Connection

Russell Norris to Humans

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

0.424
  1. Mitral Valve Prolapse Induces Regionalized Myocardial Fibrosis. J Am Heart Assoc. 2021 12 21; 10(24):e022332.
    View in: PubMed
    Score: 0.030
  2. Mitral Valve Prolapse and Its Motley Crew-Syndromic Prevalence, Pathophysiology, and Progression of a Common Heart Condition. J Am Heart Assoc. 2021 07 06; 10(13):e020919.
    View in: PubMed
    Score: 0.029
  3. DZIP1 regulates mammalian cardiac valve development through a Cby1-?-catenin mechanism. Dev Dyn. 2021 10; 250(10):1432-1449.
    View in: PubMed
    Score: 0.028
  4. Biased Opioid Receptor Ligands: Gain without Pain. Trends Endocrinol Metab. 2020 11; 31(11):801-802.
    View in: PubMed
    Score: 0.027
  5. Hypermobile Ehlers-Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes. Dev Dyn. 2021 03; 250(3):318-344.
    View in: PubMed
    Score: 0.027
  6. Primary cilia defects causing mitral valve prolapse. Sci Transl Med. 2019 05 22; 11(493).
    View in: PubMed
    Score: 0.025
  7. Inheritance Impacts Mitral Valve Insufficiency. Circ Cardiovasc Genet. 2017 10; 10(5).
    View in: PubMed
    Score: 0.022
  8. A role for primary cilia in aortic valve development and disease. Dev Dyn. 2017 08; 246(8):625-634.
    View in: PubMed
    Score: 0.022
  9. Distinct signaling pathways activated by "extracellular" and "intracellular" serotonin in heart valve development and disease. Cell Biochem Biophys. 2013; 67(3):819-28.
    View in: PubMed
    Score: 0.016
  10. Atrioventricular valve development: new perspectives on an old theme. Differentiation. 2012 Jul; 84(1):103-16.
    View in: PubMed
    Score: 0.015
  11. Expression of the familial cardiac valvular dystrophy gene, filamin-A, during heart morphogenesis. Dev Dyn. 2010 Jul; 239(7):2118-27.
    View in: PubMed
    Score: 0.013
  12. Neonatal and adult cardiovascular pathophysiological remodeling and repair: developmental role of periostin. Ann N Y Acad Sci. 2008 Mar; 1123:30-40.
    View in: PubMed
    Score: 0.011
  13. Periostin regulates collagen fibrillogenesis and the biomechanical properties of connective tissues. J Cell Biochem. 2007 Jun 01; 101(3):695-711.
    View in: PubMed
    Score: 0.011
  14. Detection of betaig-H3, a TGFbeta induced gene, during cardiac development and its complementary pattern with periostin. Anat Embryol (Berl). 2005 Aug; 210(1):13-23.
    View in: PubMed
    Score: 0.010
  15. Research Opportunities in the Treatment of Mitral Valve Prolapse: JACC Expert Panel. J Am Coll Cardiol. 2022 12 13; 80(24):2331-2347.
    View in: PubMed
    Score: 0.008
  16. PLEKHM2 Loss-of-Function Is Associated With Dilated Cardiomyopathy. Circ Genom Precis Med. 2022 08; 15(4):e003594.
    View in: PubMed
    Score: 0.008
  17. Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse. Eur Heart J. 2022 05 01; 43(17):1668-1680.
    View in: PubMed
    Score: 0.008
  18. Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse. Circ Genom Precis Med. 2021 10; 14(5):e003148.
    View in: PubMed
    Score: 0.007
  19. Chromatin Accessibility of Human Mitral Valves and Functional Assessment of MVP Risk Loci. Circ Res. 2021 03 05; 128(5):e84-e101.
    View in: PubMed
    Score: 0.007
  20. Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome. Mamm Genome. 2000 Nov; 11(11):1000-5.
    View in: PubMed
    Score: 0.007
  21. Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis. Circulation. 2019 10 15; 140(16):1331-1341.
