Results 171 to 180 of about 43,167 (288)

The X-linked intellectual disability gene product and E3 ubiquitin ligase KLHL15 degrades doublecortin proteins to constrain neuronal dendritogenesis. [PDF]

J Biol Chem, 2021
Song J, Merrill RA, Usachev AY, Strack S.   +3 more
europepmc   +1 more source

Beyond Tradition: An Integrated Toxicological, Ecological, and Public Health Perspective on Aristolochic Acids

Journal of Applied Toxicology, EarlyView.
ABSTRACT Aristolochia species have long been used in traditional medicine for their presumed anti‐inflammatory, analgesic and antimicrobial properties. However, extensive toxicological and epidemiological evidence now demonstrates that these plants contain aristolochic acids (AAs) I and II, highly potent nephrotoxic, genotoxic, and carcinogenic ...
Victor Ventura de Souza, Lara Rodrigues De Andrade, Tatiana da Silva Souza   +2 more
wiley   +1 more source

The X-Linked Intellectual Disability Gene, ZDHHC9 , Is Important for Oligodendrocyte Subtype Determination and Myelination. [PDF]

Glia
White RB, Wild AR, O'Leary TP, Thompson AJ, Flibotte S, Peng A, Rogalski JC, Mair M, Derhami N, Bamji SX.   +9 more
europepmc   +1 more source

X-linked intellectual disability, Cantagrel type [PDF]

, 2020
openaire   +1 more source

Toward an idiographic understanding of the role of sleep‐mood dynamics in adolescents' internalizing symptoms

JCPP Advances, EarlyView.
Abstract Background Adolescence is marked by increased vulnerability to sleep disturbances and mood disorders. Understanding how day‐to‐day changes in sleep and mood are linked within the same individual is crucial for clarifying sleep's role in emerging internalizing disorders. However, the extent to which an adolescent's fluctuations in sleep predict
Konstantin Drexl, Setareh Ranjbar, Sébastien Urben, Kerstin Jessica Plessen, Jennifer Glaus   +4 more
wiley   +1 more source

A New Family with X-Linked Intellectual Disability 90: A Case Report of a <i>Novel DLG3</i> Variant and Literature Review. [PDF]

Mol Syndromol
Alavanda C, Çıkı K.
europepmc   +1 more source

Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability

, 2023
Kim C, Lee Y, Thomas M, Roychaudhury A, Skinner C, Maconachie G, Crosier M, Horak H, Constantinescu C, Choi T, Kyung J, Wang T, Ku B, Chodirker B, Hammer M, Gottlob I, Norton W, Chudley A, Schwartz C.   +18 more
europepmc   +1 more source

Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability: Case report. [PDF]

Medicine (Baltimore), 2020
Bogliş A, Cosma AS, Tripon F, Bãnescu C.   +3 more
europepmc   +1 more source

X-linked intellectual disability, Turner type [PDF]

, 2020
openaire   +1 more source

Positive developmental cascades: Strength development reduces support needs in children

JCPP Advances, EarlyView.
Abstract Background Strength development in children across a range of psychiatric diagnoses may reduce needs for mental health, social, and functioning support over time. A strength‐based adjunct to child and adolescent mental health may foster the developmental context most helpful for achieving desired outcomes with positive developmental cascading ...
Melody R. Altschuler, Xiaoran Tong, Punit Shah, Edelyn Verona, Julianne M. Bowling, Robert F. Krueger, Roman Kotov, Jordan H. McAllister, Michaela Voit, Sachina Paudel, Scott C. Leon, Shashwat Kala, John S. Lyons   +12 more
wiley   +1 more source