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 *

245 related articles for article (PubMed ID: 26188006)

  • 1. Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor.
    Hor H; Francescatto L; Bartesaghi L; Ortega-Cubero S; Kousi M; Lorenzo-Betancor O; Jiménez-Jiménez FJ; Gironell A; Clarimón J; Drechsel O; Agúndez JA; Kenzelmann Broz D; Chiquet-Ehrismann R; Lleó A; Coria F; García-Martin E; Alonso-Navarro H; Martí MJ; Kulisevsky J; Hor CN; Ossowski S; Chrast R; Katsanis N; Pastor P; Estivill X
    Hum Mol Genet; 2015 Oct; 24(20):5677-86. PubMed ID: 26188006
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Han family with essential tremor caused by the P421L variant of the TENM4 gene in China.
    Chi W; Wu M; Wang HL; Wu QY; Zhang YP; Hu YN; Zhu YB; Lin XF; Chen T; Luo JW; Ruan XL; Li YF
    Neurol Sci; 2023 Jun; 44(6):2003-2015. PubMed ID: 36689009
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic testing of FUS, HTRA2, and TENM4 genes in Chinese patients with essential tremor.
    Yan YP; Xu CY; Gu LY; Zhang B; Shen T; Gao T; Tian J; Pu JL; Yin XZ; Zhang BR; Zhao GH
    CNS Neurosci Ther; 2020 Aug; 26(8):837-841. PubMed ID: 32196977
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and genetic features of dominant Essential Tremor in Tuscany, Italy: FUS, CAMTA1, ATXN1 and beyond.
    Orsucci D; Tessa A; Caldarazzo Ienco E; Trovato R; Natale G; Bilancieri G; Giuntini M; Napolitano A; Salvetti S; Vista M; Santorelli FM
    J Neurol Sci; 2024 May; 460():123012. PubMed ID: 38626532
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exome Sequencing Identifies
    Xue CB; Xu ZH; Zhu J; Wu Y; Zhuang XH; Chen QL; Wu CR; Hu JT; Zhou HS; Xie WH; Yi X; Yu SS; Peng ZY; Yang HM; Hong XH; Chen JH
    Front Genet; 2018; 9():725. PubMed ID: 30745909
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population.
    Houle G; Schmouth JF; Leblond CS; Ambalavanan A; Spiegelman D; Laurent SB; Bourassa CV; Panisset M; Chouinard S; Dupré N; Vilariño-Güell C; Rajput A; Dion PA; Rouleau GA
    Mov Disord; 2017 Feb; 32(2):292-295. PubMed ID: 28158909
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Essential tremor linked TENM4 mutation found in healthy Chinese individuals.
    Chao YX; Lin Ng EY; Tio M; Kumar P; Tan L; Au WL; Yih Y; Tan EK
    Parkinsonism Relat Disord; 2016 Oct; 31():139-140. PubMed ID: 27569844
    [No Abstract]   [Full Text] [Related]  

  • 8. A Novel
    d'Apolito M; Ceccarini C; Savino R; Adipietro I; di Bari I; Santacroce R; Curcetti M; D'Andrea G; Croce AI; Cesarano C; Polito AN; Margaglione M
    Genes (Basel); 2023 Jun; 14(7):. PubMed ID: 37510285
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of candidate genes for familial early-onset essential tremor.
    Liu X; Hernandez N; Kisselev S; Floratos A; Sawle A; Ionita-Laza I; Ottman R; Louis ED; Clark LN
    Eur J Hum Genet; 2016 Jul; 24(7):1009-15. PubMed ID: 26508575
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole genome sequencing and rare variant analysis in essential tremor families.
    Odgerel Z; Sonti S; Hernandez N; Park J; Ottman R; Louis ED; Clark LN
    PLoS One; 2019; 14(8):e0220512. PubMed ID: 31404076
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Exome sequencing identifies FUS mutations as a cause of essential tremor.
    Merner ND; Girard SL; Catoire H; Bourassa CV; Belzil VV; Rivière JB; Hince P; Levert A; Dionne-Laporte A; Spiegelman D; Noreau A; Diab S; Szuto A; Fournier H; Raelson J; Belouchi M; Panisset M; Cossette P; Dupré N; Bernard G; Chouinard S; Dion PA; Rouleau GA
    Am J Hum Genet; 2012 Aug; 91(2):313-9. PubMed ID: 22863194
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A variant in the HS1-BP3 gene is associated with familial essential tremor.
    Higgins JJ; Lombardi RQ; Pucilowska J; Jankovic J; Tan EK; Rooney JP
    Neurology; 2005 Feb; 64(3):417-21. PubMed ID: 15699368
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome-wide rare variant analysis in familial essential tremor.
    Diez-Fairen M; Houle G; Ortega-Cubero S; Bandres-Ciga S; Alvarez I; Carcel M; Ibañez L; Fernandez MV; Budde JP; Trotta JR; Tonda R; Chong JX; Bamshad MJ; Nickerson DA; ; Aguilar M; Tartari JP; Gironell A; García-Martín E; Agundez JA; Alonso-Navarro H; Jimenez-Jimenez FJ; Fernandez M; Valldeoriola F; Marti MJ; Tolosa E; Coria F; Pastor MA; Vilariño-Güell C; Rajput A; Dion PA; Cruchaga C; Rouleau GA; Pastor P
    Parkinsonism Relat Disord; 2021 Jan; 82():109-116. PubMed ID: 33279834
    [TBL] [Abstract][Full Text] [Related]  

