Pages that link to "Q24682982"
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The following pages link to Germline mutation of INI1/SMARCB1 in familial schwannomatosis (Q24682982):
Displaying 50 items.
- The SWI/SNF Subunit INI1 Contains an N-Terminal Winged Helix DNA Binding Domain that Is a Target for Mutations in Schwannomatosis (Q24338138) (← links)
- Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors (Q24643365) (← links)
- SWI/SNF chromatin remodeling complexes and cancer (Q26998657) (← links)
- Evidence of a four-hit mechanism involving SMARCB1 and NF2 in schwannomatosis-associated schwannomas (Q28260652) (← links)
- The SWI/SNF genetic blockade: effects in cell differentiation, cancer and developmental diseases (Q28292392) (← links)
- Immortalized Human Schwann Cell Lines Derived From Tumors of Schwannomatosis Patients (Q28551545) (← links)
- Quantitative assessment of whole-body tumor burden in adult patients with neurofibromatosis (Q28730289) (← links)
- A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes. (Q30252766) (← links)
- Childhood neurofibromatosis type 2 (NF2) and related disorders: from bench to bedside and biologically targeted therapies. (Q30364937) (← links)
- Neurofibromatosis type 2. (Q30391375) (← links)
- Consensus recommendations to accelerate clinical trials for neurofibromatosis type 2. (Q30406342) (← links)
- Radiographic association of schwannomas with sensory ganglia (Q30450062) (← links)
- Genetic predisposition to peripheral nerve neoplasia: diagnostic criteria and pathogenesis of neurofibromatoses, Carney complex, and related syndromes (Q30454537) (← links)
- Molecular mechanisms promoting the pathogenesis of Schwann cell neoplasms (Q30457681) (← links)
- The molecular biology of vestibular schwannomas and its association with hearing loss: a review. (Q30467803) (← links)
- Pathogenesis of vestibular schwannoma in ring chromosome 22 (Q30486093) (← links)
- Therapeutically targeting cyclin D1 in primary tumors arising from loss of Ini1. (Q30497840) (← links)
- Generation of a mouse model of atypical teratoid/rhabdoid tumor of the central nervous system through combined deletion of Snf5 and p53. (Q30671578) (← links)
- Prognostic value of MIB-1, p53, epidermal growth factor receptor, and INI1 in childhood chordomas (Q33275045) (← links)
- Imprinted CDKN1C is a tumor suppressor in rhabdoid tumor and activated by restoration of SMARCB1 and histone deacetylase inhibitors (Q33409828) (← links)
- Rapid detection of SMARCB1 sequence variation using high resolution melting (Q33517967) (← links)
- Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1 (Q33744341) (← links)
- SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis (Q33800041) (← links)
- Chromatin-regulating proteins as targets for cancer therapy (Q33907067) (← links)
- SWI/SNF chromatin remodeling enzymes in melanocyte differentiation and melanoma (Q33923821) (← links)
- Cribriform neuroepithelial tumor in the third ventricle: a case report and literature review. (Q34125544) (← links)
- Meningiomas and neurofibromatosis. (Q34131583) (← links)
- A germline missense mutation in COQ6 is associated with susceptibility to familial schwannomatosis. (Q34304972) (← links)
- Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas (Q34393793) (← links)
- Consistent SMARCB1 homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material (Q34483391) (← links)
- Congenital anomalies and rhabdoid tumor associated with 22q11 germline deletion and somatic inactivation of the SMARCB1 tumor suppressor (Q34786042) (← links)
- Educational paper: screening in cancer predisposition syndromes: guidelines for the general pediatrician (Q34915251) (← links)
- Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors (Q34915348) (← links)
- Comparative oncogenomic analysis of copy number alterations in human and zebrafish tumors enables cancer driver discovery (Q34979403) (← links)
- Segmental neurofibromatosis type 2: discriminating two hit from four hit in a patient presenting multiple schwannomas confined to one limb. (Q35025665) (← links)
- Fibroblast growth factor receptors as novel therapeutic targets in SNF5-deleted malignant rhabdoid tumors (Q35035462) (← links)
- Genome-wide approach to identify second gene targets for malignant rhabdoid tumors using high-density oligonucleotide microarrays (Q35051968) (← links)
- p16INK4A and p14ARF tumor suppressor pathways are deregulated in malignant rhabdoid tumors (Q35133362) (← links)
- TCR-dependent transformation of mature memory phenotype T cells in mice (Q35369863) (← links)
- Epithelioid malignant peripheral nerve sheath tumor arising in a schwannoma, in a patient with "neuroblastoma-like" schwannomatosis and a novel germline SMARCB1 mutation (Q35621426) (← links)
- Expanding the mutational spectrum of LZTR1 in schwannomatosis (Q35722195) (← links)
- Recent developments in brain tumor predisposing syndromes (Q35860402) (← links)
- Pediatric Non-vestibular Schwannoma (Q36350196) (← links)
- Inactivation of SNF5 cooperates with p53 loss to accelerate tumor formation in Snf5(+/-);p53(+/-) mice (Q36480038) (← links)
- Long-term survival and transmission of INI1-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndrome (Q36614782) (← links)
- Regression of schwannomas induced by adeno-associated virus-mediated delivery of caspase-1. (Q36634951) (← links)
- Tissue-specific ablation of Prkar1a causes schwannomas by suppressing neurofibromatosis protein production (Q36944177) (← links)
- Swi/Snf chromatin remodeling/tumor suppressor complex establishes nucleosome occupancy at target promoters (Q36950326) (← links)
- Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Q37130298) (← links)
- Multimerization and DNA binding properties of INI1/hSNF5 and its functional significance (Q37338970) (← links)