These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 33977026)

  • 21. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
    Lord J; McMullan DJ; Eberhardt RY; Rinck G; Hamilton SJ; Quinlan-Jones E; Prigmore E; Keelagher R; Best SK; Carey GK; Mellis R; Robart S; Berry IR; Chandler KE; Cilliers D; Cresswell L; Edwards SL; Gardiner C; Henderson A; Holden ST; Homfray T; Lester T; Lewis RA; Newbury-Ecob R; Prescott K; Quarrell OW; Ramsden SC; Roberts E; Tapon D; Tooley MJ; Vasudevan PC; Weber AP; Wellesley DG; Westwood P; White H; Parker M; Williams D; Jenkins L; Scott RH; Kilby MD; Chitty LS; Hurles ME; Maher ER;
    Lancet; 2019 Feb; 393(10173):747-757. PubMed ID: 30712880
    [TBL] [Abstract][Full Text] [Related]  

  • 22. C1QBP negatively regulates the activation of oncoprotein YBX1 in the renal cell carcinoma as revealed by interactomics analysis.
    Wang Y; Yue D; Xiao M; Qi C; Chen Y; Sun D; Zhang N; Chen R
    J Proteome Res; 2015 Feb; 14(2):804-13. PubMed ID: 25497084
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis of autosomal recessive renal tubular dysgenesis caused by variants in the ACE gene: Two fetuses with anhydramnios.
    Nguyen Thi S; Nguyen Duy A; Luong Thi Lan A; Pho Hong D; Thu HN; Huu BL; Nguyen Duc A; Thi HN; Thi CTT
    Prenat Diagn; 2024 Feb; 44(2):255-259. PubMed ID: 38091257
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Interest of chromosomal microarray analysis in the prenatal diagnosis of fetal intrauterine growth restriction.
    Brun S; Pennamen P; Mattuizzi A; Coatleven F; Vuillaume ML; Lacombe D; Arveiler B; Toutain J; Rooryck C
    Prenat Diagn; 2018 Dec; 38(13):1111-1119. PubMed ID: 30328630
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Utility of trio-based prenatal exome sequencing incorporating splice-site and mitochondrial genome assessment in pregnancies with fetal ultrasound anomalies: prospective cohort study.
    Zhu X; Gao Z; Wang Y; Huang W; Li Q; Jiao Z; Liu N; Kong X
    Ultrasound Obstet Gynecol; 2022 Dec; 60(6):780-792. PubMed ID: 35726512
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Neu-Laxova syndrome presenting prenatally with increased nuchal translucency and cystic hygroma: The utility of exome sequencing in deciphering the diagnosis.
    Bourque DK; Cloutier M; Kernohan KD; Bareke E; Grynspan D; Michaud J; ; Boycott KM
    Am J Med Genet A; 2019 May; 179(5):813-816. PubMed ID: 30838783
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
    Petrovski S; Aggarwal V; Giordano JL; Stosic M; Wou K; Bier L; Spiegel E; Brennan K; Stong N; Jobanputra V; Ren Z; Zhu X; Mebane C; Nahum O; Wang Q; Kamalakaran S; Malone C; Anyane-Yeboa K; Miller R; Levy B; Goldstein DB; Wapner RJ
    Lancet; 2019 Feb; 393(10173):758-767. PubMed ID: 30712878
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cardiomyocyte-specific loss of mitochondrial p32/C1qbp causes cardiomyopathy and activates stress responses.
    Saito T; Uchiumi T; Yagi M; Amamoto R; Setoyama D; Matsushima Y; Kang D
    Cardiovasc Res; 2017 Aug; 113(10):1173-1185. PubMed ID: 28498888
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Identification of a novel mitochondrial interacting protein of C1QBP using subcellular fractionation coupled with CoIP-MS.
    Chen R; Xiao M; Gao H; Chen Y; Li Y; Liu Y; Zhang N
    Anal Bioanal Chem; 2016 Feb; 408(6):1557-64. PubMed ID: 26753982
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel homozygous ERCC5 truncating mutation in a family with prenatal arthrogryposis--further evidence of genotype-phenotype correlation.
    Drury S; Boustred C; Tekman M; Stanescu H; Kleta R; Lench N; Chitty LS; Scott RH
    Am J Med Genet A; 2014 Jul; 164A(7):1777-83. PubMed ID: 24700531
    [TBL] [Abstract][Full Text] [Related]  

