咆哮 发表于 2025-3-26 21:51:39
Gene Transfer into Cystic Fibrosis Airway Epithelial Cells,ox 90% of deaths caused by this devastating disease are the result of infections of the respiratory tract owing to dysfunction of the Cl. transport in airway epithelial cells. Efficient transfer of the cystic fibrosis transmembrane conductance regulator (CFTR) gene into the airway epithelium of CF p龙卷风 发表于 2025-3-27 01:43:39
Genetic Analysis of Cystic Fibrosis Airway Epithelial Cells,mutation, which accounts for 30–50%;of CF chromosomes in southern European countries and for 50–80%; of CF chromosomes in the United States, Canada, Argentina, and central and northern European countriesBone-Scan 发表于 2025-3-27 08:15:53
Human Tracheal Gland Cells in Primary Culture,er ences, however, in the structure and function of the various animal airways, rendering it difficult to extrapolate to humans. In this chapter, the author describes techniques that facilitate the isolation and culture of tracheal gland cells from humans. These techniques allow high reproducibility泥瓦匠 发表于 2025-3-27 11:04:01
Human Chondrocyte Cultures as Models of Cartilage-Specific Gene Regulation,the cartilage matrix when turnover is low. The major components of the extracellular matrix synthesized by these specialized cells include highly crosslinked fibrils of the final synthesized and secreted triple helical type II collagen molecule that interact with other cartilage-specific collagens INAIVE 发表于 2025-3-27 15:12:32
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http://reply.papertrans.cn/43/4291/429043/429043_36.pngtheta-waves 发表于 2025-3-28 01:01:12
http://reply.papertrans.cn/43/4291/429043/429043_37.png准则 发表于 2025-3-28 03:59:51
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http://reply.papertrans.cn/43/4291/429043/429043_39.pngcolostrum 发表于 2025-3-28 12:15:44
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