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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 1
1982 1
1983 2
1985 3
1986 3
1987 4
1988 5
1989 9
1990 5
1991 12
1992 8
1993 9
1994 11
1995 13
1996 13
1997 13
1998 14
1999 23
2000 20
2001 19
2002 21
2003 31
2004 29
2005 37
2006 39
2007 32
2008 43
2009 52
2010 54
2011 63
2012 60
2013 49
2014 71
2015 77
2016 62
2017 54
2018 47
2019 56
2020 70
2021 61
2022 56
2023 58
2024 20

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1,144 results

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Page 1
Pediatric Brain Tumors.
Udaka YT, Packer RJ. Udaka YT, et al. Neurol Clin. 2018 Aug;36(3):533-556. doi: 10.1016/j.ncl.2018.04.009. Neurol Clin. 2018. PMID: 30072070 Review.
SMARCB1/INI1-deficient tumors of adulthood.
Parker NA, Al-Obaidi A, Deutsch JM. Parker NA, et al. F1000Res. 2020 Jun 30;9:662. doi: 10.12688/f1000research.24808.2. eCollection 2020. F1000Res. 2020. PMID: 33796273 Free PMC article. Review.
The SMARCB1/INI1 gene was first discovered in the mid-1990s, and since then it has been revealed that loss of function mutations in this gene result in aggressive rhabdoid tumors. Recently, the term "rhabdoid tumor" has become synonymous with decreased SMARCB1/INI1 …
The SMARCB1/INI1 gene was first discovered in the mid-1990s, and since then it has been revealed that loss of function mutations in this gen …
Biology and Treatment of Rhabdoid Tumor.
Geller JI, Roth JJ, Biegel JA. Geller JI, et al. Crit Rev Oncog. 2015;20(3-4):199-216. doi: 10.1615/critrevoncog.2015013566. Crit Rev Oncog. 2015. PMID: 26349416 Free PMC article. Review.
Rhabdoid tumor is a rare, highly aggressive malignancy that primarily affects infants and young children. ...The strategies for novel therapeutic approaches based on what is currently known about rhabdoid tumor biology are presented....
Rhabdoid tumor is a rare, highly aggressive malignancy that primarily affects infants and young children. ...The strategies fo
Mithramycin induces promoter reprogramming and differentiation of rhabdoid tumor.
Chasse MH, Johnson BK, Boguslawski EA, Sorensen KM, Rosien JE, Kang MH, Reynolds CP, Heo L, Madaj ZB, Beddows I, Foxa GE, Kitchen-Goosen SM, Williams BO, Triche TJ Jr, Grohar PJ. Chasse MH, et al. EMBO Mol Med. 2021 Feb 5;13(2):e12640. doi: 10.15252/emmm.202012640. Epub 2020 Dec 17. EMBO Mol Med. 2021. PMID: 33332735 Free PMC article.
Rhabdoid tumor (RT) is a pediatric cancer characterized by the inactivation of SMARCB1, a subunit of the SWI/SNF chromatin remodeling complex. ...Here we use unbiased screening of cell line panels to identify a heightened sensitivity of rhabdoid tumor
Rhabdoid tumor (RT) is a pediatric cancer characterized by the inactivation of SMARCB1, a subunit of the SWI/SNF chromatin rem
Adult Atypical Teratoid/Rhabdoid Tumors.
Wu WW, Bi WL, Kang YJ, Ramkissoon SH, Prasad S, Shih HA, Reardon DA, Dunn IF. Wu WW, et al. World Neurosurg. 2016 Jan;85:197-204. doi: 10.1016/j.wneu.2015.08.076. Epub 2015 Sep 4. World Neurosurg. 2016. PMID: 26344637 Review.
Diagnostically Challenging Epithelioid Soft Tissue Tumors.
James AW, Dry SM. James AW, et al. Surg Pathol Clin. 2015 Sep;8(3):309-29. doi: 10.1016/j.path.2015.05.002. Surg Pathol Clin. 2015. PMID: 26297059 Review.
In this article, we focus on the histologic features, differential diagnosis, and potential pitfalls in the diagnosis of epithelioid sarcoma, alveolar soft part sarcoma, clear-cell sarcoma, ossifying fibromyxoid tumor, and malignant extrarenal rhabdoid tumor. Numero …
In this article, we focus on the histologic features, differential diagnosis, and potential pitfalls in the diagnosis of epithelioid sarcoma …
Oncogenic roles of SMARCB1/INI1 and its deficient tumors.
Kohashi K, Oda Y. Kohashi K, et al. Cancer Sci. 2017 Apr;108(4):547-552. doi: 10.1111/cas.13173. Epub 2017 Apr 12. Cancer Sci. 2017. PMID: 28109176 Free PMC article. Review.
Initially, no detectable SMARCB1/INI1 protein expression was found in malignant rhabdoid tumor cells, whereas all other kinds of tumor cells and non-tumorous tissue showed SMARCB1/INI1 protein expression. ...
Initially, no detectable SMARCB1/INI1 protein expression was found in malignant rhabdoid tumor cells, whereas all other kinds …
Embryonal Tumors of the Central Nervous System: An Update.
Blessing MM, Alexandrescu S. Blessing MM, et al. Surg Pathol Clin. 2020 Jun;13(2):235-247. doi: 10.1016/j.path.2020.01.003. Epub 2020 Apr 7. Surg Pathol Clin. 2020. PMID: 32389264 Review.
Well-defined embryonal tumors include medulloblastoma, atypical teratoid/rhabdoid tumor, embryonal tumor with multilayered rosettes, C19MC-altered and embryonal tumor with multilayered rosettes, not otherwise specified, pineoblastoma, pituitary blastoma, CNS neurobl …
Well-defined embryonal tumors include medulloblastoma, atypical teratoid/rhabdoid tumor, embryonal tumor with multilayered ros …
TLE1 Expression in Malignant Rhabdoid Tumor and Atypical Teratoid/Rhabdoid Tumor.
Duncan VE, Wicker JA, Kelly DR, Li R. Duncan VE, et al. Pediatr Dev Pathol. 2018 Nov-Dec;21(6):522-527. doi: 10.1177/1093526618761720. Epub 2018 Feb 28. Pediatr Dev Pathol. 2018. PMID: 29490565
Malignant rhabdoid tumors (MRT; atypical teratoid/rhabdoid tumor [ATRT] in the central nervous system) are aggressive tumors in infants and children which can overlap with other sarcomas, such as synovial sarcoma (SS). ...
Malignant rhabdoid tumors (MRT; atypical teratoid/rhabdoid tumor [ATRT] in the central nervous system) are aggressive tumors i …
Rhabdoid tumor predisposition syndrome.
Sredni ST, Tomita T. Sredni ST, et al. Pediatr Dev Pathol. 2015 Jan-Feb;18(1):49-58. doi: 10.2350/14-07-1531-MISC.1. Epub 2014 Dec 10. Pediatr Dev Pathol. 2015. PMID: 25494491
Recently, mutations in a 2nd locus of the SWI/SNF complex, the SMARCA4 gene, also known as BRG1, were found in rhabdoid tumors with retention of SMARCB1 expression. Familial cases may occur in a condition known as rhabdoid tumor predisposition syndrome (RTPS). In RT …
Recently, mutations in a 2nd locus of the SWI/SNF complex, the SMARCA4 gene, also known as BRG1, were found in rhabdoid tumors with retentio …
1,144 results