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 *

269 related articles for article (PubMed ID: 34071368)

  • 1. Hepatic and Extrahepatic Sources and Manifestations in Endoplasmic Reticulum Storage Diseases.
    Callea F; Francalanci P; Giovannoni I
    Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34071368
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Recruitment-Secretory Block ("R-SB") Phenomenon and Endoplasmic Reticulum Storage Diseases.
    Callea F; Tomà P; Bellacchio E
    Int J Mol Sci; 2021 Jun; 22(13):. PubMed ID: 34202771
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Protein Misfolding and Aggregation: The Relatedness between Parkinson's Disease and Hepatic Endoplasmic Reticulum Storage Disorders.
    Padilla-Godínez FJ; Ramos-Acevedo R; Martínez-Becerril HA; Bernal-Conde LD; Garrido-Figueroa JF; Hiriart M; Hernández-López A; Argüero-Sánchez R; Callea F; Guerra-Crespo M
    Int J Mol Sci; 2021 Nov; 22(22):. PubMed ID: 34830348
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hepatic endoplasmic reticulum storage diseases.
    Callea F; Brisigotti M; Fabbretti G; Bonino F; Desmet VJ
    Liver; 1992 Dec; 12(6):357-62. PubMed ID: 1470006
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Mechanism of Mitochondrial Injury in Alpha-1 Antitrypsin Deficiency Mediated Liver Disease.
    Khodayari N; Wang RL; Oshins R; Lu Y; Millett M; Aranyos AM; Mostofizadeh S; Scindia Y; Flagg TO; Brantly M
    Int J Mol Sci; 2021 Dec; 22(24):. PubMed ID: 34948056
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Aberrant disulphide bonding contributes to the ER retention of alpha1-antitrypsin deficiency variants.
    Ronzoni R; Berardelli R; Medicina D; Sitia R; Gooptu B; Fra AM
    Hum Mol Genet; 2016 Feb; 25(4):642-50. PubMed ID: 26647313
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Alpha 1-antitrypsin deficiency--a hereditary storage disease of the hepatic endoplasmic reticulum].
    Stejskal J; Pijácková A; Dolezel Z; Husek K
    Cesk Pediatr; 1993 Oct; 48(10):604-7. PubMed ID: 8269534
    [No Abstract]   [Full Text] [Related]  

  • 8. Autophagy-enhancing drug carbamazepine diminishes hepatocellular death in fibrinogen storage disease.
    Puls F; Goldschmidt I; Bantel H; Agne C; Bröcker V; Dämmrich M; Lehmann U; Berrang J; Pfister ED; Kreipe HH; Baumann U
    J Hepatol; 2013 Sep; 59(3):626-30. PubMed ID: 23707368
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fibrinogen gamma375 arg-->trp mutation (fibrinogen aguadilla) causes hereditary hypofibrinogenemia, hepatic endoplasmic reticulum storage disease and cirrhosis.
    Rubbia-Brandt L; Neerman-Arbez M; Rougemont AL; Malé PJ; Spahr L
    Am J Surg Pathol; 2006 Jul; 30(7):906-11. PubMed ID: 16819336
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Alpha1-antitrypsin deficiency: liver disease associated with retention of a mutant secretory glycoprotein in the endoplasmic reticulum.
    Perlmutter DH
    Methods Mol Biol; 2003; 232():39-56. PubMed ID: 12840538
    [No Abstract]   [Full Text] [Related]  

  • 11. Elevated synthesis of human alpha 1-antitrypsin hinders the secretion of murine alpha 1-antitrypsin from hepatocytes of transgenic mice.
    Sifers RN; Rogers BB; Hawkins HK; Finegold MJ; Woo SL
    J Biol Chem; 1989 Sep; 264(26):15696-700. PubMed ID: 2788654
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mineralization of alpha-1-antitrypsin inclusion bodies in Mmalton alpha-1-antitrypsin deficiency.
    Callea F; Giovannoni I; Francalanci P; Boldrini R; Faa G; Medicina D; Nobili V; Desmet VJ; Ishak K; Seyama K; Bellacchio E
    Orphanet J Rare Dis; 2018 May; 13(1):79. PubMed ID: 29769092
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The pathological Trento variant of alpha-1-antitrypsin (E75V) shows nonclassical behaviour during polymerization.
    Miranda E; Ferrarotti I; Berardelli R; Laffranchi M; Cerea M; Gangemi F; Haq I; Ottaviani S; Lomas DA; Irving JA; Fra A
    FEBS J; 2017 Jul; 284(13):2110-2126. PubMed ID: 28504839
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Autophagy Pathway: A Critical Route in the Disposal of Alpha 1-Antitrypsin Aggregates That Holds Many Mysteries.
    Leon C; Bouchecareilh M
    Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33668611
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fibrinogen Gamma Chain Mutations Provoke Fibrinogen and Apolipoprotein B Plasma Deficiency and Liver Storage.
    Callea F; Giovannoni I; Sari S; Guldal E; Dalgic B; Akyol G; Sogo T; Al-Hussaini A; Maggiore G; Bartuli A; Boldrini R; Francalanci P; Bellacchio E
    Int J Mol Sci; 2017 Dec; 18(12):. PubMed ID: 29244742
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel fibrinogen gamma375 Arg-->Trp mutation (fibrinogen aguadilla) causes hepatic endoplasmic reticulum storage and hypofibrinogenemia.
    Brennan SO; Maghzal G; Shneider BL; Gordon R; Magid MS; George PM
    Hepatology; 2002 Sep; 36(3):652-8. PubMed ID: 12198657
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heteropolymerization of α-1-antitrypsin mutants in cell models mimicking heterozygosity.
    Laffranchi M; Berardelli R; Ronzoni R; Lomas DA; Fra A
    Hum Mol Genet; 2018 May; 27(10):1785-1793. PubMed ID: 29538751
    [TBL] [Abstract][Full Text] [Related]  

  • 18. γ375W fibrinogen-synthesizing CHO cells indicate the accumulation of variant fibrinogen within endoplasmic reticulum.
    Kobayashi T; Arai S; Ogiwara N; Takezawa Y; Nanya M; Terasawa F; Okumura N
    Thromb Res; 2014 Jan; 133(1):101-7. PubMed ID: 24210681
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A transgenic zebrafish model of hepatocyte function in human Z α1-antitrypsin deficiency.
    Yip E; Giousoh A; Fung C; Wilding B; Prakash MD; Williams C; Verkade H; Bryson-Richardson RJ; Bird PI
    Biol Chem; 2019 Nov; 400(12):1603-1616. PubMed ID: 31091192
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Alpha-1-antitrypsin deficiency: accumulation or degradation of mutant variants within the hepatic endoplasmic reticulum.
    Sifers RN; Finegold MJ; Woo SL
    Am J Respir Cell Mol Biol; 1989 Nov; 1(5):341-5. PubMed ID: 2700304
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.