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Increased Prevalence of Inflammatory Bowel Disease in Patients with Mutations in Genes Encoding the Receptor Subunits for TGFβ.

Guerrerio AL, Frischmeyer-Guerrerio PA, Huang C, Wu Y, Haritunians T, McGovern DP, MacCarrick GL, Brant SR, Dietz HC.

Inflamm Bowel Dis. 2016 Sep;22(9):2058-62. doi: 10.1097/MIB.0000000000000872.


Pregnancy and the Risk of Aortic Dissection or Rupture: A Cohort-Crossover Analysis.

Kamel H, Roman MJ, Pitcher A, Devereux RB.

Circulation. 2016 Aug 16;134(7):527-33. doi: 10.1161/CIRCULATIONAHA.116.021594. Epub 2016 Aug 4.


Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans.

Lee VS, Halabi CM, Hoffman EP, Carmichael N, Leshchiner I, Lian CG, Bierhals AJ, Vuzman D; Brigham Genomic Medicine, Mecham RP, Frank NY, Stitziel NO.

Proc Natl Acad Sci U S A. 2016 Aug 2;113(31):8759-64. doi: 10.1073/pnas.1601442113. Epub 2016 Jul 18.


A rare cause of recurrent aortic dissection.

Agrawal Y, Gupta V.

J Saudi Heart Assoc. 2016 Jul;28(3):176-9. doi: 10.1016/j.jsha.2015.11.005. Epub 2015 Nov 21.


A Case Based Approach to Clinical Genetics of Thoracic Aortic Aneurysm/Dissection.

Giusti B, Nistri S, Sticchi E, De Cario R, Abbate R, Gensini GF, Pepe G.

Biomed Res Int. 2016;2016:9579654. doi: 10.1155/2016/9579654. Epub 2016 May 25. Review.


Editorial Commentary: Understanding Marfan syndrome, or "how not to invent the light bulb".

Jones JA.

Trends Cardiovasc Med. 2016 Jul;26(5):429-32. doi: 10.1016/j.tcm.2016.02.005. Epub 2016 Feb 23. No abstract available.


Arterial Tortuosity: An Imaging Biomarker of Childhood Stroke Pathogenesis?

Wei F, Diedrich KT, Fullerton HJ, deVeber G, Wintermark M, Hodge J, Kirton A; Vascular Effects of Infection in Pediatric Stroke (VIPS) Investigators.

Stroke. 2016 May;47(5):1265-70. doi: 10.1161/STROKEAHA.115.011331. Epub 2016 Mar 22.


Cardiovascular manifestations of renovascular hypertension in diabetic mice.

Kashyap S, Engel S, Osman M, Al-Saiegh Y, Wongjarupong A, Grande JP.

PeerJ. 2016 Feb 22;4:e1736. doi: 10.7717/peerj.1736. eCollection 2016.


Genes in Thoracic Aortic Aneurysms and Dissections - Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical Practice.

De Backer J, Renard M, Campens L, François K, Callewaert B, Coucke P, De Paepe A.

Aorta (Stamford). 2013 Jul 1;1(2):135-45. doi: 10.12945/j.aorta.2013.13-024. eCollection 2013 Jul.


Structure of the Elastin-Contractile Units in the Thoracic Aorta and How Genes That Cause Thoracic Aortic Aneurysms and Dissections Disrupt This Structure.

Karimi A, Milewicz DM.

Can J Cardiol. 2016 Jan;32(1):26-34. doi: 10.1016/j.cjca.2015.11.004. Epub 2015 Nov 10. Review.


Activation of Endocannabinoid System Is Associated with Persistent Inflammation in Human Aortic Aneurysm.

Gestrich C, Duerr GD, Heinemann JC, Meertz A, Probst C, Roell W, Schiller W, Zimmer A, Bindila L, Lutz B, Welz A, Dewald O.

Biomed Res Int. 2015;2015:456582. doi: 10.1155/2015/456582. Epub 2015 Oct 11.


Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease.

Capuano A, Bucciotti F, Farwell KD, Tippin Davis B, Mroske C, Hulick PJ, Weissman SM, Gao Q, Spessotto P, Colombatti A, Doliana R.

Hum Mutat. 2016 Jan;37(1):84-97. doi: 10.1002/humu.22920. Epub 2015 Nov 4.


When flexibility is not necessarily a virtue: a review of hypermobility syndromes and chronic or recurrent musculoskeletal pain in children.

Cattalini M, Khubchandani R, Cimaz R.

Pediatr Rheumatol Online J. 2015 Oct 6;13(1):40. doi: 10.1186/s12969-015-0039-3.


Histone Deacetylase 3 Coordinates Deacetylase-independent Epigenetic Silencing of Transforming Growth Factor-β1 (TGF-β1) to Orchestrate Second Heart Field Development.

Lewandowski SL, Janardhan HP, Trivedi CM.

J Biol Chem. 2015 Nov 6;290(45):27067-89. doi: 10.1074/jbc.M115.684753. Epub 2015 Sep 29.


Arterial tortuosity in genetic arteriopathies.

Morris SA.

Curr Opin Cardiol. 2015 Nov;30(6):587-93. doi: 10.1097/HCO.0000000000000218. Review.


Clinical development of galunisertib (LY2157299 monohydrate), a small molecule inhibitor of transforming growth factor-beta signaling pathway.

Herbertz S, Sawyer JS, Stauber AJ, Gueorguieva I, Driscoll KE, Estrem ST, Cleverly AL, Desaiah D, Guba SC, Benhadji KA, Slapak CA, Lahn MM.

Drug Des Devel Ther. 2015 Aug 10;9:4479-99. doi: 10.2147/DDDT.S86621. eCollection 2015. Review.


Valve Sparing Aortic Root Replacement in Children with Loeys-Dietz Syndrome.

Sim HT, Seo DJ, Yu JJ, Baek JS, Goo HW, Park JJ.

Korean J Thorac Cardiovasc Surg. 2015 Aug;48(4):272-6. doi: 10.5090/kjtcs.2015.48.4.272. Epub 2015 Aug 5.


A Novel Mutation of SMAD3 Identified in a Chinese Family with Aneurysms-Osteoarthritis Syndrome.

Zhang W, Zhou M, Liu C, Liu C, Qiao T, Huang D, Ran F, Wang W, Liu C, Liu Z.

Biomed Res Int. 2015;2015:968135. doi: 10.1155/2015/968135. Epub 2015 Jun 29.


Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation.

Williams KW, Milner JD, Freeman AF.

Immunol Allergy Clin North Am. 2015 Aug;35(3):523-44. doi: 10.1016/j.iac.2015.05.004. Review.

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