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 *

155 related articles for article (PubMed ID: 34746377)

  • 1. Genetic and Functional Analysis of Glycosyltransferase 8 Domain-Containing Protein 1 in Taiwanese Patients With Amyotrophic Lateral Sclerosis.
    Tsai PC; Jih KY; Shen TY; Liu YH; Lin KP; Liao YC; Lee YC
    Neurol Genet; 2021 Dec; 7(6):e627. PubMed ID: 34746377
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation analysis of GLT8D1 and ARPP21 genes in amyotrophic lateral sclerosis patients from mainland China.
    Li W; Liu Z; Sun W; Yuan Y; Hu Y; Ni J; Jiao B; Fang L; Li J; Shen L; Tang B; Wang J
    Neurobiol Aging; 2020 Jan; 85():156.e1-156.e4. PubMed ID: 31653410
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the Glycosyltransferase Domain of GLT8D1 Are Associated with Familial Amyotrophic Lateral Sclerosis.
    Cooper-Knock J; Moll T; Ramesh T; Castelli L; Beer A; Robins H; Fox I; Niedermoser I; Van Damme P; Moisse M; Robberecht W; Hardiman O; Panades MP; Assialioui A; Mora JS; Basak AN; Morrison KE; Shaw CE; Al-Chalabi A; Landers JE; Wyles M; Heath PR; Higginbottom A; Walsh T; Kazoka M; McDermott CJ; Hautbergue GM; Kirby J; Shaw PJ
    Cell Rep; 2019 Feb; 26(9):2298-2306.e5. PubMed ID: 30811981
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation screening and burden analysis of GLT8D1 in Chinese patients with amyotrophic lateral sclerosis.
    Cao B; Gu X; Wei Q; Li C; Chen Y; Ou R; Hou Y; Zhang L; Li T; Song W; Zhao B; Wu Y; Chen X; Shang H
    Neurobiol Aging; 2021 May; 101():298.e17-298.e21. PubMed ID: 33581933
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosis.
    Chan Moi Fat S; McCann EP; Williams KL; Henden L; Twine NA; Bauer DC; Pamphlett R; Kiernan MC; Rowe DB; Nicholson GA; Fifita JA; Blair IP
    Neurobiol Aging; 2021 May; 101():297.e9-297.e11. PubMed ID: 33581934
    [TBL] [Abstract][Full Text] [Related]  

  • 6. GLT8D1 may not be significant in Chinese sporadic amyotrophic lateral sclerosis patients.
    Yilihamu M; He J; Liu X; Tian J; Fan D
    Neurobiol Aging; 2021 Jun; 102():224.e1-224.e3. PubMed ID: 33714647
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan.
    Tsai PC; Liao YC; Jih KY; Soong BW; Lin KP; Lee YC
    Neurobiol Aging; 2018 Dec; 72():188.e1-188.e2. PubMed ID: 30054183
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Stress signaling from the endoplasmic reticulum: A central player in the pathogenesis of amyotrophic lateral sclerosis.
    Walker AK; Atkin JD
    IUBMB Life; 2011 Sep; 63(9):754-63. PubMed ID: 21834058
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pathogenic Genome Signatures That Damage Motor Neurons in Amyotrophic Lateral Sclerosis.
    Yousefian-Jazi A; Seol Y; Kim J; Ryu HL; Lee J; Ryu H
    Cells; 2020 Dec; 9(12):. PubMed ID: 33333804
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Enzymatic activity of glycosyltransferase GLT8D1 promotes human glioblastoma cell migration.
    Ilina EI; Cialini C; Gerloff DL; Duarte Garcia-Escudero M; Jeanty C; Thézénas ML; Lesur A; Puard V; Bernardin F; Moter A; Schuster A; Dieterle M; Golebiewska A; Gérardy JJ; Dittmar G; Niclou SP; Müller T; Mittelbronn M
    iScience; 2022 Feb; 25(2):103842. PubMed ID: 35198895
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variant.
    Tsai YS; Lin KP; Jih KY; Tsai PC; Liao YC; Lee YC
    Ann Clin Transl Neurol; 2020 Jun; 7(6):965-971. PubMed ID: 32462798
    [TBL] [Abstract][Full Text] [Related]  

  • 12. GLT8D1 overexpression as a novel prognostic biomarker in human cutaneous melanoma.
    Hu H; Li Z; Zhou Y; Zhang Y; Zhao L; Zhao W; Huang Y; Song X
    Melanoma Res; 2019 Dec; 29(6):612-620. PubMed ID: 31305325
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients.
    Narain P; Padhi AK; Dave U; Mishra D; Bhatia R; Vivekanandan P; Gomes J
    Neurogenetics; 2019 Oct; 20(4):197-208. PubMed ID: 31432357
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel and Recurrent Mutations in a Cohort of Chinese Patients With Young-Onset Amyotrophic Lateral Sclerosis.
    Deng J; Wu W; Xie Z; Gang Q; Yu M; Liu J; Wang Q; Lv H; Zhang W; Huang Y; Wang T; Yuan Y; Hong D; Wang Z
    Front Neurosci; 2019; 13():1289. PubMed ID: 31866807
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The role of heat shock proteins in Amyotrophic Lateral Sclerosis: The therapeutic potential of Arimoclomol.
    Kalmar B; Lu CH; Greensmith L
    Pharmacol Ther; 2014 Jan; 141(1):40-54. PubMed ID: 23978556
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis.
    Liu ZJ; Lin HX; Wei Q; Zhang QJ; Chen CX; Tao QQ; Liu GL; Ni W; Gitler AD; Li HF; Wu ZY
    Aging Dis; 2019 Dec; 10(6):1199-1206. PubMed ID: 31788332
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic investigation of amyotrophic lateral sclerosis patients in south Italy: a two-decade analysis.
    Ungaro C; Sprovieri T; Morello G; Perrone B; Spampinato AG; Simone IL; Trojsi F; Monsurrò MR; Spataro R; La Bella V; Andò S; Cavallaro S; Conforti FL
    Neurobiol Aging; 2021 Mar; 99():99.e7-99.e14. PubMed ID: 32951934
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel Variants in the
    Liu CY; Lin JL; Feng SY; Che CH; Huang HP; Zou ZY
    J Clin Neurol; 2022 Jan; 18(1):41-47. PubMed ID: 35021275
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.
    Gijselinck I; Van Langenhove T; van der Zee J; Sleegers K; Philtjens S; Kleinberger G; Janssens J; Bettens K; Van Cauwenberghe C; Pereson S; Engelborghs S; Sieben A; De Jonghe P; Vandenberghe R; Santens P; De Bleecker J; Maes G; Bäumer V; Dillen L; Joris G; Cuijt I; Corsmit E; Elinck E; Van Dongen J; Vermeulen S; Van den Broeck M; Vaerenberg C; Mattheijssens M; Peeters K; Robberecht W; Cras P; Martin JJ; De Deyn PP; Cruts M; Van Broeckhoven C
    Lancet Neurol; 2012 Jan; 11(1):54-65. PubMed ID: 22154785
    [TBL] [Abstract][Full Text] [Related]  

  • 20. ER stress and unfolded protein response in amyotrophic lateral sclerosis.
    Kanekura K; Suzuki H; Aiso S; Matsuoka M
    Mol Neurobiol; 2009 Apr; 39(2):81-9. PubMed ID: 19184563
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.