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Items: 1 to 20 of 188

1.

Conventional chondrosarcoma in a survivor of rhabdoid tumor: enlarging the spectrum of tumors associated with SMARCB1 germline mutations.

Forest F, David A, Arrufat S, Pierron G, Ranchere-Vince D, Stephan JL, Clemenson A, Delattre O, Bourdeaut F.

Am J Surg Pathol. 2012 Dec;36(12):1892-6. doi: 10.1097/PAS.0b013e31826cbe7a.

PMID:
23154773
2.

SMARCB1 deficiency in tumors from the peripheral nervous system: a link between schwannomas and rhabdoid tumors?

Rizzo D, Fréneaux P, Brisse H, Louvrier C, Lequin D, Nicolas A, Ranchère D, Verkarre V, Jouvet A, Dufour C, Edan C, Stéphan JL, Orbach D, Sarnacki S, Pierron G, Parfait B, Peuchmaur M, Delattre O, Bourdeaut F.

Am J Surg Pathol. 2012 Jul;36(7):964-72. doi: 10.1097/PAS.0b013e31825798f1.

PMID:
22614000
3.

SMARCB1/INI1 protein expression in round cell soft tissue sarcomas associated with chromosomal translocations involving EWS: a special reference to SMARCB1/INI1 negative variant extraskeletal myxoid chondrosarcoma.

Kohashi K, Oda Y, Yamamoto H, Tamiya S, Oshiro Y, Izumi T, Taguchi T, Tsuneyoshi M.

Am J Surg Pathol. 2008 Aug;32(8):1168-74. doi: 10.1097/PAS.0b013e318161781a.

PMID:
18580682
4.

Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors.

Eaton KW, Tooke LS, Wainwright LM, Judkins AR, Biegel JA.

Pediatr Blood Cancer. 2011 Jan;56(1):7-15. doi: 10.1002/pbc.22831.

5.

Non-linkage of familial rhabdoid tumors to SMARCB1 implies a second locus for the rhabdoid tumor predisposition syndrome.

Frühwald MC, Hasselblatt M, Wirth S, Köhler G, Schneppenheim R, Subero JI, Siebert R, Kordes U, Jürgens H, Vormoor J.

Pediatr Blood Cancer. 2006 Sep;47(3):273-8.

PMID:
16206192
6.

Non-rhabdoid pediatric SMARCB1-deficient tumors: overlap between chordomas and malignant rhabdoid tumors?

Renard C, Pissaloux D, Decouvelaere AV, Bourdeaut F, Ranchère D.

Cancer Genet. 2014 Sep;207(9):384-9. doi: 10.1016/j.cancergen.2014.05.005. Epub 2014 May 23.

PMID:
25053104
7.

Malignant rhabdoid tumor of the bladder and ganglioglioma in a 14 year-old male with a germline 22q11.2 deletion.

Bosse KR, Shukla AR, Pawel B, Chikwava KR, Santi M, Tooke L, Castagna K, Biegel JA, Bagatell R.

Cancer Genet. 2014 Sep;207(9):415-9. doi: 10.1016/j.cancergen.2014.05.007. Epub 2014 May 21.

PMID:
25018128
8.

Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism.

Gigante L, Paganini I, Frontali M, Ciabattoni S, Sangiuolo FC, Papi L.

Fam Cancer. 2016 Jan;15(1):123-6. doi: 10.1007/s10689-015-9836-6.

PMID:
26342593
9.

Rhabdoid tumor predisposition syndrome.

Sredni ST, Tomita T.

Pediatr Dev Pathol. 2015 Jan-Feb;18(1):49-58. doi: 10.2350/14-07-1531-MISC.1. Epub 2014 Dec 10.

PMID:
25494491
10.

Epithelioid sarcoma is associated with a high percentage of SMARCB1 deletions.

Sullivan LM, Folpe AL, Pawel BR, Judkins AR, Biegel JA.

