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 *

262 related articles for article (PubMed ID: 25284324)

  • 41. A Pro504 --> Ser substitution in the beta-subunit of beta-hexosaminidase A inhibits alpha-subunit hydrolysis of GM2 ganglioside, resulting in chronic Sandhoff disease.
    Hou Y; McInnes B; Hinek A; Karpati G; Mahuran D
    J Biol Chem; 1998 Aug; 273(33):21386-92. PubMed ID: 9694901
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Cerebral organoids derived from Sandhoff disease-induced pluripotent stem cells exhibit impaired neurodifferentiation.
    Allende ML; Cook EK; Larman BC; Nugent A; Brady JM; Golebiowski D; Sena-Esteves M; Tifft CJ; Proia RL
    J Lipid Res; 2018 Mar; 59(3):550-563. PubMed ID: 29358305
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Plasmid-based gene transfer ameliorates visceral storage in a mouse model of Sandhoff disease.
    Yamaguchi A; Katsuyama K; Suzuki K; Kosaka K; Aoki I; Yamanaka S
    J Mol Med (Berl); 2003 Mar; 81(3):185-93. PubMed ID: 12682727
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Occurrence of an anomalous endocytic compartment in fibroblasts from Sandhoff disease patients.
    Tancini B; Magini A; Latterini L; Urbanelli L; Ciccarone V; Elisei F; Emiliani C
    Mol Cell Biochem; 2010 Feb; 335(1-2):273-82. PubMed ID: 19823769
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Abnormal epiphyseal development in a feline model of Sandhoff disease.
    McNulty MA; Prevatt PB; Nussbaum ER; Randle AN; Johnson AK; Hudson JA; Gray-Edwards HL; Sena-Esteves M; Martin DR; Carlson CS
    J Orthop Res; 2020 Dec; 38(12):2580-2591. PubMed ID: 32678923
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Tay-Sachs and Sandhoff diseases: enzymatic diagnosis in dried blood spots on filter paper: retrospective diagnoses in newborn-screening cards.
    Chamoles NA; Blanco M; Gaggioli D; Casentini C
    Clin Chim Acta; 2002 Apr; 318(1-2):133-7. PubMed ID: 11880123
    [TBL] [Abstract][Full Text] [Related]  

  • 47. GM2 ganglioside accumulation causes neuroinflammation and behavioral alterations in a mouse model of early onset Tay-Sachs disease.
    Demir SA; Timur ZK; Ateş N; Martínez LA; Seyrantepe V
    J Neuroinflammation; 2020 Sep; 17(1):277. PubMed ID: 32951593
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Therapeutic evaluation of GM2 gangliosidoses by ELISA using anti-GM2 ganglioside antibodies.
    Tsuji D; Higashine Y; Matsuoka K; Sakuraba H; Itoh K
    Clin Chim Acta; 2007 Mar; 378(1-2):38-41. PubMed ID: 17196574
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Animal models of GM2 gangliosidosis: utility and limitations.
    Lawson CA; Martin DR
    Appl Clin Genet; 2016; 9():111-20. PubMed ID: 27499644
    [TBL] [Abstract][Full Text] [Related]  

  • 50. The beta-hexosaminidase deficiency disorders: development of a clinical paradigm in the mouse.
    Tifft CJ; Proia RL
    Ann Med; 1997 Dec; 29(6):557-61. PubMed ID: 9562524
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Specific induction of macrophage inflammatory protein 1-alpha in glial cells of Sandhoff disease model mice associated with accumulation of N-acetylhexosaminyl glycoconjugates.
    Tsuji D; Kuroki A; Ishibashi Y; Itakura T; Kuwahara J; Yamanaka S; Itoh K
    J Neurochem; 2005 Mar; 92(6):1497-507. PubMed ID: 15748167
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Nonsense mutation of feline beta-hexosaminidase beta-subunit (HEXB) gene causing Sandhoff disease in a family of Japanese domestic cats.
    Kanae Y; Endoh D; Yamato O; Hayashi D; Matsunaga S; Ogawa H; Maede Y; Hayashi M
    Res Vet Sci; 2007 Feb; 82(1):54-60. PubMed ID: 16872651
    [TBL] [Abstract][Full Text] [Related]  

  • 53. GM2 Gangliosidoses: Clinical Features, Pathophysiological Aspects, and Current Therapies.
    Leal AF; Benincore-Flórez E; Solano-Galarza D; Garzón Jaramillo RG; Echeverri-Peña OY; Suarez DA; Alméciga-Díaz CJ; Espejo-Mojica AJ
    Int J Mol Sci; 2020 Aug; 21(17):. PubMed ID: 32867370
    [TBL] [Abstract][Full Text] [Related]  

  • 54. GM2 gangliosidoses: a review of cases confirmed by beta-N-acetylhexosaminidase assay.
    Christopher R; Rangaswamy GR; Shetty KT
    Indian J Pediatr; 1995; 62(4):479-83. PubMed ID: 10829909
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Ganglioside loading of cultured fibroblasts: a provocative method for the diagnosis of the GM2 gangliosidoses.
    Charrow J; Binns HJ
    Clin Chim Acta; 1986 Apr; 156(1):41-9. PubMed ID: 2938852
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Therapeutic advantages of combined gene/cell therapy strategies in a murine model of GM2 gangliosidosis.
    Sala D; Ornaghi F; Morena F; Argentati C; Valsecchi M; Alberizzi V; Di Guardo R; Bolino A; Aureli M; Martino S; Gritti A
    Mol Ther Methods Clin Dev; 2022 Jun; 25():170-189. PubMed ID: 35434178
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Characterization of the testis and epididymis in mouse models of human Tay Sachs and Sandhoff diseases and partial determination of accumulated gangliosides.
    Trasler J; Saberi F; Somani IH; Adamali HI; Huang JQ; Fortunato SR; Ritter G; Gu M; Aebersold R; Gravel RA; Hermo L
    Endocrinology; 1998 Jul; 139(7):3280-8. PubMed ID: 9645704
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported.
    Maegawa GH; Stockley T; Tropak M; Banwell B; Blaser S; Kok F; Giugliani R; Mahuran D; Clarke JT
    Pediatrics; 2006 Nov; 118(5):e1550-62. PubMed ID: 17015493
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Thymic involution and corticosterone level in Sandhoff disease model mice: new aspects the pathogenesis of GM2 gangliosidosis.
    Matsuoka K; Tsuji D; Taki T; Itoh K
    J Inherit Metab Dis; 2011 Oct; 34(5):1061-8. PubMed ID: 21598013
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases.
    Phaneuf D; Wakamatsu N; Huang JQ; Borowski A; Peterson AC; Fortunato SR; Ritter G; Igdoura SA; Morales CR; Benoit G; Akerman BR; Leclerc D; Hanai N; Marth JD; Trasler JM; Gravel RA
    Hum Mol Genet; 1996 Jan; 5(1):1-14. PubMed ID: 8789434
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.