  • 31. An exome sequencing strategy to diagnose lethal autosomal recessive disorders.
    Ellard S; Kivuva E; Turnpenny P; Stals K; Johnson M; Xie W; Caswell R; Lango Allen H
    Eur J Hum Genet; 2015 Mar; 23(3):401-4. PubMed ID: 24961629
    [TBL] [Abstract][Full Text] [Related]  

  • 32. C1QBP inhibits proliferation of porcine circovirus type 2 by restricting nuclear import of the capsid protein.
    Ma X; Lv C; Wang Q; Li C; Wang P; Luo C; Wu Y; Wei T; Liu S; Adam FEA; Yang Z; Wang X
    Arch Virol; 2021 Mar; 166(3):767-778. PubMed ID: 33420816
    [TBL] [Abstract][Full Text] [Related]  

  • 33. UPD16 itself is not a cause of intrauterine growth restriction.
    Wang H; Luo C; Liu Y; Li S; Jiang N; Zhang G; Xie J; Zhong M
    Fetal Pediatr Pathol; 2018 Dec; 37(6):452-464. PubMed ID: 30468402
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical Features, Molecular Heterogeneity, and Prognostic Implications in YARS2-Related Mitochondrial Myopathy.
    Sommerville EW; Ng YS; Alston CL; Dallabona C; Gilberti M; He L; Knowles C; Chin SL; Schaefer AM; Falkous G; Murdoch D; Longman C; de Visser M; Bindoff LA; Rawles JM; Dean JCS; Petty RK; Farrugia ME; Haack TB; Prokisch H; McFarland R; Turnbull DM; Donnini C; Taylor RW; Gorman GS
    JAMA Neurol; 2017 Jun; 74(6):686-694. PubMed ID: 28395030
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Loss of CHCHD2 Stability Coordinates with C1QBP/CHCHD2/CHCHD10 Complex Impairment to Mediate PD-Linked Mitochondrial Dysfunction.
    Ren YL; Jiang Z; Wang JY; He Q; Li SX; Gu XJ; Qi YR; Zhang M; Yang WJ; Cao B; Li JY; Wang Y; Chen YP
    Mol Neurobiol; 2024 Oct; 61(10):7968-7988. PubMed ID: 38453793
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Pathogenic variants in MRPL44 cause infantile cardiomyopathy due to a mitochondrial translation defect.
    Friederich MW; Geddes GC; Wortmann SB; Punnoose A; Wartchow E; Knight KM; Prokisch H; Creadon-Swindell G; Mayr JA; Van Hove JLK
    Mol Genet Metab; 2021 Aug; 133(4):362-371. PubMed ID: 34140213
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Added Value of Whole-Exome Sequencing for Anomalous Fetuses With Detailed Prenatal Ultrasound and Postnatal Phenotype.
    He M; Du L; Xie H; Zhang L; Gu Y; Lei T; Zheng J; Chen D
    Front Genet; 2021; 12():627204. PubMed ID: 34367232
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Utility of chromosomal microarray analysis for the exploration of isolated and severe fetal growth restriction diagnosed before 24 weeks' gestation.
    Dap M; Gicquel F; Lambert L; Perdriolle-Galet E; Bonnet C; Morel O
    Prenat Diagn; 2022 Sep; 42(10):1281-1287. PubMed ID: 35426144
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect.
    Qiao F; Wang Y; Zhang C; Zhou R; Wu Y; Wang C; Meng L; Mao P; Cheng Q; Luo C; Hu P; Xu Z
    Ultrasound Obstet Gynecol; 2021 Sep; 58(3):377-387. PubMed ID: 33142350
    [TBL] [Abstract][Full Text] [Related]  

  • 40. C1QBP regulates apoptosis of renal cell carcinoma via modulating xanthine dehydrogenase (XDH) mediated ROS generation.
    Wang Y; Liu S; Tian S; Du R; Lin T; Xiao X; Wang R; Chen R; Geng H; Subramanian S; Niu Y; Wang Y; Yue D
    Int J Med Sci; 2022; 19(5):842-857. PubMed ID: 35693733
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.