BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 35903677)

  • 21. Metachronous Wilms Tumor, Glioblastoma, and T-cell Leukemia in an Child With Constitutional Mismatch Repair Deficiency syndrome due to Novel Mutation in MSH6 (c.2590G>T).
    Citak EC; Sagcan F; Gundugan BD; Bozdogan ST; Yilmaz EB; Avci E; Balci Y; Karabulut YY
    J Pediatr Hematol Oncol; 2021 Mar; 43(2):e198-e202. PubMed ID: 31815888
    [TBL] [Abstract][Full Text] [Related]  

  • 22. An Unusual Case of Constitutional Mismatch Repair Deficiency Syndrome With Anaplastic Ganglioglioma, Colonic Adenocarcinoma, Osteosarcoma, Acute Myeloid Leukemia, and Signs of Neurofibromatosis Type 1: Case Report.
    Daou B; Zanello M; Varlet P; Brugieres L; Jabbour P; Caron O; Lavoine N; Dhermain F; Willekens C; Beuvon F; Malka D; Lechapt-Zalcmann E; Abi Lahoud G
    Neurosurgery; 2015 Jul; 77(1):E145-52; discussion E152. PubMed ID: 25850602
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Molecular Basis of Mismatch Repair Protein Deficiency in Tumors from Lynch Suspected Cases with Negative Germline Test Results.
    Olkinuora A; Gylling A; Almusa H; Eldfors S; Lepistö A; Mecklin JP; Nieminen TT; Peltomäki P
    Cancers (Basel); 2020 Jul; 12(7):. PubMed ID: 32660107
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Paediatric systemic lupus erythematosus as a manifestation of constitutional mismatch repair deficiency.
    Toledano H; Orenstein N; Sofrin E; Ruhrman-Shahar N; Amarilyo G; Basel-Salmon L; Shuldiner AR; Smirin-Yosef P; Aronson M; Al-Tarrah H; Bazak L; Gonzaga-Jauregui C; Tabori U; Wimmer K; Goldberg Y
    J Med Genet; 2020 Jul; 57(7):505-508. PubMed ID: 31501241
    [TBL] [Abstract][Full Text] [Related]  

  • 26. High-grade brain tumors in siblings with biallelic MSH6 mutations.
    Ilencikova D; Sejnova D; Jindrova J; Babal P
    Pediatr Blood Cancer; 2011 Dec; 57(6):1067-70. PubMed ID: 21674763
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Pitfalls in molecular analysis for mismatch repair deficiency in a family with biallelic pms2 germline mutations.
    Leenen CH; Geurts-Giele WR; Dubbink HJ; Reddingius R; van den Ouweland AM; Tops CM; van de Klift HM; Kuipers EJ; van Leerdam ME; Dinjens WN; Wagner A
    Clin Genet; 2011 Dec; 80(6):558-65. PubMed ID: 21204794
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Germline
    Lindsay H; Scollon S; Reuther J; Voicu H; Rednam SP; Lin FY; Fisher KE; Chintagumpala M; Adesina AM; Parsons DW; Plon SE; Roy A
    Cold Spring Harb Mol Case Stud; 2019 Oct; 5(5):. PubMed ID: 31624068
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Atypical pituitary adenoma with MEN1 somatic mutation associated with abnormalities of DNA mismatch repair genes; MLH1 germline mutation and MSH6 somatic mutation.
    Uraki S; Ariyasu H; Doi A; Furuta H; Nishi M; Sugano K; Inoshita N; Nakao N; Yamada S; Akamizu T
    Endocr J; 2017 Sep; 64(9):895-906. PubMed ID: 28701629
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome.
    Baig SM; Fatima A; Tariq M; Khan TN; Ali Z; Faheem M; Mahmood H; Killela P; Waitkus M; He Y; Zhao F; Wang S; Jiao Y; Yan H
    Fam Cancer; 2019 Apr; 18(2):261-265. PubMed ID: 30478739
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Constitutional mismatch repair deficiency (CMMRD) presenting with high-grade glioma, multiple developmental venous anomalies and malformations of cortical development-a multidisciplinary/multicentre approach and neuroimaging clues to clinching the diagnosis.
    Chhabda S; Sudhakar S; Mankad K; Jorgensen M; Carceller F; Jacques TS; Merve A; Aizpurua M; Chalker J; Garimberti E; D'Arco F
    Childs Nerv Syst; 2021 Jul; 37(7):2375-2379. PubMed ID: 33247381
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?
    Suerink M; Potjer TP; Versluijs AB; Ten Broeke SW; Tops CM; Wimmer K; Nielsen M
    Clin Genet; 2018 Jan; 93(1):134-137. PubMed ID: 28503822
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Constitutional mismatch repair deficiency and childhood leukemia/lymphoma--report on a novel biallelic MSH6 mutation.
    Ripperger T; Beger C; Rahner N; Sykora KW; Bockmeyer CL; Lehmann U; Kreipe HH; Schlegelberger B
    Haematologica; 2010 May; 95(5):841-4. PubMed ID: 20015892
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Immune Checkpoint Inhibition as Primary Adjuvant Therapy for an
    Rittberg R; Harlos C; Rothenmund H; Das A; Tabori U; Sinha N; Singh H; Chodirker B; Kim CA
    Curr Oncol; 2021 Feb; 28(1):757-766. PubMed ID: 33535600
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy.
    Suerink M; Ripperger T; Messiaen L; Menko FH; Bourdeaut F; Colas C; Jongmans M; Goldberg Y; Nielsen M; Muleris M; van Kouwen M; Slavc I; Kratz C; Vasen HF; Brugiѐres L; Legius E; Wimmer K
    J Med Genet; 2019 Feb; 56(2):53-62. PubMed ID: 30415209
    [TBL] [Abstract][Full Text] [Related]  

