Dong-Chuan Guo

Dong-Chuan Guo

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Dong-Chuan Guo

Dong-Chuan Guo

Publications by authors named "Dong-Chuan Guo"

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52Publications

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The natural history of type B aortic dissection in patients with PRKG1 mutation c.530G>A (p.Arg177Gln).

J Vasc Surg 2019 Sep 11;70(3):718-723. Epub 2019 Mar 11.

Division of Medical Genetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, Tex.

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http://dx.doi.org/10.1016/j.jvs.2018.12.032DOI Listing
September 2019

SMAD4 rare variants in individuals and families with thoracic aortic aneurysms and dissections.

Eur J Hum Genet 2019 Jul 26;27(7):1054-1060. Epub 2019 Feb 26.

Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, USA.

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http://dx.doi.org/10.1038/s41431-019-0357-xDOI Listing
July 2019

Ari-1 Regulates Myonuclear Organization Together with Parkin and Is Associated with Aortic Aneurysms.

Dev Cell 2018 04;45(2):226-244.e8

Program in Developmental Biology, Baylor College of Medicine (BCM), Houston, TX 77030, USA; Department of Molecular and Human Genetics, BCM, Houston, TX 77030, USA; Howard Hughes Medical Institute, BCM, Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital (TCH), Houston, TX 77030, USA; Department of Neuroscience, BCM, Houston, TX 77030, USA. Electronic address:

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http://dx.doi.org/10.1016/j.devcel.2018.03.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920516PMC
April 2018

Altered Smooth Muscle Cell Force Generation as a Driver of Thoracic Aortic Aneurysms and Dissections.

Arterioscler Thromb Vasc Biol 2017 01 22;37(1):26-34. Epub 2016 Nov 22.

From the Department of Internal Medicine, McGovern Medical School at The University of Texas Health Science Center at Houston (D.M.M., D.-c.G., E.R.); Department of Molecular Physiology and Biophysics, University of Vermont, Burlington (K.M.T.); Department of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville (H.L.S.); and Department of Physiology, University of Texas Southwestern Medical Center, Dallas (K.K. J.T.S.).

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http://atvb.ahajournals.org/content/early/2016/11/22/ATVBAHA
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http://dx.doi.org/10.1161/ATVBAHA.116.303229DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5222685PMC
January 2017

Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections.

Am J Hum Genet 2016 09 25;99(3):762-769. Epub 2016 Aug 25.

Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX 77030, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.06.034DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011062PMC
September 2016

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms.

J Am Heart Assoc 2016 07 14;5(7). Epub 2016 Jul 14.

Department of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands

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http://dx.doi.org/10.1161/JAHA.115.002603DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015357PMC
July 2016

Precision medical and surgical management for thoracic aortic aneurysms and acute aortic dissections based on the causative mutant gene.

J Cardiovasc Surg (Torino) 2016 Apr 2;57(2):172-7. Epub 2016 Feb 2.

Division of Medical Genetics, Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, TX, USA -

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April 2016

LOX Mutations Predispose to Thoracic Aortic Aneurysms and Dissections.

Circ Res 2016 Mar 12;118(6):928-34. Epub 2016 Jan 12.

From the Departments of Internal Medicine (D.G., E.S.R., L.G., X.D., Z.R., B.C., E.M.H., D.M.M.) and Cardiothoracic and Vascular Surgery (A.E., H.J.S.), University of Texas Health Science Center, Houston; Department of Molecular and Human Genetics, Center for Statistical Genetics, Baylor College of Medicine, Houston, TX (R.L.P.S.-C., S.M.L.); Laboratory for Vascular Translational Science, INSERM U1148, Hôpital Bichat, Paris, France (P.A., G.J., C.B.); Centre National de Référence pour le syndrome de Marfan et apparentés, Département de Génétique Moléculaire, AP-HP, Hôpital Bichat, Paris, France (P.A., C.B.); Department of Pediatrics, MetroHealth Medical Center, Cleveland, OH (R.M.); Department of Medicine, Stanford University Medical Center, CA (D.L.); and Department of Genome Sciences, University of Washington, Seattle (M.J.B., J.S., D.A.N.).

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http://dx.doi.org/10.1161/CIRCRESAHA.115.307130DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839295PMC
March 2016

SMAD2 Mutations Are Associated with Arterial Aneurysms and Dissections.

Hum Mutat 2015 Dec 10;36(12):1145-9. Epub 2015 Sep 10.

Department of Clinical Genetics, Center for Connective Tissue Research, VU University Medical Center, Amsterdam, 1007, MB, The Netherlands.

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http://dx.doi.org/10.1002/humu.22854DOI Listing
December 2015

Aortic Disease Presentation and Outcome Associated With ACTA2 Mutations.

Circ Cardiovasc Genet 2015 Jun 10;8(3):457-64. Epub 2015 Mar 10.

Departments of Internal Medicine (E.S.R., D.G., S.P., T.A.B., K.F., D.M.M.), Cardiothoracic and Vascular Surgery (A.E., H.S.), University of Texas Health Science Center at Houston; Department of Medicine, Stanford University Medical Center, CA (D.L.); Connective Tissue Gene Tests, Allentown, PA (J.H.); Department of Cardiac and Vascular Sciences, St. George's, University of London, London, United Kingdom (A.C., G.A.); AP-HP, Hôpital Bichat, Centre National de Référence pour le syndrome de Marfan et apparentés, Paris, France (C.B., G.J.), Université Paris 7, Paris, France (C.B., G.J.), AP-HP, Hôpital Bichat, Laboratoire de Génétique moléculaire, Boulogne, France (C.B.), and INSERM, U1148, Paris, France (C.B., G.J.); AP-HP, Hôpital Bichat, Service de Cardiologie, Paris, France (G.J.); Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO (A.B.); Genomic Medicine Institute, Cleveland Clinic, OH (R.M.); Department of Bioscience and Genetics, National Cerebral and Cardiovascular Center Research Institute, Osaka, Japan (T.M., H.M.); Perelman School of Medicine, University of Pennsylvania, Philadelphia (R.P.); Division of Cardiothoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX (J.C., S.L.); and Texas Heart Institute and Baylor St. Luke's Medical Center, Houston (J.C., S.L.).

