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The role of the Birt-Hogg-Dubé protein in mTOR activation and renal tumorigenesis

Oncogene, 2009-04, Vol.28 (13), p.1594-1604

2009

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Differential requirement of CAAX-mediated posttranslational processing for Rheb localization and signaling

Oncogene, 2010-01, Vol.29 (3), p.380-391

2010

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A tissue-bioengineering strategy for modeling rare human kidney diseases in vivo

Nature communications, 2021-11, Vol.12 (1), p.6496-6496, Article 6496

2021

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Loss of the Birt-Hogg-Dubé tumor suppressor results in apoptotic resistance due to aberrant TGFβ-mediated transcription

Oncogene, 2011-06, Vol.30 (22), p.2534-2546

2011

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Tuberous sclerosis-associated renal cell carcinoma. Clinical, pathological, and genetic features

The American journal of pathology, 1996-10, Vol.149 (4), p.1201-1208

1996

Volltextzugriff (PDF)

Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions

American journal of human genetics, 1996-08, Vol.59 (2), p.400-406

1996

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Tuberous sclerosis complex: linking growth and energy signaling pathways with human disease

Oncogene, 2005-11, Vol.24 (50), p.7475-7481

2005

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New developments in the neurobiology of the tuberous sclerosis complex

Neurology, 1999-10, Vol.53 (7), p.1384

1999

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Hamartin, the product of the tuberous sclerosis 1 (TSC1) gene, interacts with tuberin and appears to be localized to cytoplasmic vesicles

Cancer research (Chicago, Ill.), 1998-11, Vol.58 (21), p.4766-4770

1998

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Pulmonary lymphangioleiomyomatosis in a man

American journal of respiratory and critical care medicine, 2000-08, Vol.162 (2), p.749-752

2000

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Apparent renal cell carcinomas in tuberous sclerosis are heterogeneous : The identification of malignant epithelioid angiomyolipoma

The American journal of surgical pathology, 1998-02, Vol.22 (2), p.180-187

1998

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Evidence That Lymphangiomyomatosis Is Caused by TSC2 Mutations: Chromosome 16p13 Loss of Heterozygosity in Angiomyolipomas and Lymph Nodes from Women with Lymphangiomyomatosis

American journal of human genetics, 1998-04, Vol.62 (4), p.810-815

1998

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Loss of tuberin in both subependymal giant cell astrocytomas and angiomyolipomas supports a two-hit model for the pathogenesis of tuberous sclerosis tumors

The American journal of pathology, 1997-12, Vol.151 (6), p.1639-1647

1997

Volltextzugriff (PDF)

Frequent Estrogen and Progesterone Receptor Immunoreactivity in Renal Angiomyolipomas From Women With Pulmonary Lymphangioleiomyomatosis

Chest, 2000-01, Vol.117 (1), p.25-30

2000

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Mutational analysis of the tuberous sclerosis gene TSC2 in patients with pulmonary lymphangioleiomyomatosis

Journal of medical genetics, 2000, Vol.37 (1), p.55-57

2000

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

Cancer, 1998-11, Vol.83 (10), p.2208-2216

1998

Volltextzugriff (PDF)

Mutations in the Tuberous Sclerosis Complex Gene TSC2 Are a Cause of Sporadic Pulmonary Lymphangioleiomyomatosis

Proceedings of the National Academy of Sciences - PNAS, 2000-05, Vol.97 (11), p.6085-6090

2000

Volltextzugriff (PDF)

The spectrum of mutations in TSC1 and TSC2 in women with tuberous sclerosis and lymphangiomyomatosis

American journal of respiratory and critical care medicine, 2001-01, Vol.163 (1), p.253-258

2001

Volltextzugriff (PDF)

Autophagy: Mechanisms, regulation, and its role in tumorigenesis

Biochemistry (Moscow), 2013-04, Vol.78 (4), p.355-367

2013

Volltextzugriff (PDF)

