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Merck
CN

Heterozygous

Disease models & mechanisms (2017-02-27)
Thanushiyan Poobalasingam, Laura L Yates, Simone A Walker, Miguel Pereira, Nina Y Gross, Akmol Ali, Maria Kolatsi-Joannou, Marjo-Riitta Jarvelin, Juha Pekkanen, Eugenia Papakrivopoulou, David A Long, Mark Griffiths, Darcy Wagner, Melanie Königshoff, Matthew Hind, Cosetta Minelli, Clare M Lloyd, Charlotte H Dean
摘要

Lung diseases impose a huge economic and health burden worldwide. A key aspect of several adult lung diseases, such as idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD), including emphysema, is aberrant tissue repair, which leads to an accumulation of damage and impaired respiratory function. Currently, there are few effective treatments available for these diseases and their incidence is rising. The planar cell polarity (PCP) pathway is critical for the embryonic development of many organs, including kidney and lung. We have previously shown that perturbation of the PCP pathway impairs tissue morphogenesis, which disrupts the number and shape of epithelial tubes formed within these organs during embryogenesis. However, very little is known about the role of the PCP pathway beyond birth, partly because of the perinatal lethality of many PCP mouse mutant lines. Here, we investigate heterozygous

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Sigma-Aldrich
抗磷酸组蛋白H3(Ser10)抗体,有丝分裂标记, Upstate®, from rabbit
Sigma-Aldrich
抗-Prosurfactant蛋白C(proSP-C)抗体, serum, Chemicon®
Sigma-Aldrich
抗GAPDH 抗体, from rabbit, purified by affinity chromatography
Sigma-Aldrich
抗 GM130(C-末端) 兔抗, affinity isolated antibody, buffered aqueous solution