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http://dx.doi.org/10.1161/CIRCGENETICS.114.000943DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4601641PMC
June 2015

MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissections.

Am J Hum Genet 2014 Dec 26;95(6):736-43. Epub 2014 Nov 26.

INSERM U1148, Laboratory for Vascular Translational Science, Hôpital Bichat, Université Paris Diderot, Sorbonne Paris Cité, 75018 Paris, France; AP-HP, Département de Génétique, Hôpital Bichat, 75018 Paris, France; AP-HP, Centre de référence pour les syndromes de Marfan et apparentés, Service de Cardiologie, Hôpital Bichat, 75018 Paris, France; UFR de Médecine, Université Paris Diderot, 75018 Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.10.018DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259978PMC
December 2014

Successes and challenges of using whole exome sequencing to identify novel genes underlying an inherited predisposition for thoracic aortic aneurysms and acute aortic dissections.

Trends Cardiovasc Med 2014 Feb 15;24(2):53-60. Epub 2013 Aug 15.

Division of Medical Genetics, Department of Internal Medicine, University of Texas Health Science Center at Houston (UT Health), 6431 Fannin, Suite 6.100, Houston, TX 77030, USA.

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http://dx.doi.org/10.1016/j.tcm.2013.06.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917689PMC
February 2014

Acute aortic dissections with pregnancy in women with ACTA2 mutations.

Am J Med Genet A 2014 Jan 15;164A(1):106-12. Epub 2013 Nov 15.

Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, Texas.

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http://dx.doi.org/10.1002/ajmg.a.36208DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4012224PMC
January 2014

Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome.

Am J Med Genet A 2013 Sep 29;161A(9):2305-10. Epub 2013 Jul 29.

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

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http://dx.doi.org/10.1002/ajmg.a.36044DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829633PMC
September 2013

Treatment guidelines for thoracic aortic aneurysms and dissections based on the underlying causative gene.

J Thorac Cardiovasc Surg 2010 Dec;140(6 Suppl):S2-4; discussion S45-51

Department of Internal Medicine, the University of Texas Health Science Center at Houston, Houston, TX, USA.

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http://dx.doi.org/10.1016/j.jtcvs.2010.07.027DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3584588PMC
December 2010

An FBN1 pseudoexon mutation in a patient with Marfan syndrome: confirmation of cryptic mutations leading to disease.

J Hum Genet 2008 17;53(11-12):1007-11. Epub 2008 Sep 17.

The Department of Internal Medicine, The University of Texas Medical School at Houston, 6431 Fannin, MSB 6.100, Houston, TX 77030, USA.

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http://dx.doi.org/10.1007/s10038-008-0334-7DOI Listing
February 2009

Universal primer applications for pyrosequencing.

Methods Mol Biol 2007 ;373:57-62

Department of Internal Medicine, University of Texas Medical School ot Houston, Houston, TX, USA.

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http://dx.doi.org/10.1385/1-59745-377-3:57DOI Listing
June 2007

Pathogenesis of thoracic and abdominal aortic aneurysms.

Ann N Y Acad Sci 2006 Nov;1085:339-52

Department of Internal Medicine, University of Texas Medical School, Houston, 6431 Fannin, MSB 6.039, Houston, TX 77030, USA.

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http://doi.wiley.com/10.1196/annals.1383.013
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http://dx.doi.org/10.1196/annals.1383.013DOI Listing
November 2006

Methodology for using a universal primer to label amplified DNA segments for molecular analysis.

Biotechnol Lett 2003 Dec;25(24):2079-83

Department of Internal Medicine, University of Texas - Houston Medical School, MSB 1.410, 6431 Fannin, Houston, TX 77030, USA.

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December 2003

High throughput detection of small genomic insertions or deletions by Pyrosequencing.

Biotechnol Lett 2003 Oct;25(20):1703-7

Department of Internal Medicine, University of Texas-Houston Medical School, MSB 1.410, 6431 Fannin, Houston, TX 77030, USA.

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October 2003

Genetic susceptibility to enteroaggregative Escherichia coli diarrhea: polymorphism in the interleukin-8 promotor region.

J Infect Dis 2003 Aug 25;188(4):506-11. Epub 2003 Jul 25.

University of Texas School of Public Health, Houston, Texas, USA.

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http://dx.doi.org/10.1086/377102DOI Listing
August 2003

Mapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25.

Circulation 2003 Jul 23;107(25):3184-90. Epub 2003 Jun 23.

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

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https://www.ahajournals.org/doi/10.1161/01.CIR.0000078634.33
Publisher Site
http://dx.doi.org/10.1161/01.CIR.0000078634.33124.95DOI Listing
July 2003

Genetic basis of thoracic aortic aneurysms and dissections.

Curr Opin Cardiol 2002 Nov;17(6):677-83

Division of Medical Genetics, Department of Internal Medicine, The University of Texas Medical School at Houston, 6431 Fannin, Houston, TX 77030, USA.

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November 2002