Zobrazeno 1 - 10
of 156
pro vyhledávání: '"Natini, Jinawath"'
Autor:
Amornrat Tangprasittipap, Pawarit Innachai, Sukanya Chumchuen, Wararat Chiangjong, Natini Jinawath, Nongnuch Sirachainan, Suradej Hongeng
Publikováno v:
Stem Cell Research, Vol 79, Iss , Pp 103474- (2024)
Ten-Eleven Translocation methylcytosine dioxygenase 1 (TET1) is known to play a broad tumor suppressor role through demethylating and activating tumor suppressor genes. TET1 missense mutations are previously reported in many types of leukemia. Here,
Externí odkaz:
https://doaj.org/article/e13dd971704f41848e0ee89483288582
Autor:
Meng-Shin Shiao, Sian-Tai Liu, Ganchai Siriwatcharapibool, Supranee Thongpradit, Punnakorn Khunpanich, Sok-Keng Tong, Chih-Hsuan Huang, Natini Jinawath, Ming-Yi Chou
Publikováno v:
Heliyon, Vol 10, Iss 9, Pp e30575- (2024)
Synaptotagmin 4 (syt4) belongs to the synaptotagmin protein family, which has 17 and 28 family members in human and zebrafish, respectively. In zebrafish and rodents, syt4 is known to express abundantly in the entire central nervous system in the ear
Externí odkaz:
https://doaj.org/article/7df0aa070db74a15859b9ad246a6095e
Autor:
Yi Yang, Prapaporn Pisitkun, Wanling Yang, Natini Jinawath, Yao Lei, Yong-Fei Wang, Nattiya Hirankarn, Surakameth Mahasirimongkol, Wichai Aekplakorn, Pattarin Tangtanatakul, Krisana Jaiwan, Manon Boonbangyang, Punna Kunhapan, Pimpayao Sodsai, Jakris Eu-Ahsunthornwattana, Nareemarn Neelapaichit
Publikováno v:
Lupus Science and Medicine, Vol 11, Iss 1 (2024)
Objectives X chromosome has been considered as a risk factor for SLE, which is a prototype of autoimmune diseases with a significant sex difference (female:male ratio is around 9:1). Our study aimed at exploring the association of genetic variants in
Externí odkaz:
https://doaj.org/article/3c09ca82d0894ba284f1cb8ba925227d
Autor:
Monthira Suntiparpluacha, Jantappapa Chanthercrob, Doonyapat Sa-nguanraksa, Juthamas Sitthikornpaiboon, Amphun Chaiboonchoe, Patipark Kueanjinda, Natini Jinawath, Somponnat Sampattavanich
Publikováno v:
PeerJ, Vol 11, p e15350 (2023)
Background Triple-negative breast cancer (TNBC) is a rare and aggressive breast cancer subtype. Unlike the estrogen receptor-positive subtype, whose recurrence risk can be predicted by gene expression-based signature, TNBC is more heterogeneous, with
Externí odkaz:
https://doaj.org/article/22a3104897434dce94af55093751b24f
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
Autor:
Lalida Arsa, Teerada Siripoon, Narumol Trachu, Sasithorn Foyhirun, Duangjai Pangpunyakulchai, Suda Sanpapant, Natini Jinawath, Poompis Pattaranutaporn, Artit Jinawath, Nuttapong Ngamphaiboon
Publikováno v:
BMC Cancer, Vol 21, Iss 1, Pp 1-12 (2021)
Abstract Background Lower prevalence HPV infection has been previously reported in Thai population when compared with Western countries. p16 expression indicates HPV-associated oropharyngeal squamous cell carcinoma (OPSCC), but not non-OPSCC. We ther
Externí odkaz:
https://doaj.org/article/53f74f223beb4658b3f4ee0a8ed3d530
Autor:
Thipwimol Tim-Aroon, Khunton Wichajarn, Kamornwan Katanyuwong, Pranoot Tanpaiboon, Nithiwat Vatanavicharn, Kullasate Sakpichaisakul, Arthaporn Kongkrapan, Jakris Eu-ahsunthornwattana, Supranee Thongpradit, Kanya Moolsuwan, Nusara Satproedprai, Surakameth Mahasirimongkol, Tassanee Lerksuthirat, Bhoom Suktitipat, Natini Jinawath, Duangrurdee Wattanasirichaigoon
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background Sandhoff disease (SD) is an autosomal recessive lysosomal storage disorder, resulting in accumulation of GM2 ganglioside, particular in neuronal cells. The disorder is caused by deficiency of β-hexosaminidase B (HEX-B), due to pa
Externí odkaz:
https://doaj.org/article/5793a6bb9459425ea999df2f70d8699e
Autor:
Suttirak Pairoj, Pattareeya Damrongsak, Badin Damrongsak, Natini Jinawath, Rossukon Kaewkhaw, Chinnapat Ruttanasirawit, Tanaporn Leelawattananon, Kitsakorn Locharoenrat
Publikováno v:
Artificial Cells, Nanomedicine, and Biotechnology, Vol 49, Iss 1, Pp 120-135 (2021)
This study aimed to examine the pharmacological profiles of multiple chemo drug candidates in systematic circulation to enhance their specific interactions with five human cancer cell lines. ZnO nanoparticles were successfully bound with chemo drugs
Externí odkaz:
https://doaj.org/article/4937257bb0de4b32acc632130c944d2a
Autor:
Tananun Tanpaibule, Natini Jinawath, Aruchalean Taweewongsounton, Pimjai Niparuck, Porpon Rotjanapan
Publikováno v:
Infectious Diseases and Therapy, Vol 9, Iss 4, Pp 807-821 (2020)
Abstract Introduction The association between genetic background and the risk of invasive aspergillosis (IA) has not been addressed in Thailand. We conducted genetic risk surveillance for IA among Thai hematologic patients. Methods We conducted a pro
Externí odkaz:
https://doaj.org/article/7879d65040174ad2a799fced2ad430e8
Autor:
Pattarin Tangtanatakul, Yao Lei, Krisana Jaiwan, Wanling Yang, Manon Boonbangyang, Punna Kunhapan, Pimpayao Sodsai, Surakameth Mahasirimongkol, Prapaporn Pisitkun, Yi Yang, Jakris Eu-Ahsunthornwattana, Wichai Aekplakorn, Natini Jinawath, Nareemarn Neelapaichit, Nattiya Hirankarn, Yong-Fei Wang
Publikováno v:
Lupus Science & Medicine; 2024, Vol. 11 Issue 1, p1-8, 8p