Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Pornprot Limprasert"'
Autor:
Chariyawan Charalsawadi, Somchit Jaruratanasirikul, Areerat Hnoonual, Aussanai Chantarapong, Pornsiri Sangmanee, Sasipong Trongnit, Natini Jinawath, Pornprot Limprasert
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Chimerism is a very rare genetic finding in human. Most reported cases have a chi 46,XX/46,XY karyotype. Only three non-twin cases carrying both trisomy 21 and a normal karyotype have been reported, including two cases with a chi 47,XY,+21/46,XX kary
Externí odkaz:
https://doaj.org/article/7f3cb4dac637481ab4278b544c6bc714
Publikováno v:
Songklanakarin Journal of Science and Technology (SJST), Vol 43, Iss 3, Pp 816-823 (2021)
Fragile X (FRAXA) syndrome and fragile XE (FRAXE) syndrome are caused by the expansion of a trinucleotide repeat in the FMR1 and FMR2 genes, respectively. Currently, there are several methods available for fragile X syndrome screening in a large po
Externí odkaz:
https://doaj.org/article/6ff69f215829476e841a9ed1066d2b1c
Autor:
Areerat Hnoonual, Phawin Kor-anantakul, Chariyawan Charalsawadi, Juthamas Worachotekamjorn, Pornprot Limprasert
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Autism spectrum disorder (ASD) is a group of neurodevelopmental disorders which are etiologically heterogeneous. Chromosomal microarray is now recommended as the first-tier clinical diagnostic test for ASD. We performed chromosomal microarray in 16 T
Externí odkaz:
https://doaj.org/article/f392fe8e825b4cf4a98e489828c0998c
Publikováno v:
Medicina, Vol 58, Iss 9, p 1228 (2022)
Background and Objectives: Autism spectrum disorder (ASD) is a neurodevelopmental disorder the cause of which is not fully known. Genetic factors are believed to play a major role in the etiology of ASD. However, genetic factors have been identified
Externí odkaz:
https://doaj.org/article/833f155b8a7b4f87833515d56789aea5
Autor:
Chariyawan Charalsawadi, Sasipong Trongnit, Kanoot Jaruthamsophon, Juthamas Wirojanan, Somchit Jaruratanasirikul, Anupong Nitiruangjaras, Pornprot Limprasert
Publikováno v:
International Journal of Pediatrics, Vol 2021 (2021)
Background. Little is currently known about the genetics of pilomatricoma. A number of studies have reported some evidence that this disease may have a genetic association with mutations of CTNNB1 gene or expression of the beta-catenin protein. In th
Externí odkaz:
https://doaj.org/article/ccb0545f17274e4cb6d3ed34a4ef6946
Publikováno v:
Siriraj Medical Journal, Vol 64, Iss 6 (2020)
The case of a term Thai male infant with VACTERL anomalies including imperforate anus, atrial septal defect, tracheo-esophageal (TE) fistula, and horseshoe kidney with bilateral hydronephrosis whose chromosome study revealed an additional genomic seg
Externí odkaz:
https://doaj.org/article/e01dbe682380456a9affc9014cfb550c
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Autism spectrum disorder (ASD) is a highly heterogeneous neurodevelopmental disorder with many contributing risk genes and loci. To date, several intellectual disability (ID) susceptibility genes have frequently been identified in ASD. Here, whole ex
Externí odkaz:
https://doaj.org/article/e655817bae2c4720ab3ada5cdc52c52f
Autor:
Sauvarat Auepemkiate, Anothai Pocathikorn, Pornprot Limprasert, Paramee Thongsuksai, Kanokphorn Chiratikarnwong, Thavatchai Chuaprapaisilp, Sunisa Thaichinda, Panadda Konandana
Publikováno v:
Siriraj Medical Journal, Vol 68, Iss 5, Pp 271-276 (2016)
Background: Methotrexate (MTX) is used to treat psoriasis with various side effects and responsiveness. No predictive indicator of responsivenessor toxicityis available. Objective: Tostudytheassociationof the C677T and A1298C polymorphisms inthe me
Externí odkaz:
https://doaj.org/article/f8b0c8f9d30a443eadae614f76b04023
Autor:
Chuphong Thongnak, Areerat Hnoonual, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat, Apichaya Puangpetch, Ekawat Pasomsub, Wasun Chantratita, Pornprot Limprasert, Chonlaphat Sukasem
Publikováno v:
International Journal of Genomics, Vol 2018 (2018)
Autism spectrum disorder (ASD) has a strong genetic basis, although the genetics of autism is complex and it is unclear. Genetic testing such as microarray or sequencing was widely used to identify autism markers, but they are unsuccessful in several
Externí odkaz:
https://doaj.org/article/7c82c0961eea489080bc0dc09371a0fd
Autor:
Chariyawan Charalsawadi, Juthamas Wirojanan, Somchit Jaruratanasirikul, Nichara Ruangdaraganon, Alan Geater, Pornprot Limprasert
Publikováno v:
International Journal of Pediatrics, Vol 2017 (2017)
Background. Clinical characteristics of fragile X syndrome (FXS) have been well documented in Caucasians, whereas in Asians they have rarely been described. Those that have been conducted used small cohorts that utilized DNA for diagnosis and larger
Externí odkaz:
https://doaj.org/article/b89744f3aafa4b5e89581cedbef076a2