Pages that link to "Q24539146"
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The following pages link to Familial posterior fossa brain tumors of infancy secondary to germline mutation of the hSNF5 gene (Q24539146):
Displaying 50 items.
- Germline mutation of INI1/SMARCB1 in familial schwannomatosis (Q24682982) (← links)
- Expression of SMARCF1, a truncated form of SWI1, in neuroblastoma (Q24685907) (← links)
- Extracranial rhabdoid tumours: what we have learned so far and future directions (Q27027021) (← links)
- Transcription activator interactions with multiple SWI/SNF subunits. (Q27930422) (← links)
- Evidence of a four-hit mechanism involving SMARCB1 and NF2 in schwannomatosis-associated schwannomas (Q28260652) (← links)
- Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome (Q28262110) (← links)
- Haploinsufficiency of Snf5 (integrase interactor 1) predisposes to malignant rhabdoid tumors in mice (Q28586163) (← 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)
- Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome (Q33645991) (← links)
- Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1 (Q33744341) (← links)
- Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome (Q33909895) (← links)
- Molecular insight into medulloblastoma and central nervous system primitive neuroectodermal tumor biology from hereditary syndromes: a review (Q34051118) (← links)
- Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy. (Q34342958) (← links)
- Molecular genetics of pineal region neoplasms (Q34478051) (← links)
- Paediatric embryonic brain tumours. biological and clinical relevance of molecular genetic abnormalities (Q34578601) (← links)
- The role of genetics in the establishment and maintenance of the epigenome. (Q34649133) (← links)
- Counseling the at risk patient in the BRCA1 and BRCA2 Era. (Q34729086) (← links)
- Classifying the medulloblastoma: insights from morphology and molecular genetics (Q34783428) (← links)
- Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors (Q34915348) (← links)
- Molecular analysis of the rhabdoid predisposition syndrome in a child: a novel germline hSNF5/INI1 mutation and absence of c-myc amplification (Q35189235) (← links)
- TCR-dependent transformation of mature memory phenotype T cells in mice (Q35369863) (← links)
- Ethical issues in molecular medicine of relevance to surgeons. (Q35537370) (← links)
- The SWI/SNF complex--chromatin and cancer. (Q35667471) (← links)
- Chromosomal imbalances in choroid plexus tumors (Q35788860) (← links)
- Atypical teratoid/rhabdoid tumor evolving from an optic pathway ganglioglioma: case study (Q35800546) (← links)
- Epidemiology and genetics of childhood cancer. (Q35868038) (← links)
- Molecular pathogenesis of childhood brain tumors (Q36021571) (← links)
- Atypical teratoid rhabdoid tumors of childhood: diagnosis, treatment and challenges (Q36284530) (← links)
- New concepts in the treatment of brain tumors in very young children (Q36453264) (← links)
- Current concepts in the molecular genetics of pediatric brain tumors: implications for emerging therapies (Q36585123) (← links)
- Long-term survival and transmission of INI1-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndrome (Q36614782) (← links)
- Malignant rhabdoid tumor mimicking hepatoblastoma: a case report and literature review. (Q36968019) (← links)
- Oncogenesis caused by loss of the SNF5 tumor suppressor is dependent on activity of BRG1, the ATPase of the SWI/SNF chromatin remodeling complex. (Q37389731) (← 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)
- Molecular diagnostics of CNS embryonal tumors (Q37794829) (← links)
- The clinical implications of medulloblastoma subgroups (Q38008153) (← links)
- Rhabdoid tumors: an initial clue to the role of chromatin remodeling in cancer (Q38083797) (← links)
- Familial rhabdoid tumour 'avant la lettre'--from pathology review to exome sequencing and back again (Q38115209) (← links)
- High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor (Q38301206) (← links)
- Secondary meningioma in a long-term survivor of atypical teratoid/rhabdoid tumour with a germline INI1 mutation (Q38846896) (← links)
- Cribriform neuroepithelial tumor: molecular characterization of a SMARCB1-deficient non-rhabdoid tumor with favorable long-term outcome (Q39629867) (← links)
- hSNF5 /INI1 mutation analysis in acute myeloid leukemia. (Q40014396) (← links)
- Genomic and functional evidence for an ARID1A tumor suppressor role (Q40134611) (← links)
- Cancer-associated mutations in chromatin remodeler hSNF5 promote chromosomal instability by compromising the mitotic checkpoint. (Q40446274) (← links)
- P16INK4a is required for hSNF5 chromatin remodeler-induced cellular senescence in malignant rhabdoid tumor cells (Q40618783) (← links)
- Smarca4 ATPase mutations disrupt direct eviction of PRC1 from chromatin (Q42222276) (← links)
- Re-expression of hSNF5/INI1/BAF47 in pediatric tumor cells leads to G1 arrest associated with induction of p16ink4a and activation of RB. (Q44083876) (← links)
- A key role of the hSNF5/INI1 tumour suppressor in the control of the G1-S transition of the cell cycle (Q44134109) (← links)