Terms: = Sarcomas AND MSH2, COCA1, 4436, ENSG00000095002, HNPCC, FCC1, HNPCC1, P43246 AND Diagnosis
18 results:
1. [Clinicopathological and gene mutation characteristics of uterine carcinosarcoma].
Tu J; Xu JZ; Zhang YS; Deng LF
Zhonghua Yi Xue Za Zhi; 2023 Jun; 103(24):1864-1867. PubMed ID: 37357193
[TBL] [Abstract] [Full Text] [Related]
2. Mediastinal Myxofibrosarcoma Harboring Loss-of-Function
Jia L; Hwang H; De Las Casas L
Int J Surg Pathol; 2023 Dec; 31(8):1605-1609. PubMed ID: 37013349
[TBL] [Abstract] [Full Text] [Related]
3. Inflammatory leiomyosarcoma/rhabdomyoblastic tumor: A report of two cases with novel genetic findings.
Sukhanova M; Obeidin F; Streich L; Alexiev BA
Genes Chromosomes Cancer; 2022 Nov; 61(11):653-661. PubMed ID: 35655404
[TBL] [Abstract] [Full Text] [Related]
4. Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma.
Mirabello L; Zhu B; Koster R; Karlins E; Dean M; Yeager M; Gianferante M; Spector LG; Morton LM; Karyadi D; Robison LL; Armstrong GT; Bhatia S; Song L; Pankratz N; Pinheiro M; Gastier-Foster JM; Gorlick R; de Toledo SRC; Petrilli AS; Patino-Garcia A; Lecanda F; Gutierrez-Jimeno M; Serra M; Hattinger C; Picci P; Scotlandi K; Flanagan AM; Tirabosco R; Amary MF; Kurucu N; Ilhan IE; Ballinger ML; Thomas DM; Barkauskas DA; Mejia-Baltodano G; Valverde P; Hicks BD; Zhu B; Wang M; Hutchinson AA; Tucker M; Sampson J; Landi MT; Freedman ND; Gapstur S; Carter B; Hoover RN; Chanock SJ; Savage SA
JAMA Oncol; 2020 May; 6(5):724-734. PubMed ID: 32191290
[TBL] [Abstract] [Full Text] [Related]
5. Universal screening of both endometrial and colon cancers increases the detection of Lynch syndrome.
Adar T; Rodgers LH; Shannon KM; Yoshida M; Ma T; Mattia A; Lauwers GY; Iafrate AJ; Hartford NM; Oliva E; Chung DC
Cancer; 2018 Aug; 124(15):3145-3153. PubMed ID: 29750335
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6. Tumor development in Japanese patients with Lynch syndrome.
Saita C; Yamaguchi T; Horiguchi SI; Yamada R; Takao M; Iijima T; Wakaume R; Aruga T; Tabata T; Koizumi K
PLoS One; 2018; 13(4):e0195572. PubMed ID: 29672549
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7. MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation.
Nguyen A; Bougeard G; Koob M; Chenard MP; Schneider A; Maugard C; Entz-Werle N
Fam Cancer; 2016 Oct; 15(4):571-7. PubMed ID: 27017609
[TBL] [Abstract] [Full Text] [Related]
8. Undifferentiated Carcinoma of the Endometrium: An Expanded Immunohistochemical Analysis Including PAX-8 and Basal-Like Carcinoma Surrogate Markers.
Ramalingam P; Masand RP; Euscher ED; Malpica A
Int J Gynecol Pathol; 2016 Sep; 35(5):410-8. PubMed ID: 26598976
[TBL] [Abstract] [Full Text] [Related]
9. Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort.
Lavoine N; Colas C; Muleris M; Bodo S; Duval A; Entz-Werle N; Coulet F; Cabaret O; Andreiuolo F; Charpy C; Sebille G; Wang Q; Lejeune S; Buisine MP; Leroux D; Couillault G; Leverger G; Fricker JP; Guimbaud R; Mathieu-Dramard M; Jedraszak G; Cohen-Hagenauer O; Guerrini-Rousseau L; Bourdeaut F; Grill J; Caron O; Baert-Dusermont S; Tinat J; Bougeard G; Frébourg T; Brugières L
J Med Genet; 2015 Nov; 52(11):770-8. PubMed ID: 26318770
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10. A First Step toward Personalized Medicine in Osteosarcoma: Pharmacogenetics as Predictive Marker of Outcome after Chemotherapy-Based Treatment.
Hagleitner MM; Coenen MJ; Gelderblom H; Makkinje RR; Vos HI; de Bont ES; van der Graaf WT; Schreuder HW; Flucke U; van Leeuwen FN; Hoogerbrugge PM; Guchelaar HJ; te Loo DM
Clin Cancer Res; 2015 Aug; 21(15):3436-41. PubMed ID: 25829401
[TBL] [Abstract] [Full Text] [Related]
11. Soft tissue sarcoma and the hereditary non-polyposis colorectal cancer (hnpcc) syndrome: formulation of an hypothesis.
Urso E; Agostini M; Pucciarelli S; Bedin C; D'angelo E; Mescoli C; Viel A; Maretto I; Mammi I; Nitti D
Mol Biol Rep; 2012 Oct; 39(10):9307-10. PubMed ID: 22782591
[TBL] [Abstract] [Full Text] [Related]
12. Genealogical tree study as screening method in the Lynch syndrome prior to genetic test.
Delgado-Plasencia L; Medina-Arana V; Barrios Del Pino Y; Fernández-Peralta A; González-Aguilera JJ
Am J Clin Oncol; 2010 Aug; 33(4):376-80. PubMed ID: 20010080
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13. Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome.
Kratz CP; Holter S; Etzler J; Lauten M; Pollett A; Niemeyer CM; Gallinger S; Wimmer K
J Med Genet; 2009 Jun; 46(6):418-20. PubMed ID: 19293170
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14. sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum.
Nilbert M; Therkildsen C; Nissen A; Akerman M; Bernstein I
Fam Cancer; 2009; 8(3):209-13. PubMed ID: 19130300
[TBL] [Abstract] [Full Text] [Related]
15. Uterine carcinosarcoma associated with hereditary nonpolyposis colorectal cancer.
South SA; Hutton M; Farrell C; Mhawech-Fauceglia P; Rodabaugh KJ
Obstet Gynecol; 2007 Aug; 110(2 Pt 2):543-5. PubMed ID: 17666659
[TBL] [Abstract] [Full Text] [Related]
16. Familial sarcoma: challenging pedigrees.
Lynch HT; Deters CA; Hogg D; Lynch JF; Kinarsky Y; Gatalica Z
Cancer; 2003 Nov; 98(9):1947-57. PubMed ID: 14584079
[TBL] [Abstract] [Full Text] [Related]
17. [Molecular pathologic diagnosis in solid tumors. What is clinically relevant?].
Werner M; Cabras AD; Höfler H
Pathologe; 2002 May; 23(3):170-3. PubMed ID: 12089783
[TBL] [Abstract] [Full Text] [Related]
18. Predisposing genes in breast and ovarian cancer: an overview.
Smith SA; Ponder BA
Tumori; 1993 Oct; 79(5):291-6. PubMed ID: 8116068
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