日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

A missense variant in ASCL5 leads to lobodontia.

ASCL5基因的错义变异会导致牙叶畸形。

Theerapanon Thanakorn, Intarak Narin, Rattanapornsompong Khanti, Thaweesapphithak Sermporn, Sriwattanapong Kanokwan, Prommanee Sasiprapa, Kulvitit Sirinya, Skrinjaric Tomislav, Samaranayake Lakshman, Pongpanich Monnat, Yeetong Patra, Chaivoravitsakul Nardtiwa, Mehl Nicole Sirisopit, Assawapitaksakul Adjima, Srichomthong Chalurmpon, Chetruengchai Wanna, Porntaveetus Thantrira, Shotelersuk Vorasuk

The metagenome and metabolome signatures of dental biofilms associated with severe dental fluorosis

与严重牙齿氟斑症相关的牙菌斑的宏基因组和代谢组特征

Ajrithirong, Penpitcha; Krasaesin, Annop; Sriarj, Wannakorn; Gavila, Patcharaporn; Chetruengchai, Wanna; Sriwattanapong, Kanokwan; Manaspon, Chawan; Samaranayake, Lakshman; Porntaveetus, Thantrira

Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon

借助首届“未确诊疾病黑客马拉松”,突破罕见病诊断的界限

Delgado-Vega, Angelica Maria; Cederroth, Helene; Taylan, Fulya; Ekholm, Katja; Ek, Marlene; Thonberg, Håkan; Jemt, Anders; Nilsson, Daniel; Eisfeldt, Jesper; Bilgrav Saether, Kristine; Höijer, Ida; Akgun-Dogan, Ozlem; Asano, Yui; Barakat, Tahsin Stefan; Batkovskyte, Dominyka; Baynam, Gareth; Bodamer, Olaf; Chetruengchai, Wanna; Corcoran, Pádraic; Couse, Madeline; Danis, Daniel; Demidov, German; Dohi, Eisuke; Erhardsson, Mattias; Fernandez-Luna, Luis; Fujiwara, Toyofumi; Garg, Neha; Giugliani, Roberto; Gonzaga-Jauregui, Claudia; Grigelioniene, Giedre; Groza, Tudor; Gunnarsson, Cecilia; Hammarsjö, Anna; Hammond, Charles Kumi; Hatirnaz Ng, Özden; Hesketh, Sirisha; Hettiarachchi, Dineshani; Johansson Soller, Maria; Kirmani, Umn Ahmed; Kjellberg, Martin; Kvarnung, Malin; Kvlividze, Oleg; Lagerstedt-Robinson, Kristina; Lasko, Paul; Lassmann, Timo; Lau, Lynette Y S; Laurie, Steven; Lim, Weng Khong; Liu, Zhandong; Lysenkova Wiklander, Mariya; Makay, Prince; Maiga, Alassane Baneye; Maya-González, Carolina; Meyn, M Stephen; Neethiraj, Ramprasad; Nigro, Vincenzo; Nordgren, Felix; Nordlund, Jessica; Orrsjö, Sara; Ottosson, Jesper; Ozbek, Ugur; Özdemir, Özkan; Partin, Clyde; Pearce, David A; Peck, Raquel; Pedersen, Annie; Pettersson, Maria; Pongpanich, Monnat; Posada de la Paz, Manuel; Ramani, Arun; Romero, Juan Andres; Romero, Vanessa I; Rosenquist, Richard; Saw, Aung Min; Spencer, Matthew; Stattin, Eva-Lena; Srichomthong, Chalurmpon; Tapia-Paez, Isabel; Taruscio, Domenica; Taylor, Julie P; Tkemaladze, Tinatin; Tully, Ian; Tümer, Zeynep; van Zelst-Stams, Wendy A G; Verloes, Alain; Västerviga, Emma; Wang, Sailan; Yang, Rachel; Yamamoto, Shinya; Yépez, Vicente A; Zhang, Qing; Shotelersuk, Vorasuk; Wiafe, Samuel Agyei; Alanay, Yasemin; Botto, Lorenzo D; Kirmani, Salman; Lumaka, Aimé; Palmer, Elizabeth Emma; Puri, Ratna Dua; Wirta, Valtteri; Lindstrand, Anna; Buske, Orion J; Cederroth, Mikk; Nordgren, Ann

De novo genome assembly and transcriptome sequencing in foot and mantle tissues of Megaustenia siamensis reveals components of adhesive substances

