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| Open AccessfM to aM nucleic acid amplification for molecular diagnostics in a non-stick-coated metal microfluidic bioreactor
- Guoliang Huang
- , Qin Huang
- & Jiancheng Ye
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| Open AccessLate-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation
- Hiroshi Doi
- , Masao Ushiyama
- & Kunihiro Yoshida
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| Open AccessGlobal human frequencies of predicted nuclear pathogenic variants and the role played by protein hydrophobicity in pathogenicity potential
- Luísa Pereira
- , Pedro Soares
- & David C. Samuels
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| Open AccessA Palindromic Motif in the −2084 to −2078 Upstream Region is Essential for ABCA12 Promoter Function in Cultured Human Keratinocytes
- Yoshitaka Shimizu
- , Yasushi Ogawa
- & Masashi Akiyama
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| Open AccessVariant adiponutrin confers genetic protection against cholestatic itch
- Marcin Krawczyk
- , Malgorzata Milkiewicz
- & Frank Lammert
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| Open AccessA broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDG
- M. A. Delgado
- , G. Martinez-Domenech
- & C. G. Asteggiano
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| Open AccessWhole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death
- Zhi-Ping Tan
- , Li Xie
- & Yi-Feng Yang
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| Open AccessGenetic variations in IL1A and IL1RN are associated with the risk of preeclampsia in Chinese Han population
- Jing Li
- , Mengchun Liu
- & Xuemei Liu
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| Open AccessCumulative Effects of Variants Identified by Genome-wide Association Studies in IgA Nephropathy
- Xu-Jie Zhou
- , Yuan-Yuan Qi
- & Hong Zhang
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| Open AccessA novel de novo duplication mutation of PAX6 in a Chinese family with aniridia and other ocular abnormalities
- Jianfu Zhuang
- , Xiaole Chen
- & Juhua Yang
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Article
| Open AccessThe angiotensinogen gene polymorphism is associated with heart failure among Asians
- Wen-long Jiang
- , Hui-wei He
- & Zhi-jian Yang
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| Open AccessIdentification of a Novel GJA8 (Cx50) Point Mutation Causes Human Dominant Congenital Cataracts
- Xiang-Lian Ge
- , Yilan Zhang
- & Feng Gu
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| Open AccessGenetic variations in Toll-like receptors (TLRs 3/7/8) are associated with systemic lupus erythematosus in a Taiwanese population
- Chin-Man Wang
- , Su-Wei Chang
- & Ji-Yih Chen
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| Open AccessIdentification of Three Novel Mutations in the FRMD7 Gene for X-linked Idiopathic Congenital Nystagmus
- Xiao Zhang
- , Xianglian Ge
- & Feng Gu
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| Open AccessMutation in ST6GALNAC5 identified in family with coronary artery disease
- Kolsoum InanlooRahatloo
- , Amir Farhang Zand Parsa
- & Elahe Elahi
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| Open AccessHierarchical Modularity in ERα Transcriptional Network Is Associated with Distinct Functions and Implicates Clinical Outcomes
- Binhua Tang
- , Hang-Kai Hsu
- & Victor X. Jin
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Article
| Open AccessReversal of Aberrant Cancer Methylome and Transcriptome upon Direct Reprogramming of Lung Cancer Cells
- Dashayini Mahalingam
- , Chiou Mee Kong
- & Xueying Wang
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| Open AccessEffect of rapamycin on immunity induced by vector-mediated dystrophin expression in mdx skeletal muscle
- Saman Eghtesad
- , Siddharth Jhunjhunwala
- & Paula R. Clemens
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Article
| Open AccessTherapeutic potential of HIV protease-activable CASP3
- Kosuke Miyauchi
- , Emiko Urano
- & Jun Komano