Mod Pathol. 2013 Mar;26(3):385-92. doi: 10.1038/modpathol.2012.175. Epub 2012 Oct 12.

11.

Premature termination of SMARCB1 translation may be followed by reinitiation in schwannomatosis-associated schwannomas, but results in absence of SMARCB1 expression in rhabdoid tumors.

Hulsebos TJ, Kenter S, Verhagen WI, Baas F, Flucke U, Wesseling P.

Acta Neuropathol. 2014 Sep;128(3):439-48. doi: 10.1007/s00401-014-1281-3. Epub 2014 Apr 17.

PMID:
24740647
12.

Infrequent SMARCB1/INI1 gene alteration in epithelioid sarcoma: a useful tool in distinguishing epithelioid sarcoma from malignant rhabdoid tumor.

Kohashi K, Izumi T, Oda Y, Yamamoto H, Tamiya S, Taguchi T, Iwamoto Y, Hasegawa T, Tsuneyoshi M.

Hum Pathol. 2009 Mar;40(3):349-55. doi: 10.1016/j.humpath.2008.08.007. Epub 2008 Oct 29.

PMID:
18973917
13.

Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1.

Swensen JJ, Keyser J, Coffin CM, Biegel JA, Viskochil DH, Williams MS.

J Med Genet. 2009 Jan;46(1):68-72. doi: 10.1136/jmg.2008.060152.

14.

Congenital anomalies and rhabdoid tumor associated with 22q11 germline deletion and somatic inactivation of the SMARCB1 tumor suppressor.

Toth G, Zraly CB, Thomson TL, Jones C, Lapetino S, Muraskas J, Zhang J, Dingwall AK.

Genes Chromosomes Cancer. 2011 Jun;50(6):379-88. doi: 10.1002/gcc.20862. Epub 2011 Mar 15.

15.

SMARCB1 mutations in schwannomatosis and genotype correlations with rhabdoid tumors.

Smith MJ, Wallace AJ, Bowers NL, Eaton H, Evans DG.

Cancer Genet. 2014 Sep;207(9):373-8. doi: 10.1016/j.cancergen.2014.04.001. Epub 2014 Apr 8.

PMID:
24933152
16.

Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor.

Kordes U, Gesk S, Frühwald MC, Graf N, Leuschner I, Hasselblatt M, Jeibmann A, Oyen F, Peters O, Pietsch T, Siebert R, Schneppenheim R.

Genes Chromosomes Cancer. 2010 Feb;49(2):176-81. doi: 10.1002/gcc.20729.

PMID:
19902524
17.

Predisposition to atypical teratoid/rhabdoid tumor due to an inherited INI1 mutation.

Janson K, Nedzi LA, David O, Schorin M, Walsh JW, Bhattacharjee M, Pridjian G, Tan L, Judkins AR, Biegel JA.

Pediatr Blood Cancer. 2006 Sep;47(3):279-84.

PMID:
16261613
18.

SMARCB1 (INI1)-negative rhabdoid carcinomas of the gastrointestinal tract: clinicopathologic and molecular study of a highly aggressive variant with literature review.

Agaimy A, Rau TT, Hartmann A, Stoehr R.

Am J Surg Pathol. 2014 Jul;38(7):910-20. doi: 10.1097/PAS.0000000000000173. Review.

PMID:
24503755
19.

Favorable outcome of patients affected by rhabdoid tumors due to rhabdoid tumor predisposition syndrome (RTPS).

Kordes U, Bartelheim K, Modena P, Massimino M, Biassoni V, Reinhard H, Hasselblatt M, Schneppenheim R, Frühwald MC.

Pediatr Blood Cancer. 2014 May;61(5):919-21. doi: 10.1002/pbc.24793. Epub 2013 Oct 3.

PMID:
24123847
20.

Rapid detection of SMARCB1 sequence variation using high resolution melting.

Dagar V, Chow CW, Ashley DM, Algar EM.

BMC Cancer. 2009 Dec 13;9:437. doi: 10.1186/1471-2407-9-437.

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