Terms: = Testicular cancer AND SMARCB1, Ini1, 6598, ENSG00000099956, Snr1, SNF5L1, RDT, BAF47, hSNFS, SNF5, INI1, Sfh1p, Q12824
8 results:
1. smarcb1-Deficient Skull Base Chondrosarcoma with 12p Duplication Presenting as Somatic-Type Malignancy Arising from Metastatic Seminoma.
Argyris PP; Challa B; Satturwar S; VanKoevering KK; Wakely PE
Head Neck Pathol; 2024 Jan; 18(1):1. PubMed ID: 38236556
[TBL] [Abstract] [Full Text] [Related]
2. The 2022 World Health Organization Classification of Tumours of the Urinary System and Male Genital Organs-Part A: Renal, Penile, and testicular Tumours.
Moch H; Amin MB; Berney DM; Compérat EM; Gill AJ; Hartmann A; Menon S; Raspollini MR; Rubin MA; Srigley JR; Hoon Tan P; Tickoo SK; Tsuzuki T; Turajlic S; Cree I; Netto GJ
Eur Urol; 2022 Nov; 82(5):458-468. PubMed ID: 35853783
[TBL] [Abstract] [Full Text] [Related]
3. Cyclin Pathway Genomic Alterations Across 190,247 Solid Tumors: Leveraging Large-Scale Data to Inform Therapeutic Directions.
Jardim DL; Millis SZ; Ross JS; Woo MS; Ali SM; Kurzrock R
Oncologist; 2021 Jan; 26(1):e78-e89. PubMed ID: 32885893
[TBL] [Abstract] [Full Text] [Related]
4. KBG syndrome patient due to 16q24.3 microdeletion presenting with a paratesticular rhabdoid tumor: Coincidence or cancer predisposition?
Behnert A; Auber B; Steinemann D; Frühwald MC; Huisinga C; Hussein K; Kratz C; Ripperger T
Am J Med Genet A; 2018 Jun; 176(6):1449-1454. PubMed ID: 29696793
[TBL] [Abstract] [Full Text] [Related]
5. Sinonasal smarcb1 (ini1) Deficient Carcinoma With Yolk Sac Tumor Differentiation: Report of a Case and Comparison With ini1 Expression in Gonadal Germ Cell Tumors.
Zamecnik M; Rychnovsky J; Syrovatka J
Int J Surg Pathol; 2018 May; 26(3):245-249. PubMed ID: 29166820
[TBL] [Abstract] [Full Text] [Related]
6. [A CASE OF PRIMITIVE NEUROECTODERMAL TUMOR OF THE TESTIS].
Goto T; Sato M; Fujii S; Itoh J; Soma F
Nihon Hinyokika Gakkai Zasshi; 2015 Jan; 106(1):53-8. PubMed ID: 26399133
[TBL] [Abstract] [Full Text] [Related]
7. Primitive neuroectodermal tumors in patients with testicular germ cell tumors usually resemble pediatric-type central nervous system embryonal neoplasms and lack chromosome 22 rearrangements.
Ulbright TM; Hattab EM; Zhang S; Ehrlich Y; Foster RS; Einhorn LH; Cheng L
Mod Pathol; 2010 Jul; 23(7):972-80. PubMed ID: 20348883
[TBL] [Abstract] [Full Text] [Related]
8. Loss of ini1 expression is characteristic of both conventional and proximal-type epithelioid sarcoma.
Hornick JL; Dal Cin P; Fletcher CD
Am J Surg Pathol; 2009 Apr; 33(4):542-50. PubMed ID: 19033866
[TBL] [Abstract] [Full Text] [Related]
