BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Lymphoma AND MLH1, COCA2, 4292, ENSG00000076242, hMLH1, FCC2, HNPCC2, P40692, MGC5172, HNPCC AND Diagnosis
24 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. 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]  

  • 3. [Un- and dedifferentiated endometrial carcinoma : A rare entity with a wide range of differential diagnosis].
    Höhn AK; Brambs CE; Opitz S; Erber R; Hartmann A; Horn LC
    Pathologe; 2019 Nov; 40(6):609-618. PubMed ID: 31578630
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. [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]  

  • 5. 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]  

  • 6. Hypertriglyceridemia during asparaginase treatment in children with acute lymphoblastic leukemia correlates with antithrombin activity in adolescents.
    Persson L; Harila-Saari A; Hed Myrberg I; Heyman M; Nilsson A; Ranta S
    Pediatr Blood Cancer; 2017 Oct; 64(10):. PubMed ID: 28440015
    [TBL] [Abstract] [Full Text] [Related]  

  • 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. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Primary intraocular lymphoma.
    Sagoo MS; Mehta H; Swampillai AJ; Cohen VM; Amin SZ; Plowman PN; Lightman S
    Surv Ophthalmol; 2014; 59(5):503-16. PubMed ID: 24560125
    [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. Endometrial and ovarian carcinomas with undifferentiated components: clinically aggressive and frequently underrecognized neoplasms.
    Tafe LJ; Garg K; Chew I; Tornos C; Soslow RA
    Mod Pathol; 2010 Jun; 23(6):781-9. PubMed ID: 20305618
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Aberrant methylation in promoter-associated CpG islands of multiple genes in relapsed childhood acute lymphoblastic leukemia.
    Matsushita C; Yang Y; Takeuchi S; Matsushita M; Van Dongen JJ; Szczepanski T; Bartram CR; Seo H; Koeffler HP; Taguchi H
    Oncol Rep; 2004 Jul; 12(1):97-9. PubMed ID: 15201966
    [TBL] [Abstract] [Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  


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