RSPH1 抗体

Yin, Livraghi-Butrico, Sears, Rogers, Burns, Grubb, Ostrowski: "Mice with a Deletion of Rsph1 Exhibit a Low Level of Mucociliary Clearance and Develop a PCD Phenotype." in: American journal of respiratory cell and molecular biology, (2019) (PubMed).

Li, Sha, Wang, Ding, Liu, Ji, Mei, Huang, Lin, Kong, Lu, Qin, Zhang, Zhuang, Tang, Lu: "DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella." in: Clinical genetics, Vol. 95, Issue 5, pp. 590-600, (2019) (PubMed).

Onoufriadis, Shoemark, Schmidts, Patel, Jimenez, Liu, Thomas, Dixon, Hirst, Rutman, Burgoyne, Williams, Scully, Bolard, Lafitte, Beales, Hogg, Yang, Chung, Emes, OCallaghan, Bouvagnet, Mitchison: "Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects." in: Human molecular genetics, Vol. 23, Issue 13, pp. 3362-74, (2014) (PubMed).

Kott, Legendre, Copin, Papon, Dastot-Le Moal, Montantin, Duquesnoy, Piterboth, Amram, Bassinet, Beucher, Beydon, Deneuville, Houdouin, Journel, Just, Nathan, Tamalet, Collot, Jeanson, Le Gouez et al.: "Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects. ..." in: American journal of human genetics, Vol. 93, Issue 3, pp. 561-70, (2013) (PubMed).

Uhlén, Oksvold, Älgenäs, Hamsten, Fagerberg, Klevebring, Lundberg, Odeberg, Pontén, Kondo, Sivertsson: "Antibody-based protein profiling of the human chromosome 21." in: Molecular & cellular proteomics : MCP, Vol. 11, Issue 3, pp. M111.013458, (2012) (PubMed).

Shetty, Klotz, Wolkowicz, Flickinger, Herr: "Radial spoke protein 44 (human meichroacidin) is an axonemal alloantigen of sperm and cilia." in: Gene, Vol. 396, Issue 1, pp. 93-107, (2007) (PubMed).