Kinase mTOR: Regulation and role in maintenance of cellular homeostasis, tumor development, and aging

Biochemistry (Moscow), 2014-02, Vol.79 (2), p.88-101

2014

Volltextzugriff (PDF)

Estradiol promotes pentose phosphate pathway addiction and cell survival via reactivation of Akt in mTORC1 hyperactive cells

Cell death & disease, 2014-05, Vol.5 (5), p.e1231-e1231

2014

Volltextzugriff (PDF)

Metastasis of benign tumor cells in tuberous sclerosis complex

Genes chromosomes & cancer, 2003-12, Vol.38 (4), p.376-381

Henske, Elizabeth Petri

2003

Volltextzugriff (PDF)

Chromosome 16 Loss of Heterozygosity in Tuberous Sclerosis and Sporadic Lymphangiomyomatosis

American journal of respiratory and critical care medicine, 2001-10, Vol.164 (8), p.1537-1540

2001

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Aggressive variants of chromophobe renal cell carcinoma

Cancer, 1996-10, Vol.78 (8), p.1756-1761

1996

Volltextzugriff (PDF)

Tuberin, the tuberous sclerosis complex 2 tumor suppressor gene product, regulates Rho activation, cell adhesion and migration

Oncogene, 2002-12, Vol.21 (55), p.8470-8476

2002

Volltextzugriff (PDF)

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The role of the Birt-Hogg-Dubé protein in mTOR activation and renal tumorigenesis

Differential requirement of CAAX-mediated posttranslational processing for Rheb localization and signaling

A tissue-bioengineering strategy for modeling rare human kidney diseases in vivo

Loss of the Birt-Hogg-Dubé tumor suppressor results in apoptotic resistance due to aberrant TGFβ-mediated transcription

Tuberous sclerosis-associated renal cell carcinoma. Clinical, pathological, and genetic features

Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions

Tuberous sclerosis complex: linking growth and energy signaling pathways with human disease

New developments in the neurobiology of the tuberous sclerosis complex

Hamartin, the product of the tuberous sclerosis 1 (TSC1) gene, interacts with tuberin and appears to be localized to cytoplasmic vesicles

Pulmonary lymphangioleiomyomatosis in a man

Apparent renal cell carcinomas in tuberous sclerosis are heterogeneous : The identification of malignant epithelioid angiomyolipoma

Evidence That Lymphangiomyomatosis Is Caused by TSC2 Mutations: Chromosome 16p13 Loss of Heterozygosity in Angiomyolipomas and Lymph Nodes from Women with Lymphangiomyomatosis

Loss of tuberin in both subependymal giant cell astrocytomas and angiomyolipomas supports a two-hit model for the pathogenesis of tuberous sclerosis tumors

Frequent Estrogen and Progesterone Receptor Immunoreactivity in Renal Angiomyolipomas From Women With Pulmonary Lymphangioleiomyomatosis

Mutational analysis of the tuberous sclerosis gene TSC2 in patients with pulmonary lymphangioleiomyomatosis

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

Mutations in the Tuberous Sclerosis Complex Gene TSC2 Are a Cause of Sporadic Pulmonary Lymphangioleiomyomatosis

The spectrum of mutations in TSC1 and TSC2 in women with tuberous sclerosis and lymphangiomyomatosis

Autophagy: Mechanisms, regulation, and its role in tumorigenesis

Kinase mTOR: Regulation and role in maintenance of cellular homeostasis, tumor development, and aging

Estradiol promotes pentose phosphate pathway addiction and cell survival via reactivation of Akt in mTORC1 hyperactive cells

Metastasis of benign tumor cells in tuberous sclerosis complex

Chromosome 16 Loss of Heterozygosity in Tuberous Sclerosis and Sporadic Lymphangiomyomatosis

Aggressive variants of chromophobe renal cell carcinoma

Tuberin, the tuberous sclerosis complex 2 tumor suppressor gene product, regulates Rho activation, cell adhesion and migration

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