Found: 25
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Macrophage autophagy protects against hepatocellular carcinogenesis in mice.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98203-5
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- Publication type:
- Article
Unknown Circovirus in Immunosuppressed Patient with Hepatitis, France, 2022.
- Published in:
- Emerging Infectious Diseases, 2023, v. 29, n. 5, p. 1051, doi. 10.3201/eid2905.221485
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- Publication type:
- Article
Persistent SARS-CoV-2 Alpha Variant Infection in Immunosuppressed Patient, France, February 2022.
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- Emerging Infectious Diseases, 2022, v. 28, n. 7, p. 1512, doi. 10.3201/eid2807.220467
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- Publication type:
- Article
Novel SARS-CoV-2 Variant Derived from Clade 19B, France.
- Published in:
- 2021
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- Publication type:
- journal article
Fatal Measles Inclusion-Body Encephalitis in Adult with Untreated AIDS, France.
- Published in:
- 2020
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- Publication type:
- journal article
Fatal Encephalitis Caused by Cristoli Virus, an Emerging Orthobunyavirus, France.
- Published in:
- 2020
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- Publication type:
- journal article
Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlation.
- Published in:
- 2015
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- Publication type:
- journal article
Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 15, p. 7875, doi. 10.3390/ijms22157875
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- Publication type:
- Article
Phenotype Analysis of Retinal Dystrophies in Light of the Underlying Genetic Defects: Application to Cone and Cone-Rod Dystrophies.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 19, p. 4854, doi. 10.3390/ijms20194854
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- Publication type:
- Article
Expanding the Mutation Spectrum in ABCA4: Sixty Novel Disease Causing Variants and Their Associated Phenotype in a Large French Stargardt Cohort.
- Published in:
- International Journal of Molecular Sciences, 2018, v. 19, n. 8, p. 2196, doi. 10.3390/ijms19082196
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- Publication type:
- Article
Omicron induced distinct immune respiratory transcriptomics signatures compared to pre‐existing variants in critically ill COVID‐19 patients.
- Published in:
- Journal of Medical Virology, 2023, v. 95, n. 12, p. 1, doi. 10.1002/jmv.29268
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- Publication type:
- Article
Case Report: Cerebral Nocardiosis Caused by Nocardia cyriacigeorgica Detected by Metagenomics in an Apparently Immunocompetent Patient.
- Published in:
- 2022
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- Publication type:
- Case Study
Fitness‐associated substitutions following failure of direct‐acting antivirals assessed by deep sequencing of full‐length hepatitis C virus genomes.
- Published in:
- Alimentary Pharmacology & Therapeutics, 2020, v. 52, n. 10, p. 1583, doi. 10.1111/apt.16054
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- Publication type:
- Article
Prospective Comparison Between Shotgun Metagenomics and Sanger Sequencing of the 16S rRNA Gene for the Etiological Diagnosis of Infections.
- Published in:
- Frontiers in Microbiology, 2022, v. 13, p. 1, doi. 10.3389/fmicb.2022.761873
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- Publication type:
- Article
Viral genomic, metagenomic and human transcriptomic characterization and prediction of the clinical forms of COVID-19.
- Published in:
- PLoS Pathogens, 2021, v. 17, n. 3, p. 1, doi. 10.1371/journal.ppat.1009416
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- Publication type:
- Article
Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B.
- Published in:
- 2019
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- Publication type:
- journal article
WDR34, a candidate gene for non‐syndromic rod‐cone dystrophy.
- Published in:
- Clinical Genetics, 2021, v. 99, n. 2, p. 298, doi. 10.1111/cge.13872
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- Publication type:
- Article
BNT162b2 Messenger RNA Vaccination Did Not Prevent an Outbreak of Severe Acute Respiratory Syndrome Coronavirus 2 Variant 501Y.V2 in an Elderly Nursing Home but Reduced Transmission and Disease Severity.
- Published in:
- Clinical Infectious Diseases, 2022, v. 74, n. 3, p. 517, doi. 10.1093/cid/ciab446
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- Publication type:
- Article
Interleukin-17 programs liver progenitor cell transformation into cancer stem cells through miR-122 downregulation with increased risk of primary liver cancer initiation.
- Published in:
- International Journal of Biological Sciences, 2022, v. 18, n. 5, p. 1944, doi. 10.7150/ijbs.70408
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- Publication type:
- Article
Fatal encephalitis caused by Newcastle disease virus in a child.
- Published in:
- Acta Neuropathologica, 2021, v. 142, n. 3, p. 605, doi. 10.1007/s00401-021-02344-w
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- Publication type:
- Article
CHM mutation spectrum and disease: An update at the time of human therapeutic trials.
- Published in:
- Human Mutation, 2021, v. 42, n. 4, p. 323, doi. 10.1002/humu.24174
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- Publication type:
- Article
MERTK mutation update in inherited retinal diseases.
- Published in:
- Human Mutation, 2018, v. 39, n. 7, p. 887, doi. 10.1002/humu.23431
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- Publication type:
- Article
Analysis of Microbiota and Mycobiota in Fungal Ball Rhinosinusitis: Specific Interaction between Aspergillus fumigatus and Haemophilus influenza?
- Published in:
- Journal of Fungi, 2021, v. 7, n. 7, p. 1, doi. 10.3390/jof7070550
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- Publication type:
- Article
Ultra-deep sequencing improves the detection of drug resistance in cellular DNA from HIV-infected patients on ART with suppressed viraemia.
- Published in:
- 2018
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- Publication type:
- journal article
Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy.
- Published in:
- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/485624
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- Publication type:
- Article