Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Nusara Satproedprai"'
Autor:
Narongsak Nakwan, Surakameth Mahasirimongkol, Nusara Satproedprai, Tassamonwan Chaiyasung, Punna Kunhapan, Cheep Charoenlap, Kamonnut Singkhamanan, Chariyawan Charalsawadi
Publikováno v:
Jornal de Pediatria, Vol 98, Iss 4, Pp 383-389 (2022)
Objective: To explore possible genes related to the development of persistent pulmonary hypertension of the newborn (PPHN). Methods: The authors identified 285 single nucleotide polymorphisms (SNPs) of 11 candidate genes (BMPR2, EPAS1, PDE3A, VEGFA,
Externí odkaz:
https://doaj.org/article/7fdd30fb30de4594ad41ea01c3096055
Autor:
Phyu Thwe Soe, Jariya Hanthamrongwit, Chutiphon Saelee, Soe Paing Kyaw, Prasong Khaenam, Saradee Warit, Nusara Satproedprai, Surakameth Mahasirimongkol, Hideki Yanai, Patchanee Chootong, Chaniya Leepiyasakulchai
Publikováno v:
International Journal of Infectious Diseases, Vol 110, Iss , Pp 75-82 (2021)
Objective: To elucidate the antigenic potential of dormancy-associated antigens Rv2659c and Rv3128c of Mycobacterium tuberculosis by examining the persistence of specific IgG and IgA memory B cells (MBCs) among patients with active tuberculosis (TB),
Externí odkaz:
https://doaj.org/article/b48995d318e5478ca236b57f47613ca4
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:
Pattarin Tangtanatakul, Chisanu Thumarat, Nusara Satproedprai, Punna Kunhapan, Tassamonwan Chaiyasung, Siriwan Klinchanhom, Yong-Fei Wang, Wei Wei, Jeerapat Wongshinsri, Direkrit Chiewchengchol, Pongsawat Rodsaward, Pintip Ngamjanyaporn, Thanitta Suangtamai, Surakameth Mahasirimongkol, Prapaporn Pisitkun, Nattiya Hirankarn
Publikováno v:
Arthritis Research & Therapy, Vol 22, Iss 1, Pp 1-13 (2020)
Abstract Background Differences in the expression of variants across ethnic groups in the systemic lupus erythematosus (SLE) patients have been well documented. However, the genetic architecture in the Thai population has not been thoroughly examined
Externí odkaz:
https://doaj.org/article/d955c3a74043429487f121f1f780a0a8
Autor:
Noppadol Chanhom, Sukanya Wattanapokayakit, Nusara Satproedprai, Supharat Suvichapanich, Surakameth Mahasirimongkol, Usa Chaikledkaew, Wanvisa Udomsinprasert, Taisei Mushiroda, Jiraphun Jittikoon
Publikováno v:
Heliyon, Vol 7, Iss 4, Pp e06852- (2021)
Antituberculosis drug-induced liver injury (ATDILI) is the common adverse reaction of antituberculosis drugs. Glutathione S-transferases (GSTs), which are phase II metabolizing enzymes for detoxification, are recognized as potential mediators of hepa
Externí odkaz:
https://doaj.org/article/8f4f4884bd864234a2ec5801481db618
Autor:
Narongsak Nakwan, Punna Kunhapan, Tassamonwan Chaiyasung, Nusara Satproedprai, Kamonnut Singkhamanan, Surakameth Mahasirimongkol, Chariyawan Charalsawadi
Publikováno v:
Translational Pediatrics. 12:1-12
Autor:
Surakameth Mahasirimongkol, Fei Hou, Pattarin Tangtanatakul, Wei Wei, Qin Song, Yan Zhang, Zhiming Lin, Xinyu Zhang, Yao Lei, Yu-Lung Lau, Xiao Qin, Prapaporn Pisitkun, Nusara Satproedprai, Lichuan Zheng, Chengmin Qian, Li Shao, Nattiya Hirankarn, Wanling Yang, Yong-Fei Wang
Publikováno v:
Arthritis & Rheumatology. 74:840-848
Objectives Systemic lupus erythematosus (SLE) is a prototype autoimmune disease with differences in prevalence and severity among ancestral groups. This study aims to identify novel genetic components either shared or distinct between Asian and Europ
Autor:
Chalurmpon Srichomthong, Keswadee Lapphra, Surakameth Mahasirimongkol, Thantrira Porntaveetus, Sissades Tongsima, Vorasuk Shotelersuk, Wanna Chetruengchai, Wichittra Tassaneeyakul, Sujiraporn Pakchuen, Kanya Suphapeetiporn, Verayuth Praphanphoj, Pattarapong Makarawate, Rujipat Wasitthankasem, Adjima Assawapitaksakul, Athiphat Khuninthong, Duangdao Wichadakul, Nusara Satproedprai, Pongsakorn Wangkumhang, Prapaporn Pisitkun, Vorthunju Nakhonsri, Piranit Nik Kantaputra, Alisa Wilantho, Chureerat Phokaew, Philip J. Shaw, Jittima Piriyapongsa, Chumpol Ngamphiw
Publikováno v:
Clinical Genetics. 100:703-712
To maximize the potential of genomics in medicine, it is essential to establish databases of genomic variants for ethno-geographic groups that can be used for filtering and prioritizing candidate pathogenic variants. Populations with non-European anc
Autor:
Surakameth Mahasirimongkol, Kamonnut Singkhamanan, Nusara Satproedprai, Chariyawan Charalsawadi, Punna Kunhapan, Narongsak Nakwan, Cheep Charoenlap, Tassamonwan Chaiyasung
Publikováno v:
Jornal de Pediatria v.98 n.4 2022
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Volume: 98, Issue: 4, Pages: 383-389, Published: 25 JUL 2022
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Volume: 98, Issue: 4, Pages: 383-389, Published: 25 JUL 2022
Objective: To explore possible genes related to the development of persistent pulmonary hypertension of the newborn (PPHN). Methods: The authors identified 285 single nucleotide polymorphisms (SNPs) of 11 candidate genes (BMPR2, EPAS1, PDE3A, VEGFA,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afb7f310a119585fc9844d75b7f2edb4
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572022000400383
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572022000400383
Autor:
Duangrurdee Wattanasirichaigoon, Natini Jinawath, Tassanee Lerksuthirat, Nithiwat Vatanavicharn, Nusara Satproedprai, Arthaporn Kongkrapan, Kamornwan Katanyuwong, Pranoot Tanpaiboon, Bhoom Suktitipat, Thipwimol Tim-Aroon, Surakameth Mahasirimongkol, Kanya Moolsuwan, Jakris Eu-ahsunthornwattana, Khunton Wichajarn, Supranee Thongpradit, Kullasate Sakpichaisakul
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-9 (2021)
BMC Pediatrics
BMC Pediatrics
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 pathogenic