Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Amornrat Tangprasittipap"'
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
Publikováno v:
Stem Cell Research, Vol 80, Iss , Pp 103514- (2024)
The human leukocyte antigen (HLA) system comprises cell-surface proteins responsible for the presentation of peptide antigens. HLAs play an essential role in the regulation of the human immune system, and their studies have been crucial to its unders
Externí odkaz:
https://doaj.org/article/2952282e716247de962a61fea551bfa4
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:
Chokdee Wongborisuth, Sukanya Chumchuen, Orapan Sripichai, Usanarat Anurathaphan, Nuankanya Sathirapongsasuti, Duantida Songdej, Amornrat Tangprasittipap, Suradej Hongeng
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Reactivating of fetal hemoglobin (HbF; α2γ2) can ameliorate the severity of β-thalassemia disease by compensating for adult hemoglobin deficiency in patients. Previously, microarray analysis revealed that zinc finger protein (ZNF)802 (als
Externí odkaz:
https://doaj.org/article/5be5abf3bdcf4e058589c3c34b0fffe1
Autor:
Wasinee Wongkummool, Pirut Tong-ngam, Thongperm Munkongdee, Amornrat Tangprasittipap, Kittiphong Paiboonsukwong, Suradej Hongeng, Suthat Fucharoen, Pimlak Charoenkwan, Alisa Tubsuwan
Publikováno v:
Stem Cell Research, Vol 65, Iss , Pp 102979- (2022)
Hemoglobin Constant Spring (HbCS) is unstable hemoglobin resulting from a nucleotide substitution at the termination codon of the HBA2 gene (c.427 T > C). The homozygous state for HbCS is non-transfusion dependent in adults. Nevertheless, severe anem
Externí odkaz:
https://doaj.org/article/8730a4909dbe49a19074434f86306681
Publikováno v:
Stem Cell Research, Vol 60, Iss , Pp 102675- (2022)
MUi028-A human induced pluripotent stem cell (hiPSC) line was generated from normal fetal skin fibroblasts using a non-integrative reprogramming method. Reprogramming factors OCT4, SOX2, KLF4, L-MYC, and LIN28, and TP53 shRNA in three episomal vector
Externí odkaz:
https://doaj.org/article/c5f3f6cb9ac94d89a2eaa0136d449913
Autor:
Amornrat Tangprasittipap, Sukanya Chumchuen, Gunn Pornratananont, Narisorn Kitiyanant, Suradej Hongeng
Publikováno v:
Stem Cell Research, Vol 52, Iss , Pp 102211- (2021)
The 13q deletion syndrome is a rare chromosomal disorder caused by loss of the long arm of chromosome 13, and usually entails developmental delay, intellectual disability, behavioral problems and distinctive facial features. In this study, we success
Externí odkaz:
https://doaj.org/article/70882109b6424516b536346b49a40734
Autor:
Chokdee Wongborisuth, Sukanya Chumchuen, Orapan Sripichai, Usanarat Anurathaphan, Nuankanya Sathirapongsasuti, Duantida Songdej, Amornrat Tangprasittipap, Suradej Hongeng
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/cab3ea3f1c42469cb010fb22b9c47ad0
Autor:
Wasinee Wongkummool, Warun Maneepitasut, Pirut Tong-ngam, Amornrat Tangprasittipap, Thongperm Munkongdee, Chanikarn Boonchuay, Saovaros Svasti, Narisorn Kitiyanant, Kittiphong Paiboonsukwong, Suthat Fucharoen, Alisa Tubsuwan
Publikováno v:
Stem Cell Research, Vol 20, Iss C, Pp 80-83 (2017)
The thalassemias are a group of genetic disorders characterized by a deficiency in the synthesis of globin chains. In this study the MUi009-A human induced pluripotent stem cell line was successfully generated from peripheral blood CD34+ haematopoiet
Externí odkaz:
https://doaj.org/article/b12438ab650b480bb44089f3df049bbc
Autor:
Wasinee Wongkummool, Warun Maneepitasut, Thongperm Munkongdee, Pirut Tong-ngam, Amornrat Tangprasittipap, Saovaros Svasti, Narisorn Kitiyanant, Kittiphong Paiboonsukwong, Suthat Fucharoen, Alisa Tubsuwan
Publikováno v:
Stem Cell Research, Vol 20, Iss C, Pp 84-87 (2017)
Hemoglobin Constant Spring (HbCS, HBA2: c.427T>C) is a common nondeletional α-thalassemia resulting from a nucleotide substitution at the termination codon of the HBA2 gene. Homozygosity for HbCS is characterized with mild anemia, jaundice, and sple
Externí odkaz:
https://doaj.org/article/0be3b5bcc43540e4a17c7afd092f51db