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Items: 9

1.
MR lymphangiography of lymphatic abnormalities in children and adults with Noonan syndrome
C. C. Pieper, J. Wagenpfeil, A. Henkel, S. Geiger, T. Köster, K. Hoss, J. A. Luetkens, C. Hart, U. I. Attenberger, A. Müller
Sci Rep. 2022; 12: 11164. Published online 2022 Jul 1. doi: 10.1038/s41598-022-13806-w
PMCID:
PMC9249771
ArticlePubReaderPDF–1.9MCite
2.
Increased Mutagen Sensitivity and DNA Damage in Pulmonary Arterial Hypertension
Chiara Federici, Kylie M. Drake, Christina M. Rigelsky, Lauren N. McNelly, Sirena L. Meade, Suzy A. A. Comhair, Serpil C. Erzurum, Micheala A. Aldred
Am J Respir Crit Care Med. 2015 Jul 15; 192(2): 219–228. Published online 2015 Jul 15. doi: 10.1164/rccm.201411-2128OC
PMCID:
PMC4532823
ArticlePubReaderPDF–1.3MCite
3.
Targeted Deletion of Tsc1 Causes Fatal Cardiomyocyte Hyperplasia Independently of Afterload
Usamah S. Kayyali, Christopher G. Larsen, Sarah Bashiruddin, Sara L. Lewandowski, Chinmay M. Trivedi, Rod R. Warburton, Andrey A. Parkhitko, Tasha A. Morrison, Elizabeth P. Henske, Yvonne Chekaluk, David J. Kwiatkowski, Geraldine A. Finlay
Cardiovasc Pathol. Author manuscript; available in PMC 2016 Mar 1.
Published in final edited form as: Cardiovasc Pathol. 2015 Mar-Apr; 24(2): 80–93. Published online 2014 Nov 7. doi: 10.1016/j.carpath.2014.10.005
PMCID:
PMC4344870
ArticlePubReaderPDF–2.4MCite
4.
Bicuspid aortic valve and aortic coarctation are linked to deletion of the X chromosome short arm in Turner syndrome
Carolyn Bondy, Vladimir K Bakalov, Clara Cheng, Laura Olivieri, Douglas R Rosing, Andrew E Arai
J Med Genet. 2013 Oct; 50(10): 662–665. Published online 2013 Jul 3. doi: 10.1136/jmedgenet-2013-101720
PMCID:
PMC3786649
ArticlePubReaderPDF–353KCite
5.
Schimke immuno‐osseous dysplasia: a clinicopathological correlation
J Marietta Clewing, Barbara C Antalfy, Thomas Lücke, Behzad Najafian, Katja M Marwedel, Akira Hori, Ralph M Powel, A F Safo Do, Lydia Najera, Karen SantaCruz, M John Hicks, Dawna L Armstrong
J Med Genet. 2007 Feb; 44(2): 122–130. doi: 10.1136/jmg.2006.044313
PMCID:
PMC2598061
ArticlePubReaderPDF–5.4MCite
6.
Endoglin Expression Is Reduced in Normal Vessels but Still Detectable in Arteriovenous Malformations of Patients with Hereditary Hemorrhagic Telangiectasia Type 1
Annie Bourdeau, Urszula Cymerman, Marie-Eve Paquet, Wendy Meschino, Wendy C. McKinnon, Alan E. Guttmacher, Laurence Becker, Michelle Letarte
Am J Pathol. 2000 Mar; 156(3): 911–923. doi: 10.1016/S0002-9440(10)64960-7
PMCID:
PMC1876827
ArticlePubReaderPDF–744KCite
7.
Monosomy 22q11 in patients with pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries
M. Hofbeck, A. Rauch, G. Buheitel, G. Leipold, J. von der Emde, R. Pfeiffer, H. Singer
Heart. 1998 Feb; 79(2): 180–185. doi: 10.1136/hrt.79.2.180
PMCID:
PMC1728610
SummaryPDF–127KCite
8.
A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome.
R D Jefferson, J Burn, K L Gaunt, S Hunter, E V Davison
J Med Genet. 1986 Oct; 23(5): 474–477. doi: 10.1136/jmg.23.5.474
PMCID:
PMC1049789
SummaryPage BrowsePDF–824KCite
9.
Detection of neuropeptide Y and its mRNA in megakaryocytes: enhanced levels in certain autoimmune mice.
A Ericsson, M Schalling, K R McIntyre, J M Lundberg, D Larhammar, K Seroogy, T Hökfelt, H Persson
Proc Natl Acad Sci U S A. 1987 Aug; 84(16): 5585–5589. doi: 10.1073/pnas.84.16.5585
PMCID:
PMC298907
SummaryPage BrowsePDF–1.5MCite

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