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Blood and lymphatic systems are segregated by the FLCN tumor suppressor

Nature communications, 2020-12, Vol.11 (1), p.6314-6314, Article 6314

2020

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Birt-Hogg-Dubé syndrome: Clinical and molecular aspects of recently identified kidney cancer syndrome

International journal of urology, 2016-03, Vol.23 (3), p.204-210

2016

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An open-label, prospective, single-arm study of switching from infliximab to cyclosporine for refractory uveitis in patients with Behçet’s disease in long-term remission

Japanese journal of ophthalmology, 2021-11, Vol.65 (6), p.843-848

2021

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HLA-DRB104:05 is involved in the development of Vogt–Koyanagi–Harada disease-like immune-related adverse events in patients receiving immune checkpoint inhibitors

Scientific reports, 2023-08, Vol.13 (1), p.13580-13580, Article 13580

2023

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Folliculin-interacting proteins Fnip1 and Fnip2 play critical roles in kidney tumor suppression in cooperation with Flcn

Proceedings of the National Academy of Sciences - PNAS, 2015-03, Vol.112 (13), p.E1624-E1631

2015

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Homozygous Loss of BHD Causes Early Embryonic Lethality and Kidney Tumor Development with Activation of mTORC1 and mTORC2

Proceedings of the National Academy of Sciences - PNAS, 2009-11, Vol.106 (44), p.18722-18727

2009

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Regulation of mitochondrial oxidative metabolism by tumor suppressor FLCN

JNCI : Journal of the National Cancer Institute, 2012-11, Vol.104 (22), p.1750-1764

2012

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Identification and characterization of a novel folliculin-interacting protein FNIP2

Gene, 2008-05, Vol.415 (1), p.60-67

2008

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Folliculin (Flcn) inactivation leads to murine cardiac hypertrophy through mTORC1 deregulation

Human molecular genetics, 2014-11, Vol.23 (21), p.5706-5719

2014

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Loss of Folliculin Disrupts Hematopoietic Stem Cell Quiescence and Homeostasis Resulting in Bone Marrow Failure

Stem cells (Dayton, Ohio), 2016-04, Vol.34 (4), p.1068-1082

2016

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The folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dubé syndrome is required for murine B-cell development

Blood, 2012-08, Vol.120 (6), p.1254-1261

2012

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Abstract 3527: Clarification of the molecular mechanism for cancer development in Xp11.2 translocation renal cell carcinoma

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.3527-3527

2017

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BHD-associated kidney cancer exhibits unique molecular characteristics and a wide variety of variants in chromatin remodeling genes

Human molecular genetics, 2018-08, Vol.27 (15), p.2712-2724

2018

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H255Y and K508R missense mutations in tumour suppressor folliculin (FLCN) promote kidney cell proliferation

Human molecular genetics, 2017-01, Vol.26 (2), p.354-366

2017

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Abstract LB-113: Genome-wide mapping of TFE3-fusion target genes

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.LB-113-LB-113

2013

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Regulation of Mitochondria Oxidative Metabolism by Tumor Suppressor FLCN

JNCI : Journal of the National Cancer Institute, 2012-11, Vol.104 (22), p.1750

2012

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Regulation of Mitochondrial Oxidative Metabolism byTumor Suppressor FLCN

JNCI : Journal of the National Cancer Institute, 2012, Vol.104 (22), p.1750-1764

2012

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Polymorphism of IFN-gamma gene and Vogt-Koyanagi-Harada disease

Molecular vision, 2007-12, Vol.13, p.2334-2338

2007

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Tyrosinase gene family and Vogt-Koyanagi-Harada disease in Japanese patients

Molecular vision, 2006-12, Vol.12, p.1601-1605

2006

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Analysis of single nucleotide polymorphisms at 13 loci within the transforming growth factor-induced factor gene shows no association with high myopia in Japanese subjects

Immunogenetics (New York), 2006-12, Vol.58 (12), p.947-953

2006

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Guidelines for the Diagnosis of Ocular Sarcoidosis

Ocular immunology and inflammation, 2008-05, Vol.16 (3), p.77-81

2008

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Case of neurosarcoidosis with rapid visual field defect progression

Nippon Ganka Gakkai zasshi, 2007-09, Vol.111 (9), p.728

2007

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Investigation of the Appropriate Use of Antiseptics with Cotton Swabs

Japanese Journal of Hospital Pharmacy, 2000/12/10, Vol.26(6), pp.647-651

2000

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Investigation of the Appropriate Use of Antiseptics with Cotton Swabs

Byōin yakugaku, 2000, Vol.26 (6), p.647-651

2000

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Blood and lymphatic systems are segregated by the FLCN tumor suppressor

Birt-Hogg-Dubé syndrome: Clinical and molecular aspects of recently identified kidney cancer syndrome

An open-label, prospective, single-arm study of switching from infliximab to cyclosporine for refractory uveitis in patients with Behçet’s disease in long-term remission

HLA-DRB104:05 is involved in the development of Vogt–Koyanagi–Harada disease-like immune-related adverse events in patients receiving immune checkpoint inhibitors

Folliculin-interacting proteins Fnip1 and Fnip2 play critical roles in kidney tumor suppression in cooperation with Flcn

TFE3 Xp11.2 Translocation Renal Cell Carcinoma Mouse Model Reveals Novel Therapeutic Targets and Identifies GPNMB as a Diagnostic Marker for Human Disease

Homozygous Loss of BHD Causes Early Embryonic Lethality and Kidney Tumor Development with Activation of mTORC1 and mTORC2

Regulation of mitochondrial oxidative metabolism by tumor suppressor FLCN

Identification and characterization of a novel folliculin-interacting protein FNIP2

Folliculin (Flcn) inactivation leads to murine cardiac hypertrophy through mTORC1 deregulation

Loss of Folliculin Disrupts Hematopoietic Stem Cell Quiescence and Homeostasis Resulting in Bone Marrow Failure

The folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dubé syndrome is required for murine B-cell development

Abstract 3527: Clarification of the molecular mechanism for cancer development in Xp11.2 translocation renal cell carcinoma

BHD-associated kidney cancer exhibits unique molecular characteristics and a wide variety of variants in chromatin remodeling genes

H255Y and K508R missense mutations in tumour suppressor folliculin (FLCN) promote kidney cell proliferation

Abstract LB-113: Genome-wide mapping of TFE3-fusion target genes

Regulation of Mitochondria Oxidative Metabolism by Tumor Suppressor FLCN

Regulation of Mitochondrial Oxidative Metabolism byTumor Suppressor FLCN

Polymorphism of IFN-gamma gene and Vogt-Koyanagi-Harada disease

Tyrosinase gene family and Vogt-Koyanagi-Harada disease in Japanese patients

Analysis of single nucleotide polymorphisms at 13 loci within the transforming growth factor-induced factor gene shows no association with high myopia in Japanese subjects

Guidelines for the Diagnosis of Ocular Sarcoidosis

Case of neurosarcoidosis with rapid visual field defect progression

Investigation of the Appropriate Use of Antiseptics with Cotton Swabs

Investigation of the Appropriate Use of Antiseptics with Cotton Swabs

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