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Nasal ciliated cells are primary targets for SARS-CoV-2 replication in the early stage of COVID-19.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-11492-2
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- Publication type:
- Article
The genome-wide landscape of C:G > T:A polymorphism at the CpG contexts in the human population.
- Published in:
- BMC Genomics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12864-020-6674-1
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- Publication type:
- Article
Clinical and genetic characteristics of three patients with congenital insensitivity to pain with anhidrosis: Case reports and a review of the literature.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 4, p. 1, doi. 10.1002/mgg3.2430
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- Publication type:
- Article
Author Correction: Heterogeneous genetic landscape of congenital neutropenia in Korean patients revealed by whole exome sequencing: genetic, phenotypic and histologic correlations.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Mutalisk: a web-based somatic MUTation AnaLyIS toolKit for genomic, transcriptional and epigenomic signatures.
- Published in:
- Nucleic Acids Research, 2018, v. 46, n. W1, p. W102, doi. 10.1093/nar/gky406
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- Publication type:
- Article
TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology.
- Published in:
- Nucleic Acids Research, 2011, v. 39, n. suppl_1, p. D883, doi. 10.1093/nar/gkq1101
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- Publication type:
- Article
Reference-unbiased copy number variant analysis using CGH microarrays.
- Published in:
- Nucleic Acids Research, 2010, v. 38, n. 20, p. e190, doi. 10.1093/nar/gkq730
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- Publication type:
- Article
Weight-bearing activity impairs nuclear membrane and genome integrity via YAP activation in plantar melanoma.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29925-x
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- Publication type:
- Article
Weight-bearing activity impairs nuclear membrane and genome integrity via YAP activation in plantar melanoma.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29925-x
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- Publication type:
- Article
Publisher Correction: Weight-bearing activity impairs nuclear membrane and genome integrity via YAP activation in plantar melanoma.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Weight-bearing activity impairs nuclear membrane and genome integrity via YAP activation in plantar melanoma.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29925-x
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- Publication type:
- Article
Single-cell transcriptome of bronchoalveolar lavage fluid reveals sequential change of macrophages during SARS-CoV-2 infection in ferrets.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24807-0
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- Publication type:
- Article
A family-based association study after genome-wide linkage analysis identified two genetic loci for renal function in a Mongolian population.
- Published in:
- Kidney International, 2013, v. 83, n. 2, p. 285, doi. 10.1038/ki.2012.389
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- Publication type:
- Article
Subclonal diversification of primary breast cancer revealed by multiregion sequencing.
- Published in:
- Nature Medicine, 2015, v. 21, n. 7, p. 751, doi. 10.1038/nm.3886
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- Publication type:
- Article
Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals.
- Published in:
- Nature Genetics, 2011, v. 43, n. 8, p. 745, doi. 10.1038/ng.872
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- Publication type:
- Article
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing.
- Published in:
- Nature Genetics, 2010, v. 42, n. 5, p. 400, doi. 10.1038/ng.555
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- Publication type:
- Article
Low-level brain somatic mutations in exonic regions are collectively implicated in autism with germline mutations in autism risk genes.
- Published in:
- Experimental & Molecular Medicine EMM, 2024, v. 56, n. 8, p. 1750, doi. 10.1038/s12276-024-01284-1
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- Publication type:
- Article
Dissecting single-cell genomes through the clonal organoid technique.
- Published in:
- Experimental & Molecular Medicine EMM, 2021, v. 53, n. 10, p. 1503, doi. 10.1038/s12276-021-00680-1
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- Publication type:
- Article
Mutational spectrum of SARS-CoV-2 during the global pandemic.
- Published in:
- Experimental & Molecular Medicine EMM, 2021, v. 53, n. 8, p. 1229, doi. 10.1038/s12276-021-00658-z
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- Publication type:
- Article
Publisher Correction: Serotonin signals through a gut-liver axis to regulate hepatic steatosis.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-08085-x
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- Publication type:
- Article
Serotonin signals through a gut-liver axis to regulate hepatic steatosis.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07287-7
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- Publication type:
- Article
Cerebral Cavernous Malformation 1 Determines YAP/TAZ Signaling-Dependent Metastatic Hallmarks of Prostate Cancer Cells.
