Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Narisorn Kitiyanant"'
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:
Panetha Pansri, Phetcharat Phanthong, Nopparat Suthprasertporn, Yindee Kitiyanant, Alisa Tubsuwan, Andras Dinnyes, Julianna Kobolak, Narisorn Kitiyanant
Publikováno v:
PeerJ, Vol 9, p e11388 (2021)
Background Several pieces of evidence from in vitro studies showed that brain-derived neurotrophic factor (BDNF) promotes proliferation and differentiation of neural stem/progenitor cells (NSCs) into neurons. Moreover, the JAK2 pathway was proposed t
Externí odkaz:
https://doaj.org/article/2985f7da4e544c078c690bbc1c0a6cc6
Autor:
Warun Maneepitasut, Wasinee Wongkummool, Pirut Tong-ngam, Kornkanok Promthep, Alisa Tubsuwan, Aung Khine Linn, Bunyong Phakdeekitcharoen, Suparerk Borwornpinyo, Narisorn Kitiyanant, Phetcharat Phanthong, Suradej Hongeng
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102306- (2021)
Autosomal dominant polycystic kidney disease (ADPKD) is one of the common genetic kidney disorders that are caused by mutations in PKD1 or PKD2 gene. In this report, the MUi026-A human induced pluripotent stem cell (hiPSC) line was established from t
Externí odkaz:
https://doaj.org/article/de85bf9e20904b65a2365d17cb6e45f4
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:
Abinaya Chandrasekaran, Hasan X. Avci, Anna Ochalek, Lone N. Rösingh, Kinga Molnár, Lajos László, Tamás Bellák, Annamária Téglási, Krisztina Pesti, Arpad Mike, Phetcharat Phanthong, Orsolya Bíró, Vanessa Hall, Narisorn Kitiyanant, Karl-Heinz Krause, Julianna Kobolák, András Dinnyés
Publikováno v:
Stem Cell Research, Vol 25, Iss C, Pp 139-151 (2017)
Neural progenitor cells (NPCs) from human induced pluripotent stem cells (hiPSCs) are frequently induced using 3D culture methodologies however, it is unknown whether spheroid-based (3D) neural induction is actually superior to monolayer (2D) neural
Externí odkaz:
https://doaj.org/article/cab47fd19054428793390b890e26170a
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
Autor:
Amornrat Tangprasittipap, Bunyada Jittorntrum, Praguywan Kadegasem, Werasak Sasanakul, Nongnuch Sirachainan, Narisorn Kitiyanant, Suradej Hongeng
Publikováno v:
Stem Cell Research, Vol 36, Iss , Pp - (2019)
Mutations in MYH9 gene is one of the major causes of inherited thrombocytopenia resulted from nonfunctional myosin-9 protein. We have generated a human induced pluripotent stem cell line MUi010-A from skin fibroblasts of a patient who had a point mut
Externí odkaz:
https://doaj.org/article/bb697fcca6cc4c37b429a787959c1e05
Autor:
Amornrat Tangprasittipap, Bunyada Jittorntrum, Wasinee Wongkummool, Narisorn Kitiyanant, Alisa Tubsuwan
Publikováno v:
Stem Cell Research, Vol 20, Iss C, Pp 91-93 (2017)
The MUi019-A human induced pluripotent stem cell line was generated from peripheral blood CD34+ hematopoietic progenitors of a healthy woman using a non-integrative reprogramming method. Episomal vectors carrying reprogramming factors OCT4, SOX2, KLF
Externí odkaz:
https://doaj.org/article/72f087f19040448299c2926ead227e1f
Autor:
Amornrat Tangprasittipap, Chonthicha Satirapod, Bunyada Jittorntrum, Sassawat Lertritanan, Usanarat Anurathaphan, Phetcharat Phanthong, Suparerk Borwornpinyo, Narisorn Kitiyanant, Suradej Hongeng
Publikováno v:
Stem Cell Research, Vol 15, Iss 3, Pp 506-509 (2015)
Human iPSC line MU011.A-hiPS was generated from homozygous α-thalassemia (−SEA/−SEA) fetal skin fibroblasts using a non-integrative reprogramming method. Reprogramming factors OCT3/4, SOX2, KLF4, L-MYC, LIN28, and shRNA of TP53 contained in thre
Externí odkaz:
https://doaj.org/article/b3ec16e6d5674fb9b9feb06e9336a1f0