Megaustenia siamensis 足部和外套膜组织的从头基因组组装和转录组测序揭示了粘合物质的成分

Wanna Chetruengchai #, Parin Jirapatrasilp #, Chalurmpon Srichomthong, Adjima Assawapitaksakul, Arthit Pholyotha, Piyoros Tongkerd, Vorasuk Shotelersuk, Somsak Panha

Comprehensive genome assembly reveals genetic diversity and carcass consumption insights in critically endangered Asian king vultures

综合基因组组装揭示了极度濒危的亚洲王鹫的遗传多样性和尸体消费见解

Wannapol Buthasane, Vorasuk Shotelersuk, Wanna Chetruengchai, Chalurmpon Srichomthong, Adjima Assawapitaksakul, Sithichoke Tangphatsornruang, Wirulda Pootakham, Chutima Sonthirod, Sissades Tongsima, Pongsakorn Wangkumhang, Alisa Wilantho, Ampika Thongphakdee, Saowaphang Sanannu, Chaianan Poksawat, T

Carrier frequency estimation of pathogenic variants of autosomal recessive and X-linked recessive mendelian disorders using exome sequencing data in 1,642 Thais

利用1642名泰国人的外显子组测序数据,对常染色体隐性遗传和X连锁隐性遗传孟德尔疾病的致病变异携带者频率进行估计

Chetruengchai, Wanna; Phowthongkum, Prasit; Shotelersuk, Vorasuk

XLI Annual Meeting of the Indian Academy of Neurosciences and International Conference on BRAIN: CHEMISTRY TO COGNITION

印度神经科学学会第41届年会暨脑:化学与认知国际会议

Boonsimma, Ponghatai; Ittiwut, Chupong; Kamolvisit, Wuttichart; Ittiwut, Rungnapa; Chetruengchai, Wanna; Phokaew, Chureerat; Srichonthong, Chalurmpon; Poonmaksatit, Sathida; Desudchit, Tayard; Suphapeetiporn, Kanya; Shotelersuk, Vorasuk

Comparative genomics and genome-wide SNPs of endangered Eld's deer provide breeder selection for inbreeding avoidance

濒危坡鹿的比较基因组学和全基因组SNP分析为育种者避免近亲繁殖提供了选择依据。

Pumpitakkul, Vichayanee; Chetruengchai, Wanna; Srichomthong, Chalurmpon; Phokaew, Chureerat; Pootakham, Wirulda; Sonthirod, Chutima; Nawae, Wanapinun; Tongsima, Sissades; Wangkumhang, Pongsakorn; Wilantho, Alisa; Utara, Yongchai; Thongpakdee, Ampika; Sanannu, Saowaphang; Maikaew, Umaporn; Khuntawee, Suphattharaphonnaphan; Changpetch, Wirongrong; Phromwat, Phairot; Raschasin, Kacharin; Sarnkhaeveerakul, Phunyaphat; Supapannachart, Pannawat; Buthasane, Wannapol; Pukazhenthi, Budhan S; Koepfli, Klaus-Peter; Suriyaphol, Prapat; Tangphatsornruang, Sithichoke; Suriyaphol, Gunnaporn; Shotelersuk, Vorasuk

HLA-B*46:01:01:01 and HLA-DRB1*09:01:02:01 are associated with anti-rHuEPO-induced pure red cell aplasia

HLA-B*46:01:01:01 和 HLA-DRB1*09:01:02:01 与抗 rHuEPO 诱导的纯红细胞再生障碍性贫血相关。

Suttichet, Thitima Benjachat; Chamnanphon, Monpat; Pongpanich, Monnat; Chokyakorn, Sarun; Kupatawintu, Pawinee; Srichomthong, Chalurmpon; Chetruengchai, Wanna; Chuntakaruk, Hathaichanok; Rungrotmongkol, Thanyada; Chariyavilaskul, Pajaree; Shotelersuk, Vorasuk; Praditpornsilpa, Kearkiat

A LILRB1 variant with a decreased ability to phosphorylate SHP-1 leads to autoimmune diseases

LILRB1 变体磷酸化 SHP-1 的能力下降会导致自身免疫性疾病

Thivaratana Sinthuwiwat, Supranee Buranapraditkun, Wuttichart Kamolvisit, Siraprapa Tongkobpetch, Wanna Chetruengchai, Chalurmpon Srichomthong, Adjima Assawapitaksakul, Chureerat Phokaew, Patipark Kueanjinda, Tanapat Palaga, Tadech Boonpiyathad, Kanya Suphapeetiporn, Nattiya Hirankarn, Vorasuk Shote