Two cases of compound heterozygosity for Hb Hekinan [α27(B8)Glu→ Asp (α1)] and α-thalassemia in Thailand

بواسطة Lukana Ngiwsara, Chantragan Srisomsap, Pranee Winichagoon, Suthat Fucharoen, Jisnuson Svasti
منشور في 2018

Hb Kodaira II [β146(HC3)His→Gln] detected in Thailand

بواسطة Lukana Ngiwsara, Chantragan Srisomsap, Pranee Winichagoon, Suthat Fucharoen, Jisnuson Svasti
منشور في 2018

Hb Kurosaki [α7(A5)Lys→Glu (4AG→GAG)]: An α2-globin gene mutation found in Thailand

بواسطة Lukana Ngiwsara, Chantragan Srisomsap, Pranee Winichagoon, Suthat Fucharoen, Bussara Sae-Ngow, Jisnuson Svasti
منشور في 2018

Comparison of membrane-associated proteins in human cholangiocarcinoma and hepatocellular carcinoma cell lines

بواسطة Chantragan Srisomsap, Pantipa Subhasitanont, Phannee Sawangareetrakul, Daranee Chokchaichamnankit, Lukana Ngiwsara, Khajeelak Chiablaem, Jisnuson Svasti
منشور في 2018

Molecular analysis of the novel IDS allele in a thai family with mucopolysaccharidosis type II: The c.928C>T (p.Gln310*) transcript is sensitive to nonsense-mediated mRNA decay

بواسطة Lukana Ngiwsara, Kitiwan Rojnueangnit, Duangrurdee Wattanasirichaigoon, Thipwimol Tim-Aroon, Phannee Sawangareetrakul, Voraratt Champattanachai, James R. Ketudat-Cairns, Jisnuson Svasti
منشور في 2018

Biodecolorization of a food azo dye by the deep sea Dermacoccus abyssi MT1.1^Tstrain from the Mariana Trench

بواسطة Weeranuch Lang, Sarote Sirisansaneeyakul, Lígia O. Martins, Lukana Ngiwsara, Nobuo Sakairi, Wasu Pathom-aree, Masayuki Okuyama, Haruhide Mori, Atsuo Kimura
منشور في 2018

Biodecolorization of a food azo dye by the deep sea Dermacoccus abyssi MT1.1^Tstrain from the Mariana Trench

بواسطة Weeranuch Lang, Sarote Sirisansaneeyakul, Lígia O. Martins, Lukana Ngiwsara, Nobuo Sakairi, Wasu Pathom-aree, Masayuki Okuyama, Haruhide Mori, Atsuo Kimura
منشور في 2018

Proteomic profiling of cholangiocarcinoma cell line treated with pomiferin from Derris malaccensis

بواسطة Jisnuson Svasti, Chantragan Srisomsap, Pantipa Subhasitanont, Siriporn Keeratichamroen, Daranee Chokchaichamnankit, Lukana Ngiwsara, Nitirat Chimnoi, Somchai Pisutjaroenpong, Supanna Techasakul, Shui Tein Chen
منشور في 2018

Synthesis of Isocryptolepine-Triazole Adducts and Evaluation of Their Cytotoxic Activity

بواسطة Warabhorn Rodphon, Pavitra Laohapaisan, Nantamon Supantanapong, Onrapak Reamtong, Lukana Ngiwsara, Kriengsak Lirdprapamongkol, Charnsak Thongsornkleeb, Nisachon Khunnawutmanotham, Jumreang Tummatorn, Jisnuson Svasti, Somsak Ruchirawat
منشور في 2022

p.X654R IDUA variant among Thai individuals with intermediate mucopolysaccharidosis type I and its residual activity as demonstrated in COS-7 cells

بواسطة Lukana Ngiwsara, James R. Ketudat-Cairns, Phannee Sawangareetrakul, Ratana Charoenwattanasatien, Voraratt Champattanachai, Chulaluck Kuptanon, Suthipong Pangkanon, Thipwimol Tim-Aroon, Duangrurdee Wattanasirichaigoon, Jisnuson Svasti
منشور في 2019

Molecular characterization of Thai patients with phenylalanine hydroxylase deficiency and in vitro functional study of two novel PAH variants

بواسطة Lukana Ngiwsara, Nithiwat Vatanavicharn, Phannee Sawangareetrakul, Somporn Liammongkolkul, Pisanu Ratanarak, Boonchai Boonyawat, Chantragan Srisomsap, Voraratt Champattanachai, James Ketudat-Cairns, Pornswan Wasant, Jisnuson Svasti
منشور في 2022

The molecular basis of mucopolysaccharidosis type I in two Thai patients

بواسطة James R. Ketudat Cairns, Siriporn Keeratichamroen, Supattra Sukcharoen, Voraratt Champattanachai, Lukana Ngiwsara, Kriengsak Lirdprapamongkol, Somporn Liammongkolkul, Chantragan Srisomsap, Rudee Surarit, Pornswan Wasant, Jisnuson Svasti
منشور في 2018

Aberrant proteins expressed in skin fibroblasts of Parkinson's disease patients carrying heterozygous variants of glucocerebrosidase and parkin genes

بواسطة Phannee Sawangareetrakul, Lukana Ngiwsara, Voraratt Champattanachai, Daranee Chokchaichamnankit, Kittirat Saharat, James R. Ketudat Cairns, Chantragan Srisomsap, Kawinthra Khwanraj, Permphan Dharmasaroja, Teeratorn Pulkes, Jisnuson Svasti
منشور في 2022

Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2

بواسطة Piranit Nik Kantaputra, Prapai Dejkhamron, Sissades Tongsima, Chumpol Ngamphiw, Worrachet Intachai, Lukana Ngiwsara, Phannee Sawangareetrakul, Jisnuson Svasti, Bjorn Olsen, James R.Ketudat Cairns, Kanokkan Bumroongkit
منشور في 2020

Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in Thailand

بواسطة Lukana Ngiwsara, Duangrurdee Wattanasirichaigoon, Thipwimol Tim-Aroon, Kitiwan Rojnueangnit, Saisuda Noojaroen, Arthaporn Khongkraparn, Phannee Sawangareetrakul, James R. Ketudat-Cairns, Ratana Charoenwattanasatien, Voraratt Champattanachai, Chulaluck Kuptanon, Suthipong Pangkanon, Jisnuson Svasti
منشور في 2020

Clinical and molecular characterization of an extended family with fabry disease

بواسطة Duangrurdee Wattanasirichaigoon, Jisnuson Svasti, James R. Ketudat Cairns, Kanchana Tangnararatchakit, Anannit Visudtibhan, Siriporn Keeratichamroen, Lukana Ngiwsara, Pongsakdi Khowsathit, Tassanee Onkoksoong, Apatsa Lekskul, Dowruang Mongkolsiri, Chanchai Jariengprasert, Cheamchit Thawil, Suwimol Ruencharoen
منشور في 2018