Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Alisa Tubsuwan"'
Autor:
Keatdamrong Janpipatkul, Nareerat Sutjarit, Amornrat Tangprasittipap, Tai Chaiamarit, Pawarit Innachai, Kanoknetr Suksen, Tanida Chokpanuwat, Thipwimol Tim-Aroon, Usanarat Anurathapan, Natee Jearawiriyapaisarn, Alisa Tubsuwan, Supareak Bowornpinyo, Nithi Asavapanumas, Arthit Chairoungdua, Kanit Bhukhai, Suradej Hongeng
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-14 (2024)
Abstract Background Gaucher disease (GD) is one of the most common types of lysosomal storage diseases (LSDs) caused by pathogenic variants of lysosomal β-glucocerebrosidase gene (GBA1), resulting in the impairment of Glucocerebrosidase (GCase) enzy
Externí odkaz:
https://doaj.org/article/59a850ee25e242c784be1f2144fdcbd3
Autor:
Varit Jan-ngam, Siriraj Boontha, Alisa Tubsuwan, Somsakul Pop Wongpalee, Kanda Fanhchaksai, Adisak Tantiworawit, Pimlak Charoenkwan, Pinyaphat Khamphikham
Publikováno v:
Heliyon, Vol 10, Iss 18, Pp e38020- (2024)
Reactivation of fetal hemoglobin (HbF, α2γ2) potentially alleviates clinical presentation in β-thalassemia. Prolyl hydroxylase domain enzymes (PHDs) play roles in the canonical oxygen-sensing pathway and maintain the stability of cellular hypoxia-
Externí odkaz:
https://doaj.org/article/e639dce5a1d3423e9be7472e82a74b31
Autor:
Tanapat Pornsukjantra, Nongluk Saikachain, Nareerat Sutjarit, Arthaporn Khongkrapan, Alisa Tubsuwan, Kanit Bhukhai, Thipwimol Tim-Aroon, Usanarat Anurathapan, Suradej Hongeng, Nithi Asavapanumas
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract Gaucher disease (GD) is a lysosomal storage disorder caused by a mutation in the GBA1 gene, responsible for encoding the enzyme Glucocerebrosidase (GCase). Although neuronal death and neuroinflammation have been observed in the brains of ind
Externí odkaz:
https://doaj.org/article/0f6e96ed824b4ccca62b25c09c125f40
Autor:
Umnuaychoke Thongsa-ad, Anongnat Wongpan, Wasinee Wongkummool, Phaewa Chaiwijit, Kwanchanok Uppakara, Gorawin Chaiyakitpattana, Passanan Singpant, Pirut Tong-ngam, Amnat Chukhan, Wachirachai Pabuprappap, Sirapope Wongniam, Apichart Suksamrarn, Suradej Hongeng, Usanarat Anurathapan, Kasem Kulkeaw, Alisa Tubsuwan, Kanit Bhukhai
Publikováno v:
Stem Cell Research & Therapy, Vol 15, Iss 1, Pp 1-20 (2024)
Abstract Background The diarylheptanoid ASPP 049 has improved the quality of adult hematopoietic stem cell (HSC) expansion ex vivo through long-term reconstitution in animal models. However, its effect on hematopoietic regeneration from human induced
Externí odkaz:
https://doaj.org/article/1307d64570604af68cd78ca8bd7b61ed
Autor:
Sudarat Wongkidakarn, Chonlada Yodtup, Danai Jantapalaboon, Panapat Phairoh, Supaporn Suparak, Panadda Dhepakson, Alisa Tubsuwan, Kobkaew Bumroongthai
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103605- (2024)
Hematopoietic stem cell isolated from a healthy 39-year-old woman were successfully reprogrammed and transformed into induced pluripotent stem cell (iPSCs) by using the integration-free episomal vector included OCT3/4/shp53, Sox2/KLF4, L-MYC/LIN28 an
Externí odkaz:
https://doaj.org/article/bdc002eb018d47b8aa3b1985677159dc
Autor:
Phitchapa Pongpaksupasin, Pirut Tong-Ngam, Natee Jearawiriyapaisarn, Kittiphong Paiboonsukwong, Siripakorn Sangkitporn, Adisak Trinavarat, Alisa Tubsuwan, La-Ongsri Atchaneeyasakul
Publikováno v:
Stem Cell Research, Vol 78, Iss , Pp 103448- (2024)
Mutations in the eyes shut homolog (EYS) gene are one of the common causes of autosomal recessive retinitis pigmentosa (RP). The lack of suitable animal models hampers progress understanding of the disease mechanism and drug development. This study r
Externí odkaz:
https://doaj.org/article/3273ffd9fb6c4cfaae40779c7c245672
Autor:
Pirut Tong-ngam, Wasinee Wongkummool, Phitchapa Pongpaksupasin, Nongnaphat Rawara, Duangnapa Kovanich, Narisorn Kitiyanant, Thongperm Munkongdee, Kittiphong Paiboonsukwong, Suthat Fucharoen, Alisa Tubsuwan
Publikováno v:
Stem Cell Research, Vol 73, Iss , Pp 103228- (2023)
Hemoglobin E (HbE), a common variant in Southeast Asian populations, results from a G to A substitution at codon 26 of the HBB gene, causing abnormal Hb and mild β-thalassemia-like symptoms. Here, we derived an induced pluripotent stem cell (iPSC) l
Externí odkaz:
https://doaj.org/article/7051fa372e814cda8b01e2f7ad0576b3
Autor:
Kitsada Kangboonruang, Tanapat Pornsukjantra, Pirut Tong-Ngam, Tanida Chokpanuwat, Thipwimol Tim-Aroon, Duangrurdee Wattanasirichaigoon, Usanarat Anurathapan, Suradej Hongeng, Nithi Asavapanumas, Kanit Bhukhai, Alisa Tubsuwan
Publikováno v:
Stem Cell Research, Vol 73, Iss , Pp 103229- (2023)
Gaucher disease (GD) is a common lysosomal storage disease resulting from mutations in the glucocerebrosidase (GBA1) gene. This genetic disorder manifests with symptoms affecting multiple organs, yet the underlying mechanisms leading to pathology rem
Externí odkaz:
https://doaj.org/article/7d6440b83bd94cfe949e746889387da2
Autor:
Sujira Mukda, Tanya Prasertporn, Jiraporn Panmanee, Alisa Tubsuwan, Nopphon Petchyam, Ittipat Meewan, Kornkanok Promthep, Surapon Piboonpocanun
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S284- (2023)
Externí odkaz:
https://doaj.org/article/9da851a2590e41b6b8dddc23eaf78fd3
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S288- (2023)
Externí odkaz:
https://doaj.org/article/239e5749c5ec4b50ad71858afd2fa6d6