Found: 14
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Machine learning phenomics (MLP) combining deep learning with time-lapse-microscopy for monitoring colorectal adenocarcinoma cells gene expression and drug-response.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-12364-5
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- Article
Isolation of CF cell lines corrected at δF508-CFTR locus by SFHR-mediated targeting.
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- Gene Therapy, 2002, v. 9, n. 11, p. 683, doi. 10.1038/sj.gt.3301741
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- Article
AFM nano‐mechanical study of the beating profile of hiPSC‐derived cardiomyocytes beating bodies WT and DM1.
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- Journal of Molecular Recognition, 2018, v. 31, n. 10, p. 1, doi. 10.1002/jmr.2725
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- Article
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosis.
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- Clinical Genetics, 2016, v. 89, n. 1, p. 93, doi. 10.1111/cge.12674
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- Article
SARS‐COV‐2 and infectivity: Possible increase in infectivity associated to integrin motif expression.
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- Journal of Medical Virology, 2020, v. 92, n. 10, p. 1741, doi. 10.1002/jmv.25831
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- Article
Gene expression profile study in CFTR mutated bronchial cell lines.
- Published in:
- Clinical & Experimental Medicine, 2006, v. 6, n. 4, p. 157, doi. 10.1007/s10238-006-0116-5
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- Article
Evidence for an association between the SRD5A2 (type II steroid 5.
- Published in:
- Disease Markers, 2000, v. 16, n. 3-4, p. 147, doi. 10.1155/2000/683607
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- Article
Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 809, doi. 10.1038/sj.ejhg.5200547
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- Article
Cloning and molecular characterization of three Ubiquitin Fusion Degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster.
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- Cytogenetics & Cell Genetics, 2001, v. 92, n. 3/4, p. 279, doi. 10.1159/000056916
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- Article
Isolation and cloning by a polymerase chain reaction of a genomic DNA fragment of the human slow skeletal troponin (TNNT1) gene.
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- Cell Biochemistry & Function, 1993, v. 11, n. 3, p. 187, doi. 10.1002/cbf.290110306
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- Article
Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscle.
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- Cell Biochemistry & Function, 1992, v. 10, n. 4, p. 251, doi. 10.1002/cbf.290100407
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- Article
Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita.
- Published in:
- Human Mutation, 1998, v. 11, n. 4, p. 331, doi. 10.1002/(SICI)1098-1004(1998)11:4<331::AID-HUMU13>3.0.CO;2-0
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- Article
Identification of Three Novel Cystic Fibrosis Mutations in a Sample of Italian Cystic Fibrosis Patients.
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- Human Heredity, 1993, v. 43, n. 5, p. 295, doi. 10.1159/000154147
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- Article
Forensic Applications of Molecular Genetic Analysis: An Italian Collaborative Study on Paternity Testing by the Determination of Variable Number of Tandem Repeat DNA Polymorphisms.
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- Human Heredity, 1991, v. 41, n. 3, p. 174, doi. 10.1159/000153997
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- Article