Search Results - "next generation sequencing"

Heightened cocaine-seeking in male rats associates with a distinct transcriptomic profile in the medial prefrontal cortex by Christina R. Merritt, Christina R. Merritt, Ashley E. Smith, Ashley E. Smith, Kamil Khanipov, Kamil Khanipov, George Golovko, George Golovko, Kelly T. Dineley, Kelly T. Dineley, Noelle C. Anastasio, Noelle C. Anastasio, Kathryn A. Cunningham, Kathryn A. Cunningham

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Response to PD-1 inhibitor in SMARCB1‑deficient undifferentiated rectal carcinoma with low TMB, proficient MMR and BRAF V600E mutation: a case report and literature review by Wenjuan Shen, Yi Pan, Shuangmei Zou

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Acquisition, Divergence, and Personalization of the Female Perineal Microbiomes Are Driven by Developmental Milestones and Disrupted by Urinary Tract Infection: A Pilot Study by Elizabeth J. Lucas, Christina B. Ching, Christina B. Ching, Shweta Saraswat, Shareef M. Dabdoub, Purnima P. Kumar, Sheryl S. Justice

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Urothelial carcinoma of the graft kidney with molecular analyses: a rare case report by Joyce M. Chen, G. Kenneth Haines, William Lam, Asha Reddy, Meenakshi Mehrotra, Jane Houldsworth, Qiusheng Si

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Sperm deoxyribonucleic acid fragmentation index at the time of intracytoplasmic sperm injection and standard in vitro fertilization is correlated with lower fertilization but not w... by Alicia L. Broussard, Ph.D., H.C.L.D, Benjamin Leader, M.D, Edna Tirado, Ph.D, Helena Russell, M.S, Hind Beydoun, Ph.D, Robert Colver, M.D, Laura Reuter, M.D, Bradford Bopp, M.D, Matthew Will, M.D, Erica Anspach Will, M.D, Glen Adaniya, Ph.D., H.C.L.D

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Factors affecting biochemical pregnancy loss (BPL) in preimplantation genetic testing for aneuploidy (PGT-A) cycles: machine learning-assisted identification by José A. Ortiz, B. Lledó, R. Morales, A. Máñez-Grau, A. Cascales, A. Rodríguez-Arnedo, Juan C. Castillo, A. Bernabeu, R. Bernabeu

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Kidney microRNA Expression Pattern in Type 2 Diabetic Nephropathy in BTBR Ob/Ob Mice by Lucas Opazo-Ríos, Lucas Opazo-Ríos, Antonio Tejera-Muñoz, Manuel Soto Catalan, Vanessa Marchant, Carolina Lavoz, Sebastián Mas Fontao, Juan Antonio Moreno, Marta Fierro Fernandez, Ricardo Ramos, Beatriz Suarez-Alvarez, Carlos López-Larrea, Carlos López-Larrea, Marta Ruiz-Ortega, Jesús Egido, Raúl R. Rodrigues-Díez, Raúl R. Rodrigues-Díez

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Reverse Expression of Aging-Associated Molecules through Transfection of miRNAs to Aged Mice by Jung-Hee Kim, Bo-Ram Lee, Eun-Sook Choi, Kyeong-Min Lee, Seong-Kyoon Choi, Jung Hoon Cho, Won Bae Jeon, Eunjoo Kim

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Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation by Jiaping Wang, Qingping Zhang, Yan Chen, Shujie Yu, Xiru Wu, Xinhua Bao, Yongxin Wen

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Tumor Type Agnostic Therapy Carrying BRAF Mutation: Case Reports and Review of Literature by Ottavia Bernocchi, Marianna Sirico, Silvia Paola Corona, Carla Strina, Manuela Milani, Maria Rosa Cappelletti, Giuseppina Ferrero, Nicoletta Ziglioli, Valeria Cervoni, Andrea Macchiavelli, Giandomenico Roviello, Daniele Generali

