Results 81 to 90 of about 1,751 (156)

Molecular Insights into Outer Dynein Arm Defects in Primary Ciliary Dyskinesia: Involvement of ZMYND10 and GRP78. [PDF]

Cells
Erdem İL, Kaya ZB, Atilla P, Emiralioğlu N, Eylem CC, Nemutlu E, Özçelik U, Büyükşahin HN, Daniş A, Karakoç E.   +9 more
europepmc   +1 more source

Cryo-EM single-particle analysis expanding towards increasingly native samples. [PDF]

Acta Crystallogr D Struct Biol
Moecking J, Zeev-Ben-Mordehai T.
europepmc   +1 more source

Axonemal dynein contributions to flagellar beat types and waveforms

Fochler S, Doran MH, Beneke T, Smith J, Fort C, Walker BJ, Brown A, Gluenz E, Wheeler RJ.   +8 more
europepmc   +1 more source

A novel frameshift variant in AXDND1 may cause multiple morphological abnormalities of the sperm flagella in a consanguineous Pakistani family. [PDF]

Asian J Androl
Ali I, Yang ML, Rahim F, Ali H, Zeb A, Ahmad N, Raza Y, Yue W, Shoaib M, Abbas T, Shah W, Ma H, Zhang H, Yin H, Shi QH.   +14 more
europepmc   +1 more source

The Increase in the Frequency and Amplitude of the Beating of Isolated Mouse Tracheal Cilia Reactivated by ATP and cAMP with Elevation in pH. [PDF]

Int J Mol Sci
Kobayashi A, Kawaguchi K, Asano S, Wu H, Nakano T, Inui T, Marunaka Y, Nakahari T.   +7 more
europepmc   +1 more source

<i>Chlamydomonas</i> FBB18 is a ubiquitin-like protein essential for the cytoplasmic preassembly of various ciliary dyneins. [PDF]

Proc Natl Acad Sci U S A
Yamamoto R, Sahashi Y, Shimo-Kon R, Sakato-Antoku M, Suzuki M, Luo L, Tanaka H, Ishikawa T, Yagi T, King SM, Kurisu G, Kon T.   +11 more
europepmc   +1 more source

Genetic spectrum and genotype-phenotype correlations in DNAH5-mutated primary ciliary dyskinesia: a systematic review. [PDF]

Orphanet J Rare Dis
Dong M, Shi X, Zhou Y, Duan J, He L, Song X, Huang Z, Chen R, Li J, Jia N.   +9 more
europepmc   +1 more source

Methylation of ciliary dynein motors involves the essential cytosolic assembly factor DNAAF3/PF22. [PDF]

Proc Natl Acad Sci U S A
Sakato-Antoku M, Patel-King RS, Balsbaugh JL, King SM.   +3 more
europepmc   +1 more source

An amino acid-resolution interactome for motile cilia identifies the structure and function of ciliopathy protein complexes. [PDF]

Dev Cell
McCafferty CL, Papoulas O, Lee C, Bui KH, Taylor DW, Marcotte EM, Wallingford JB, Wallingford JB.   +7 more
europepmc   +1 more source

Novel compound heterozygous mutation in <i>DNAH9</i> causes complex congenital heart disease. [PDF]

Mol Med Rep
Liu X, Zhou JL, Yang CY, Zhou HY, He WB, Yang J.   +5 more
europepmc   +1 more source