BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Lymphoma AND MSH2, COCA1, 4436, ENSG00000095002, HNPCC, FCC1, HNPCC1, P43246 AND Diagnosis
20 results:

  • 1. Constitutional Mismatch Repair Deficiency Syndrome as a Cause of Numerous Malignancies in a Teenage Patient-A Case Report.
    Samborska M; Galli D; Achkar R; Thambyrajah S; Derwich K
    J Pediatr Hematol Oncol; 2023 Oct; 45(7):e917-e920. PubMed ID: 37526375
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. Genomics improves risk stratification of adults with T-cell acute lymphoblastic leukemia enrolled in measurable residual disease-oriented trials.
    González-Gil C; Morgades M; Lopes T; Fuster-Tormo F; García-Chica J; Zhao R; Montesinos P; Torrent A; Diaz-Beya M; Coll R; Hermosín L; Mercadal S; González-Campos J; Zamora L; Artola T; Vall-Llovera F; Tormo M; Gil-Cortés C; Barba P; Novo A; Ribera J; Bernal T; De Ugarriza PL; Queipo MP; Martínez-Sánchez P; Giménez A; González-Martínez T; Cladera A; Cervera J; Fernández-Martín R; Ardaiz MÁ; Vidal MJ; Baena Á; López-Bigas N; Bigas A; Maciejewski J; Orfao A; Ribera JM; Genescà E
    Haematologica; 2023 Apr; 108(4):969-980. PubMed ID: 36325893
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. Double heterozygotes of BRCA1/BRCA2 and mismatch repair gene pathogenic variants: case series and clinical implications.
    Laish I; Friedman E; Levi-Reznick G; Kedar I; Katz L; Levi Z; Halpern N; Parnasa S; Abu-Shatya A; Half E; Goldberg Y
    Breast Cancer Res Treat; 2021 Aug; 188(3):685-694. PubMed ID: 34086170
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. Clinicopathological features and risk factors for developing colorectal neoplasia in Hodgkin's lymphoma survivors.
    Ykema BLM; Rigter LS; Spaander MCW; Moons LMG; Bisseling TM; Aleman BMP; Dekker E; Verbeek WHM; Kuipers EJ; de Boer JP; Lugtenburg PJ; Janus CPM; Petersen EJ; Roesink JM; van der Maazen RWM; Meijer GA; Schaapveld M; van Leeuwen FE; Carvalho B; Snaebjornsson P; van Leerdam ME
    Dig Endosc; 2022 Jan; 34(1):163-170. PubMed ID: 33928678
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. Therapy-induced mutations drive the genomic landscape of relapsed acute lymphoblastic leukemia.
    Li B; Brady SW; Ma X; Shen S; Zhang Y; Li Y; Szlachta K; Dong L; Liu Y; Yang F; Wang N; Flasch DA; Myers MA; Mulder HL; Ding L; Liu Y; Tian L; Hagiwara K; Xu K; Zhou X; Sioson E; Wang T; Yang L; Zhao J; Zhang H; Shao Y; Sun H; Sun L; Cai J; Sun HY; Lin TN; Du L; Li H; Rusch M; Edmonson MN; Easton J; Zhu X; Zhang J; Cheng C; Raphael BJ; Tang J; Downing JR; Alexandrov LB; Zhou BS; Pui CH; Yang JJ; Zhang J
    Blood; 2020 Jan; 135(1):41-55. PubMed ID: 31697823
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. [Constitutional MMR deficiency: Genetic bases and clinical implications].
    Buecher B; Le Mentec M; Doz F; Bourdeaut F; Gauthier-Villars M; Stoppa-Lyonnet D; Colas C
    Bull Cancer; 2019 Feb; 106(2):162-172. PubMed ID: 30551794
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. ALK-positive gastric inflammatory myofibroblastic tumor in an adult with familial adenomatous polyposis and diffuse fundic polyposis.
    Fan J; Huang B; Yang X; Yang M; He J; Nie X
    Diagn Pathol; 2017 Sep; 12(1):68. PubMed ID: 28923119
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. 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]  

