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Tuberous sclerosis causing mutants of the TSC2 gene product affect proliferation and p27 expression
ONCOGENE
Multifocal micronodular pneumocyte hyperplasia and lymphangioleiomyomatosis in tuberous sclerosis with a TSC2 gene
MODERN PATHOLOGY
Hamartin and tuberin expression in human tissues
MODERN PATHOLOGY
Carcinogenicity of a nephrotoxic metabolite of the "nongenotoxic" carcinogen hydroquinone
CHEMICAL RESEARCH IN TOXICOLOGY
Neuropathology of tuberous sclerosis
BRAIN & DEVELOPMENT
Tuberous sclerosis complex genes: from flies to human genetics
ARCHIVES OF DERMATOLOGICAL RESEARCH
Mutational analysis of TSC1 and TSC2 genes in gangliogliomas
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
Biological behavior and tumorigenesis of subependymal giant cell astrocytomas
JOURNAL OF NEURO-ONCOLOGY
Hamartin and tuberin interaction with the G2/M cyclin-dependent kinase CDK1 and its regulatory cyclins A and B
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomassuggests different genetic mechanisms for pathogenesis of TSC lesions
AMERICAN JOURNAL OF HUMAN GENETICS
Developmental expression of the tuberous sclerosis proteins tuberin and hamartin
ACTA NEUROPATHOLOGICA
Interaction between LIS1 and doublecortin, two lissencephaly gene products
HUMAN MOLECULAR GENETICS
Tuberin expression in ganglioglioma
ULTRASTRUCTURAL PATHOLOGY
Novel cerebral lesions in the Eker rat model of tuberous sclerosis: Cortical tuber and anaplastic ganglioglioma
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
National Institutes of Health consensus conference: Tuberous sclerosis complex
ARCHIVES OF NEUROLOGY
A new Western blotting method using polymer immunocomplexes: Detection of Tsc1 and Tsc2 expression in various cultured cell lines
ANALYTICAL BIOCHEMISTRY
Simultaneous loss of hamartin and tuberin from the cerebrum, kidney and heart with tuberous sclerosis
ACTA NEUROPATHOLOGICA
Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex
JOURNAL OF HUMAN GENETICS
Mutation screening of the entire coding regions of the TSC1 and the TSC2 gene with the protein truncation test PTT identifies frequent splicing defects
HUMAN MUTATION
Analysis of both TCS1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosis
HUMAN MUTATION
Distribution of Tsc2 protein in various normal rat tissues and renal tumours of Tsc2 mutant (Eker) rat detected by immunohistochemistry
VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
The expression of hamartin, the product of the TSC1 gene, in normal human tissues and in TSC1- and TSC2-linked angiomyolipomas
MODERN PATHOLOGY
New developments in the neurobiology of the tuberous sclerosis complex
NEUROLOGY
Loss of the TSC2 product tuberin in subependymal giant-cell tumors
ACTA NEUROPATHOLOGICA
EXON SCANNING OF THE ENTIRE TSC2 GENE FOR GERMLINE MUTATIONS IN 40 UNRELATED PATIENTS WITH TUBEROUS SCLEROSIS
Human mutation
A ROLE OF THE TUBEROUS SCLEROSIS GENE-2 PRODUCT DURING NEURONAL DIFFERENTIATION
Oncogene
TUBEROUS SCLEROSIS-RELATED GENE-EXPRESSION IN NORMAL AND DYSPLASTIC BRAIN
Epilepsy research
MICRONODULAR PNEUMOCYTE HYPERPLASIA
The American journal of surgical pathology
THE IDENTIFICATION OF A CONSERVED BINDING MOTIF WITHIN HUMAN-PAPILLOMAVIRUS TYPE-16 E6 BINDING PEPTIDES, E6AP AND E6BP
Journal of General Virology
CONGENITAL OLIVOPONTOCEREBELLAR ATROPHY - REPORT OF 2 SIBLINGS WITH PALEOCEREBELLAR AND NEOCEREBELLAR ATROPHY
Acta Neuropathologica
DELETION OF 11 AMINO-ACIDS IN TUBERIN ASSOCIATED WITH SEVERE TUBEROUSSCLEROSIS PHENOTYPES - EVIDENCE FOR A NEW ESSENTIAL DOMAIN IN THE FIRST 3RD OF THE PROTEIN
European journal of human genetics
ALTERATIONS IN THE RAP1 SIGNALING PATHWAY ARE COMMON IN HUMAN GLIOMAS
Oncogene
INTRAGENIC TSC2 SOMATIC MUTATIONS AS KNUDSON 2ND-HIT IN SPONTANEOUS AND CHEMICALLY-INDUCED RENAL CARCINOMAS IN THE EKER RAT MODEL
Japanese journal of cancer research
HMB-45 AND TUBERIN IN HAMARTOMAS ASSOCIATED WITH TUBEROUS SCLEROSIS
Modern pathology
SUSTAINED CARDIOMYOCYTE DNA-SYNTHESIS IN WHOLE-EMBRYO CULTURES LACKING THE TSC2 GENE-PRODUCT
American journal of physiology. Heart and circulatory physiology
TUBEROUS SCLEROSIS IN A 20-WEEK GESTATION FETUS - IMMUNOHISTOCHEMICALSTUDY
Acta Neuropathologica
COLOCALIZATION OF THE TSC2 PRODUCT TUBERIN WITH ITS TARGET RAP1 IN THE GOLGI-APPARATUS
Oncogene
TISSUE AND CELL-TYPE-SPECIFIC EXPRESSION OF THE TUBEROUS SCLEROSIS GENE, TSC2, IN HUMAN TISSUES
Modern pathology
HISTORY OF THE TUBEROUS SCLEROSIS COMPLEX
Brain & development