Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Peng-Xiang Zuo"'
Publikováno v:
Neural Regeneration Research, Vol 12, Iss 2, Pp 259-266 (2017)
Developmental dyslexia is a complex reading and writing disorder with strong genetic components. In previous genetic studies about dyslexia, a number of candidate genes have been identified. These include DCDC2, which has repeatedly been associated w
Externí odkaz:
https://doaj.org/article/8a4442c9f6214907990bdf825e6cff8a
Publikováno v:
Current medical science. 41(6)
This study aimed to explore the orthographic processing of simplified Chinese characters in developmental dyslexic children in Kashgar, Xinjiang, China, and provide a theoretical basis for intervention strategies for developmental dyslexia in Chinese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57f32b953b660a798649a2d31766f10a
https://pubmed.ncbi.nlm.nih.gov/34874487
https://pubmed.ncbi.nlm.nih.gov/34874487
Publikováno v:
Asia Pacific Journal of Public Health. 30:378-386
We explored the association between maternal nutrition knowledge, attitude, and practice (KAP) and 25-hydroxyvitamin D (25(OH)D) values in children with rickets in Xinjiang, People’s Republic of China. We recruited 514 mothers with children (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3955802495f7149a62ed09209b5f89f5
https://doi.org/10.1177/1010539518768034
https://doi.org/10.1177/1010539518768034
Publikováno v:
Neural Regeneration Research, Vol 12, Iss 2, Pp 259-266 (2017)
Neural Regeneration Research
Neural Regeneration Research
Developmental dyslexia is a complex reading and writing disorder with strong genetic components. In previous genetic studies about dyslexia, a number of candidate genes have been identified. These include DCDC2, which has repeatedly been associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad2396e24cae4800fed8f987ef669ffb
http://www.nrronline.org/article.asp?issn=1673-5374
http://www.nrronline.org/article.asp?issn=1673-5374
Publikováno v:
Journal of genetics. 98(1)
The aetiology of developmental dyslexia (DD) is complex; although candidate genes have been suggested, the molecular mechanism and risk factors remain unknown. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f33ff3a229e75f73065faa039ef90098
https://pubmed.ncbi.nlm.nih.gov/31204720
https://pubmed.ncbi.nlm.nih.gov/31204720
Publikováno v:
Journal of Genetics. 98
The aetiology of developmental dyslexia (DD) is complex; although candidate genes have been suggested, the molecular mechanism and risk factors remain unknown. The KIAA0319 gene is functionally related to neuronal migration and axon growth, and sever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::947687210f3826d13b904aa0f0a00d0e
https://doi.org/10.1007/s12041-019-1103-4
https://doi.org/10.1007/s12041-019-1103-4
Publikováno v:
Journal of Human Genetics
The gene KIAA0319 has been reported to be associated with developmental dyslexia (DD) in previous studies, although the results have not always been consistent. However, few studies have been conducted in Uyghur populations. In the present study, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01947bfc36bb3107b853ef2d83004dde
https://doi.org/10.1038/jhg.2016.40
https://doi.org/10.1038/jhg.2016.40
Publikováno v:
Physica C: Superconductivity. 486:17-22
The hysteretic behavior of the levitation force between a permanent magnet and a melt-textured-growth YBCO bulk has been investigated under both zero-field cooling (ZFC) and field cooling (FC) processes. It is found that both in ZFC and FC measuremen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d74df219e4c9604022168852079706a
https://doi.org/10.1016/j.physc.2012.12.006
https://doi.org/10.1016/j.physc.2012.12.006
To investigate the association of KIAA0319 gene polymorphisms and developmental dyslexia in individuals of Uyghurian descent. Eighteen single nucleotide polymorphisms (SNP) of gene KIAA0319 were screened in a group of 196 patients with dyslexia and 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bdd2d3547b9f343ae4d45db57a8521a
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 7, p e0159042 (2016)
PLoS ONE, Vol 11, Iss 7, p e0159042 (2016)
Background Several studies have been conducted to explore risk factors for dyslexia. However, most studies examining dyslexia have been skewed toward Western countries, and few have considered two nationalities simultaneously. This study focused on d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db9330f2d17c181f73e8a49f16556489
https://pubmed.ncbi.nlm.nih.gov/27416106
https://pubmed.ncbi.nlm.nih.gov/27416106