Connection

Naohiro Yamaguchi to Humans

This is a "connection" page, showing publications Naohiro Yamaguchi has written about Humans.
Connection Strength

0.191
  1. Do CPVT-linked mutations alter RYR2 regulation by cytosolic Ca2+ in cardiomyocytes? J Gen Physiol. 2022 09 05; 154(9).
    View in: PubMed
    Score: 0.032
  2. CRISPR/Cas9 Gene Editing of RYR2 in Human iPSC-Derived Cardiomyocytes to Probe Ca2+ Signaling Aberrancies of CPVT Arrhythmogenesis. Methods Mol Biol. 2022; 2573:41-52.
    View in: PubMed
    Score: 0.031
  3. A central core disease mutation in the Ca2+-binding site of skeletal muscle ryanodine receptor impairs single-channel regulation. Am J Physiol Cell Physiol. 2019 08 01; 317(2):C358-C365.
    View in: PubMed
    Score: 0.026
  4. Two EF-hand motifs in ryanodine receptor calcium release channels contribute to isoform-specific regulation by calmodulin. Cell Calcium. 2017 09; 66:62-70.
    View in: PubMed
    Score: 0.022
  5. Malignant hyperthermia-associated mutations in the S2-S3 cytoplasmic loop of type 1 ryanodine receptor calcium channel impair calcium-dependent inactivation. Am J Physiol Cell Physiol. 2016 Nov 01; 311(5):C749-C757.
    View in: PubMed
    Score: 0.021
  6. Two regions of the ryanodine receptor calcium channel are involved in Ca(2+)-dependent inactivation. Biochemistry. 2014 Mar 04; 53(8):1373-9.
    View in: PubMed
    Score: 0.018
  7. Different regions in skeletal and cardiac muscle ryanodine receptors are involved in transducing the functional effects of calmodulin. J Biol Chem. 2004 Aug 27; 279(35):36433-9.
    View in: PubMed
    Score: 0.009
  8. Ca2+-mediated activation of the skeletal-muscle ryanodine receptor ion channel. J Biol Chem. 2018 12 14; 293(50):19501-19509.
    View in: PubMed
    Score: 0.006
  9. CRISPR/Cas9 Gene editing of RyR2 in human stem cell-derived cardiomyocytes provides a novel approach in investigating dysfunctional Ca2+ signaling. Cell Calcium. 2018 07; 73:104-111.
    View in: PubMed
    Score: 0.006
  10. Mechanical regulation of native and the recombinant calcium channel. Cell Calcium. 2013 Apr; 53(4):264-74.
    View in: PubMed
    Score: 0.004
  11. Thermodynamics of calmodulin binding to cardiac and skeletal muscle ryanodine receptor ion channels. Proteins. 2009 Jan; 74(1):207-11.
    View in: PubMed
    Score: 0.003
  12. Single channel properties of heterotetrameric mutant RyR1 ion channels linked to core myopathies. J Biol Chem. 2008 Mar 07; 283(10):6321-9.
    View in: PubMed
    Score: 0.003
  13. Characterization of recessive RYR1 mutations in core myopathies. Hum Mol Genet. 2006 Sep 15; 15(18):2791-803.
    View in: PubMed
    Score: 0.003
  14. Calmodulin regulation and identification of calmodulin binding region of type-3 ryanodine receptor calcium release channel. Biochemistry. 2005 Nov 15; 44(45):15074-81.
    View in: PubMed
    Score: 0.003
  15. Characterization of recombinant skeletal muscle (Ser-2843) and cardiac muscle (Ser-2809) ryanodine receptor phosphorylation mutants. J Biol Chem. 2003 Dec 19; 278(51):51693-702.
    View in: PubMed
    Score: 0.002
  16. Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptor. Hum Mol Genet. 2003 Feb 15; 12(4):379-88.
    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.