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NS4A protein as a marker of HCV history suggests that different HCV genotypes originally evolved from genotype 1b.
- Published in:
- Virology Journal, 2011, v. 8, n. 1, p. 317, doi. 10.1186/1743-422X-8-317
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- Publication type:
- Article
HCV genotype-specific correlation with serum markers: Higher predictability for genotype 4a.
- Published in:
- Virology Journal, 2011, v. 8, n. 1, p. 293, doi. 10.1186/1743-422X-8-293
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- Publication type:
- Article
Claudin-1 required for HCV virus entry has high potential for phosphorylation and O-glycosylation.
- Published in:
- Virology Journal, 2011, v. 8, n. 1, p. 229, doi. 10.1186/1743-422X-8-229
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- Publication type:
- Article
Serine 204 phosphorylation and O-b-GlcNAC interplay of IGFBP-6 as therapeutic indicator to regulate IGF-II functions in viral mediated hepatocellular carcinoma.
- Published in:
- Virology Journal, 2011, v. 8, n. 1, p. 208, doi. 10.1186/1743-422X-8-208
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- Publication type:
- Article
A brief review on molecular, genetic and imaging techniques for HCV fibrosis evaluation.
- Published in:
- Virology Journal, 2011, v. 8, n. 1, p. 53, doi. 10.1186/1743-422X-8-53
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- Publication type:
- Article
A comparison of four fibrosis indexes in chronic HCV: development of new fibrosis-cirrhosis index (FCI).
- Published in:
- 2011
- By:
- Publication type:
- journal article
Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short stature.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 7, p. 1132, doi. 10.1093/hmg/ddaa032
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- Publication type:
- Article
Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 6, p. 972, doi. 10.1093/hmg/ddy406
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- Publication type:
- Article