Application of heteroduplex analysis for CALR mutation screening detection in patients with Ph-myeloproliferative neoplasms by T. N. Subbotina, D. V. Kurochkin, I. E. Maslyukova, A. S. Khazieva, E. V. Vasiliev, M. A. Mikhalev, E. A. Dunaeva, K. O. Mironov

Subjects: Get full text

A 3D-printed Sanger sequencing activity addresses student misconceptions by Phillip E. Brown, Stefanie H. Chen

Subjects: “…Sanger sequencing…”
Get full text

Porcine Sample Type Characteristics Associated with Sequencing and Isolation of Influenza A Virus by Daniel C. A. Moraes, Onyekachukwu H. Osemeke, Michael A. Zeller, Amy L. Baker, Gustavo S. Silva, Giovani Trevisan, Daniel C. L. Linhares, Phillip C. Gauger

Subjects: Get full text

Association of functional variants in miRNA genes with the risk of coronary heart disease by Taqweem Ul Haq, Muhammad Riaz Khan, Sajjad Ali, Tariq Aziz, Thamer H. Albekairi, Aftab Ali Shah

Subjects: Get full text

Sanger sequencing reveals Pseudomonas aeruginosa was the most common cross-contamination of gastrointestinal endoscopy by Zainab hameed

Subjects: “…Pseudomonas aeroginusa, Pseudomonas nitroreducens, gastrointestinal endoscopy contamination, Sanger sequencing.…”
Get full text

Archived HIV-1 Drug Resistance Mutations: Role of Proviral HIV-1 DNA Genotype for the Management of Virological Responder People Living with HIV by Roberta Campagna, Chiara Nonne, Guido Antonelli, Ombretta Turriziani

Subjects: Get full text

ANALYSIS OF MUTATIONS IN KRAS AND BRAF GENES IN COLORECTAL CANCER IN RUSSIAN PATIENTS by E. E. Pisareva, L. N. Ljubchenko, S. P. Kovalenko, V. A. Shamanin

Subjects: Get full text

Dynamics and genetic variation of dengue virus serotypes circulating during the 2022 outbreak in Karachi by Faaria Tariq, Muhammad Irfan, Saba Farooq, Hana’a Iqbal, Atia-tul-Wahab, Ishtiaq Ahmad Khan, Thomas Iftner, M. Iqbal Choudhary

Subjects: Get full text

Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosis by Aurélien Palmyre, Fairouz Koraichi, Flavie Ader, Erwan Donal, Céline Bordet, Pascal de Groote, Laurence Faivre, Patricia Reant, Annick Toutain, Karine Nguyen, Bertrand Isidor, Anne-Claire Brehin, Lise Legrand, Estelle Gandjbakhch, Julie Proukhnitzky, Richard Isnard, Nicolas Mansencal, Jean-François Pruny, Jean-Pierre Rabes, Bruno Francou, Catherine Caillaud, Pascale Richard, Philippe Charron

Subjects: Get full text

DNA Testing Methodology for the Evaluation of Susceptibility to Scrapie in Tsurcana Sheep by Dana-Iuliana Neață, Maria-Mihaela Antofie, Teodor Vintilă

Subjects: Get full text

IHH gene variants in North Indian individuals with brachydactyly A1 by Shalini Dhiman, Inusha Panigrahi, Shifali Gupta, Harvinder Kaur

Subjects: Get full text

FBN2 pathogenic mutation in congenital contractural arachnodactyly with severe skeletal manifestations by Yazhou Huang, Xingxin Fang, Linya Ma, Jibo Zhang, Chao Wang, Taoran Gao, Dan Peng

Subjects: Get full text

Unexpected Pediatric Cluster of Enterovirus C105, Verona, Italy by Elena Pomari, Simone Malagò, Guglielmo Ferrari, Greta Romano, Antonio Mori, Andrea Matucci, Rebecca Feletti, Paolo Bonetti, Fausto Baldanti, Concetta Castilletti, Antonio Piralla

Subjects: Get full text

Scifer: An R/Bioconductor package for large-scale integration of Sanger sequencing and flow cytometry data of index-sorted single cells by Rodrigo Arcoverde Cerveira, Klara Lenart, Marcel Martin, Matthew James Hinchcliff, Fredrika Hellgren, Kewei Ye, Juliana Assis Geraldo, Taras Kreslavsky, Sebastian Ols, Karin Loré

Subjects: Get full text

Spectrum of VHL mutations in clear cell renal cell carcinoma by N. N. Mazurenko, I. V. Tsyganova, V. V. Strelnikov, A. V. Balbutsky, T. F. Malivanova, E. B. Kuznetsova, V. A. Draudin-Krilenko, O. V. Shangina, A. F. Mukeria, V. B. Matveev, D. G. Zaridze

Subjects: Get full text

Genetic screening of malay familial hypercholesterolemia patient for LDLRAP1/PCSK9/APOB mutations via whole exome sequencing by Muhammad-Redha Abdullah-Zawawi, Zam Zureena Mohd Rani, Nur Syakeera Seeni Ahamed Mydeen, Ryia Illani Mohd Yunos, Siti Aishah Sulaiman, Izzatul ‘Aliaa Badaruddin, Rose Ismet, Norlaila Mustafa, Syahidatun Najwa Abu Zahid, Rahman Jamal, Azrul Azlan Hamzah, Nor Azian Abdul Murad

Subjects: Get full text

Results of <em>UGT1A1</em> gene sequencing in individuals with the Gilbert syndrome phenotype by A. A. Ivanova, N. E. Apartseva, A. P. Kashirina, E. G. Nemcova, Ju. V. Ivanova, M. V. Kruchinina, S. A. Kurilovich, V. N. Maksimov

Subjects: Get full text

Silent but significant: Functional elucidation of a synonymous ATP7B mutation in Wilson’s disease pedigrees by Qi Zhang, Qi Zhang, Xiaoming Xie, Hairong Li, Yulei Li, Hongyao Huang, Hongyao Huang

Subjects: Get full text

Targeting malignant adenomyoepithelioma of the breast: clinical insights on multimodal therapy and disease-free survival by Hung-Liang Pai, Wei-Ting Hsu, Chia-Chi Chang, Ming-Hsin Yeh

Subjects: Get full text

Discovery of a novel lymphocytic choriomeningitis virus strain associated with severe human disease in immunocompetent patient, New Mexico by Jordan T. Gass, Robert A. Nofchissey, Frances M. Twohig, Chunyan Ye, Samuel M. Goodfellow, Kimiknu Mentore, Marcos Burgos, Oscar Negrete, Shannon Whitmer, John D. Klena, Deborah Cannon, Leanna Sayyad, Steven B. Bradfute

Subjects: Get full text