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 *

101 related articles for article (PubMed ID: 24643038)

  • 1. Human glycosylation disorders.
    Krasnewich D
    Cancer Biomark; 2014 Jan; 14(1):3-16. PubMed ID: 24643038
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing.
    Timal S; Hoischen A; Lehle L; Adamowicz M; Huijben K; Sykut-Cegielska J; Paprocka J; Jamroz E; van Spronsen FJ; Körner C; Gilissen C; Rodenburg RJ; Eidhof I; Van den Heuvel L; Thiel C; Wevers RA; Morava E; Veltman J; Lefeber DJ
    Hum Mol Genet; 2012 Oct; 21(19):4151-61. PubMed ID: 22492991
    [TBL] [Abstract][Full Text] [Related]  

  • 3. More than 40 years of glycobiology in Regensburg.
    Tanner W; Lehle L
    Biochem Biophys Res Commun; 2012 Aug; 425(3):578-82. PubMed ID: 22925677
    [No Abstract]   [Full Text] [Related]  

  • 4. Congenital disorders of glycosylation: a concise chart of glycocalyx dysfunction.
    Hennet T; Cabalzar J
    Trends Biochem Sci; 2015 Jul; 40(7):377-84. PubMed ID: 25840516
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital disorders of glycosylation.
    Jaeken J
    Ann N Y Acad Sci; 2010 Dec; 1214():190-8. PubMed ID: 21175687
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The clinical relevance of glycobiology.
    Schachter H
    J Clin Invest; 2001 Dec; 108(11):1579-82. PubMed ID: 11733552
    [No Abstract]   [Full Text] [Related]  

  • 7. Congenital disorders of glycosylation. Part II. Defects of protein O-glycosylation.
    Cylwik B; Lipartowska K; Chrostek L; Gruszewska E
    Acta Biochim Pol; 2013; 60(3):361-8. PubMed ID: 24051442
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ALG1-CDG: a new case with early fatal outcome.
    Rohlfing AK; Rust S; Reunert J; Tirre M; Du Chesne I; Wemhoff S; Meinhardt F; Hartmann H; Das AM; Marquardt T
    Gene; 2014 Jan; 534(2):345-51. PubMed ID: 24157261
    [TBL] [Abstract][Full Text] [Related]  

  • 9. DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy.
    Barone R; Aiello C; Race V; Morava E; Foulquier F; Riemersma M; Passarelli C; Concolino D; Carella M; Santorelli F; Vleugels W; Mercuri E; Garozzo D; Sturiale L; Messina S; Jaeken J; Fiumara A; Wevers RA; Bertini E; Matthijs G; Lefeber DJ
    Ann Neurol; 2012 Oct; 72(4):550-8. PubMed ID: 23109149
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Congenital disorders of glycosylation: sweet news.
    Theodore M; Morava E
    Curr Opin Pediatr; 2011 Dec; 23(6):581-7. PubMed ID: 21970833
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation.
    Lübbehusen J; Thiel C; Rind N; Ungar D; Prinsen BH; de Koning TJ; van Hasselt PM; Körner C
    Hum Mol Genet; 2010 Sep; 19(18):3623-33. PubMed ID: 20605848
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Significance of sugar chain recognition by galectins and its involvement in disease-associated glycosylation.
    Arikawa T; Simamura E; Shimada H; Nakamura T; Hatta T; Shoji H
    Congenit Anom (Kyoto); 2014 May; 54(2):77-81. PubMed ID: 24450300
    [TBL] [Abstract][Full Text] [Related]  

  • 13. MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.
    Schenk B; Imbach T; Frank CG; Grubenmann CE; Raymond GV; Hurvitz H; Korn-Lubetzki I; Revel-Vik S; Raas-Rotschild A; Luder AS; Jaeken J; Berger EG; Matthijs G; Hennet T; Aebi M
    J Clin Invest; 2001 Dec; 108(11):1687-95. PubMed ID: 11733564
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation.
    Ashikov A; Abu Bakar N; Wen XY; Niemeijer M; Rodrigues Pinto Osorio G; Brand-Arzamendi K; Hasadsri L; Hansikova H; Raymond K; Vicogne D; Ondruskova N; Simon MEH; Pfundt R; Timal S; Beumers R; Biot C; Smeets R; Kersten M; Huijben K; ; Linders PTA; van den Bogaart G; van Hijum SAFT; Rodenburg R; van den Heuvel LP; van Spronsen F; Honzik T; Foulquier F; van Scherpenzeel M; Lefeber DJ; ; Mirjam W; Han B; Helen M; Helen M; Peter VH; Jiddeke VK; Diego M; Lars M; Katja BH; Jozef H; Majid A; Kevin C; Johann TWN
    Hum Mol Genet; 2018 Sep; 27(17):3029-3045. PubMed ID: 29878199
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital disorders of glycosylation.
    Jaeken J
    Handb Clin Neurol; 2013; 113():1737-43. PubMed ID: 23622397
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Defining the phenotype in congenital disorder of glycosylation due to ALG1 mutations.
    Morava E; Vodopiutz J; Lefeber DJ; Janecke AR; Schmidt WM; Lechner S; Item CB; Sykut-Cegielska J; Adamowicz M; Wierzba J; Zhang ZH; Mihalek I; Stockler S; Bodamer OA; Lehle L; Wevers RA
    Pediatrics; 2012 Oct; 130(4):e1034-9. PubMed ID: 22966035
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PMM2-CDG: phenotype and genotype in four affected family members.
    Bortot B; Cosentini D; Faletra F; Biffi S; De Martino E; Carrozzi M; Severini GM
    Gene; 2013 Dec; 531(2):506-9. PubMed ID: 23988505
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie.
    Imbach T; Schenk B; Schollen E; Burda P; Stutz A; Grunewald S; Bailie NM; King MD; Jaeken J; Matthijs G; Berger EG; Aebi M; Hennet T
    J Clin Invest; 2000 Jan; 105(2):233-9. PubMed ID: 10642602
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Distinct features of congenital disorder of glycosylation type IIx in Kuwait: a case report.
    Makhseed N; Dhaunsi G; Jaeken J
    J Child Neurol; 2012 Feb; 27(2):222-4. PubMed ID: 21960674
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inherited disorders of glycosylation.
    Sparks SE
    Mol Genet Metab; 2006 Jan; 87(1):1-7. PubMed ID: 16511948
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.