  • 9. Acute lymphoblastic leukemia and lymphoma in the context of constitutional mismatch repair deficiency syndrome.
    Ripperger T; Schlegelberger B
    Eur J Med Genet; 2016 Mar; 59(3):133-42. PubMed ID: 26743104
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity.
    Baris HN; Barnes-Kedar I; Toledano H; Halpern M; Hershkovitz D; Lossos A; Lerer I; Peretz T; Kariv R; Cohen S; Half EE; Magal N; Drasinover V; Wimmer K; Goldberg Y; Bercovich D; Levi Z
    Pediatr Blood Cancer; 2016 Mar; 63(3):418-27. PubMed ID: 26544533
    [TBL] [Abstract] [Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.
    Bodo S; Colas C; Buhard O; Collura A; Tinat J; Lavoine N; Guilloux A; Chalastanis A; Lafitte P; Coulet F; Buisine MP; Ilencikova D; Ruiz-Ponte C; Kinzel M; Grandjouan S; Brems H; Lejeune S; Blanché H; Wang Q; Caron O; Cabaret O; Svrcek M; Vidaud D; Parfait B; Verloes A; Knappe UJ; Soubrier F; Mortemousque I; Leis A; Auclair-Perrossier J; Frébourg T; Fléjou JF; Entz-Werle N; Leclerc J; Malka D; Cohen-Haguenauer O; Goldberg Y; Gerdes AM; Fedhila F; Mathieu-Dramard M; Hamelin R; Wafaa B; Gauthier-Villars M; Bourdeaut F; Sheridan E; Vasen H; Brugières L; Wimmer K; Muleris M; Duval A;
    Gastroenterology; 2015 Oct; 149(4):1017-29.e3. PubMed ID: 26116798
    [TBL] [Abstract] [Full Text] [Related]  

  • 13. [Management of hereditary non-polyposis syndrome (Lynch syndrome)].
    Kariv R; Goldberg Y; Soler I; Rosner G; Half E; Moshkowitz M; Vilkin A; Levi Z; Niv Y
    Harefuah; 2011 Apr; 150(4):392-6, 416. PubMed ID: 22164924
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. The mechanisms underlying MMR deficiency in immunodeficiency-related non-Hodgkin lymphomas are different from those in other sporadic microsatellite instable neoplasms.
    Borie C; Colas C; Dartigues P; Lazure T; Rince P; Buhard O; Folliot P; Chalastanis A; Muleris M; Hamelin R; Mercier D; Oliveira C; Seruca R; Chadburn A; Leblond V; Barete S; Gaïdano G; Martin A; Gaulard P; Fléjou JF; Raphael M; Duval A
    Int J Cancer; 2009 Nov; 125(10):2360-6. PubMed ID: 19551857
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. Familial T-cell non-Hodgkin lymphoma caused by biallelic msh2 mutations.
    Scott RH; Homfray T; Huxter NL; Mitton SG; Nash R; Potter MN; Lancaster D; Rahman N
    J Med Genet; 2007 Jul; 44(7):e83. PubMed ID: 17601929
    [TBL] [Abstract] [Full Text] [Related]  

  • 16. Neurofibromatosis von Recklinghausen type I phenotype and early onset of cancers in siblings compound heterozygous for mutations in MSH6.
    Ostergaard JR; Sunde L; Okkels H
    Am J Med Genet A; 2005 Dec; 139A(2):96-105; discussion 96. PubMed ID: 16283678
    [TBL] [Abstract] [Full Text] [Related]  

  • 17. Colorectal malignancies in HIV-positive patients.
    Yegüez JF; Martinez SA; Sands DR; Sands LR; Hellinger MD
    Am Surg; 2003 Nov; 69(11):981-7. PubMed ID: 14627261
    [TBL] [Abstract] [Full Text] [Related]  

  • 18. Café-au-lait spots and early onset colorectal neoplasia: a variant of hnpcc?
    Trimbath JD; Petersen GM; Erdman SH; Ferre M; Luce MC; Giardiello FM
    Fam Cancer; 2001; 1(2):101-5. PubMed ID: 14574005
    [TBL] [Abstract] [Full Text] [Related]  

  • 19. Analysis of mismatch repair defects in the familial occurrence of lymphoma and colorectal cancer.
    Teruya-Feldstein J; Greene J; Cohen L; Popplewell L; Ellis NA; Offit K
    Leuk Lymphoma; 2002 Aug; 43(8):1619-26. PubMed ID: 12400605
    [TBL] [Abstract] [Full Text] [Related]  

  • 20. Association of a duodenal follicular lymphoma and hereditary nonpolyposis colorectal cancer.
    Rosty C; Brière J; Cellier C; Delabesse E; Carnot F; Barbier JP; Laurent-Puig P
    Mod Pathol; 2000 May; 13(5):586-90. PubMed ID: 10824932
    [TBL] [Abstract] [Full Text] [Related]  


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