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PreviewIssue DateTitleAuthor(s)
2016TBC1D24 genotype-phenotype correlationBalestrini, S.; Milh, M.; Castiglioni, C.; Lüthy, K.; Finelli, M.; Verstreken, P.; Cardon, A.; Stražišar, B.; Holder, J.; Lesca, G.; Mancardi, M.; Poulat, A.; Repetto, G.; Banka, S.; Bilo, L.; Birkeland, L.; Bosch, F.; Brockmann, K.; Cross, J.; Doummar, D.; et al.
1995Activating point mutations in the common beta subunit of the human GM-CSF, IL-3 and IL-5 receptors suggest the involvement of beta subunit dimerization and cell type-specific molecules in signallingJenkins, B.; D'Andrea, R.; Gonda, T.
1998Osteoclast-mediated bone resorption is stimulated during short-term administration of granulocyte colony-stimulating factor but is not responsible for hematopoietic progenitor cell mobilisationTakamatsu, Y.; Simmons, P.; Moore, R.; Morris, H.; To, L.; Leuesque, J.
2014BAFF regulates activation of self-reactive T cells through B-cell dependent mechanisms and mediates protection in NOD miceMariño, E.; Walters, S.N.; Villanueva, J.E.; Richards, J.L.; Mackay, C.R.; Grey, S.T.
2017ProBDNF Accelerates Brain Amyloid-β Deposition and Learning and Memory Impairment in APPswePS1dE9 Transgenic MiceChen, J.; Zhang, T.; Jiao, S.; Zhou, X.; Zhong, J.; Wang, Y.; Liu, J.; Deng, J.; Wang, S.; Xu, Z.
1996Physiological Levels of Calcitonin Regulate the Mouse Osteoclast Calcitonin Receptor by a Protein Kinase A-Mediated MechanismWada, S.; Udagawa, N.; Nagata, N.; Martin, T.; Findlay, D.
1996Calcitonin Receptor Down-Regulation Relates to Calcitonin Resistance in Mature Mouse OsteoclastsWada, S.; Udagawa, N.; Nagata, N.; Martin, T.; Findlay, D.
1999Identification of a 14-3-3 binding sequence in the common B chain of the granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-3 (IL-3), and IL-5 receptors that is serine-phosphorylated by GM-CSFStomski, F.; Dottore, M.; Winnall, W.; Guthridge, M.; Woodcock, J.; Bagley, C.; Thomas, D.; Andrews, R.; Berndt, M.; Lopez, A.
2019CBE1 is a manchette- and mitochondria-associated protein with a potential role in somatic cell proliferationPleuger, C.; Lehti, M.S.; Cooper, M.; O'Connor, A.E.; Merriner, D.J.; Smyth, I.M.; Cottle, D.L.; Fietz, D.; Bergmann, M.; O'Bryan, M.K.
2022Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial diseaseLee, R.G.; Balasubramaniam, S.; Stentenbach, M.; Kralj, T.; McCubbin, T.; Padman, B.; Smith, J.; Riley, L.G.; Priyadarshi, A.; Peng, L.; Nuske, M.R.; Webster, R.; Peacock, K.; Roberts, P.; Stark, Z.; Lemire, G.; Ito, Y.A.; Boycott, K.M.; Geraghty, M.T.; Van Klinken, J.B.; et al.