Results 101 to 110 of about 6,697 (138)

A homozygous splice-site variant in <i>ZMYND10</i> causes primary ciliary dyskinesia with primary infertility in a Chinese family. [PDF]

Front Med (Lausanne)
He J, Lu X, Guo M, Yang B, Zhou X, Liu Y, Fan H, Yang D, Luo H.   +8 more
europepmc   +1 more source

Emerging Roles of Tubulin Isoforms and Their Post-Translational Modifications in Microtubule-Based Transport and Cellular Functions. [PDF]

Biomolecules
Nair AR, Saroj N, Kunwar A.
europepmc   +1 more source

Challenges in postoperative management of a patient with primary ciliary dyskinesia and Joubert syndrome and related disorders with congenital heart disease. [PDF]

BMJ Case Rep
Kumasaka I, Takushi H, Watanabe T, Ota C.   +3 more
europepmc   +1 more source

Ccdc57 regulates cilia and left-right patterning in Xenopus. [PDF]

Biol Open
Yang B, Mis EK, Zhou X, Aslam F, He J, Lu X, Fan H, Guo T, Deniz E, Luo H, Khokha MK.   +10 more
europepmc   +1 more source

Functional Diversity and Emerging Roles of Human NME/NDPK Group II Proteins. [PDF]

Int J Mol Sci
Proust B, Ćetković H, Jazvinšćak Jembrek M, Šutić M, Vrbančić L, Bosnar MH.   +5 more
europepmc   +1 more source

Cilia Dynamics in Primary Ciliary Dyskinesia: A Biophysical Characterization of the <i>RSPH4A</i> Founder Variant. [PDF]

Cells
Rosario-Ortiz G, Muñiz-Hernández J, Ortiz-Pérez NM, Ramos-Benitez MJ, Mosquera RA, De Jesús-Rojas W.   +5 more
europepmc   +1 more source

Primary cilia dysfunction: A critical driver of metabolic diseases (Review). [PDF]

Int J Mol Med
Wang X, Jin Y, Xie K, Yao P, Song L, Liu H, Tan Y.   +6 more
europepmc   +1 more source

Centrosomal JAK2 Tyrosine Kinase Regulates Primary Cilia Length, Cell Proliferation, and Cilia Orientation During Cell Migration. [PDF]

FASEB J
Karki G, Boone L, Klaiber T, Lambert T, Kimball B, Burkhart B, Youssef M, Diakonova M.   +7 more
europepmc   +1 more source

The Long Haul: Microtubule Motors as the Essential Supply Line for Neuronal Longevity. [PDF]

J Neurochem
Turner ED, Twelvetrees AE.
europepmc   +1 more source

Biallelic Truncating DNAH14 Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review. [PDF]

Int J Mol Sci
Baris S, Dogan M, Terali K, Gezdirici A, Eroz R, Yucel PP, Kilic H, Yavas C, Yildirim G, Baris I.   +9 more
europepmc   +1 more source