BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 34491919)

  • 1. Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion.
    Quiggle A; Charng WL; Antunes L; Nikolov M; Bledsoe X; Hecht JT; Dobbs MB; Gurnett CA
    Clin Orthop Relat Res; 2022 Feb; 480(2):421-430. PubMed ID: 34491919
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients.
    Girisha KM; Bidchol AM; Graul-Neumann L; Gupta A; Hehr U; Lessel D; Nader S; Shah H; Wickert J; Kutsche K
    BMC Med Genet; 2016 Apr; 17():27. PubMed ID: 27048506
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CORR Insights®: Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion.
    Slullitel GA
    Clin Orthop Relat Res; 2022 Feb; 480(2):431-432. PubMed ID: 34704968
    [No Abstract]   [Full Text] [Related]  

  • 4. Three novel missense mutations in the filamin B gene are associated with isolated congenital talipes equinovarus.
    Yang H; Zheng Z; Cai H; Li H; Ye X; Zhang X; Wang Z; Fu Q
    Hum Genet; 2016 Oct; 135(10):1181-9. PubMed ID: 27395407
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exome sequencing of 1190 non-syndromic clubfoot cases reveals
    Charng WL; Nikolov M; Shrestha I; Seeley MA; Josyula NS; Justice AE; Dobbs MB; Gurnett CA
    J Med Genet; 2024 Apr; ():. PubMed ID: 38663984
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exome sequencing analysis identifies frequent oligogenic involvement and
    Jiang H; Liang S; He K; Hu J; Xu E; Lin T; Meng Y; Zhao J; Ma J; Gao R; Wang C; Yang F; Zhou X
    J Med Genet; 2020 Jun; 57(6):405-413. PubMed ID: 32381728
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel in-frame
    Hickey SE; Koboldt DC; Mosher TM; Brennan P; Schmalz BA; Crist E; McBride KL; Adler BH; White P; Wilson RK
    Cold Spring Harb Mol Case Stud; 2019 Dec; 5(6):. PubMed ID: 31836586
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.
    Bicknell LS; Farrington-Rock C; Shafeghati Y; Rump P; Alanay Y; Alembik Y; Al-Madani N; Firth H; Karimi-Nejad MH; Kim CA; Leask K; Maisenbacher M; Moran E; Pappas JG; Prontera P; de Ravel T; Fryns JP; Sweeney E; Fryer A; Unger S; Wilson LC; Lachman RS; Rimoin DL; Cohn DH; Krakow D; Robertson SP
    J Med Genet; 2007 Feb; 44(2):89-98. PubMed ID: 16801345
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach.
    S UK; Sankar S; Younes S; D TK; Ahmad MN; Okashah SS; Kamaraj B; Al-Subaie AM; C GPD; Zayed H
    Molecules; 2020 Nov; 25(23):. PubMed ID: 33255942
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of a de novo heterozygous missense FLNB mutation in lethal atelosteogenesis type I by exome sequencing.
    Jeon GW; Lee MN; Jung JM; Hong SY; Kim YN; Sin JB; Ki CS
    Ann Lab Med; 2014 Mar; 34(2):134-8. PubMed ID: 24624349
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
    Yang CF; Wang CH; Siong H'ng W; Chang CP; Lin WD; Chen YT; Wu JY; Tsai FJ
    Hum Mutat; 2017 May; 38(5):540-547. PubMed ID: 28145000
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic association of ARHGAP21 gene variant with mandibular prognathism.
    Perillo L; Monsurrò A; Bonci E; Torella A; Mutarelli M; Nigro V
    J Dent Res; 2015 Apr; 94(4):569-76. PubMed ID: 25691070
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cell-Dependent Pathogenic Roles of Filamin B in Different Skeletal Malformations.
    Wu H; Wang Y; Chen X; Yao Y; Zhao W; Fang L; Sun X; Wang N; Jiang J; Gao L; Zhao J; Xu C
    Oxid Med Cell Longev; 2022; 2022():8956636. PubMed ID: 35832491
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The variants at FLNA and FLNB contribute to the susceptibility of hypertension and stroke with differentially expressed mRNA.
    Liu C; Tang W; Zhao H; Yang S; Ren Z; Li J; Chen Y; Zhao X; Xu D; Zhao Y; Shen C
    Pharmacogenomics J; 2021 Aug; 21(4):458-466. PubMed ID: 33649519
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.
    Cameron-Christie SR; Wells CF; Simon M; Wessels M; Tang CZN; Wei W; Takei R; Aarts-Tesselaar C; Sandaradura S; Sillence DO; Cordier MP; Veenstra-Knol HE; Cassina M; Ludwig K; Trevisson E; Bahlo M; Markie DM; Jenkins ZA; Robertson SP
    Am J Hum Genet; 2018 Jun; 102(6):1115-1125. PubMed ID: 29805041
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families.
    Shahi RB; De Brakeleer S; Caljon B; Pauwels I; Bonduelle M; Joris S; Fontaine C; Vanhoeij M; Van Dooren S; Teugels E; De Grève J
    BMC Cancer; 2019 Apr; 19(1):313. PubMed ID: 30947698
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Filamin B: The next hotspot in skeletal research?
    Xu Q; Wu N; Cui L; Wu Z; Qiu G
    J Genet Genomics; 2017 Jul; 44(7):335-342. PubMed ID: 28739045
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.
    Norton N; Li D; Rieder MJ; Siegfried JD; Rampersaud E; Züchner S; Mangos S; Gonzalez-Quintana J; Wang L; McGee S; Reiser J; Martin E; Nickerson DA; Hershberger RE
    Am J Hum Genet; 2011 Mar; 88(3):273-82. PubMed ID: 21353195
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes.
    Gowans LJJ; Al Dhaheri N; Li M; Busch T; Obiri-Yeboah S; Oti AA; Sabbah DK; Arthur FKN; Awotoye WO; Alade AA; Twumasi P; Agbenorku P; Plange-Rhule G; Naicker T; Donkor P; Murray JC; Sobreira NLM; Butali A
    Mol Genet Genomic Med; 2021 Apr; 9(4):e1655. PubMed ID: 33719213
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.