Dongchuan Guo

Dongchuan Guo

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Dongchuan Guo

Dongchuan Guo

Publications by authors named "Dongchuan Guo"

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16Publications

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Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic Dissection.

Circ Genom Precis Med 2019 Jun 18;12(6):e002476. Epub 2019 Jun 18.

University of Michigan (B.N.W., W.E.H., L.F., J.M., A.D., X.W., M.R.M., S.K.G., N.J.D., C.M.B., J.K., Y.E.C., K.K., G.M.D., H.P., K.A.E., C.J.W., B.Y.), Michigan Medicine, University of Michigan, Ann Arbor.

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http://dx.doi.org/10.1161/CIRCGEN.118.002476DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582991PMC
June 2019

Variants of Unknown Significance in Genes Associated with Heritable Thoracic Aortic Disease Can Be Low Penetrant "Risk Variants".

Am J Hum Genet 2018 07 28;103(1):138-143. Epub 2018 Jun 28.

Division of Medical Genetics and Cardiology, Department of Internal Medicine, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), 6431 Fannin Street, MSB 6.100, Houston, TX 77030, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00029297183017
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http://dx.doi.org/10.1016/j.ajhg.2018.05.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035370PMC
July 2018

Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections.

PLoS One 2016 19;11(4):e0153543. Epub 2016 Apr 19.

Department of Internal Medicine, Division of Medical Genetics, University of Texas Health Science Center at Houston, Houston, Texas, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0153543PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836726PMC
August 2016

Deficiency of MMP17/MT4-MMP proteolytic activity predisposes to aortic aneurysm in mice.

Circ Res 2015 Jul 11;117(2):e13-26. Epub 2015 May 11.

From the Department of Vascular Biology and Inflammation (M.M.-A., A.A., N.M.-B., A.P., J.M.R., A.G.A.), Proteomics Unit (E.C., J.V.) and Bioinformatics Unit (F.M.), Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain; Department of Pharmacology/Nephrology, Faculty of Medicine, Universidad Autónoma de Madrid, Madrid, Spain (A.B.G.-R., M.S.); Department of Internal Medicine, University of Texas Health Science Center at Houston, TX (D.G., D.M.); Department of Basic Biomedical Sciences, Universidad Europea de Madrid, Villaviciosa de Odón, Madrid, Spain (C.S.-C.); Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ (D.T.D.); and Division of Cancer Cell Research, Institute of Medical Science, University of Tokyo, Minato-ku, Tokyo, Japan (M.S.).

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http://circres.ahajournals.org/content/early/2015/05/11/CIRC
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http://circres.ahajournals.org/lookup/doi/10.1161/CIRCRESAHA
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http://dx.doi.org/10.1161/CIRCRESAHA.117.305108DOI Listing
July 2015

RNF213 rare variants in an ethnically diverse population with Moyamoya disease.

Stroke 2014 Nov 2;45(11):3200-7. Epub 2014 Oct 2.

From the Division of Medical Genetics, Department of Internal Medicine, University of Texas Health Science Center, Houston (A.C.C., D.G., Z.R., K.F., E.S.R., H.P., D.M.M.); Department of Molecular and Human Genetics, Center for Statistical Genetics, Baylor College of Medicine, Houston, TX (R.L.P.S.-C., S.M.L., G.T.W.); Department of Genome Sciences (J.S., M.J.B., D.A.N.) and Department of Pediatrics (M.J.B.), University of Washington, Seattle; Department of Neurosurgery, Stanford University, CA (G.K.S.); and Clinical Innovation and Research Institute, Memorial Hermann Hospital, Houston, TX (J.C.G.).

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http://dx.doi.org/10.1161/STROKEAHA.114.006244DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4420622PMC
November 2014

Single-nucleotide polymorphism array genotyping is equivalent to metaphase cytogenetics for diagnosis of Turner syndrome.

Genet Med 2014 Jan 6;16(1):53-9. Epub 2013 Jun 6.

National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.

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http://www.nature.com/articles/gim201377
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http://dx.doi.org/10.1038/gim.2013.77DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883919PMC
January 2014

MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II.

Hum Mol Genet 2007 Oct 31;16(20):2453-62. Epub 2007 Jul 31.

Department of Internal Medicine and Institute of Molecular Medicine, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.

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http://dx.doi.org/10.1093/hmg/ddm201DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2905218PMC
October 2007

The role of MMP-2 and MMP-9 polymorphisms in sporadic intracranial aneurysms.

J Neurosurg 2006 Sep;105(3):418-23

Department of Internal Medicine and Neurosurgery, The University of Texas Medical School at Houston, USA.

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http://dx.doi.org/10.3171/jns.2006.105.3.418DOI Listing
September 2006

Familial thoracic aortic aneurysms and dissections: three families with early-onset ascending and descending aortic dissections in women.

Am J Med Genet A 2006 Jun;140(11):1196-202

Department of Internal Medicine, Division of Medical Genetics, The University of Texas Medical School at Houston, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1002/ajmg.a.31236DOI Listing
June 2006