  • 36. No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency.
    Tesch VK; IJspeert H; Raicht A; Rueda D; Dominguez-Pinilla N; Allende LM; Colas C; Rosenbaum T; Ilencikova D; Baris HN; Nathrath MHM; Suerink M; Januszkiewicz-Lewandowska D; Ragab I; Azizi AA; Wenzel SS; Zschocke J; Schwinger W; Kloor M; Blattmann C; Brugieres L; van der Burg M; Wimmer K; Seidel MG
    Front Immunol; 2018; 9():1506. PubMed ID: 30013564
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis.
    Vargas-Parra GM; González-Acosta M; Thompson BA; Gómez C; Fernández A; Dámaso E; Pons T; Morak M; Del Valle J; Iglesias S; Velasco À; Solanes A; Sanjuan X; Padilla N; de la Cruz X; Valencia A; Holinski-Feder E; Brunet J; Feliubadaló L; Lázaro C; Navarro M; Pineda M; Capellá G
    Int J Cancer; 2017 Oct; 141(7):1365-1380. PubMed ID: 28577310
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.
    van der Klift HM; Mensenkamp AR; Drost M; Bik EC; Vos YJ; Gille HJ; Redeker BE; Tiersma Y; Zonneveld JB; García EG; Letteboer TG; Olderode-Berends MJ; van Hest LP; van Os TA; Verhoef S; Wagner A; van Asperen CJ; Ten Broeke SW; Hes FJ; de Wind N; Nielsen M; Devilee P; Ligtenberg MJ; Wijnen JT; Tops CM
    Hum Mutat; 2016 Nov; 37(11):1162-1179. PubMed ID: 27435373
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Patterns of germline and somatic mutations in 16 genes associated with mismatch repair function or containing tandem repeat sequences.
    Chang SC; Lan YT; Lin PC; Yang SH; Lin CH; Liang WY; Chen WS; Jiang JK; Lin JK
    Cancer Med; 2020 Jan; 9(2):476-486. PubMed ID: 31769227
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Constitutional mismatch repair-deficiency syndrome (CMMR-D) - a case report of a family with biallelic MSH6 mutation].
    Ilenčíková D
    Klin Onkol; 2012; 25 Suppl():S34-8. PubMed ID: 22920205
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.