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Novel variants in 3 kb of 5'UTR of the beta 1-adrenergic receptor gene (-93C>T, -210C>T, and -2146T>C): -2146C homozygotes present in patients with idiopathic dilated cardiomyopathy and coronary heart disease.
Wenzel K, Felix SB, Bauer D, Heere P, Flachmeier C, Podlowski S, Köpke K, Hoehe MR. Wenzel K, et al. Among authors: flachmeier c. Hum Mutat. 2000 Dec;16(6):534. doi: 10.1002/1098-1004(200012)16:6<534::AID-HUMU24>3.0.CO;2-X. Hum Mutat. 2000. PMID: 11102996 No abstract available.
SMARCAD1 Haploinsufficiency Underlies Huriez Syndrome and Associated Skin Cancer Susceptibility.
Günther C, Lee-Kirsch MA, Eckhard J, Matanovic A, Kerscher T, Rüschendorf F, Klein B, Berndt N, Zimmermann N, Flachmeier C, Thuß T, Lucas N, Marenholz I, Esparza-Gordillo J, Hübner N, Traupe H, Delaporte E, Lee YA. Günther C, et al. Among authors: flachmeier c. J Invest Dermatol. 2018 Jun;138(6):1428-1431. doi: 10.1016/j.jid.2018.01.015. Epub 2018 Feb 1. J Invest Dermatol. 2018. PMID: 29409814 Free article. No abstract available.
Use of cyanuric chloride-activated paper for detection of subpicogram quantities of specific DNA sequences and its application to linked restriction fragment length polymorphism analysis in a Duchenne muscular dystrophy affected family.
Hunger HD, Speer A, Flachmeier C, Hanke R, Behrendt G, Coutelle C. Hunger HD, et al. Among authors: flachmeier c. Anal Biochem. 1987 Aug 15;165(1):45-55. doi: 10.1016/0003-2697(87)90199-0. Anal Biochem. 1987. PMID: 2891319
12 results