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 *

177 related articles for article (PubMed ID: 32219895)

  • 21. Intravenous delivery of adeno-associated viral gene therapy in feline GM1 gangliosidosis.
    Gross AL; Gray-Edwards HL; Bebout CN; Ta NL; Nielsen K; Brunson BL; Lopez Mercado KR; Osterhoudt DE; Batista AR; Maitland S; Seyfried TN; Sena-Esteves M; Martin DR
    Brain; 2022 Apr; 145(2):655-669. PubMed ID: 34410345
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical and molecular characteristics of 11 Chinese probands with GM1 gangliosidosis.
    Feng Y; Huang Y; Zhao X; Sheng H; Feng Y; Zhang W; Liu L
    Metab Brain Dis; 2018 Dec; 33(6):2051-2057. PubMed ID: 30267299
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Sialidase NEU3 action on GM1 ganglioside is neuroprotective in GM1 gangliosidosis.
    Allende ML; Lee YT; Byrnes C; Li C; Tuymetova G; Bakir JY; Nicoli ER; James VK; Brodbelt JS; Tifft CJ; Proia RL
    J Lipid Res; 2023 Dec; 64(12):100463. PubMed ID: 37871851
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Phenotype determining alleles in GM1 gangliosidosis patients bearing novel GLB1 mutations.
    Hofer D; Paul K; Fantur K; Beck M; Roubergue A; Vellodi A; Poorthuis BJ; Michelakakis H; Plecko B; Paschke E
    Clin Genet; 2010 Sep; 78(3):236-46. PubMed ID: 20175788
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A computational approach to analyse the amino acid variants of GLB1 protein causing GM1 Gangliosidosis.
    Priyanka K; Madhana Priya N; Magesh R
    Metab Brain Dis; 2021 Mar; 36(3):499-508. PubMed ID: 33394287
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Biochemical and molecular characterization of novel mutations in GLB1 and NEU1 in patient cells with lysosomal storage disorders.
    Kwak JE; Son MY; Son YS; Son MJ; Cho YS
    Biochem Biophys Res Commun; 2015 Feb; 457(4):554-60. PubMed ID: 25600812
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Comprehensive behavioral and biochemical outcomes of novel murine models of GM1-gangliosidosis and Morquio syndrome type B.
    Przybilla MJ; Ou L; Tăbăran AF; Jiang X; Sidhu R; Kell PJ; Ory DS; O'Sullivan MG; Whitley CB
    Mol Genet Metab; 2019 Feb; 126(2):139-150. PubMed ID: 30528226
    [TBL] [Abstract][Full Text] [Related]  