  • 14. SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential Tremor.
    Sánchez E; Bergareche A; Krebs CE; Gorostidi A; Makarov V; Ruiz-Martinez J; Chorny A; Lopez de Munain A; Marti-Masso JF; Paisán-Ruiz C
    ASN Neuro; 2015; 7(4):. PubMed ID: 26297037
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The impact of rare variants in FUS in essential tremor.
    Hopfner F; Stevanin G; Müller SH; Mundwiller E; Bungeroth M; Durr A; Pendziwiat M; Anheim M; Schneider SA; Tittmann L; Klebe S; Lorenz D; Deuschl G; Brice A; Kuhlenbäumer G
    Mov Disord; 2015 Apr; 30(5):721-4. PubMed ID: 25631824
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Parkinson's Disease in Teneurin Transmembrane Protein 4 (
    Pu JL; Gao T; Si XL; Zheng R; Jin CY; Ruan Y; Fang Y; Chen Y; Song Z; Yin XZ; Yan YP; Tian J; Zhang BR
    Front Genet; 2020; 11():598064. PubMed ID: 33414808
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia.
    Bolar NA; Golzio C; Živná M; Hayot G; Van Hemelrijk C; Schepers D; Vandeweyer G; Hoischen A; Huyghe JR; Raes A; Matthys E; Sys E; Azou M; Gubler MC; Praet M; Van Camp G; McFadden K; Pediaditakis I; Přistoupilová A; Hodaňová K; Vyleťal P; Hartmannová H; Stránecký V; Hůlková H; Barešová V; Jedličková I; Sovová J; Hnízda A; Kidd K; Bleyer AJ; Spong RS; Vande Walle J; Mortier G; Brunner H; Van Laer L; Kmoch S; Katsanis N; Loeys BL
    Am J Hum Genet; 2016 Jul; 99(1):174-87. PubMed ID: 27392076
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Candidate variants in TUB are associated with familial tremor.
    Sailani MR; Jahanbani F; Abbott CW; Lee H; Zia A; Rego S; Winkelmann J; Hopfner F; Khan TN; Katsanis N; Müller SH; Berg D; Lyman KM; Mychajliw C; Deuschl G; Bernstein JA; Kuhlenbäumer G; Snyder MP
    PLoS Genet; 2020 Sep; 16(9):e1009010. PubMed ID: 32956375
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DGAT2 Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease.
    Hong YB; Kang J; Kim JH; Lee J; Kwak G; Hyun YS; Nam SH; Hong HD; Choi YR; Jung SC; Koo H; Lee JE; Choi BO; Chung KW
    Hum Mutat; 2016 May; 37(5):473-80. PubMed ID: 26786738
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family.
    Audo I; Bujakowska K; Orhan E; El Shamieh S; Sennlaub F; Guillonneau X; Antonio A; Michiels C; Lancelot ME; Letexier M; Saraiva JP; Nguyen H; Luu TD; Léveillard T; Poch O; Dollfus H; Paques M; Goureau O; Mohand-Saïd S; Bhattacharya SS; Sahel JA; Zeitz C
    Hum Mol Genet; 2014 Jan; 23(2):491-501. PubMed ID: 24026677
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.