Establishment and characterization of BHD-F59RSVT, an immortalized cell line derived from a renal cell carcinoma in a patient with Birt-Hogg-Dubé syndrome. (Q38725502)

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scientific article published on 19 December 2016

Language	Label	Description	Also known as
English	Establishment and characterization of BHD-F59RSVT, an immortalized cell line derived from a renal cell carcinoma in a patient with Birt-Hogg-Dubé syndrome.	scientific article published on 19 December 2016

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27991910%20AND%20SRC:MED&resulttype=core&format=json

30 March 2020

Establishment and characterization of BHD-F59RSVT, an immortalized cell line derived from a renal cell carcinoma in a patient with Birt-Hogg-Dubé syndrome (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27991910%20AND%20SRC:MED&resulttype=core&format=json

30 March 2020

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renal cell carcinoma

1 reference

based on heuristic

inferred from title

3

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30 March 2020

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Mitsuko Furuya

1

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30 March 2020

Hisashi Hasumi

2

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30 March 2020

Reiko Tanaka

4

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30 March 2020

Yasuhiro Iribe

5

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30 March 2020

Takahiro Onishi

6

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30 March 2020

Yoji Nagashima

7

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30 March 2020

Yukio Nakatani

8

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30 March 2020

Yasuhiro Isono

9

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30 March 2020

Masahiro Yao

10

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30 March 2020

publication date

19 December 2016

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30 March 2020

Laboratory Investigation

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30 March 2020

97

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30 March 2020

3

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30 March 2020

343-351

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30 March 2020

describes a project that uses

0 references

Birt-Hogg-Dubé syndrome: diagnosis and management

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Identification and characterization of a novel folliculin-interacting protein FNIP2

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Interaction of folliculin (Birt-Hogg-Dubé gene product) with a novel Fnip1-like (FnipL/Fnip2) protein

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

The International Society of Urological Pathology (ISUP) Vancouver Classification of Renal Neoplasia

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Kidney-targeted Birt-Hogg-Dube gene inactivation in a mouse model: Erk1/2 and Akt-mTOR activation, cell hyperproliferation, and polycystic kidneys

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Deficiency of FLCN in mouse kidney led to development of polycystic kidneys and renal neoplasia

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Inactivation of the FLCN tumor suppressor gene induces TFE3 transcriptional activity by increasing its nuclear localization

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Absence of the Birt-Hogg-Dubé gene product is associated with increased hypoxia-inducible factor transcriptional activity and a loss of metabolic flexibility

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

The UOK 257 cell line: a novel model for studies of the human Birt-Hogg-Dubé gene pathway

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Renal cell tumour characteristics in patients with the Birt-Hogg-Dubé cancer susceptibility syndrome: a retrospective, multicentre study

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Immunohistochemical characterization of renal tumors in patients with Birt-Hogg-Dubé syndrome

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Clinical and genetic spectrum of Birt-Hogg-Dube syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting feature

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Pulmonary cysts of Birt-Hogg-Dubé syndrome: a clinicopathologic and immunohistochemical study of 9 families.

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Genome-Wide Uniparental Disomy and Copy Number Variations in Renal Cell Carcinomas Associated with Birt-Hogg-Dubé Syndrome

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Fluorescent and chromogenic in situ hybridization of CEN17q as a potent useful diagnostic marker for Birt-Hogg-Dubé syndrome-associated chromophobe renal cell carcinomas.

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

Renal Tumors in the Birt-Hogg-Dubé Syndrome

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

7 January 2021

based on heuristic

inferred from DOI database lookup

Eosinophilic and classic chromophobe renal cell carcinomas have similar frequent losses of multiple chromosomes from among chromosomes 1, 2, 6, 10, and 17, and this pattern of genetic abnormality is not present in renal oncocytoma

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.2016.137

7 January 2021

based on heuristic

inferred from DOI database lookup

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