  • 28. GM1 gangliosidosis: molecular analysis of nine patients and development of an RT-PCR assay for GLB1 gene expression profiling.
    Caciotti A; Donati MA; Procopio E; Filocamo M; Kleijer W; Wuyts W; Blaumeiser B; d'Azzo A; Simi L; Orlando C; McKenzie F; Fiumara A; Zammarchi E; Morrone A
    Hum Mutat; 2007 Feb; 28(2):204. PubMed ID: 17221873
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Systemic AAV9 gene transfer in adult GM1 gangliosidosis mice reduces lysosomal storage in CNS and extends lifespan.
    Weismann CM; Ferreira J; Keeler AM; Su Q; Qui L; Shaffer SA; Xu Z; Gao G; Sena-Esteves M
    Hum Mol Genet; 2015 Aug; 24(15):4353-64. PubMed ID: 25964428
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The Arg482His mutation in the beta-galactosidase gene is responsible for a high frequency of GM1 gangliosidosis carriers in a Cypriot village.
    Georgiou T; Stylianidou G; Anastasiadou V; Caciotti A; Campos Y; Zammarchi E; Morrone A; D'azzo A; Drousiotou A
    Genet Test; 2005; 9(2):126-32. PubMed ID: 15943552
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assay.
    Myers KA; Bennett MF; Chow CW; Carden SM; Mandelstam SA; Bahlo M; Scheffer IE
    Am J Med Genet A; 2018 Jan; 176(1):230-234. PubMed ID: 29160035
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of a novel
    Zubaida B; Almas Hashmi M; Arshad Cheema H; Naeem M
    J Genet; 2018 Dec; 97(5):1445-1449. PubMed ID: 30555092
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Recurrent and novel GLB1 mutations in India.
    Bidchol AM; Dalal A; Trivedi R; Shukla A; Nampoothiri S; Sankar VH; Danda S; Gupta N; Kabra M; Hebbar SA; Bhat RY; Matta D; Ekbote AV; Puri RD; Phadke SR; Gowrishankar K; Aggarwal S; Ranganath P; Sharda S; Kamate M; Datar CA; Bhat K; Kamath N; Shah H; Krishna S; Gopinath PM; Verma IC; Nagarajaram HA; Satyamoorthy K; Girisha KM
    Gene; 2015 Aug; 567(2):173-81. PubMed ID: 25936995
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Complete correction of enzymatic deficiency and neurochemistry in the GM1-gangliosidosis mouse brain by neonatal adeno-associated virus-mediated gene delivery.
    Broekman ML; Baek RC; Comer LA; Fernandez JL; Seyfried TN; Sena-Esteves M
    Mol Ther; 2007 Jan; 15(1):30-7. PubMed ID: 17164772
    [TBL] [Abstract][Full Text] [Related]  

  • 35. beta-galactosidase gene mutations affecting the lysosomal enzyme and the elastin-binding protein in GM1-gangliosidosis patients with cardiac involvement.
    Morrone A; Bardelli T; Donati MA; Giorgi M; Di Rocco M; Gatti R; Parini R; Ricci R; Taddeucci G; D'Azzo A; Zammarchi E
    Hum Mutat; 2000; 15(4):354-66. PubMed ID: 10737981
    [TBL] [Abstract][Full Text] [Related]  

  • 36. GM1 gangliosidosis type II: Results of a 10-year prospective study.
    D'Souza P; Farmer C; Johnston JM; Han ST; Adams D; Hartman AL; Zein W; Huryn LA; Solomon B; King K; Jordan CP; Myles J; Nicoli ER; Rothermel CE; Mojica Algarin Y; Huang R; Quimby R; Zainab M; Bowden S; Crowell A; Buckley A; Brewer C; Regier DS; Brooks BP; Acosta MT; Baker EH; Vézina G; Thurm A; Tifft CJ
    Genet Med; 2024 Jul; 26(7):101144. PubMed ID: 38641994
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Clinical and Molecular Spectrum of GM1 Gangliosidosis.
    Arash-Kaps L; Komlosi K; Seegräber M; Diederich S; Paschke E; Amraoui Y; Beblo S; Dieckmann A; Smitka M; Hennermann JB
    J Pediatr; 2019 Dec; 215():152-157.e3. PubMed ID: 31761138
    [TBL] [Abstract][Full Text] [Related]  

  • 38. GM1 gangliosidosis: patients with different phenotypic features and novel mutations.
    Emecen Sanli M; Dogan M
    J Pediatr Endocrinol Metab; 2023 Jun; 36(6):602-607. PubMed ID: 37042746
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Beta-galactosidase-deficient mouse as an animal model for GM1-gangliosidosis.
    Matsuda J; Suzuki O; Oshima A; Ogura A; Noguchi Y; Yamamoto Y; Asano T; Takimoto K; Sukegawa K; Suzuki Y; Naiki M
    Glycoconj J; 1997 Sep; 14(6):729-36. PubMed ID: 9337086
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Identification and pathogenicity prediction of a novel GLB1 variant c.101T>C (p.Ile34Thr) in an infant with GM1 gangliosidosis].
    Lan XR; Qiu JW; Li H; Cai XR; Song YZ
    Zhongguo Dang Dai Er Ke Za Zhi; 2019 Jan; 21(1):71-76. PubMed ID: 30675867
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.