    View in: PubMed
    Score: 0.006
  22. Genome-Wide Association Study-Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse. Circ Genom Precis Med. 2019 05; 12(5):e002497.
    View in: PubMed
    Score: 0.006
  23. Human pre-valvular endocardial cells derived from pluripotent stem cells recapitulate cardiac pathophysiological valvulogenesis. Nat Commun. 2019 04 26; 10(1):1929.
    View in: PubMed
    Score: 0.006
  24. The exocyst acting through the primary cilium is necessary for renal ciliogenesis, cystogenesis, and tubulogenesis. J Biol Chem. 2019 04 26; 294(17):6710-6718.
    View in: PubMed
    Score: 0.006
  25. Role of Periostin in Cardiac Valve Development. Adv Exp Med Biol. 2019; 1132:177-191.
    View in: PubMed
    Score: 0.006
  26. New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study. Eur Heart J. 2018 04 14; 39(15):1269-1277.
    View in: PubMed
    Score: 0.006
  27. MEF2C regulates outflow tract alignment and transcriptional control of Tdgf1. Development. 2016 Mar 01; 143(5):774-9.
    View in: PubMed
    Score: 0.005
  28. The Living Scar--Cardiac Fibroblasts and the Injured Heart. Trends Mol Med. 2016 Feb; 22(2):99-114.
    View in: PubMed
    Score: 0.005
  29. Mitral valve disease--morphology and mechanisms. Nat Rev Cardiol. 2015 Dec; 12(12):689-710.
    View in: PubMed
    Score: 0.005
  30. Genetic association analyses highlight biological pathways underlying mitral valve prolapse. Nat Genet. 2015 Oct; 47(10):1206-11.
    View in: PubMed
    Score: 0.005
  31. Mutations in DCHS1 cause mitral valve prolapse. Nature. 2015 Sep 03; 525(7567):109-13.
    View in: PubMed
    Score: 0.005
  32. Angiotensin II-dependent TGF-? signaling contributes to Loeys-Dietz syndrome vascular pathogenesis. J Clin Invest. 2014 Jan; 124(1):448-60.
    View in: PubMed
    Score: 0.004
  33. Cadherin-11 expression patterns in heart valves associate with key functions during embryonic cushion formation, valve maturation and calcification. Cells Tissues Organs. 2013; 198(4):300-10.
    View in: PubMed
    Score: 0.004
  34. Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation. Biochim Biophys Acta. 2014 Feb; 1843(2):234-44.
    View in: PubMed
    Score: 0.004
  35. miR-21 represses Pdcd4 during cardiac valvulogenesis. Development. 2013 May; 140(10):2172-80.
    View in: PubMed
    Score: 0.004
  36. Mutations in the TGF-? repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm. Nat Genet. 2012 Nov; 44(11):1249-54.
    View in: PubMed
    Score: 0.004
  37. Transforming growth factor ?, bone morphogenetic protein, and vascular endothelial growth factor mediate phenotype maturation and tissue remodeling by embryonic valve progenitor cells: relevance for heart valve tissue engineering. Tissue Eng Part A. 2010 Nov; 16(11):3375-83.
    View in: PubMed
    Score: 0.003
  38. Developmental basis of adult cardiovascular diseases: valvular heart diseases. Ann N Y Acad Sci. 2010 Feb; 1188:177-83.
    View in: PubMed
    Score: 0.003
  39. Periostin mediates vascular smooth muscle cell migration through the integrins alphavbeta3 and alphavbeta5 and focal adhesion kinase (FAK) pathway. Atherosclerosis. 2010 Feb; 208(2):358-65.
    View in: PubMed
    Score: 0.003
  40. Periostin promotes atrioventricular mesenchyme matrix invasion and remodeling mediated by integrin signaling through Rho/PI 3-kinase. Dev Biol. 2007 Feb 01; 302(1):256-66.
    View in: PubMed
    Score: 0.003
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.