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

Hereditary papillary renal cell carcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.UCL.2008.07.014

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.UCL.2008.07.014

1 reference

19 August 2017

1 reference

PubMed ID

18992610