Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Oranud Praditsap"'
Autor:
Narissara Kaewboonlert, Methichit Wattanapanitch, Oranud Praditsap, Nipaporn Deejai, Chutima Chanprasert, Nunghathai Sawasdee, Choochai Nettuwakul, Wanchai Wanachiwanawin, Suchai Sritippayawan, Prapaporn Jungtrakoon Thamtarana, Pa-thai Yenchitsomanus, Nanyawan Rungroj
Publikováno v:
Stem Cell Research, Vol 67, Iss , Pp 103043- (2023)
Distal renal tubular acidosis (dRTA), a disease characterized by the failure of the distal nephron to secrete acid into the urine, can be caused by mutations in SLC4A1 gene encoding erythroid and kidney anion exchanger 1 (AE1). Here, an induced pluri
Externí odkaz:
https://doaj.org/article/18db16af51b54239b14c96026c571b77
Autor:
Nanyawan Rungroj, Nirinya Sudtachat, Choochai Nettuwakul, Nunghathai Sawasdee, Oranud Praditsap, Prapaporn Jungtrakoon, Suchai Sritippayawan, Duangporn Chuawattana, Sombat Borvornpadungkitti, Chagkrapan Predanon, Wattanachai Susaengrat, Pa-Thai Yenchitsomanus
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e45533 (2012)
We previously reported the association between prothrombin (F2), encoding a stone inhibitor protein - urinary prothrombin fragment 1 (UPTF1), and the risk of kidney stone disease in Northeastern Thai patients. To identify specific F2 variation respon
Externí odkaz:
https://doaj.org/article/c6aeba930e52495a8de80133ba445f39
Autor:
Piranit Kantaputra, Yeliz Guven, Tugba Kalayci, Pelin Karaca Özer, Wannakamon Panyarak, Worrachet Intachai, Bjorn Olsen, Bruce M. Carlson, Oranud Praditsap, Sissades Tongsima, Chumpol Ngamphiw, Peeranat Jatooratthawichot, Abigail S. Tucker, James R. Ketudat Cairns
Publikováno v:
Clinical geneticsREFERENCES. 102(1)
Mutations in LTBP3 are associated with Dental Anomalies and Short Stature syndrome (DASS; MIM 601216), which is characterized by hypoplastic type amelogenesis imperfecta, hypodontia, underdeveloped maxilla, short stature, brachyolmia, aneurysm and di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c0e8fdbe05f8bd898eb76fe29c6a24b
https://pubmed.ncbi.nlm.nih.gov/35352826
https://pubmed.ncbi.nlm.nih.gov/35352826
Autor:
Pa-thai Yenchitsomanus, Thanyaporn Dechtawewat, Oranud Praditsap, Suchai Sritippayawan, Nipaporn Deejai, Santi Rojsatapong, Arnat Pasena, Choochai Nettuwakul, Wipada Chaowagul, Nanyawan Rungroj, Nunghathai Sawasdee
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Scientific Reports
Scientific Reports
Kidney stone disease (KSD) is a prevalent disorder that causes human morbidity worldwide. The etiology of KSD is heterogeneous, ranging from monogenic defect to complex interaction between genetic and environmental factors. Since mutations of genes r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03918ad3c1c82954772c4b0189ff5928
http://link.springer.com/article/10.1038/s41598-020-66936-4
http://link.springer.com/article/10.1038/s41598-020-66936-4
Genomics and Genetics, 15, 1, 1-15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7258b86073366900f1f0109b8c3dfc72
Autor:
Sittideth Sangnual, Oranud Praditsap, Duangporn Chuawattana, Katesirin Ruamyod, Suchai Sritippayawan, Mutita Junking, Santi Rojsatapong, Wipada Chaowagul, Stephen G. Waxman, Pa-thai Yenchitsomanus, Nanyawan Rungroj, Nunghathai Sawasdee, Boonyarit Cheunsuchon, Sulayman D. Dib-Hajj, Wattana B. Watanapa, Choochai Nettuwakul
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
Scientific Reports
Scientific Reports
Human kidney stone disease (KSD) causes significant morbidity and public health burden worldwide. The etiology of KSD is heterogeneous, ranging from monogenic defects to complex interaction between genetic and environmental factors. However, the gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6884adfbe23478cf8113599e9fa62492
https://doi.org/10.1038/s41598-018-28623-3
https://doi.org/10.1038/s41598-018-28623-3
Autor:
Nunghathai Sawasdee, Pa-thai Yenchitsomanus, Suchai Sritippayawan, Nanyawan Rungroj, Nirinya Sudtachat, Choochai Nettuwakul, Oranud Praditsap, Duangporn Chuawattana
Publikováno v:
BMC Medical Genetics
Background Kidney stone disease (KSD) is a complex disorder with unknown etiology in majority of the patients. Genetic and environmental factors may cause the disease. In the present study, we used DNA microarray to genotype single nucleotide polymor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a84d749c522e0bd0a75ab21c93ae68c
https://doi.org/10.1186/1471-2350-15-50
https://doi.org/10.1186/1471-2350-15-50
Autor:
Nanyawan Rungroj, Sittideth Sangnual, Oranud Praditsap, Choochai Nettuwakul, Nunghathai Sawasdee, Pa-Thai Yenchitsomanus
1, 7, Thai Journal of Genetics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65fc88095763a89ac8ba5b7706eff83e
Autor:
Nunghathai Sawasdee, Wattanachai Susaengrat, Nirinya Sudtachat, Choochai Nettuwakul, Oranud Praditsap, Pa-thai Yenchitsomanus, Nanyawan Rungroj, Sombat Borvornpadungkitti, Suchai Sritippayawan, Duangporn Chuawattana, Chagkrapan Predanon, Prapaporn Jungtrakoon
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e45533 (2012)
PLoS ONE
PLoS ONE
We previously reported the association between prothrombin (F2), encoding a stone inhibitor protein - urinary prothrombin fragment 1 (UPTF1), and the risk of kidney stone disease in Northeastern Thai patients. To identify specific F2 variation respon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbafd73386bbef0b311f2abd06e48f93
http://europepmc.org/articles/PMC3446884?pdf=render
http://europepmc.org/articles/PMC3446884?pdf=render
Autor:
Anunchai Assawamakin, Chumpol Ngamphiw, Oranud Praditsap, Chanin Linwongse, Sissades Tongsima
1, 3, Thai Journal of Genetics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10419b551ae8877dbc757ee65de8f1e4