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Year | Number of Results |
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2019 | 1 |
2020 | 2 |
2021 | 1 |
2024 | 0 |
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Page 1
A common SNP risk variant MT1-MMP causative for Dupuytren's disease has a specific defect in collagenolytic activity.
Matrix Biol. 2021 Mar;97:20-39. doi: 10.1016/j.matbio.2021.02.003. Epub 2021 Feb 13.
Matrix Biol. 2021.
PMID: 33592276
Molecular and cellular correlates of human nerve regeneration: ADCYAP1/PACAP enhance nerve outgrowth.
Baskozos G, Sandy-Hindmarch O, Clark AJ, Windsor K, Karlsson P, Weir GA, McDermott LA, Burchall J, Wiberg A, Furniss D, Bennett DLH, Schmid AB.
Baskozos G, et al.
Brain. 2020 Jul 1;143(7):2009-2026. doi: 10.1093/brain/awaa163.
Brain. 2020.
PMID: 32651949
Free PMC article.
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Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis.
Allen RJ, Guillen-Guio B, Oldham JM, Ma SF, Dressen A, Paynton ML, Kraven LM, Obeidat M, Li X, Ng M, Braybrooke R, Molina-Molina M, Hobbs BD, Putman RK, Sakornsakolpat P, Booth HL, Fahy WA, Hart SP, Hill MR, Hirani N, Hubbard RB, McAnulty RJ, Millar AB, Navaratnam V, Oballa E, Parfrey H, Saini G, Whyte MKB, Zhang Y, Kaminski N, Adegunsoye A, Strek ME, Neighbors M, Sheng XR, Gudmundsson G, Gudnason V, Hatabu H, Lederer DJ, Manichaikul A, Newell JD Jr, O'Connor GT, Ortega VE, Xu H, Fingerlin TE, Bossé Y, Hao K, Joubert P, Nickle DC, Sin DD, Timens W, Furniss D, Morris AP, Zondervan KT, Hall IP, Sayers I, Tobin MD, Maher TM, Cho MH, Hunninghake GM, Schwartz DA, Yaspan BL, Molyneaux PL, Flores C, Noth I, Jenkins RG, Wain LV.
Allen RJ, et al.
Am J Respir Crit Care Med. 2020 Mar 1;201(5):564-574. doi: 10.1164/rccm.201905-1017OC.
Am J Respir Crit Care Med. 2020.
PMID: 31710517
Free PMC article.
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Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI.
Major M, Freund MK, Burch KS, Mancuso N, Ng M, Furniss D, Pasaniuc B, Ophoff RA.
Major M, et al.
Genet Epidemiol. 2019 Sep;43(6):629-645. doi: 10.1002/gepi.22209. Epub 2019 May 13.
Genet Epidemiol. 2019.
PMID: 31087417
Free PMC article.
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