BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

216 related articles for article (PubMed ID: 29231814)

  • 1. A homozygous
    Fouquet B; Pawlikowska P; Caburet S; Guigon C; Mäkinen M; Tanner L; Hietala M; Urbanska K; Bellutti L; Legois B; Bessieres B; Gougeon A; Benachi A; Livera G; Rosselli F; Veitia RA; Misrahi M
    Elife; 2017 Dec; 6():. PubMed ID: 29231814
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia.
    Bogliolo M; Bluteau D; Lespinasse J; Pujol R; Vasquez N; d'Enghien CD; Stoppa-Lyonnet D; Leblanc T; Soulier J; Surrallés J
    Genet Med; 2018 Apr; 20(4):458-463. PubMed ID: 28837157
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M.
    Singh TR; Bakker ST; Agarwal S; Jansen M; Grassman E; Godthelp BC; Ali AM; Du CH; Rooimans MA; Fan Q; Wahengbam K; Steltenpool J; Andreassen PR; Williams DA; Joenje H; de Winter JP; Meetei AR
    Blood; 2009 Jul; 114(1):174-80. PubMed ID: 19423727
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia.
    Kasak L; Punab M; Nagirnaja L; Grigorova M; Minajeva A; Lopes AM; Punab AM; Aston KI; Carvalho F; Laasik E; Smith LB; ; Conrad DF; Laan M
    Am J Hum Genet; 2018 Aug; 103(2):200-212. PubMed ID: 30075111
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Novel Phenotype Combining Primary Ovarian Insufficiency Growth Retardation and Pilomatricomas With MCM8 Mutation.
    Heddar A; Beckers D; Fouquet B; Roland D; Misrahi M
    J Clin Endocrinol Metab; 2020 Jun; 105(6):. PubMed ID: 32242235
    [TBL] [Abstract][Full Text] [Related]  

  • 6. FANCM of the Fanconi anemia core complex is required for both monoubiquitination and DNA repair.
    Xue Y; Li Y; Guo R; Ling C; Wang W
    Hum Mol Genet; 2008 Jun; 17(11):1641-52. PubMed ID: 18285517
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility.
    Catucci I; Osorio A; Arver B; Neidhardt G; Bogliolo M; Zanardi F; Riboni M; Minardi S; Pujol R; Azzollini J; Peissel B; Manoukian S; De Vecchi G; Casola S; Hauke J; Richters L; Rhiem K; Schmutzler RK; Wallander K; Törngren T; Borg Å; Radice P; Surrallés J; Hahnen E; Ehrencrona H; Kvist A; Benitez J; Peterlongo P
    Genet Med; 2018 Apr; 20(4):452-457. PubMed ID: 28837162
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in MSH5 in primary ovarian insufficiency.
    Guo T; Zhao S; Zhao S; Chen M; Li G; Jiao X; Wang Z; Zhao Y; Qin Y; Gao F; Chen ZJ
    Hum Mol Genet; 2017 Apr; 26(8):1452-1457. PubMed ID: 28175301
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Differential contribution of the Fanconi anemia-related proteins to repair of several types of DNA damage in cultured silkworm cells.
    Sugahara R; Mon H; Lee JM; Shiotsuki T; Kusakabe T
    FEBS Lett; 2014 Nov; 588(21):3959-63. PubMed ID: 25240201
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FANCL gene mutations in premature ovarian insufficiency.
    Yang Y; Guo T; Liu R; Ke H; Xu W; Zhao S; Qin Y
    Hum Mutat; 2020 May; 41(5):1033-1041. PubMed ID: 32048394
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.
    Caburet S; Todeschini AL; Petrillo C; Martini E; Farran ND; Legois B; Livera G; Younis JS; Shalev S; Veitia RA
    EBioMedicine; 2019 Apr; 42():524-531. PubMed ID: 31000419
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A homozygous FANCM frameshift pathogenic variant causes male infertility.
    Yin H; Ma H; Hussain S; Zhang H; Xie X; Jiang L; Jiang X; Iqbal F; Bukhari I; Jiang H; Ali A; Zhong L; Li T; Fan S; Zhang B; Gao J; Li Y; Nazish J; Khan T; Khan M; Zubair M; Hao Q; Fang H; Huang J; Huleihel M; Sha J; Pandita TK; Zhang Y; Shi Q
    Genet Med; 2019 Jan; 21(1):62-70. PubMed ID: 29895858
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rare variants in FANCA induce premature ovarian insufficiency.
    Yang X; Zhang X; Jiao J; Zhang F; Pan Y; Wang Q; Chen Q; Cai B; Tang S; Zhou Z; Chen S; Yin H; Fu W; Luo Y; Li D; Li G; Shang L; Yang J; Jin L; Shi Q; Wu Y
    Hum Genet; 2019 Dec; 138(11-12):1227-1236. PubMed ID: 31535215
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
    Fan S; Jiao Y; Khan R; Jiang X; Javed AR; Ali A; Zhang H; Zhou J; Naeem M; Murtaza G; Li Y; Yang G; Zaman Q; Zubair M; Guan H; Zhang X; Ma H; Jiang H; Ali H; Dil S; Shah W; Ahmad N; Zhang Y; Shi Q
    Am J Hum Genet; 2021 Feb; 108(2):324-336. PubMed ID: 33508233
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel homozygous mutation in the FSHR gene is causative for primary ovarian insufficiency.
    Liu H; Xu X; Han T; Yan L; Cheng L; Qin Y; Liu W; Zhao S; Chen ZJ
    Fertil Steril; 2017 Dec; 108(6):1050-1055.e2. PubMed ID: 29157895
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24.
    Daschkey S; Bienemann K; Schuster V; Kreth HW; Linka RM; Hönscheid A; Fritz G; Johannes C; Fleckenstein B; Kempkes B; Gombert M; Ginzel S; Borkhardt A
    J Clin Immunol; 2016 Oct; 36(7):684-92. PubMed ID: 27473539
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Fanconi anemia ortholog FANCM ensures ordered homologous recombination in both somatic and meiotic cells in Arabidopsis.
    Knoll A; Higgins JD; Seeliger K; Reha SJ; Dangel NJ; Bauknecht M; Schröpfer S; Franklin FC; Puchta H
    Plant Cell; 2012 Apr; 24(4):1448-64. PubMed ID: 22547783
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosomal instability in women with primary ovarian insufficiency.
    Katari S; Aarabi M; Kintigh A; Mann S; Yatsenko SA; Sanfilippo JS; Zeleznik AJ; Rajkovic A
    Hum Reprod; 2018 Mar; 33(3):531-538. PubMed ID: 29425284
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetic instability in ovarian epithelial cells from women at risk of ovarian cancer.
    Pejovic T; Yates JE; Liu HY; Hays LE; Akkari Y; Torimaru Y; Keeble W; Rathbun RK; Rodgers WH; Bale AE; Ameziane N; Zwaan CM; Errami A; Thuillier P; Cappuccini F; Olson SB; Cain JM; Bagby GC
    Cancer Res; 2006 Sep; 66(18):9017-25. PubMed ID: 16982743
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole-exome sequencing identifies a homozygous donor splice-site mutation in STAG3 that causes primary ovarian insufficiency.
    He WB; Banerjee S; Meng LL; Du J; Gong F; Huang H; Zhang XX; Wang YY; Lu GX; Lin G; Tan YQ
    Clin Genet; 2018 Feb; 93(2):340-344. PubMed ID: 28393351
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.