Results 141 to 150 of about 7,199,374 (204)

<i>Fmr1</i> mutation is associated with gut microbiome structure and diversity as well as intestinal barrier integrity and function in a sex- and genotype-dependent manner. [PDF]

mSphere
Alam S, Shaughnessy CA, Lucas EA, Olawale F, Fathepure BZ, McCullagh EA.   +5 more
europepmc   +1 more source

Autonomic Nervous System Function and Sensory Sensitivity in 12-Month-Old Infants with the <i>FMR1</i> Premutation. [PDF]

Int J Mol Sci
Morton A, Arnold H, Hamrick L, Chase A, Cobb S, Roberts J.   +5 more
europepmc   +1 more source

HK2 drives synaptic dysfunction in fragile X syndrome via epigenetic regulation of H3K18 lactylation. [PDF]

Front Pharmacol
Luan Y, Zhang H, Ma N, Zhang Y, Xu Z, Zhang W, Zhang X, Liu Y.   +7 more
europepmc   +1 more source

Autonomic Function in Fragile X Syndrome: A Systematic Review. [PDF]

J Intellect Disabil Res
Weissgold S, Eley SEA, Wright D, McKechanie AG, Stanfield AC.   +4 more
europepmc   +1 more source

Capturing Phenotypic Heterogeneity in Differentiated Sensory Processing Profiles: Non-Syndromic Autism and Fragile X Syndrome. [PDF]

Autism
Knott CE, Roberts JE, Will EA.
europepmc   +1 more source

Mis-spliced FMR1 transcripts in human fragile X syndrome neural progenitors and neurons. [PDF]

J Neurodev Disord
Hourani SM, Utami KH, Oh SL, Castrén ML, Pouladi MA.   +4 more
europepmc   +1 more source

Clinical Trial Designs for Rare Disorders: A Scoping Review of the Effectiveness of Pharmacologic Interventions in Fragile X Syndrome. [PDF]

Neurol Genet
Van Steenbergen A, Kaur M, Rubanarayana K, Bolduc F.   +3 more
europepmc   +1 more source

Caregiver-perceived behavioral challenges in fragile X syndrome and implications for measuring treatment benefit in clinical trials. [PDF]

J Patient Rep Outcomes
Merikle E, Tich N, Sebree T, Hagerman R, O'Quinn S, Nomikos G, Bzdek K.   +6 more
europepmc   +1 more source

Impaired Activity-Regulated Proteostasis: A Shared Mechanism in Neurodevelopmental Disorders. [PDF]

Biol Psychiatry
Pandey K.
europepmc   +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