Results 221 to 230 of about 164,456 (390)

3D-printed low-voltage-driven ciliary hydrogel microactuators. [PDF]

open access: yesNature
Liu Z   +11 more
europepmc   +1 more source

Co-expression of xenopsin and rhabdomeric opsin in photoreceptors bearing microvilli and cilia

open access: gold, 2017
Oliver Vöcking   +3 more
openalex   +1 more source

The role of primary cilia in the molecular pathogenesis of phaeochromocytoma [PDF]

open access: bronze, 2016
Samuel O’Toole   +3 more
openalex   +1 more source

Evaluation of Acute Exposure to Combustible and Novel Tobacco Products Using an In Vitro Human Airway Organ Tissue Equivalent Model

open access: yesJournal of Applied Toxicology, EarlyView.
ABSTRACT Despite the well‐known risks of tobacco use, tobacco exposure remains a major contributor to morbidity and mortality worldwide. Although cigarette use has declined, the popularity of novel tobacco products (NTPs), such as electronic cigarettes (ECs) and heated tobacco products (HTPs), has increased.
Timothy S. Leach   +8 more
wiley   +1 more source

A protein complex in the extreme distal tip of vertebrate motile cilia controls their organization, length, and function. [PDF]

open access: yesNat Commun
Hong J   +15 more
europepmc   +1 more source

DOCK8 deficiency presenting with sclerosing cholangitis, raised immunoglobulin E, and bronchiectasis: A fatal pediatric case report

open access: yesJPGN Reports, EarlyView.
Abstract Dedicator of cytokinesis 8 (DOCK8) deficiency is a rare autosomal recessive primary immunodeficiency. Patients with DOCK8 deficiency typically present at early age with allergic manifestations, cutaneous and respiratory infections, raised immunoglobulin E, and they have an increased risk of developing malignancies.
Natalia Nedelkopoulou   +4 more
wiley   +1 more source

Case series: Joubert syndrome and eosinophilic esophagitis

open access: yesJPGN Reports, EarlyView.
Abstract Joubert syndrome (JS) is a rare genetic disorder characterized by developmental abnormalities, particularly in the brainstem and cerebellar vermis, alongside multisystem manifestations such as kidney and liver anomalies, polydactyly, cleft lip or palate, and tongue defects.
Jonathon Schening   +5 more
wiley   +1 more source

Lack of ANKMY2 suppresses kidney cystogenesis in embryonic- and adult-onset polycystic kidney disease. [PDF]

open access: yesPLoS Genet
Hwang SH   +7 more
europepmc   +1 more source

Comparative Study of Accommodative Function and Binocular Vision in Patients With Primary Angle‐Closure Disease

open access: yesThe Kaohsiung Journal of Medical Sciences, EarlyView.
ABSTRACT The age‐related decline in accommodative function after the age of 50 years corresponds with an increasing incidence of primary angle‐closure disease (PACD); however, the interaction between this decline and PACD remains unexamined. Additionally, refractive error‐accommodation associations in elderly individuals, which are critical for PACD ...
Feng‐Rui Yang   +6 more
wiley   +1 more source

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