Results 251 to 260 of about 36,064 (332)

NME7 maintains primary cilium assembly, ciliary microtubule stability, and Hedgehog signaling. [PDF]

Life Sci Alliance
Ji M, Cui W, Feng Q, Qi J, Wang X, Zhu H, Zhang W, Fu W.   +7 more
europepmc   +1 more source

The primary cilium as a dual sensor of mechanochemical signals in chondrocytes

, 2012
Hayat Muhammad, Yoach Rais, Nicolai Miosge, Efrat Monsonego‐Ornan   +3 more
openalex   +1 more source

Genetic Risk Factors in Normal Pressure Hydrocephalus: What We Know and What Is Next

Movement Disorders, EarlyView.
Abstract Knowledge of the genetic factors in normal pressure hydrocephalus (NPH) is rapidly evolving, with significant advances in recent years. We conducted a systematic review examining genetic contributions to NPH risk. Ovid Embase, Ovid Medline, Web of Science, and Cochrane Central were searched from inception through October 14, 2024, for human ...
Camila C. Piccinin, Saar Anis, Jeryl Ritzi T. Yu, Philippe A. Salles, Henry Mauricio Chaparro‐Solano, Avery Kundrick, Shelley Ivary, James Y. Liao, Sean J. Nagel, Ignacio F. Mata   +9 more
wiley   +1 more source

Polycystins recruit cargo to distinct ciliary extracellular vesicle subtypes in C. elegans. [PDF]

Nat Commun
Nikonorova IA, desRanleau E, Jacobs KC, Saul J, Walsh JD, Wang J, Barr MM.   +6 more
europepmc   +1 more source

INPP5E interacts with AURKA, linking phosphoinositide signalling to primary cilium stability [PDF]

, 2014
Olga V. Plotnikova, Seongjin Seo, Denny L. Cottle, Sarah E. Conduit, Sandra Hakim, Jennifer M. Dyson, Christina A. Mitchell, Ian Smyth   +7 more
openalex   +1 more source

Platelet‐Rich Plasma for Rhinitis Medicamentosa: A Promising Histopathological Study in an Animal Model

Otolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective To investigate whether platelet‐rich plasma (PRP) has an efficacy on histopathologic changes in rhinitis medicamentosa (RM) in a rat model. Study Design Experimental animal study. Setting University animal laboratory. Methods Forty Wistar albino rats were randomly assigned to five groups to assess the effects of various treatments on
Kamil Gokce Tulaci, Salih Yayman, Erhan Arslan, Hasan Canakci, Tugba Tulaci, Gülay Turan, Omer Hizli, Hasmet Yazici   +7 more
wiley   +1 more source

Ciliary G-Protein Coupled Receptor Signaling in Polycystic Kidney Disease. [PDF]

Int J Mol Sci
Buqaileh R, Alshriem LA, AbouAlaiwi W.
europepmc   +1 more source

CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium

, 2012
Ji Eun Lee, Jennifer L. Silhavy, Maha S. Zaki, Jana Schroth, Stephanie Bielas, Sarah Marsh, Jesus Olvera, Francesco Brancati, Miriam Iannicelli, Koji Ikegami, Andrew M Schlossman, Barry Merriman, Tania Attié‐Bitach, Clare V. Logan, Ian Glass, Andrew Cluckey, Carrie M Louie, Jeong Ho Lee, Hilary R Raynes, Isabelle Rapin, Ignacio P Castroviejo, Mitsutoshi Setou, Clara Barbot, Eugen Boltshauser, Stanley F. Nelson, Friedhelm Hildebrandt, Colin A. Johnson, Daniel Doherty, Enza Maria Valente, Joseph G. Gleeson   +29 more
openalex   +2 more sources

Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter Study

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To investigate the clinical outcome of fetuses with ventriculomegaly (VM), and to identify risk factors for progression of fetal VM in order to improve prenatal counseling. This was a multicenter, retrospective cohort study, comprising 229 cases with VM.
Anouk Moens, Zoe Albersnagel, Marieke B. Veenhof, Phebe N. Adama van Scheltema, Esther Sikkel, Mariëtte J. V. Hoffer, Brigitte H. W. Faas, Dineke Westra, Ilse Feenstra, Emilia K. Bijlsma, Gijs W. E. Santen, Corrie E. Erasmus, Cacha M. P. C. D. Peeters‐Scholte   +12 more
wiley   +1 more source

NEK8, a NIMA-family protein kinase at the core of the ciliary INV complex. [PDF]

Cell Commun Signal
Roig J.
europepmc   +1 more source