Fused Supernumerary Kidneys with S-shaped Configuration: A Case Series by Sai Shankar Mankuzhy Gopalakrishnan, Jenikar Paulraj, R Remya, Nillohit Saha, Harshavardhan Balaganesan

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A novel mutation, Ile344Asn, in microsomal triglyceride transfer protein abolishes binding to protein disulfide isomerase by Swati Valmiki, Cindy Bredefeld, M. Mahmood Hussain

Subjects: “…variants…”
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Association between the aromatase (CYP19A1) gene variant rs10046 and cardiovascular risk in postmenopausal women by Betânia Rodrigues dos Santos, Gislaine Casanova, Thais Rasia da Silva, Karen Oppermann, Poli Mara Spritzer

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Designing the trajectories of variant teaching of the basics of artificial intelligence in the school course of computer science taking into account the possibilities of project-re... by Sergey D. Karakozov, Nadezhda N. Samylkina

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Research on the characteristics of 18F-FDG PET/CT in mantle cell lymphoma and the discrimination between cellular morphological variants by REN Yixuan, CHEN Cheng, CAI Mingci, CHEN Jiamin, YANG Xinxin, WANG Chao, LIN Xiaozhu, CHENG Shu, JIANG Xufeng, CHEN Dongxu

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Runoff Simulation Study of Ganjiang River Basin Based on Distributed Time-varying Gain Hydrological Model and CN05.1 Precipitation Data by ZHONG Qi, FU Xiaolei, JIANG Xiaolei, ZHANG Yuchen, HU Leyi, ZHANG Liping

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Genomic and Metabolomic Analyses of <i>Streptomyces albulus</i> with Enhanced ε-Poly-<span style="font-variant: small-caps">l</span>-lysine Production Through Adaptive Laboratory E... by Xidong Ren, Xinjie Sun, Yan Chen, Xiangheng Xi, Yunzhe Ma, Xinyue Jiang, Xian Zhang, Chenying Wang, Deqiang Zhu, Xinli Liu

Subjects: “…ε-poly-<span style="font-variant: small-caps">l</span>-lysine…”
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Atypical hemolytic uremic syndrome with a C3 variant following COVID-19: a case report by Masato Ando, Kazuo Kubota, Kazuo Kubota, Saori Kadowaki, Minako Kawamoto, Norio Kawamoto, Haruka Okamoto, Soichiro Nagaya, Yuki Miwa, Hidenori Ohnishi, Hidenori Ohnishi

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DEL phenotype in RhD-negative North Indian blood donors by Paramjit Kaur, Ravneet K. Bedi, Tanvi Sood, Kshitija Mittal, Gagandeep Kaur

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Prolegómenos a una edición crítica contemporánea de «La Circe», de Lope de Vega: a propósito de su transmisión textual, seis variantes y dos voces by Cipriano López Lorenzo

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Unraveling the genetic connections for mitochondrial DNA control region and breast cancer susceptibility by Namra Khalid, Muhammad Umer Khan, Raima Rehman, Shamsa Kanwal, Tazeen Zahid, Muhammad Usman Ghani, Ayesha Iftikhar, Qurban Ali, Muhammad Arshad Javed

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Wilson Disease in a Turkish Population: Molecular Insights into an Old Disease with Reported and Novel Variants by Abdullatif Bakır, Vehap Topçu, Büşranur Çavdarlı

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Encoding of Variant Taxonomies in TEI by Helena Bermúdez Sabel

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Divergence of gut bacteria through the selection of genomic variants implicated in the metabolism of sugars, amino acids, and purines by small extracellular vesicles in milk by Fang Zhou, Peerzada Tajamul Mumtaz, Haluk Dogan, Roland Madadjim, Juan Cui, Janos Zempleni

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Comparative Analysis of COVID‐19 Severity and Mortality Among Vaccinated and Unvaccinated Individuals During the Delta Variant Surge in a Tertiary Care Center: A Cohort Study by Fatemeh Hasani, Zahra Norouzi, Kimia Jazi, Gholamreza Roshandel, Alireza Norouzi

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Heterogeneous clinical phenotypes of sporadic early-onset Alzheimer’s disease: a neuropsychological data-driven approach by Deepti Putcha, Yuta Katsumi, Alexandra Touroutoglou, Ani Eloyan, Alexander Taurone, Maryanne Thangarajah, Paul Aisen, Jeffrey L. Dage, Tatiana Foroud, Clifford R. Jack, Joel H. Kramer, Kelly N. H. Nudelman, Rema Raman, Prashanthi Vemuri, Alireza Atri, Gregory S. Day, Ranjan Duara, Neill R. Graff-Radford, Ian M. Grant, Lawrence S. Honig, Erik C. B. Johnson, David T. Jones, Joseph C. Masdeu, Mario F. Mendez, Erik Musiek, Chiadi U. Onyike, Meghan Riddle, Emily Rogalski, Stephen Salloway, Sharon Sha, R. Scott Turner, Thomas S. Wingo, David A. Wolk, Kyle Womack, Maria C. Carrillo, Gil D. Rabinovici, Bradford C. Dickerson, Liana G. Apostolova, Dustin B. Hammers, the LEADS Consortium

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Identification of Houge type of X-linked syndromic mental retardation caused by CNKSR2 truncated variants by Si-Hua Chang, Jie-Yuan Jin, Yi-Qiao Hu, Run-Yan Wang, Rong Xiang, Xia Wang

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Étude comparée du fonctionnement des parenthèses et des tirets by Guillaume François

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Nigmat Hakim, manuscript, “Idegey”, dastan, variability, textual studies, written sources, version by Fazlutdinov I.I.

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Functional annotation of variants from healthy individuals by Jean Lee, Sung Eun Hong

Subjects: “…variants…”
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