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Emerging Infectious Diseases|February 24, 2022
Mycobacterium leprae Infection in a Wild Nine-Banded Armadillo, Nuevo León, MexicoLucio Vera-Cabrera, Cesar J Ramos-Cavazos, Nathan A Youssef, et al.
Clinical Genetics|May 21, 2013
Could a patient with SMC1A duplication be classified as a human cohesinopathy?C Baquero-Montoya, M C Gil-Rodríguez, M E Teresa-Rodrigo, et al.
Plos Pathogens|April 8, 2021
High-throughput, single-copy sequencing reveals SARS-CoV-2 spike variants coincident with mounting humoral immunity during acute COVID-19Sung Hee Ko, Elham Bayat Mokhtari, Prakriti Mudvari, et al.
Archives of Pathology & Laboratory Medicine|July 31, 2024
A Droplet Digital Polymerase Chain Reaction-Based Tool to Aid in Melanoma Diagnosis: Development of a 4-Gene Panel Using 164 Melanocytic NeoplasmsJason R McFadden, Iman Salem, Mirjana Stevanovic, et al.
Antonie Van Leeuwenhoek|July 15, 2014
Reference genes for RT-qPCR studies in Corynebacterium pseudotuberculosis identified through analysis of RNA-seq dataDaiane M Carvalho, Pablo H de Sá, Thiago L P Castro, et al.
Journal of Investigational Allergology & Clinical Immunology|October 27, 2025
Identification of Dual Super-Response in Patients With Asthma and CRSwNP Treated With MepolizumabM Estravís, D Carreiras-Quintas, J C Triviño, et al.
Genome Announcements|August 13, 2016
Genome Sequence of Corynebacterium pseudotuberculosis Strain PA02 Isolated from an Ovine Host in the AmazonGabriel R S Muge, Adonney A O Veras, Pablo H C G de Sá, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2021
High-Throughput, Single-Copy Sequencing Reveals SARS-CoV-2 Spike Variants Coincident with Mounting Humoral Immunity during Acute COVID-19Sung Hee Ko, Elham Bayat Mokhtari, Prakriti Mudvari, et al.
Epilepsia|December 3, 2003
Recent developments in the quest for myoclonic epilepsy genesAntonio V Delgado-Escueta, Katerina B Perez-Gosiengfiao, Dongsheng Bai, et al.
American Journal of Human Genetics|February 3, 2007
Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardationMatthew A Deardorff, Maninder Kaur, Dinah Yaeger, et al.
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