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收藏Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity神经元细胞粘附分子中的双等位基因变体会导致神经发育障碍,其特征是发育迟缓,肌张力低下,神经病/痉挛
Kurolap, Alina; Kreuder, Florian; Gonzaga-Jauregui, Claudia; Duvdevani, Morasha Plesser; Harel, Tamar; Tammer, Luna; Xin, Baozhong; Bakhtiari, Somayeh; Rice, James; van Eyk, Clare L.; Gecz, Jozef; Mah, Jean K.; Atkinson, Derek; Cope, Heidi; Sullivan, Jennifer A.; Douek, Alon M.; Colquhoun, Daniel; Henry, Jason; Wlodkowic, Donald; Parman, Yesim; Candayan, Ayse; Kocasoy-Orhan, Elif; Ilivitzki, Anat; Soudry, Shiri; Leibu, Rina; Glaser, Fabian; Sency, Valerie; Ast, Gil; Shashi, Vandana; Fahey, Michael C.; Battalog, Esra; Jordanova, Albena; Meiner, Vardiella; Innes, A. Micheil; Wang, Heng; Elpeleg, Orly; Kruer, Michael C.; Kaslin, Jan; Feldman, Hagit Baris
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收藏PR1P Stabilizes VEGF and Upregulates Its Signaling to Reduce Elastase-induced Murine Emphysema
Adini, Avner; Wu, Hao; Dao, Duy T.; Ko, Victoria H.; Yu, Lumeng J.; Pan, Amy; Puder, Mark; Mitiku, Selome Z.; Potla, Ratnakar; Chen, Hong; Rice, James M.; Matthews, Benjamin D.
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收藏Rodent tumors of urinary bladder, renal cortex, and thyroid gland in IARC Monographs evaluations of carcinogenic risk to humans
Rice, JM; Baan, RA; Blettner, M; Genevois-Charmeau, C; Grosse, Y; McGregor, DB; Partensky, C; Wilbourn, JD
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