Results 171 to 180 of about 5,920 (201)

Diversity and complexity of auditory representation in the hearing systems of <i>Aedes aegypti</i> mosquitoes. [PDF]

Sci Adv
Ohashi TS, Xu YYJ, Shigaki S, Nakamura Y, Lee TT, Loh YM, Mishiro-Sato E, Eberl DF, Su MP, Kamikouchi A.   +9 more
europepmc   +1 more source

The roles of cytoplasmic dynein complex in various ocular disorders. [PDF]

Mol Med
Zhou X, Xie J, Tong W, Fu J.
europepmc   +1 more source

A novel compound heterozygous mutation in the DYNC2H1 gene in a Chinese family with Jeune syndrome. [PDF]

Hereditas
Xiong S, Hu G, Zhou Y, Sun F, Ma Y.
europepmc   +1 more source

Chlamydomonas dynein-preassembly-deficient mutants exhibit characteristic ciliary responses to viscous media. [PDF]

MicroPubl Biol
Yamamoto R, Kitamura Y, Kon T.
europepmc   +1 more source

Roles of microtubules and LIS1 in dynein transport machinery assembly. [PDF]

Nature
Rao Q, Yang J, Chai P, Markus S, Zhang K.   +4 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

Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephaly. [PDF]

Orphanet J Rare Dis
Proepper CR, Schwarz LM, Schuetz SM, von Au K, Bast T, Beaud N, Borggraefe I, Bosch F, Busse M, Chung J, Debus O, Diepold K, Fries T, von Gersdorff G, Haeussler M, Hahn A, Hartlieb T, Heiming R, Herkenrath P, Kluger G, Kreth JH, Kurlemann G, Moeller P, Morris-Rosendahl DJ, Panzer A, Philippi H, Ruegner S, Toepfer C, Vieker S, Wiemer-Kruel A, Winter A, Schuierer G, Hehr U, Geis T.   +33 more
europepmc   +1 more source

The mechanochemical cycle of reactive full-length human dynein 1. [PDF]

Nat Struct Mol Biol
Chai P, Yang J, Geohring IC, Markus SM, Wang Y, Zhang K.   +5 more
europepmc   +1 more source

Base editing-derived models of human WDR34 and WDR60 disease alleles replicate retrograde intraflagellar transport (IFT) and hedgehog signaling defects. [PDF]

Commun Biol
Antony D, Güleç EY, Klawonn A, Bakey Z, Schüle I, Kim GJ, Cathomen T, Skatulla I, Brunner HG, Arnold SJ, Schmidts M.   +10 more
europepmc   +1 more source

Analysis of the <i>DYNC1H1</i> Gene Polymorphic Variants' Association with ASD Occurrence and Clinical Phenotype of Affected Children. [PDF]

Genes (Basel)
Balcerzyk-Matić A, Iwanicki T, Jarosz A, Nowak T, Emich-Widera E, Kazek B, Kapinos-Gorczyca A, Kapinos M, Iwanicka J, Gawron K, Likus W, Niemiec P.   +11 more
europepmc   +1 more source