Results 61 to 70 of about 9,852,555 (389)

Establishment of inclusive single-cell transcriptome atlases from mouse and human tooth as powerful resource for dental research

open access: yesFrontiers in Cell and Developmental Biology, 2022
Single-cell (sc) omics has become a powerful tool to unravel a tissue’s cell landscape across health and disease. In recent years, sc transcriptomic interrogation has been applied to a variety of tooth tissues of both human and mouse, which has ...
Florian Hermans   +6 more
doaj   +1 more source

CNS phenotype in X linked Charcot- Marie-Tooth disease

open access: yesJournal of Neurology Neurosurgery & Psychiatry, 2018
We read with interest the study by Koutsis et al reporting an increased prevalence of multiple sclerosis (MS) in their cohort of patients with X linked Charcot-Marie-Tooth disease (CMTX1).1 CMTX1 is a neurological condition with significant disability ...
Vinojini Vivekanandam   +3 more
semanticscholar   +1 more source

Infant and child oral health risk status correlated to behavioral habits of parents or caregivers: a survey in central Italy [PDF]

open access: yes, 2017
Aim: The aim of this survey was to evaluate the knowledge and awareness of parents and caregivers about potential oral health risk factors for their children in their first months of life (3–30 months).
American   +13 more
core   +2 more sources

Cell Calcification Models and Their Implications for Medicine and Biomaterial Research

open access: yesAdvanced Healthcare Materials, EarlyView.
Calcification, is the process by which the tissues containing minerals are formed, occurring during normal physiological processes, or in pathological conditions. Here, it is aimed to give a comprehensive overview of the range of cell models available, and the approaches taken by these models, highlighting when and how methodological divergences arise,
Luke Hunter   +5 more
wiley   +1 more source

Rehabilitation in Charcot-Marie-Tooth disease type 1

open access: yesAdvances in Clinical Neuroscience & Rehabilitation, 2014
Charcot-Marie-Tooth disease is the most common inherited peripheral neuropathy with a prevalence of approximately 1 in 2,500 [1]. The most common subtype is the autosomal dominant type 1A, which is caused by an intrachromosomal duplication on chromosome ...
Manoj Mannil   +3 more
doaj   +1 more source

A novel missense mutation in PLEKHG5 gene causing an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease in an Iraqi family

open access: yesEgyptian Journal of Medical Human Genetics, 2023
Background Charcot–Marie–Tooth disease comprises a large spectrum of clinically heterogeneous disorders. PLEKHG5 variants have shown an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease C and distal spinal muscular atrophy IV.
Mostafa Neissi   +4 more
doaj   +1 more source

A role for the GDAP1 gene in the molecular pathogenesis of Charcot‑Marie‑Tooth disease.

open access: yesActa Neurobiologiae Experimentalis, 2018
In 2002 a series of mutations in the GDAP1 gene were reported in patients suffering from Charcot‑Marie‑Tooth disease manifesting as early-onset, progressive distal‑muscle wasting and weakness.
Weronika Rzepnikowska, A. Kochański
semanticscholar   +1 more source

Metronidazole‐Loaded Cyclodextrin Nanogels for Antibacterial Therapy and Microbiota Regulation in Periodontitis

open access: yesAdvanced Healthcare Materials, EarlyView.
A methacrylamide β‐cyclodextrin‐based nanogel (MACD nGel) is developed to load the antimicrobial drug Metronidazole (MNZ) for topical delivery for the treatment of periodontitis. It is demonstrated that cyclodextrin nanogel (nGel) loaded with metronidazole provides an efficient drug delivery route but also has potential clinical applications and offers
Yanjing Ji   +8 more
wiley   +1 more source

Sodium nitrate protects against metabolic syndrome by sialin-mediated macrophage rebalance

open access: yesSignal Transduction and Targeted Therapy
Metabolic syndrome, characterized by metabolic dysfunction-associated steatotic liver disease (MASLD) and type 2 diabetes mellitus (T2DM), poses a significant threat to patients’ health worldwide; however, efficient treatment is currently unavailable ...
Shaorong Li   +20 more
doaj   +1 more source

A case report of Parry Romberg Syndrome initially presenting as periodontitis [PDF]

open access: yes, 2018
Parry Romberg Syndrome (PRS) is a rare disorder of progressive hemifacial atrophy, involving soft tissues, fat and occasionally bone. It can co-exist with presentations of Morphea.
Bramley   +14 more
core   +1 more source

Home - About - Disclaimer - Privacy