Articles

Case report: A novel PTCH1 frameshift mutation leading to nevoid basal cell carcinoma syndrome

in Dermatology

• Xiaoqing Lang
• Ting Wang
• Shuping Guo
• Yao Dang
• Yingjie Zhang
• Hongye Liu
• Hongxia He
• Li Li
• Huajie Yuan
• Ting He

New Putative Antimicrobial Candidates: In silico Design of Fish-Derived Antibacterial Peptide-Motifs

in Synthetic Biology

• Hedmon Okella
• John J. Georrge
• Sylvester Ochwo
• Christian Ndekezi
• Kevin Tindo Koffi
• Jacqueline Aber
• Clement Olusoji Ajayi
• Fatoumata Gnine Fofana
• Hilda Ikiriza
• Andrew G. Mtewa

Mechanistic Insight Into the Interaction Between Helicobacter pylori Urease Subunit α and Its Molecular Chaperone Hsp60

in Infectious Agents and Disease

• Huilin Zhao
• Yulong Wu
• Zheng Xu
• Ran Ma
• Yunfei Ding
• Xuelian Bai
• Qianyu Rong
• Ying Zhang
• Boqing Li
• Xiaofei Ji

Identifying natural inhibitors against FUS protein in dementia through machine learning, molecular docking, and dynamics simulation

• Darwin Li

A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia

in Genetics of Common and Rare Diseases

• Danxia Guo
• Yingchun Zheng
• Zhongzhi Gan
• Yingying Guo
• Sijie Jiang
• Fang Yang
• Fu Xiong
• Hua Zheng

Comprehensive structural and functional analyses of RAD50 nsSNPs: from prediction to impact assessment

in Drug Discovery in Bioinformatics

• Samina Malik
• Mirza Jawad Ul Hasnain
• Gul Zaib
• Haleema Saadia
• Arif Malik
• Ayesha Zahid

A novel variant c.A527G in ITGB4 leads to autosomal dominant epidermolysis bullosa in China

in Dermatology

• Juyi Li
• Xiawen Yang
• Yimin He
• Peng Cheng
• Hengfei Li
• Aiping Deng
• Xiufang Wang
• Wei Cai
• Jifa Hu
• Qiu Tang

Structure Prediction and Potential Inhibitors Docking of Enterovirus 2C Proteins

in Virology

• Daoqun Li
• Leiliang Zhang

A Rare Heterozygous TINF2 Deletional Frameshift Mutation in a Chinese Pedigree With a Spectrum of TBDs Phenotypes

in Genetics of Common and Rare Diseases

• Hai-Long Ren
• Ying-Chun Zheng
• Guo-Qian He
• Ju Gao
• Xia Guo

Genetic analysis of acute intermittent porphyria caused by novel classical splicing variant in the insertion region of 29-residue specific to human HMBS protein

in Biological Modeling and Simulation

• Lei Liang
• Haixia Meng
• Haotian Wu
• Jianrong Zhao

Identification and Characterization of a Gene stp17 Located on the Linear Plasmid pBSSB1 as an Enhanced Gene of Growth and Motility in Salmonella enterica Serovar Typhi

in Molecular Bacterial Pathogenesis

• Haifang Zhang
• Yunxia Zhu
• Xiaofang Xie
• Min Wang
• Hong Du
• Shungao Xu
• Ying Zhang
• Mingyu Gong
• Bin Ni
• Huaxi Xu

Molecular analysis of three DNA mismatch repair protein variants in Chinese families with suspected Lynch syndrome

in Precision Medicine

• Juyi Li
• Haichun Ni
• Peng Cheng
• Yujia Peng
• Lei Liu
• Xiangyang Wang
• Wei Cheng
• Hengfei Li
• Xiufang Wang
• Hongfeng Zhang

Molecular Architecture of the Antiophidic Protein DM64 and its Binding Specificity to Myotoxin II From Bothrops asper Venom

in Structural Biology

• Barbara S. Soares
• Surza Lucia G. Rocha
• Viviane A. Bastos
• Diogo B. Lima
• Paulo C. Carvalho
• Fabio C. Gozzo
• Borries Demeler
• Tayler L. Williams
• Janelle Arnold
• Amy Henrickson

Molecular modeling, simulation and docking of Rv1250 protein from Mycobacterium tuberculosis

in Drug Discovery in Bioinformatics

• Sumita Choudhary
• Anup Kumar Kesavan
• Vijay Juneja
• Sheetal Thakur