Connection

HAMED JAFAR-NEJAD to Humans

This is a "connection" page, showing publications HAMED JAFAR-NEJAD has written about Humans.
Connection Strength

0.277
  1. The glycosyltransferase POGLUT1 regulates muscle stem cell development and maintenance in mice. PLoS Genet. 2025 Aug; 21(8):e1011806.
    View in: PubMed
    Score: 0.025
  2. Adeno-associated Virus-mediated Silencing of Sox4 Leads to Long-Term Amelioration of Liver Phenotypes in Mouse Models of Alagille Syndrome. Gastroenterology. 2025 10; 169(5):1000-1016.
    View in: PubMed
    Score: 0.024
  3. NGLY1 Deficiency, a Congenital Disorder of Deglycosylation: From Disease Gene Function to Pathophysiology. Cells. 2022 03 29; 11(7).
    View in: PubMed
    Score: 0.020
  4. Tracing the NGLY1 footprints: insights from Drosophila. J Biochem. 2022 Feb 21; 171(2):153-160.
    View in: PubMed
    Score: 0.019
  5. Multifaceted regulation of Notch signaling by glycosylation. Glycobiology. 2021 01 09; 31(1):8-28.
    View in: PubMed
    Score: 0.018
  6. A conserved role for AMP-activated protein kinase in NGLY1 deficiency. PLoS Genet. 2020 12; 16(12):e1009258.
    View in: PubMed
    Score: 0.018
  7. Sox9 Is a Modifier of the Liver Disease Severity in a Mouse Model of Alagille Syndrome. Hepatology. 2020 04; 71(4):1331-1349.
    View in: PubMed
    Score: 0.017
  8. The Roles of Notch Signaling in Liver Development and Disease. Biomolecules. 2019 10 14; 9(10).
    View in: PubMed
    Score: 0.017
  9. Unbiased glycomics: a powerful tool in rare disease diagnosis and research. Transl Res. 2019 04; 206:1-4.
    View in: PubMed
    Score: 0.016
  10. Sensitized genetic backgrounds reveal differential roles for EGF repeat xylosyltransferases in Drosophila Notch signaling. Glycobiology. 2018 11 01; 28(11):849-859.
    View in: PubMed
    Score: 0.016
  11. Jagged1 heterozygosity in mice results in a congenital cholangiopathy which is reversed by concomitant deletion of one copy of Poglut1 (Rumi). Hepatology. 2016 Feb; 63(2):550-65.
    View in: PubMed
    Score: 0.013
  12. The multiple roles of epidermal growth factor repeat O-glycans in animal development. Glycobiology. 2015 Oct; 25(10):1027-42.
    View in: PubMed
    Score: 0.012
  13. The protein O-glucosyltransferase Rumi modifies eyes shut to promote rhabdomere separation in Drosophila. PLoS Genet. 2014 Nov; 10(11):e1004795.
    View in: PubMed
    Score: 0.012
  14. Negative regulation of notch signaling by xylose. PLoS Genet. 2013 Jun; 9(6):e1003547.
    View in: PubMed
    Score: 0.011
  15. Role of glycans and glycosyltransferases in the regulation of Notch signaling. Glycobiology. 2010 Aug; 20(8):931-49.
    View in: PubMed
    Score: 0.009
  16. Regulation of notch signaling via O-glucosylation insights from Drosophila studies. Methods Enzymol. 2010; 480:375-98.
    View in: PubMed
    Score: 0.008
  17. Gfi/Pag-3/senseless zinc finger proteins: a unifying theme? Mol Cell Biol. 2004 Oct; 24(20):8803-12.
    View in: PubMed
    Score: 0.006
  18. POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, a-dystroglycan hypoglycosylation and a distinctive radiological pattern. Acta Neuropathol. 2020 03; 139(3):565-582.
    View in: PubMed
    Score: 0.004
  19. Generation of an induced pluripotent stem cell line (CSCRMi001-A) from a patient with a new type of limb-girdle muscular dystrophy (LGMD) due to a missense mutation in POGLUT1 (Rumi). Stem Cell Res. 2017 10; 24:102-105.
    View in: PubMed
    Score: 0.004
  20. A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss. EMBO Mol Med. 2016 11; 8(11):1289-1309.
    View in: PubMed
    Score: 0.003
  21. A congenital disorder of deglycosylation: Biochemical characterization of N-glycanase 1 deficiency in patient fibroblasts. Glycobiology. 2015 Aug; 25(8):836-44.
    View in: PubMed
    Score: 0.003
  22. Rumi functions as both a protein O-glucosyltransferase and a protein O-xylosyltransferase. Proc Natl Acad Sci U S A. 2011 Oct 04; 108(40):16600-5.
    View in: PubMed
    Score: 0.002
  23. Differential repression by freud-1/CC2D1A at a polymorphic site in the dopamine-D2 receptor gene. J Biol Chem. 2007 Jul 20; 282(29):20897-905.
    View in: PubMed
    Score: 0.002
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.