- Published in:
- Cancers, 2021, v. 13, n. 5, p. 1125, doi. 10.3390/cancers13051125
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- Publication type:
- Article
TIARA genome database: update 2013.
- Published in:
- Database: The Journal of Biological Databases & Curation, 2013, v. 2013, p. 1, doi. 10.1093/database/bat003
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- Publication type:
- Article
Patient-derived organoids as a preclinical platform for precision medicine in colorectal cancer.
- Published in:
- Molecular Oncology, 2022, v. 16, n. 12, p. 2396, doi. 10.1002/1878-0261.13144
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- Publication type:
- Article
Single Cell Analysis of Human Thyroid Reveals the Transcriptional Signatures of Aging.
- Published in:
- Endocrinology, 2023, v. 164, n. 4, p. 1, doi. 10.1210/endocr/bqad029
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- Publication type:
- Article
Severe protein C deficiency in a newborn caused by a homozygous pathogenic variant in the PROC gene: a case report.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Severe protein C deficiency in a newborn caused by a homozygous pathogenic variant in the PROC gene: a case report.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Implication of CD69<sup>+</sup>CD103<sup>+</sup> tissue‐resident‐like CD8<sup>+</sup> T cells as a potential immunotherapeutic target for cholangiocarcinoma.
- Published in:
- Liver International, 2021, v. 41, n. 4, p. 764, doi. 10.1111/liv.14814
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- Publication type:
- Article
A highly annotated whole-genome sequence of a Korean individual.
- Published in:
- Nature, 2009, v. 460, n. 7258, p. 1011, doi. 10.1038/nature08211
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- Publication type:
- Article
Fine-scale mapping of meiotic recombination in Asians.
- Published in:
- BMC Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2156-14-19
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- Publication type:
- Article
Ultra‐Low Level Somatic Mutations and Structural Variations in Focal Cortical Dysplasia Type II.
- Published in:
- Annals of Neurology, 2023, v. 93, n. 6, p. 1082, doi. 10.1002/ana.26609
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- Publication type:
- Article
Genomic features of renal cell carcinoma developed during end-stage renal disease and dialysis.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 2, p. 290, doi. 10.1093/hmg/ddac180
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- Publication type:
- Article
Clinical Utility of Whole-Genome Analysis as One-for-All Test for Breast Cancer: A Case Series.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
A fusion of CD63-BCAR4 identified in lung adenocarcinoma promotes tumorigenicity and metastasis.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Recurrent fusion transcripts detected by whole-transcriptome sequencing of 120 primary breast cancer samples.
- Published in:
- Genes, Chromosomes & Cancer, 2015, v. 54, n. 11, p. 681, doi. 10.1002/gcc.22279
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- Publication type:
- Article
Patterns and mechanisms of structural variations in human cancer.
- Published in:
- Experimental & Molecular Medicine EMM, 2018, v. 50, n. 8, p. 1, doi. 10.1038/s12276-018-0112-3
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- Publication type:
- Article
A male mouse model for metabolic dysfunction-associated steatotic liver disease and hepatocellular carcinoma.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-50660-y
- By:
- Publication type:
- Article
FX: an RNA-Seq analysis tool on the cloud.
- Published in:
- Bioinformatics, 2012, v. 28, n. 5, p. 721, doi. 10.1093/bioinformatics/bts023
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- Publication type:
- Article
Combined linkage and association analyses identify a novel locus for obesity near PROX1 in Asians.
- Published in:
- Obesity (19307381), 2013, v. 21, n. 11, p. 2405, doi. 10.1002/oby.20153
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- Publication type:
- Article
FIREVAT: finding reliable variants without artifacts in human cancer samples using etiologically relevant mutational signatures.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s13073-019-0695-x
- By:
- Publication type:
- Article
PRMT1 Is Required for the Maintenance of Mature β-Cell Identity.
- Published in:
- 2020
- By:
- Publication type:
- journal article