Comprehensive genomic and phenotypic characterization of germline FH deletion in hereditary leiomyomatosis and renal cell carcinoma.

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Hereditary kidney cancer syndromes: Genetic disorders driven by alterations in metabolism and epigenome regulation.

P2860

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Comprehensive genomic and phenotypic characterization of germline FH deletion in hereditary leiomyomatosis and renal cell carcinoma.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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name

Comprehensive genomic and phen ...... osis and renal cell carcinoma.

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Comprehensive genomic and phen ...... osis and renal cell carcinoma.

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type

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Comprehensive genomic and phen ...... osis and renal cell carcinoma.

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Comprehensive genomic and phen ...... osis and renal cell carcinoma.

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Comprehensive genomic and phen ...... osis and renal cell carcinoma.

@en

Comprehensive genomic and phen ...... osis and renal cell carcinoma.

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P1476

Comprehensive genomic and phen ...... tosis and renal cell carcinoma

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P2093

Adam R Metwalli

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Cathy D Vocke

http://www.w3.org/2001/XMLSchema#string

Christopher J Ricketts

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James Peterson

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Lindsay A Middelton

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Maria J Merino

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Ramaprasad Srinivasan

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Youfeng Yang

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P2860

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

Metabolic reprogramming for producing energy and reducing power in fumarate hydratase null cells from hereditary leiomyomatosis renal cell carcinoma

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

Hereditary leiomyomatosis and renal cell carcinoma.

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

An antioxidant response phenotype shared between hereditary and sporadic type 2 papillary renal cell carcinoma.

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

Inherited susceptibility to uterine leiomyomas and renal cell cancer

Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer.

Identification of intragenic deletions and duplication in the FLCN gene in Birt-Hogg-Dubé syndrome.

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484-492

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scholarly article

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10.1002/GCC.22452

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W Marston Linehan

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2017-03-31T00:00:00Z

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28196407

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6637959

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Comprehensive genomic and phenotypic characterization of germline FH deletion in hereditary leiomyomatosis and renal cell carcinoma.

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P2860

P2860

Comprehensive genomic and phenotypic characterization of germline FH deletion in hereditary leiomyomatosis and renal cell carcinoma.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932