Search Results - "gene"

Identification of a compound heterozygote in LYST gene: a case report on Chediak-Higashi syndrome by Yinsen Song, Zhengping Dong, Shuying Luo, Junmei Yang, Yuebing Lu, Bo Gao, Tianli Fan

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Identification of Hub Gene TIMP1 and Relative ceRNAs Regulatory Network in Colorectal Cancer by Qin YF, Li GM, Wang G, Kong DJ, Wang HD, Zhao YM, Hao JP, Qin H, Sun DQ, Wang H

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Rare presentation of Rothmund-Thomson syndrome with novel compound heterozygous mutations of the RECQL4 gene, by Xinyue Zhang, Songmei Geng, Yi Zheng

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Glycogen Storage Disease Type IX due to a Novel Mutation in PHKA2 Gene by Hamza Hassan Khan, Lauren Parr, Allison Jay, Saleem Raza, Hernando Lyons, Sanjay Kumar

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ABCB1 Gene Is Associated With Clinical Response to SNRIs in a Local Chinese Han Population by Xiao-Xiao Shan, Xiao-Xiao Shan, Yan Qiu, Yan Qiu, Wei-Wei Xie, Ren-Rong Wu, Ren-Rong Wu, Yan Yu, Hai-Shan Wu, Hai-Shan Wu, Le-Hua Li, Le-Hua Li

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High-Throughput Identification of Epigenetic Compounds to Enhance Chicken Host Defense Peptide Gene Expression by Zhuo Deng, Wentao Lyu, Guolong Zhang

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Antifungal activity of eugenol on Cryptococcus neoformans biological activity and Cxt1p gene expression by Parviz Hassanpour, Masoomeh Shams-Ghahfarokhi, Mehdi Razzaghi-Abyaneh

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Analysis of BCL11A gene polymorphisms and hemolysis parameters in patients with sickle-cell disease by Marilia R. Laurentino, Maritza C. Barbosa, Talyta Ellen J. Santos, Anne Caroline B. Perdigão, Fernanda M. C. Araújo, Romelia P. G. Lemes

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Establishment of Risk Model and Analysis of Immunoinfiltration Based on Mitophagy-Related Associated Genes in Atrial Fibrillation by Sang W, Wang L, Yan X, Sun H, Han Y, Wang F, Tang B, Li Y

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Autosomal dominant hereditary spastic paraplegia: Novel mutations in the <it>REEP1 </it>gene (SPG31) by Epplen Joerg T, Arning Larissa, Schlang Katharina J, Stemmler Susanne

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Recent Advances of Nanotechnology-Facilitated Bacteria-Based Drug and Gene Delivery Systems for Cancer Treatment by Chaojie Zhu, Zhiheng Ji, Junkai Ma, Zhijie Ding, Jie Shen, Qiwen Wang

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The Alu-insertion progesterone receptor gene polymorphism is not associated with breast cancer: a meta-analysis by Jun Yao, Xing-ling Qi, Yong Zhang

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Expression deregulation of matrix metalloproteinases and vasoconstriction related genes in Pakistani females with abnormal uterine bleeding by Zertashia Akram, Ishrat Mahjabeen, Faiza Irshad, Malik Waqar Ahmed, Sadaf Rehman, Muhammad Rizwan, Amna Shafqat, Aniqa Kiran, Asma Saeed

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Genome editing-mediated knock-in of therapeutic genes ameliorates the disease phenotype in a model of hemophilia by Jeong Hyeon Lee, Hye-Kyung Oh, Beom Seok Choi, Ho Hyeon Lee, Kyu Jun Lee, Un Gi Kim, Jina Lee, Hyerim Lee, Geon Seong Lee, Se Jun Ahn, Jeong Pil Han, Seokjoong Kim, Su Cheong Yeom, Dong Woo Song

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Degradation of Bacterial Antibiotic Resistance Genes during Exposure to Non-Thermal Atmospheric Pressure Plasma by Ibtissam Courti, Cristina Muja, Thomas Maho, Florent P. Sainct, Philippe Guillot

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Screening of key genes in the pathogenesis of muscle atrophy in CKD-PEW children based on RNA sequencing by Liang Ying, Jiang Yeping, Wang Hui, Zhou Nan, FuQian, Shen Ying

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Association of differential gene expression with imatinib mesylate and omacetaxine mepesuccinate toxicity in lymphoblastoid cell lines by Kulkarni Hemant, Göring Harald H H, Diego Vincent, Cole Shelley, Walder Ken R, Collier Greg R, Blangero John, Carless Melanie A

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The molecular mechanisms and pharmacotherapy of ATP-sensitive potassium channel gene mutations underlying neonatal diabetes by Veronica Lang, Peter E Light

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Novel Candidate Single Nucleotide Polymorphisms of ERCC2 Gene that Influence Colorectal Cancer Susceptibility by Rand Farhad, Eman Saadi Saleh, Ahmed Zuhair Alsammarraie

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A novel mutation in <it>STK11 </it>gene is associated with Peutz-Jeghers Syndrome in Indian patients by Singh Lalji, Mohankrishna P, Rao G, Reddy D, Thakur Nikita, Chandak Giriraj R

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