Results 181 to 190 of about 7,289,232 (294)

Deficits in Forelimb Reach Learning in a Mouse Model of Fragile X Syndrome. [PDF]

eNeuro
Young LF, Derham A, Zhu R, Suvrathan A.
europepmc   +1 more source

Loose Anagen Hair Syndrome: A Scoping Review

Pediatric Dermatology, EarlyView.
ABSTRACT Loose anagen hair syndrome (LAHS) is a rare, non‐scarring alopecia that may occur sporadically or follow autosomal dominant inheritance. The objective of this study was to review the etiology, clinical presentation, diagnostic features (including trichoscopy, trichogram, and microscopy), natural history, and treatment outcomes of LAHS.
Romy Shenderey, Hailey Land, Eric McMullen, Daniela Giansante, Grace Xiong, Katya Peri, Raquel Ocvirk, Justin Trasolini, Laurence Mainville, Shireen Dumont, Narachai Julanon, Cathryn Sibbald, Jeffrey Donovan   +12 more
wiley   +1 more source

Loss of Fmr1 reorganizes the multi-elemental composition across tissues in Fragile X Syndrome mice. [PDF]

PLoS One
Alam S, Reeves JT, Wilder SM, McCullagh EA.   +3 more
europepmc   +1 more source

Genetic risk variants implicate impaired maintenance and repair of periodontal tissues as causal for periodontitis—A synthesis of recent findings

Periodontology 2000, EarlyView.
AbstractPeriodontitis is a complex inflammatory disease in which the host genome, in conjunction with extrinsic factors, determines susceptibility and progression. Genetic predisposition is the strongest risk factor in the first decades of life. As people age, chronic exposure to the periodontal microbiome puts a strain on the proper maintenance of ...
Arne S. Schaefer, Luigi Nibali, Noha Zoheir, Niki M. Moutsopoulos, Bruno G. Loos   +4 more
wiley   +1 more source

Electroretinography biomarkers indicate disrupted visual processing in Fragile X syndrome. [PDF]

J Neurodev Disord
Pu Q, Bennett N, Sekhar TC, Stanley MT, Berry-Kravis E.   +4 more
europepmc   +1 more source

Fragile X-syndrome: literature review and report of two cases

Fragile X-syndrome is caused by a mutation in chromosome X. It is one of the most frequent causes of learning disability. The most frequent manifestations of fragile X-syndrome are learning disability, different orofacial morphological alterations and an
Gay Escoda, Cosme, Quinteros Borgarello, Milva, Berini Aytés, Leonardo, Ridaura Ruiz, Lourdes   +3 more
core  

Shared molecular framework and bidirectional effects of osteoporosis on periodontal disease and dental implant therapy in the elderly

Periodontology 2000, EarlyView.
Abstract Objectives This review synthesizes evidence regarding the prevalence, epidemiological associations, and mechanistic pathways between osteoporosis, periodontal disease, and dental implant therapy. Materials and Methods A literature review was conducted to identify studies focused on: osteoporosis, periodontal disease, and dental implants ...
Samin Sirous, Jaclyn C. Chalmers, Pin‐Ying Li, Yumna Subhani, Yvonne L. Hernandez‐Kapila   +4 more
wiley   +1 more source

Knowledge, attitudes, and perspectives on gene therapy for Fragile X syndrome: results from two community and caregiver surveys. [PDF]

Front Mol Neurosci
Chen V, Vomvos M, De Sonia A, Rosselot H, Lozano R.   +4 more
europepmc   +1 more source

Understanding extracellular vesicles in antiaging

Periodontology 2000, EarlyView.
Abstract Background Aging is a multifactorial process marked by gradual cellular dysregulation, regulated by hallmarks, including genomic instability, mitochondrial dysregulation, and chronic inflammation. Extracellular vesicles (EVs), especially exosomes, have emerged as pivotal mediators of cell‐to‐cell communication with potential roles in both ...
Paras Ahmad, Nathan E. Estrin, Anton Sculean, Richard J. Miron   +3 more
wiley   +1 more source

Cerebral Cortex Morphometry and Relaxometry in Male Children With Fragile X Syndrome and Autism. [PDF]

Brain Behav
Guerrero-Gonzalez JM, Lowe AK, Kecskemeti SR, Travers BG, Alexander AL, Sterling AM.   +5 more
europepmc   +1 more source