Results 221 to 230 of about 2,259,944 (347)

Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation. [PDF]

Commun Biol, 2021
Stavsky A, Stoler O, Kostic M, Katoshevsky T, Assali EA, Savic I, Amitai Y, Prokisch H, Leiz S, Daumer-Haas C, Fleidervish I, Perocchi F, Gitler D, Sekler I.   +13 more
europepmc   +1 more source

The future in a bubble: Supporting Finnish early childhood professionals working in diverse settings

British Educational Research Journal, EarlyView.
Abstract The purpose of this study was to contribute to the knowledge about early childhood education and care (ECEC) personnel's perception of the support structures that are most effective in assisting them in their work with culturally and linguistically diverse children.
Alexandra C. Anton, Juli‐Anna Aerila, Elizabeth A. Steed   +2 more
wiley   +1 more source

G-quadruplex stabilizer CX-5461 effectively combines with radiotherapy to target α-thalassemia/mental retardation X-linked-deficient malignant glioma. [PDF]

Neuro Oncol
Dharmaiah S, Malgulwar PB, Johnson WE, Chen BA, Sharin V, Whitfield BT, Alvarez C, Tadimeti V, Farooqi AS, Huse JT.   +9 more
europepmc   +1 more source

CNKSR2 gene mutation leads to Houge type of X-linked syndromic mental retardation: A case report and review of literature. [PDF]

Medicine (Baltimore), 2021
Kang Q, Yang L, Liao H, Wu L, Chen B, Yang S, Kuang X, Yang H, Liao C.   +8 more
europepmc   +1 more source

Sustaining the teaching profession: Innovating the ‘golden thread’ in university‐led teacher education

British Educational Research Journal, EarlyView.
Abstract This paper examines the implications of England's ‘golden thread’ policy framework for teacher education, which describes a state‐mandated, linear model of professional learning from initial teacher training and education through to continuing professional development.
Amanda Nuttall, Ed Podesta, Aimee Quickfall, Megan Stephenson   +3 more
wiley   +1 more source

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

Nature Genetics, 2008
A. Sharp, H. Mefford, Kelly Li, Carl A. Baker, C. Skinner, R. Stevenson, R. Schroer, F. Novara, M. Gregori, R. Ciccone, A. Broomer, I. Casuga, Yu Wang, Chunling Xiao, Catalin C. Barbacioru, G. Gimelli, B. Bernardina, C. Torniero, R. Giorda, R. Regan, V. Murday, S. Mansour, M. Fichera, L. Castiglia, P. Failla, M. Ventura, Zhaoshi Jiang, G. Cooper, S. Knight, C. Romano, O. Zuffardi, Caifu Chen, C. Schwartz, E. Eichler   +33 more
semanticscholar   +1 more source

Homozygous PGAP2 Mutation Causes Hyperphosphatasia with Mental Retardation Syndrome-3: Genetic and Clinical Evaluation of the Ultra-Rare Inherited Glycosylphosphatidylinositol Biosynthesis Defect. [PDF]

Mol Syndromol
Küçükçongar Yavaş A, Özbey SZ, Ergin B, Ünal Y, Bilginer Gürbüz B, Karaatmaca B, Özyürek H, Oflaz O, Basan H, Kasapkara ÇS.   +9 more
europepmc   +1 more source

Author Correction: Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation. [PDF]

Commun Biol, 2021
Stavsky A, Stoler O, Kostic M, Katoshevsky T, Assali EA, Savic I, Amitai Y, Prokisch H, Leiz S, Daumer-Haas C, Fleidervish I, Perocchi F, Gitler D, Sekler I.   +13 more
europepmc   +1 more source

Making teaching an attractive profession: What are the challenges and opportunities for minority ethnic teachers in England?

British Educational Research Journal, EarlyView.
Abstract This paper explores the challenges and opportunities surrounding the recruitment and retention of minority ethnic teachers in England. Drawing on interview data from 33 teachers and school leaders of diverse ethnic backgrounds, it investigates whether racialised barriers identified in earlier research have shifted in the current context of ...
Antonina Tereshchenko, Feyisa Demie, Stephen Gorard, Yiyang Gao, Beng Huat See, Nadia Siddiqui   +5 more
wiley   +1 more source

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males.

American Journal of Human Genetics, 2005
H. Van Esch, Marijke Bauters, J. Ignatius, M. Jansen, M. Raynaud, K. Hollanders, D. Lugtenberg, T. Bienvenu, L. Jensen, J. Gécz, C. Moraine, P. Marynen, J. Fryns, G. Froyen   +13 more
semanticscholar   +1 more source