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 *

241 related articles for article (PubMed ID: 26637975)

  • 41. Fibulin-5 mutations: mechanisms of impaired elastic fiber formation in recessive cutis laxa.
    Hu Q; Loeys BL; Coucke PJ; De Paepe A; Mecham RP; Choi J; Davis EC; Urban Z
    Hum Mol Genet; 2006 Dec; 15(23):3379-86. PubMed ID: 17035250
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway.
    Tian G; Jaglin XH; Keays DA; Francis F; Chelly J; Cowan NJ
    Hum Mol Genet; 2010 Sep; 19(18):3599-613. PubMed ID: 20603323
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Mutation of the α-tubulin Tuba1a leads to straighter microtubules and perturbs neuronal migration.
    Belvindrah R; Natarajan K; Shabajee P; Bruel-Jungerman E; Bernard J; Goutierre M; Moutkine I; Jaglin XH; Savariradjane M; Irinopoulou T; Poncer JC; Janke C; Francis F
    J Cell Biol; 2017 Aug; 216(8):2443-2461. PubMed ID: 28687665
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Familial Michelin tire baby syndrome.
    Hayashi M; Wataya-Kaneda M; Koguchi-Yoshioka H; Arase N; Kubo T; Nakano H; Fujimoto M
    J Dermatol; 2022 Jul; 49(7):e219-e220. PubMed ID: 35277884
    [No Abstract]   [Full Text] [Related]  

  • 45. Cutis Laxa.
    Mohamed M; Voet M; Gardeitchik T; Morava E
    Adv Exp Med Biol; 2014; 802():161-84. PubMed ID: 24443027
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Mutations in TUBGCP4 alter microtubule organization via the γ-tubulin ring complex in autosomal-recessive microcephaly with chorioretinopathy.
    Scheidecker S; Etard C; Haren L; Stoetzel C; Hull S; Arno G; Plagnol V; Drunat S; Passemard S; Toutain A; Obringer C; Koob M; Geoffroy V; Marion V; Strähle U; Ostergaard P; Verloes A; Merdes A; Moore AT; Dollfus H
    Am J Hum Genet; 2015 Apr; 96(4):666-74. PubMed ID: 25817018
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Mutations in TUBB8 and Human Oocyte Meiotic Arrest.
    Feng R; Sang Q; Kuang Y; Sun X; Yan Z; Zhang S; Shi J; Tian G; Luchniak A; Fukuda Y; Li B; Yu M; Chen J; Xu Y; Guo L; Qu R; Wang X; Sun Z; Liu M; Shi H; Wang H; Feng Y; Shao R; Chai R; Li Q; Xing Q; Zhang R; Nogales E; Jin L; He L; Gupta ML; Cowan NJ; Wang L
    N Engl J Med; 2016 Jan; 374(3):223-32. PubMed ID: 26789871
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A proteomic survey of microtubule-associated proteins in a R402H TUBA1A mutant mouse.
    Leca I; Phillips AW; Hofer I; Landler L; Ushakova L; Cushion TD; Dürnberger G; Stejskal K; Mechtler K; Keays DA
    PLoS Genet; 2020 Nov; 16(11):e1009104. PubMed ID: 33137126
    [TBL] [Abstract][Full Text] [Related]  

  • 49. ADP ribosylation factor-like protein 2 (Arl2) regulates the interaction of tubulin-folding cofactor D with native tubulin.
    Bhamidipati A; Lewis SA; Cowan NJ
    J Cell Biol; 2000 May; 149(5):1087-96. PubMed ID: 10831612
    [TBL] [Abstract][Full Text] [Related]  

  • 50. TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes.
    Curiel J; Rodríguez Bey G; Takanohashi A; Bugiani M; Fu X; Wolf NI; Nmezi B; Schiffmann R; Bugaighis M; Pierson T; Helman G; Simons C; van der Knaap MS; Liu J; Padiath Q; Vanderver A
    Hum Mol Genet; 2017 Nov; 26(22):4506-4518. PubMed ID: 28973395
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A dominant tubulin mutation causes cerebellar neurodegeneration in a genetic model of tubulinopathy.
    Fertuzinhos S; Legué E; Li D; Liem KF
    Sci Adv; 2022 Feb; 8(7):eabf7262. PubMed ID: 35171680
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Cutis laxa of the autosomal recessive type in a consanguineous family.
    de Schepper S; Loeys B; de Paepe A; Lambert J; Naeyaert JM
    Eur J Dermatol; 2003; 13(6):529-33. PubMed ID: 14721770
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa.
    Fischer-Zirnsak B; Escande-Beillard N; Ganesh J; Tan YX; Al Bughaili M; Lin AE; Sahai I; Bahena P; Reichert SL; Loh A; Wright GD; Liu J; Rahikkala E; Pivnick EK; Choudhri AF; Krüger U; Zemojtel T; van Ravenswaaij-Arts C; Mostafavi R; Stolte-Dijkstra I; Symoens S; Pajunen L; Al-Gazali L; Meierhofer D; Robinson PN; Mundlos S; Villarroel CE; Byers P; Masri A; Robertson SP; Schwarze U; Callewaert B; Reversade B; Kornak U
    Am J Hum Genet; 2015 Sep; 97(3):483-92. PubMed ID: 26320891
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Kinetic analysis of tubulin exchange at microtubule ends at low vinblastine concentrations.
    Jordan MA; Wilson L
    Biochemistry; 1990 Mar; 29(11):2730-9. PubMed ID: 2346745
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Dynamic localization of CLIP-170 to microtubule plus ends is coupled to microtubule assembly.
    Diamantopoulos GS; Perez F; Goodson HV; Batelier G; Melki R; Kreis TE; Rickard JE
    J Cell Biol; 1999 Jan; 144(1):99-112. PubMed ID: 9885247
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Aurora A site specific TACC3 phosphorylation regulates astral microtubule assembly by stabilizing γ-tubulin ring complex.
    Rajeev R; Singh P; Asmita A; Anand U; Manna TK
    BMC Mol Cell Biol; 2019 Dec; 20(1):58. PubMed ID: 31823729
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Loss of zebrafish atp6v1e1b, encoding a subunit of vacuolar ATPase, recapitulates human ARCL type 2C syndrome and identifies multiple pathobiological signatures.
    Pottie L; Van Gool W; Vanhooydonck M; Hanisch FG; Goeminne G; Rajkovic A; Coucke P; Sips P; Callewaert B
    PLoS Genet; 2021 Jun; 17(6):e1009603. PubMed ID: 34143769
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Congenital generalized cutis laxa: 5 cases].
    Rybojad M; Baumann C; Godeau G; Moraillon I; Prigent F; Morel P; Bourrat E
    Ann Dermatol Venereol; 1999 Apr; 126(4):317-9. PubMed ID: 10421933
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Presence of an expressed beta-tubulin gene (TUBB) in the HLA class I region may provide the genetic basis for HLA-linked microtubule dysfunction.
    Volz A; Weiss E; Trowsdale J; Ziegler A
    Hum Genet; 1994 Jan; 93(1):42-6. PubMed ID: 8270253
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Tubulin: Structure, Functions and Roles in Disease.
    Binarová P; Tuszynski J
    Cells; 2019 Oct; 8(10):. PubMed ID: 31652491
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.