Pages that link to "Q81684801"
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The following pages link to Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis (Q81684801):
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)
- Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome (Q28262110) (← links)
- Unilateral vestibular schwannoma in a patient with schwannomatosis in the absence of LZTR1 mutation (Q30277398) (← links)
- Therapeutic advances for the tumors associated with neurofibromatosis type 1, type 2, and schwannomatosis (Q30357776) (← links)
- Superficial neurofibromas in the setting of schwannomatosis: nosologic implications (Q30400778) (← links)
- miRNA-7 Attenuation in Schwannoma Tumors Stimulates Growth by Upregulating Three Oncogenic Signaling Pathways (Q30428483) (← links)
- A novel imaging-compatible sciatic nerve schwannoma model (Q30471189) (← links)
- Plexiform schwannoma involving the trachea and recurrent laryngeal nerve: a case report (Q30663724) (← 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)
- Oncogenic roles of SMARCB1/INI1 and its deficient tumors (Q33607443) (← 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)
- Meningiomas and neurofibromatosis. (Q34131583) (← links)
- Tandem Intercostal Thoracic Schwannomas Resected Using a Thoracoscopic Nerve-Sparing Technique: Case Report (Q34204131) (← links)
- Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas (Q34393793) (← 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)
- 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)
- 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)
- Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome (Q36406904) (← links)
- The role of SMARCB1/INI1 in development of rhabdoid tumor. (Q37420245) (← links)
- The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis (Q37601480) (← links)
- Incidence of atypical teratoid/rhabdoid tumors in children: a population-based study by the Austrian Brain Tumor Registry, 1996-2006. (Q37782304) (← links)
- SWI/SNF nucleosome remodellers and cancer. (Q37886668) (← links)
- Revisiting neurofibromatosis type 2 diagnostic criteria to exclude LZTR1-related schwannomatosis. (Q39179434) (← links)
- Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development. (Q41464099) (← links)
- Expression of SMARCB1 (INI1) mutations in familial schwannomatosis (Q41904124) (← links)
- Identification of genetic susceptibility to childhood cancer through analysis of genes in parallel (Q42013225) (← links)
- SMARCB1/INI1 alterations and hepatoblastoma: another extrarenal rhabdoid tumor revealed? (Q42087788) (← links)
- Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri (Q44718402) (← links)
- Schwannomatosis, sporadic schwannomatosis, and familial schwannomatosis: a surgical series with long-term follow-up (Q45820823) (← links)
- Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosis. (Q48510274) (← links)
- Pain correlates with germline mutation in schwannomatosis (Q49557868) (← links)
- Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria. (Q53116195) (← links)
- RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomas. (Q53154025) (← links)
- Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor. (Q54455194) (← links)
- CTF meeting 2012: Translation of the basic understanding of the biology and genetics of NF1, NF2, and schwannomatosis toward the development of effective therapies. (Q55638662) (← links)
- A recurrent de novo missense pathogenic variant in SMARCB1 causes severe intellectual disability and choroid plexus hyperplasia with resultant hydrocephalus (Q56538973) (← links)
- Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomas (Q57207010) (← links)
- Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis (Q57266550) (← links)
- What's new in neurofibromatosis? Proceedings from the 2009 NF Conference: new frontiers (Q57657390) (← links)
- Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation (Q57737866) (← links)
- Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities: a meta-analysis (Q64004323) (← links)
- Podoplanin and CD34 in peripheral nerve sheath tumours: focus on neurofibromatosis 1-associated atypical neurofibroma (Q84990314) (← links)
- Malignant progression of a peripheral nerve sheath tumor in the setting of rhabdoid tumor predisposition syndrome (Q87986889) (← links)
- Co-occurrence of schwannomatosis and rhabdoid tumor predisposition syndrome 1 (Q88739307) (← links)