A. Tubsuwan

发表

Innovative Therapies for Hemoglobin Disorders

E. Payen, O. Nègre, K. Sii-Felice, 2020, BioDrugs.

Parallel assessment of globin lentiviral transfer in induced pluripotent stem cells and adult hematopoietic stem cells derived from the same transplanted β‐thalassemia patient

C. Eaves, A. Cheung, S. Fucharoen, 2013, Stem Cells.

Establishment and Characterization of MUi027-A: A Novel Patient-Derived Cell Line of Polycystic Kidney Disease with PKD1 Mutation

S. Borwornpinyo, S. Hongeng, B. Phakdeekitcharoen, 2022, Journal of personalized medicine.

Increased autophagy leads to decreased apoptosis during β-thalassaemic mouse and patient erythropoiesis

J. Vadolas, S. Fucharoen, Duncan R. Smith, 2022, Scientific Reports.

Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of βE pre‐mRNA splicing determine disease severity

S. Fucharoen, S. Svasti, T. Munkongdee, 2011, British journal of haematology.

Generation of human liver organoids from pluripotent stem cell-derived hepatic endoderms

K. Kulkeaw, A. Tubsuwan, Nongnat Tongkrajang, 2020, PeerJ.

Construction of thalassemic mouse induced pluripotent stem cells for disease modeling

S. Svasti, Natee Jearawiriyapaisarn, A. Tubsuwan, 2015 .

GRP78/BiP determines senescence evasion cell fate after cisplatin-based chemotherapy

P. Chanvorachote, Preedakorn Chunhacha, A. Tubsuwan, 2021, Scientific Reports.

Lab resource: Stem cell lineGeneration of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1

G. Waldemar, T. Nielsen, J. Nielsen, 2016 .

Generation of induced pluripotent stem cells from peripheral blood CD34+ hematopoietic progenitors of a 31year old healthy woman.

A. Tubsuwan, Narisorn Kitiyanant, A. Tangprasittipap, 2017, Stem cell research.

Derivation of the human induced pluripotent stem cell line MUi017-A from a patient with homozygous Hemoglobin Constant Spring.

S. Fucharoen, S. Svasti, T. Munkongdee, 2017, Stem cell research.

Transplantation of Macaca cynomolgus iPS-derived hematopoietic cells in NSG immunodeficient mice

G. Daley, In-Hyun Park, L. Tosca, 2015, Haematologica.

Generation of human induced pluripotent stem cell line (MUi034-A) from an unusual case of hydrops fetalis associated with homozygous hemoglobin Constant Spring.

P. Charoenkwan, S. Fucharoen, T. Munkongdee, 2022, Stem cell research.

Tetraspanins are involved in Burkholderia pseudomallei-induced cell-to-cell fusion of phagocytic and non-phagocytic cells

P. Monk, N. Chantratita, L. Partridge, 2020, Scientific Reports.

Transcriptional response to the host cell environment of a multidrug-resistant Mycobacterium tuberculosis clonal outbreak Beijing strain reveals its pathogenic features

S. Borwornpinyo, B. VanderVen, P. Prombutara, 2021, Scientific Reports.

Brain-derived neurotrophic factor increases cell number of neural progenitor cells derived from human induced pluripotent stem cells

A. Dinnyés, J. Kobolák, Y. Kitiyanant, 2021, PeerJ.

POTENT INHIBITION OF Peperomia pellucida EXTRACTS TOWARDS RANKL-INDUCED OSTEOCLAST FORMATION THROUGH M1 MACROPHAGE POLARIZATION

N. Charoenphandhu, K. Paiboonsukwong, C. Riani, 2021 .

Novel Potent Autophagy Inhibitor Ka-003 Inhibits Dengue Virus Replication

S. Borwornpinyo, S. Ubol, A. Tubsuwan, 2023, Viruses.

Recombinant Cas9 protein production in an endotoxin-free system and evaluation with editing the BCL11A gene in human cells.

C. Saisawang, A. Ketterman, R. Kurita, 2023, Protein expression and purification.

Tetraspanins are involved in Burkholderia pseudomallei (cid:486)induced cell(cid:486)to(cid:486)cell fusion of phagocytic and non(cid:486)phagocytic cells

A. Tubsuwan, Natnaree Saiprom, P. Monk, 2020 .

An increase in ER stress and unfolded protein response in iPSCs-derived neuronal cells from neuronopathic Gaucher disease patients

S. Hongeng, U. Anurathapan, Nithi Asavapanumas, 2024, Scientific reports.

Establishment of MUi030-A: A human induced pluripotent stem cell line carrying homozygous L444P mutation in the GBA1 gene to study type-3 Gaucher disease.

D. Wattanasirichaigoon, S. Hongeng, U. Anurathapan, 2023, Stem cell research.

Generation of human induced pluripotent stem cell line (MUi033-A) from a male with homozygous for Hemoglobin E.

D. Kovanich, T. Munkongdee, K. Paiboonsukwong, 2023, Stem cell research.

A generation of human-induced pluripotent stem cell line (MUi032-A) from a Choroideremia disease patient carrying a hemizygous mutation on the CHM gene.

L. Atchaneeyasakul, K. Paiboonsukwong, Natee Jearawiriyapaisarn, 2022, Stem cell research.

A generation of human induced pluripotent stem cell line (MUi031-A) from a type-3 Gaucher disease patient carrying homozygous mutation on GBA1 gene.

D. Wattanasirichaigoon, S. Hongeng, U. Anurathapan, 2022, Stem cell research.

Generation of human induced pluripotent stem cell line (MUi026-A) from a patient with autosomal dominant polycystic kidney disease carrying PKD1 point mutation.

S. Borwornpinyo, S. Hongeng, B. Phakdeekitcharoen, 2021, Stem cell research.

Establishment of MUi009 - A human induced pluripotent stem cells from a 32year old male with homozygous β°-thalassemia coinherited with heterozygous α-thalassemia 2.

S. Fucharoen, S. Svasti, T. Munkongdee, 2017, Stem cell research.

Generation of spinocerebellar ataxia type 2 patient-derived iPSC line H196.

T. Nielsen, J. Nielsen, P. Hyttel, 2016, Stem cell research.

Generation of spinocerebellar ataxia type 2 patient-derived iPSC line H271.

T. Nielsen, J. Nielsen, P. Hyttel, 2016, Stem cell research.

Generation of spinocerebellar ataxia type 2 patient-derived iPSC line H266.

T. Nielsen, J. Nielsen, P. Hyttel, 2016, Stem cell research.

Lab resource: Stem cell lineGeneration of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1

G. Waldemar, T. Nielsen, J. Nielsen, 2016 .

Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H196.

U. Mau-Holzmann, Alexander F Engelbrecht, T. Nielsen, 2016, Stem cell research.

Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H271.

U. Mau-Holzmann, Alexander F Engelbrecht, T. Nielsen, 2016, Stem cell research.

Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H266.

U. Mau-Holzmann, Alexander F Engelbrecht, T. Nielsen, 2016, Stem cell research.