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Experimental Dermatology|May 25, 2012
Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 (P2RY5) gene in a Turkish family with hypotrichosis and woolly hairHassnaa Mahmoudi, Esra Tug, Ali Haydar Parlak, et al.
Nano Letters|February 12, 2016
Gate-Sensing Coherent Charge Oscillations in a Silicon Field-Effect TransistorM Fernando Gonzalez-Zalba, Sergey N Shevchenko, Sylvain Barraud, et al.
Acta Anaesthesiologica Scandinavica|July 20, 2007
Anti-inflammatory effects of sevoflurane and mild hypothermia in endotoxemic ratsC Hofstetter, K A Boost, M Flondor, et al.
European Journal of Cell Biology|April 3, 2007
Identification of a keratin-associated protein with a putative role in vesicle transportLaura Planko, Karsten Böhse, Jörg Höhfeld, et al.
The British Journal of Dermatology|April 23, 2002
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approachA M Hillmer, R Kruse, F Macciardi, et al.
Plos One|September 10, 2021
Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldnessLara M Hochfeld, Marta Bertolini, David Broadley, et al.
BMC Genomics|July 23, 2004
The FU gene and its possible protein isoformsTorben Østerlund, David B Everman, Regina C Betz, et al.
Nano Letters|June 6, 2015
Dispersively Detected Pauli Spin-Blockade in a Silicon Nanowire Field-Effect TransistorA C Betz, R Wacquez, M Vinet, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|October 6, 2011
[Galli-Galli disease. Clinical and histopathological investigation using a case series of 18 patients]S Hanneken, A Rütten, S Eigelshoven, et al.
Klinische Padiatrie|August 24, 2012
A premature termination mutation in a patient with Lowe syndrome without congenital cataracts: dropping the "O" in OCRLS M Pasternack, D Böckenhauer, M Refke, et al.
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