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 *

240 related articles for article (PubMed ID: 31067307)

  • 21. Rab1-dependent ER-Golgi transport dysfunction is a common pathogenic mechanism in SOD1, TDP-43 and FUS-associated ALS.
    Soo KY; Halloran M; Sundaramoorthy V; Parakh S; Toth RP; Southam KA; McLean CA; Lock P; King A; Farg MA; Atkin JD
    Acta Neuropathol; 2015 Nov; 130(5):679-97. PubMed ID: 26298469
    [TBL] [Abstract][Full Text] [Related]  

  • 22. RNA and Protein Interactors with TDP-43 in Human Spinal-Cord Lysates in Amyotrophic Lateral Sclerosis.
    Volkening K; Keller BA; Leystra-Lantz C; Strong MJ
    J Proteome Res; 2018 Apr; 17(4):1712-1729. PubMed ID: 29513014
    [TBL] [Abstract][Full Text] [Related]  

  • 23. ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis.
    Parakh S; Jagaraj CJ; Vidal M; Ragagnin AMG; Perri ER; Konopka A; Toth RP; Galper J; Blair IP; Thomas CJ; Walker AK; Yang S; Spencer DM; Atkin JD
    Hum Mol Genet; 2018 Apr; 27(8):1311-1331. PubMed ID: 29409023
    [TBL] [Abstract][Full Text] [Related]  

  • 24. ALS/FTLD-linked TDP-43 regulates neurite morphology and cell survival in differentiated neurons.
    Han JH; Yu TH; Ryu HH; Jun MH; Ban BK; Jang DJ; Lee JA
    Exp Cell Res; 2013 Aug; 319(13):1998-2005. PubMed ID: 23742895
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Endogenous TDP-43 mislocalization in a novel knock-in mouse model reveals DNA repair impairment, inflammation, and neuronal senescence.
    Mitra J; Dharmalingam P; Kodavati M; Guerrero EN; Rao KS; Garruto RM; Hegde ML
    Res Sq; 2024 Mar; ():. PubMed ID: 38343852
    [TBL] [Abstract][Full Text] [Related]  

  • 26. APTX acts in DNA double-strand break repair in a manner distinct from XRCC4.
    Imamura R; Saito M; Shimada M; Kobayashi J; Ishiai M; Matsumoto Y
    J Radiat Res; 2023 May; 64(3):485-495. PubMed ID: 36940705
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Coexistence of perseveration and apathy in the TDP-43
    Kim E; White MA; Phillips BU; Lopez-Cruz L; Kim H; Heath CJ; Lee JE; Saksida LM; Sreedharan J; Bussey TJ
    Transl Psychiatry; 2020 Nov; 10(1):377. PubMed ID: 33149110
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Dysregulation of chromatin remodelling complexes in amyotrophic lateral sclerosis.
    Tibshirani M; Zhao B; Gentil BJ; Minotti S; Marques C; Keith J; Rogaeva E; Zinman L; Rouaux C; Robertson J; Durham HD
    Hum Mol Genet; 2017 Nov; 26(21):4142-4152. PubMed ID: 28973294
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Tar DNA binding protein of 43 kDa (TDP-43), 14-3-3 proteins and copper/zinc superoxide dismutase (SOD1) interact to modulate NFL mRNA stability. Implications for altered RNA processing in amyotrophic lateral sclerosis (ALS).
    Volkening K; Leystra-Lantz C; Yang W; Jaffee H; Strong MJ
    Brain Res; 2009 Dec; 1305():168-82. PubMed ID: 19815002
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Lysine 271 but not lysine 210 of XRCC4 is required for the nuclear localization of XRCC4 and DNA ligase IV.
    Fukuchi M; Wanotayan R; Liu S; Imamichi S; Sharma MK; Matsumoto Y
    Biochem Biophys Res Commun; 2015 Jun; 461(4):687-94. PubMed ID: 25934149
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutant FUS causes DNA ligation defects to inhibit oxidative damage repair in Amyotrophic Lateral Sclerosis.
    Wang H; Guo W; Mitra J; Hegde PM; Vandoorne T; Eckelmann BJ; Mitra S; Tomkinson AE; Van Den Bosch L; Hegde ML
    Nat Commun; 2018 Sep; 9(1):3683. PubMed ID: 30206235
    [TBL] [Abstract][Full Text] [Related]  

  • 32. TARDBP pathogenic mutations increase cytoplasmic translocation of TDP-43 and cause reduction of endoplasmic reticulum Ca²⁺ signaling in motor neurons.
    Mutihac R; Alegre-Abarrategui J; Gordon D; Farrimond L; Yamasaki-Mann M; Talbot K; Wade-Martins R
    Neurobiol Dis; 2015 Mar; 75():64-77. PubMed ID: 25526708
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Loss of TDP-43 function contributes to genomic instability in amyotrophic lateral sclerosis.
    Fang M; Deibler SK; Nana AL; Vatsavayai SC; Banday S; Zhou Y; Almeida S; Weiss A; Brown RH; Seeley WW; Gao FB; Green MR
    Front Neurosci; 2023; 17():1251228. PubMed ID: 37849894
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The molecular link between inefficient GluA2 Q/R site-RNA editing and TDP-43 pathology in motor neurons of sporadic amyotrophic lateral sclerosis patients.
    Yamashita T; Kwak S
    Brain Res; 2014 Oct; 1584():28-38. PubMed ID: 24355598
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Crosstalk between BER and NHEJ in XRCC4-Deficient Cells Depending on hTERT Overexpression.
    Sergeeva SV; Loshchenova PS; Oshchepkov DY; Orishchenko KE
    Int J Mol Sci; 2024 Sep; 25(19):. PubMed ID: 39408734
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Extensive phenotypic characterisation of a human TDP-43
    Watkins JA; Alix JJP; Shaw PJ; Mead RJ
    Sci Rep; 2021 Aug; 11(1):16659. PubMed ID: 34404845
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids.
    Tamaki Y; Ross JP; Alipour P; Castonguay CÉ; Li B; Catoire H; Rochefort D; Urushitani M; Takahashi R; Sonnen JA; Stifani S; Dion PA; Rouleau GA
    PLoS Genet; 2023 Feb; 19(2):e1010606. PubMed ID: 36745687
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Immunoreactivity of valosin-containing protein in sporadic amyotrophic lateral sclerosis and in a case of its novel mutant.
    Ayaki T; Ito H; Fukushima H; Inoue T; Kondo T; Ikemoto A; Asano T; Shodai A; Fujita T; Fukui S; Morino H; Nakano S; Kusaka H; Yamashita H; Ihara M; Matsumoto R; Kawamata J; Urushitani M; Kawakami H; Takahashi R
    Acta Neuropathol Commun; 2014 Dec; 2():172. PubMed ID: 25492614
    [TBL] [Abstract][Full Text] [Related]  

  • 39. MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis.
    MacNair L; Xiao S; Miletic D; Ghani M; Julien JP; Keith J; Zinman L; Rogaeva E; Robertson J
    Brain; 2016 Jan; 139(Pt 1):86-100. PubMed ID: 26525917
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ligase 3-mediated end-joining maintains genome stability of human embryonic stem cells.
    Kohutova A; Raška J; Kruta M; Seneklova M; Barta T; Fojtik P; Jurakova T; Walter CA; Hampl A; Dvorak P; Rotrekl V
    FASEB J; 2019 Jun; 33(6):6778-6788. PubMed ID: 30807703
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.