Worrachet相关文献与解析，生知库 | 链接生命科学的每一步

肿瘤免疫

炎症

T细胞

线粒体

凋亡

转录调控

巨噬细胞

自噬

传染病

氧化应激

肠道菌群

磷酸化

血管生成

囊泡

3D/类器官

单细胞

中性粒细胞

外泌体

DNA甲基化

miRNA

药物研究

铁死亡

细胞衰老

乙酰化

缺氧低氧

泛素化

树突状细胞

组蛋白修饰

炎性小体

肿瘤微环境

lncRNA

代谢重编程

焦亡

m6A/m5C/m7G

内质网应激

空间多组学

细胞基因治疗

治疗耐药

相分离

Treg

上皮间质转化

免疫代谢

染色质重塑

脂质过氧化

脂代谢

蛋白质稳态

铁代谢

细胞极性

氨基酸代谢

碱基编辑

cGAS-STING

肠脑轴

蛋白降解

乳酸化

翻译调控

circRNA

piRNA

肿瘤异质性

NK 细胞

氧化脂质

MDSC

NETosis

低氧缺氧

溶酶体功能

细胞干性

琥珀酰化

CAR-NK

RNA 编辑

冷应激

Tfh

巴豆酰化

器官芯片

表观遗传记忆

铜死亡

器官纤维化

线粒体未折叠蛋白反应

空间代谢组

程序性坏死

自噬流

肠肝轴

丙酰化

MAIT 细胞

日期影响因子

Correction: Kularbkaew et al. Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis. Int. J. Mol. Sci. 2024, 25, 8867

更正：Kularbkaew 等人，《TBC1D2B 基因的遗传变异与拉蒙综合征和遗传性牙龈纤维瘤病相关》，《国际分子科学杂志》，2024 年，25 卷，8867 页。

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms26073228

Kularbkaew, Thatphicha; Thongmak, Tipaporn; Sandeth, Phan; Daroontum, Teerada; Durward, Callum S; Vittayakittipong, Pichai; Duke, Paul; Iamaroon, Anak; Kintarak, Sompid; Intachai, Worrachet; Ngamphiw, Chumpol; Tongsima, Sissades; Jatooratthawichot, Peeranat; Cox, Timothy C; Ketudat Cairns, James R; Kantaputra, Piranit

发表日期：2025

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Rare Filaggrin Variants Are Associated with Pustular Skin Diseases in Asians

罕见丝聚蛋白变异体与亚洲人的脓疱性皮肤病相关

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms25126466

Lo Piccolo, Luca; Wongkummool, Wasinee; Jantaree, Phatcharida; Daroontum, Teerada; Chaowattanapanit, Suteeraporn; Choonhakarn, Charoen; Amornpinyo, Warayuwadee; Chaiwarith, Romanee; Kiratikanon, Salin; Rujiwetpongstorn, Rujira; Tovanabutra, Napatra; Chiewchanvit, Siri; Ngamphiw, Chumpol; Intachai, Worrachet; Kantaputra, Piranit; Chuamanochan, Mati

发表日期：2024

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Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis

TBC1D2B基因的遗传变异与拉蒙综合征和遗传性牙龈纤维瘤病相关。

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms25168867

Kularbkaew, Thatphicha; Thongmak, Tipaporn; Sandeth, Phan; Daroontum, Teerada; Durward, Callum S; Vittayakittipong, Pichai; Duke, Paul; Iamaroon, Anak; Kintarak, Sompid; Intachai, Worrachet; Ngamphiw, Chumpol; Tongsima, Sissades; Jatooratthawichot, Peeranat; Cox, Timothy C; Ketudat Cairns, James R; Kantaputra, Piranit

发表日期：2024

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Human Leukocyte Antigen Markers for Distinguishing Pustular Psoriasis and Adult-Onset Immunodeficiency with Pustular Reaction