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Sox9-Increased miR-322-5p Facilitates BMP2-Induced Chondrogenic Differentiation by Targeting Smad7 in Mesenchymal Stem Cells by Yongsheng Zeng, Chengcheng Du, Pengcheng Xiao, Yiting Lei, Piao Zhao, Zhenglin Zhu, Shengqiang Gao, Bowen Chen, Shengwen Cheng, Wei Huang, Chen Zhao

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Comparison of aneuploidy rates between conventional in vitro fertilization and intracytoplasmic sperm injection in in vitro fertilization-intracytoplasmic sperm injection split ins... by Jie Deng, M.D., Ph.D, Olutunmike Kuyoro, M.D, Qianying Zhao, M.S, Barry Behr, Ph.D, Ruth B. Lathi, M.D

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Mutations in the NUP93, NUP107 and NUP160 genes cause steroid-resistant nephrotic syndrome in Chinese children by Yanxinli Han, Hongyu Sha, Yuan Yang, Zhuowei Yu, Lanqi Zhou, Yi Wang, Fengjie Yang, Liru Qiu, Yu Zhang, Jianhua Zhou

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Expanding the Phenotypic Spectrum of <i>ECEL1</i>-Associated Distal Arthrogryposis by Akshata Huddar, Kiran Polavarapu, Veeramani Preethish-Kumar, Mainak Bardhan, Gopikrishnan Unnikrishnan, Saraswati Nashi, Seena Vengalil, Priyanka Priyadarshini, Karthik Kulanthaivelu, Gautham Arunachal, Hanns Lochmüller, Atchayaram Nalini

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Geographic characteristics of HTLV-1 molecular subgroups and genetic substitutions in East Asia: Insights from complete genome sequencing of HTLV-1 strains isolated in Taiwan and J... by Satoshi Nozuma, Akiko Yoshimura, Shun-Chung Pai, Hung-Jen Chen, Eiji Matsuura, Masakazu Tanaka, Daisuke Kodama, Mika Dozono, Toshio Matsuzaki, Hiroshi Takashima, Ya-Chien Yang, Ryuji Kubota

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Case report: Durable response of ensartinib targeting EML4-ALK fusion in osimertinib-resistant non-small cell lung cancer by Yongkuan Guo, Ran Zhang, Yiran Meng, Li Wang, Liuqing Zheng, Jian You

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Genomic characterization of high-recurrence risk papillary thyroid carcinoma in a southern Chinese population by Min Li, Haitao Jia, Qiuqin Qian, Peng Wen, Chuan Chen, Yaqiong Hua, Kai Wang, Wenyong Zhang, Feng Shi

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Exploring Variability in Rifampicin Plasma Exposure and Development of Anti-Tuberculosis Drug-Induced Liver Injury among Patients with Pulmonary Tuberculosis from the Pharmacogenet... by Agnija Kivrane, Viktorija Ulanova, Solveiga Grinberga, Eduards Sevostjanovs, Anda Viksna, Iveta Ozere, Ineta Bogdanova, Maksims Zolovs, Renate Ranka

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Evaluation of Rapid Library Preparation Protocols for Whole Genome Sequencing Based Outbreak Investigation by Helena M. B. Seth-Smith, Helena M. B. Seth-Smith, Helena M. B. Seth-Smith, Ferdinando Bonfiglio, Ferdinando Bonfiglio, Aline Cuénod, Aline Cuénod, Josiane Reist, Adrian Egli, Adrian Egli, Daniel Wüthrich, Daniel Wüthrich, Daniel Wüthrich

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CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability by Louise Montagne, Mehdi Derhourhi, Amélie Piton, Bénédicte Toussaint, Emmanuelle Durand, Emmanuel Vaillant, Dorothée Thuillier, Stefan Gaget, Franck De Graeve, Iandry Rabearivelo, Amélie Lansiaux, Bruno Lenne, Sylvie Sukno, Rachel Desailloud, Miriam Cnop, Ramona Nicolescu, Lior Cohen, Jean-François Zagury, Mélanie Amouyal, Jacques Weill, Jean Muller, Olivier Sand, Bruno Delobel, Philippe Froguel, Amélie Bonnefond

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