BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 29887954)

  • 1. Comparative analysis of the two extremes of
    Xu Q; Wu N; Cui L; Lin M; Thirumal Kumar D; George Priya Doss C; Wu Z; Shen J; Song X; Qiu G
    Am J Transl Res; 2018; 10(5):1400-1412. PubMed ID: 29887954
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Disruption of
    Xu Q; Cui L; Lin Y; Cui LA; Xia W
    Bone Rep; 2024 Mar; 20():101746. PubMed ID: 38463381
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in FLNB cause boomerang dysplasia.
    Bicknell LS; Morgan T; Bonafé L; Wessels MW; Bialer MG; Willems PJ; Cohn DH; Krakow D; Robertson SP
    J Med Genet; 2005 Jul; 42(7):e43. PubMed ID: 15994868
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Filamin B mutations cause chondrocyte defects in skeletal development.
    Lu J; Lian G; Lenkinski R; De Grand A; Vaid RR; Bryce T; Stasenko M; Boskey A; Walsh C; Sheen V
    Hum Mol Genet; 2007 Jul; 16(14):1661-75. PubMed ID: 17510210
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Disease-associated substitutions in the filamin B actin binding domain confer enhanced actin binding affinity in the absence of major structural disturbance: Insights from the crystal structures of filamin B actin binding domains.
    Sawyer GM; Clark AR; Robertson SP; Sutherland-Smith AJ
    J Mol Biol; 2009 Jul; 390(5):1030-47. PubMed ID: 19505475
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development.
    Zhou X; Tian F; Sandzén J; Cao R; Flaberg E; Szekely L; Cao Y; Ohlsson C; Bergo MO; Borén J; Akyürek LM
    Proc Natl Acad Sci U S A; 2007 Mar; 104(10):3919-24. PubMed ID: 17360453
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome.
    Farrington-Rock C; Kirilova V; Dillard-Telm L; Borowsky AD; Chalk S; Rock MJ; Cohn DH; Krakow D
    Hum Mol Genet; 2008 Mar; 17(5):631-41. PubMed ID: 17635842
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biallelic mutations in FLNB cause a skeletal dysplasia with 46,XY gonadal dysgenesis by activating β-catenin.
    Upadhyay K; Loke J; O V; Taragin B; Ostrer H
    Clin Genet; 2018 Feb; 93(2):412-416. PubMed ID: 29095481
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibit.
    Rehder H; Laccone F; Kircher SG; Schild RL; Rapp C; Bald R; Schulze B; Behunova J; Neesen J; Schoner K
    Am J Med Genet A; 2018 Jul; 176(7):1559-1568. PubMed ID: 29797497
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Disease-associated mutations in the actin-binding domain of filamin B cause cytoplasmic focal accumulations correlating with disease severity.
    Daniel PB; Morgan T; Alanay Y; Bijlsma E; Cho TJ; Cole T; Collins F; David A; Devriendt K; Faivre L; Ikegawa S; Jacquemont S; Jesic M; Krakow D; Liebrecht D; Maitz S; Marlin S; Morin G; Nishikubo T; Nishimura G; Prescott T; Scarano G; Shafeghati Y; Skovby F; Tsutsumi S; Whiteford M; Zenker M; Robertson SP
    Hum Mutat; 2012 Apr; 33(4):665-73. PubMed ID: 22190451
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in two regions of FLNB result in atelosteogenesis I and III.
    Farrington-Rock C; Firestein MH; Bicknell LS; Superti-Furga A; Bacino CA; Cormier-Daire V; Le Merrer M; Baumann C; Roume J; Rump P; Verheij JB; Sweeney E; Rimoin DL; Lachman RS; Robertson SP; Cohn DH; Krakow D
    Hum Mutat; 2006 Jul; 27(7):705-10. PubMed ID: 16752402
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Seven additional families with spondylocarpotarsal synostosis syndrome with novel biallelic deleterious variants in FLNB.
    Salian S; Shukla A; Shah H; Bhat SN; Bhat VR; Nampoothiri S; Shenoy R; Phadke SR; Hariharan SV; Girisha KM
    Clin Genet; 2018 Jul; 94(1):159-164. PubMed ID: 29566257
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Insulin-like growth factor-1 rescues the mutated FGF receptor 3 (G380R) expressing ATDC5 cells from apoptosis through phosphatidylinositol 3-kinase and MAPK.
    Koike M; Yamanaka Y; Inoue M; Tanaka H; Nishimura R; Seino Y
    J Bone Miner Res; 2003 Nov; 18(11):2043-51. PubMed ID: 14606518
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical diagnosis of Larsen syndrome, Stickler syndrome and Loeys-Dietz syndrome in a 19-year old male: a case report.
    Riise N; Lindberg BR; Kulseth MA; Fredwall SO; Lundby R; Estensen ME; Drolsum L; Merckoll E; Krohg-Sørensen K; Paus B
    BMC Med Genet; 2018 Aug; 19(1):155. PubMed ID: 30170566
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.