人类白细胞抗原标志物在区分脓疱型银屑病和成人发病型脓疱反应免疫缺陷中的应用

影响因子:2.8

doi:10.3390/genes15030278

Sangphukieo, Apiwat; Thongkumkoon, Patcharawadee; Noisagul, Pitiporn; Lo Piccolo, Luca; O'Brien, Timothy E; Chaowattanapanit, Suteeraporn; Choonhakarn, Charoen; Amornpinyo, Warayuwadee; Chaiwarith, Romanee; Kiratikanon, Salin; Rujiwetpongstorn, Rujira; Tovanabutra, Napatra; Chiewchanvit, Siri; Kantaputra, Piranit; Intachai, Worrachet; Dissook, Sivamoke; Chuamanochan, Mati

发表日期：2024

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Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth

人类APC基因的罕见遗传变异与正中牙和孤立性多生牙有关。

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms24054255

Panyarat, Chomchanok; Nakornchai, Siriruk; Chintakanon, Kanoknart; Leelaadisorn, Niramol; Intachai, Worrachet; Olsen, Bjorn; Tongsima, Sissades; Adisornkanj, Ploy; Ngamphiw, Chumpol; Cox, Timothy C; Kantaputra, Piranit

发表日期：2023

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Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas

FREM2基因杂合变异与正中牙、多生牙、口腔骨疣和牙瘤相关。

期刊:Diagnostics

影响因子:3.3

doi:10.3390/diagnostics13071214

Kantaputra, Piranit Nik; Tripuwabhrut, Kanich; Anthonappa, Robert P; Chintakanon, Kanoknart; Ngamphiw, Chumpol; Adisornkanj, Ploy; Porntrakulseree, Nop; Olsen, Bjorn; Intachai, Worrachet; Hennekam, Raoul C; Vieira, Alexandre R; Tongsima, Sissades

发表日期：2023

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A Mutation in CACNA1S Is Associated with Multiple Supernumerary Cusps and Root Maldevelopment

CACNA1S基因突变与多生牙尖和牙根发育不良有关

期刊:Diagnostics

影响因子:3.3

doi:10.3390/diagnostics13050895

Kantaputra, Piranit; Leelaadisorn, Niramol; Hatsadaloi, Athiwat; Quarto, Natalina; Intachai, Worrachet; Tongsima, Sissades; Kawasaki, Katsushige; Ohazama, Atsushi; Ngamphiw, Chumpol; Wiriyakijja, Paswach

发育与干细胞

发表日期：2023

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A Founder Intronic Variant in P3H1 Likely Results in Aberrant Splicing and Protein Truncation in Patients of Karen Descent with Osteogenesis Imperfecta Type VIII

P3H1基因中的一个创始内含子变异可能导致Karen血统的VIII型成骨不全患者出现异常剪接和蛋白质截短。

影响因子:2.8

doi:10.3390/genes14020322

Kantaputra, Piranit Nik; Angkurawaranon, Salita; Intachai, Worrachet; Ngamphiw, Chumpol; Olsen, Bjorn; Tongsima, Sissades; Cox, Timothy C; Ketudat Cairns, James R

发表日期：2023

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Genetic Variants in Protein Tyrosine Phosphatase Non-Receptor Type 23 Are Responsible for Mesiodens Formation

蛋白酪氨酸磷酸酶非受体型 23 的遗传变异是导致中间型白斑形成的原因

期刊:Biology-Basel

doi:10.3390/biology12030393

Ploy Adisornkanj, Rajit Chanprasit, Steven Eliason, Juan M Fons, Worrachet Intachai, Sissades Tongsima, Bjorn Olsen, Stefan T Arold, Chumpol Ngamphiw, Brad A Amendt, Abigail S Tucker, Piranit Kantaputra

发表日期：2023

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SERPINB3, Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis

SERPINB3、成人发病的免疫缺陷和全身性脓疱性银屑病

doi:10.3390/genes14020266

Piranit Kantaputra, Teerada Daroontum, Mati Chuamanochan, Suteeraporn Chaowattanapanit, Salin Kiratikanon, Charoen Choonhakarn, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, Chumpol Ngamphiw, Patrizia Pontisso, Timothy C Cox, Puey Ounjai

发表日期：2023

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