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TUBEROUS SCLEROSIS 2 (disorder)
Known as:
TSC2
, TUBEROUS SCLEROSIS 2
Tuberous sclerosis mapped to chromosome 16p13.3 (TSC2 gene).
National Institutes of Health
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Related topics
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31 relations
Attention Deficit Disorder
Autistic Disorder
Autosomal dominant inheritance
Cardiac rhabdomyoma
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Broader (1)
Tuberous Sclerosis
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
An Australian tuberous sclerosis cohort: Are surveillance guidelines being met?
M. Chopra
,
J. Lawson
,
+8 authors
D. Mowat
Journal of Paediatrics and Child Health
2011
Corpus ID: 41308118
Aim: This study aims to describe the phenotypic and genotypic characteristics of 45 Australian patients with tuberous sclerosis…
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2009
2009
Renal and liver tumors in Tsc2+/− mice, a model of tuberous sclerosis complex, do not respond to treatment with atorvastatin, a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor
G. Finlay
,
Amy J. Malhowski
,
K. Polizzi
,
Izabela Malinowska-Kołodziej
,
D. Kwiatkowski
Molecular Cancer Therapeutics
2009
Corpus ID: 19172899
Inactivating mutations of the tumor suppressor gene TSC2 are associated with tumorigenesis in tuberous sclerosis complex (TSC…
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2009
2009
Growth Factors , Cytokines , Cell Cycle Molecules The Methylation of the TSC 2 Promoter Underlies the Abnormal Growth of TSC 2 Angiomyolipoma-Derived Smooth Muscle Cells
E. Lesma
,
S. Sirchia
,
+6 authors
A. Gorio
2009
Corpus ID: 37403122
From the Laboratory of Pharmacology,* the Medical Genetic Unit, the Division of Pathology, the Disabled Advanced Medical…
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2008
2008
Toponomics Analysis of Functional Interactions of the Ubiquitin Ligase PAM (Protein Associated with Myc) during Spinal Nociceptive Processing*S
Sandra C. Pierre
,
C. Mäurer
,
+6 authors
K. Scholich
Molecular & Cellular Proteomics
2008
Corpus ID: 18389100
Protein associated with Myc (PAM) is a giant E3 ubiquitin ligase of 510 kDa. Although the role of PAM during neuronal development…
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2005
2005
Distinct Allelic Variants of TSC1 and TSC2 in Epilepsy-Associated Cortical Malformations Without Balloon Cells
M. Majores
,
I. Blümcke
,
+9 authors
A. Becker
Journal of Neuropathology and Experimental…
2005
Corpus ID: 17991472
Epilepsy-associated malformations of cortical development (MCDs) comprise a variety of dysplastic and neoplastic lesions of yet…
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Review
2005
Review
2005
Clinical and molecular insights into lymphangioleiomyomatosis.
W. Steagall
,
A. Taveira-DaSilva
,
J. Moss
Sarcoidosis Vasculities and Diffuse Lung Diseases
2005
Corpus ID: 32004756
Lymphangioleiomyomatosis (LAM) is a rare disease of women that is characterized by a proliferation of abnormal smooth muscle-like…
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2001
2001
Cells derived from tuberous sclerosis show a prolonged S phase of the cell cycle and increased apoptosis
M. Wataya-Kaneda
,
Y. Kaneda
,
+5 authors
K. Yoshikawa
Archives of Dermatological Research
2001
Corpus ID: 2100292
Abstract Tuberous sclerosis complex (TSC) is a multisystemic disorder characterized by systemic hamartomas. Although the disease…
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1998
1998
Biallelic mutations of the Tsc2 gene in chemically induced rat renal cell carcinoma
N. Satake
,
S. Urakami
,
Y. Hirayama
,
K. Izumi
,
O. Hino
International Journal of Cancer
1998
Corpus ID: 26777718
A number of cancer genes have been identified by the study of hereditary human cancers and shown to be involved in sporadic…
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1995
1995
Molecular genetic basis of renal carcinogenesis in the Eker rat model of tuberous sclerosis(Tsc2)
O. Hino
,
E. Kobayashi
,
+5 authors
H. Mitani
Molecular Carcinogenesis
1995
Corpus ID: 19948411
We have recently identified on rat chromosome 10q a germline mutation in the tuberous sclerosis gene(Tsc2), the gene predisposing…
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Highly Cited
1994
Highly Cited
1994
The predisposing gene of the Eker rat inherited cancer syndrome is tightly linked to the tuberous sclerosis (TSC2) gene.
Okio Hino
,
Toshiyuki Kobayashi
,
+4 authors
Y. Hirayama
Biochemical and Biophysical Research…
1994
Corpus ID: 8912104
The Eker rat is a promising animal model of cancer predisposition syndromes. In this study, using 129 backcross animals, we have…
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