BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 34815695)

  • 1. Whole Exome Sequencing Study in a Family with Type 2 Diabetes Mellitus.
    Zhou X; Guo W; Yin H; Chen J; Ma L; Yang Q; Zhao Y; Li S; Liu W; Li H
    Int J Gen Med; 2021; 14():8217-8229. PubMed ID: 34815695
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Screening of Candidate Pathogenic Genes for Spontaneous Abortion Using Whole Exome Sequencing.
    Zhu Q; Liu J; Chen L; Zhou Y; Zhou T; Bian W; Ding G; Li G; Ding J
    Comb Chem High Throughput Screen; 2022; 25(9):1462-1473. PubMed ID: 34225611
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Combined analysis of whole-exome sequencing and RNA sequencing in type 2 diabetes mellitus patients with thirst and fatigue.
    Lv B; Yang X; An T; Wu Y; He Z; Li B; Wang Y; Tan F; Wang T; Zhu J; Hu Y; Liu X; Jiang G
    Diabetol Metab Syndr; 2022 Aug; 14(1):111. PubMed ID: 35941691
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Combined analysis of whole-exon sequencing and lncRNA sequencing in type 2 diabetes mellitus patients with obesity.
    An T; Zhang J; Liu YF; Wu YX; Lian J; Wang TY; Hu YY; Zhu JJ; Huang J; Zhao DD; Mo FF; Gao SH; Jiang GJ
    J Cell Mol Med; 2020 Feb; 24(4):2451-2463. PubMed ID: 31957265
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism.
    Johnson SR; Leo PJ; McInerney-Leo AM; Anderson LK; Marshall M; McGown I; Newell F; Brown MA; Conwell LS; Harris M; Duncan EL
    Pediatr Diabetes; 2018 Jun; 19(4):656-662. PubMed ID: 29417725
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
    Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
    Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency.
    Wang L; Tsutsumi S; Kawaguchi T; Nagasaki K; Tatsuno K; Yamamoto S; Sang F; Sonoda K; Sugawara M; Saiura A; Hirono S; Yamaue H; Miki Y; Isomura M; Totoki Y; Nagae G; Isagawa T; Ueda H; Murayama-Hosokawa S; Shibata T; Sakamoto H; Kanai Y; Kaneda A; Noda T; Aburatani H
    Genome Res; 2012 Feb; 22(2):208-19. PubMed ID: 22156295
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evaluation of whole-genome sequencing of four Chinese crested dogs for variant detection using the ion proton system.
    Viluma A; Sayyab S; Mikko S; Andersson G; Bergström TF
    Canine Genet Epidemiol; 2015; 2():16. PubMed ID: 26457193
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Optimized detection of insertions/deletions (INDELs) in whole-exome sequencing data.
    Kim BY; Park JH; Jo HY; Koo SK; Park MH
    PLoS One; 2017; 12(8):e0182272. PubMed ID: 28792971
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of Two Cases of Ciliopathy-Associated Diabetes and Their Mutation Analysis Using Whole Exome Sequencing.
    Kim MK; Kwak SH; Kang S; Jung HS; Cho YM; Kim SY; Park KS
    Diabetes Metab J; 2015 Oct; 39(5):439-43. PubMed ID: 26566502
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide SNP and InDel mutations in Mycobacterium tuberculosis associated with rifampicin and isoniazid resistance.
    Li H; Guo H; Chen T; Yu L; Chen Y; Zhao J; Yan H; Chen M; Sun Q; Zhang C; Zhou L; Chen L
    Int J Clin Exp Pathol; 2018; 11(8):3903-3914. PubMed ID: 31949778
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Next generation sequencing exome data analysis aids in the discovery of SNP and INDEL patterns in Parkinson's disease.
    Odumpatta R; Mohanapriya A
    Genomics; 2020 Sep; 112(5):3722-3728. PubMed ID: 32348865
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Screening of familial primary biliary cholangitis and research on low-frequency mutations by whole-exome sequencing].
    Zhang S; Guo GY; Zhou X; Han Y
    Zhonghua Gan Zang Bing Za Zhi; 2018 May; 26(5):388-392. PubMed ID: 29996209
    [No Abstract]   [Full Text] [Related]  

  • 14. A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family.
    Jelani M; Kang C; Mohamoud HS; Al-Rehaili R; Almramhi MM; Serafi R; Yang H; Al-Aama JY; Naeem M; Alkhiary YM
    Arch Oral Biol; 2016 Jul; 67():28-33. PubMed ID: 27019138
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Somatic Genetic Variation in Solid Pseudopapillary Tumor of the Pancreas by Whole Exome Sequencing.
    Guo M; Luo G; Jin K; Long J; Cheng H; Lu Y; Wang Z; Yang C; Xu J; Ni Q; Yu X; Liu C
    Int J Mol Sci; 2017 Jan; 18(1):. PubMed ID: 28054945
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family.
    Gu JM; Ke YH; Yue H; Liu YJ; Zhang Z; Zhang H; Hu WW; Wang C; He JW; Hu YQ; Li M; Fu WZ; Zhang ZL
    Bone; 2013 Jan; 52(1):9-16. PubMed ID: 23000505
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exome sequencing identifies DLG1 as a novel gene for potential susceptibility to Crohn's disease in a Chinese family study.
    Xu S; Zhou F; Tao J; Song L; Ng SC; Wang X; Chen L; Yi F; Ran Z; Zhou R; Xia B
    PLoS One; 2014; 9(6):e99807. PubMed ID: 24937328
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa.
    Méndez-Vidal C; González-Del Pozo M; Vela-Boza A; Santoyo-López J; López-Domingo FJ; Vázquez-Marouschek C; Dopazo J; Borrego S; Antiñolo G
    Mol Vis; 2013; 19():2187-95. PubMed ID: 24227914
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing.
    Hollegaard MV; Grauholm J; Nielsen R; Grove J; Mandrup S; Hougaard DM
    Mol Genet Metab; 2013; 110(1-2):65-72. PubMed ID: 23830478
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United States.
    Lim SH; Tran-Viet KN; Yanovitch TL; Freedman SF; Klemm T; Call W; Powell C; Ravichandran A; Metlapally R; Nading EB; Rozen S; Young TL
    Am J Ophthalmol; 2013 Mar; 155(3):508-517.e5. PubMed ID: 23218701
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.