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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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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

Volltextzugriff (PDF)

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

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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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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

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Autophagy: Mechanisms, regulation, and its role in tumorigenesis

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

2013

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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

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)

Frequent Progesterone Receptor Immunoreactivity in Tuberous Sclerosis-Associated Renal Angiomyolipomas

The Journal of urology, 1999-08, p.638

1999

Volltextzugriff (PDF)

Cell Cycle-regulated Phosphorylation of Hamartin, the Product of the Tuberous Sclerosis Complex 1 Gene, by Cyclin-dependent Kinase 1/Cyclin B

The Journal of biological chemistry, 2003-12, Vol.278 (51), p.51372-51379

2003

Volltextzugriff (PDF)

Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1

Annals of human genetics, 1995-01, Vol.59 (1), p.25-37

1995

Volltextzugriff (PDF)

Construction of a GT polymorphism map of human 9q

Genomics (San Diego, Calif.), 1992-02, Vol.12 (2), p.229-240

1992

Volltextzugriff (PDF)

A novel missense mutation in the GTPase activating protein homology region of TSC2 in two large families with tuberous sclerosis complex

Journal of medical genetics, 2001-05, Vol.38 (5), p.347-349

2001

Volltextzugriff (PDF)

Pulmonary manifestations in tuberous sclerosis complex

American journal of medical genetics. Part C, Seminars in medical genetics, 2018-09, Vol.178 (3), p.326-337

2018

Volltextzugriff (PDF)

Tuberous Sclerosis Complex Diagnostic Criteria Update: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference

Pediatric neurology, 2013-10, Vol.49 (4), p.243-254

2013

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

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

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

Mutational analysis of the tuberous sclerosis gene TSC2 in patients with 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

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

Frequent Progesterone Receptor Immunoreactivity in Tuberous Sclerosis-Associated Renal Angiomyolipomas

Cell Cycle-regulated Phosphorylation of Hamartin, the Product of the Tuberous Sclerosis Complex 1 Gene, by Cyclin-dependent Kinase 1/Cyclin B

Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1

Construction of a GT polymorphism map of human 9q

A novel missense mutation in the GTPase activating protein homology region of TSC2 in two large families with tuberous sclerosis complex

Pulmonary manifestations in tuberous sclerosis complex

Tuberous Sclerosis Complex Diagnostic Criteria Update: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference

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