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UnknownEvaluation of the prognostic value of liver stiffness in patients with hepatitis C virus treated with triple or dual antiviral therapy: A prospective pilot study.
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S-EPMC4356922 | biostudies-literature
UnknownSite-specific, covalent incorporation of Tus, a DNA-binding protein, on ionic-complementary self-assembling peptide hydrogels using transpeptidase Sortase A as a conjugation tool†Dedicated to the memory of Joachim H. G. Steinke.‡Electronic supplementary information (ESI) available: Further experimental data. See DOI: 10.1039/c3sm00131hClick here for additional data file.
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S-EPMC3705885 | biostudies-literature
UnknownMuscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations.
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S-EPMC3179367 | biostudies-literature
UnknownNext generation sequencing (NGS) strategies for the genetic testing of myopathies.
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S-EPMC3631804 | biostudies-literature
UnknownInteraction of vault particles with estrogen receptor in the MCF-7 breast cancer cell.
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S-EPMC2132791 | biostudies-literature
UnknownA Novel Missense Variant in <i>LHX4</i> in Three Children with Multiple Pituitary Hormone Deficiency Belonging to Two Unrelated Families and Contribution of Additional <i>GLI2</i> and <i>IGFR1</i> Variant.
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S-EPMC11941417 | biostudies-literature
UnknownTocilizumab for patients with COVID-19 pneumonia. The single-arm TOCIVID-19 prospective trial.
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S-EPMC7576974 | biostudies-literature
UnknownPatients carrying Arg1809 substitution with no choroidal abnormalities: a further proof of a "Quasi-Incomplete" NF1 phenotype.
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S-EPMC9905567 | biostudies-literature
UnknownNeurofibromatosis Type 1: Pediatric Aspects and Review of Genotype-Phenotype Correlations.
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S-EPMC9954221 | biostudies-literature
UnknownA Novel Homozygous Loss-of-Function Variant in SPRED2 Causes Autosomal Recessive Noonan-like Syndrome.
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S-EPMC10815364 | biostudies-literature
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