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Human Molecular Genetics|March 12, 2020
Knockin mouse model of the human CFL2 p.A35T mutation results in a unique splicing defect and severe myopathy phenotypeSamantha M Rosen, Mugdha Joshi, Talia Hitt, et al.Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 26, 2012
Thiazolidinedione response in familial lipodystrophy patients with LMNA mutations: a case seriesA Luedtke, M Boschmann, C Colpe, et al.Clinical Radiology|February 3, 2009
Chronic left ventricular failure: the role of imaging in diagnosis and planning of conventional and novel therapiesE T D Hoey, D Gopalan, S K B Agrawal, et al.Journal of Medicinal Chemistry|October 28, 2005
Design and studies of novel 5-substituted alkynylpyrimidine nucleosides as potent inhibitors of mycobacteriaDinesh Rai, Monika Johar, Tracey Manning, et al.International Journal of Pediatric Otorhinolaryngology|August 11, 2020
Familial and genetic factors in laryngeal cleft: Have we learned anything?Natasha D Dombrowski, Youjin Li, Cher X Zhao, et al.The American Journal of Cardiology|April 4, 1998
Angiotensin-converting enzyme and angiotensinogen gene polymorphisms and heart rate variability in twinsA Busjahn, A Voss, H Knoblauch, et al.Clinical Genetics|March 25, 2000
Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German familiesW Pei, H Baron, B Müller-Myhsok, et al.Blood Pressure|April 18, 2003
Genetic influence on blood pressure and lipid parameters in a sample of Polish twinsP Jedrusik, A Januszewicz, A Busjahn, et al.Hypertension (Dallas, Tex. : 1979)|March 7, 2001
Endothelial dysfunction and xanthine oxidoreductase activity in rats with human renin and angiotensinogen genesE M Mervaala, Z J Cheng, I Tikkanen, et al.Hypertension (Dallas, Tex. : 1979)|January 21, 2000
NF-kappaB inhibition ameliorates angiotensin II-induced inflammatory damage in ratsD N Muller, R Dechend, E M Mervaala, et al.Pageof 83