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HBV DNA Integration into Telomerase or MLL4 Genes and TERT Promoter Point Mutation as Three Independent Signatures in Subgrouping HBV-Related HCC with Distinct Features.
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- Liver Cancer (2235-1795), 2024, v. 13, n. 1, p. 41, doi. 10.1159/000530699
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- Article
Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese.
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- Journal of Human Genetics, 2008, v. 53, n. 5, p. 419, doi. 10.1007/s10038-008-0265-3
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- Article
Novel mutations involving the NF1 gene coding sequence in neurofibromatosis type 1 patients from Taiwan.
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- Journal of Human Genetics, 2003, v. 48, n. 10, p. 545, doi. 10.1007/s10038-003-0066-7
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- Article
A persistent level of Cisd2 extends healthy lifespan and delays aging in mice.
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- Human Molecular Genetics, 2012, v. 21, n. 18, p. 3956, doi. 10.1093/hmg/dds210
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- Article
Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48).
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- Journal of Biomedical Science, 2021, v. 28, n. 1, p. 1, doi. 10.1186/s12929-021-00763-1
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- Article
Disclosing an In-Frame Deletion of the Titin Gene as the Possible Predisposing Factor of Anthracycline-Induced Cardiomyopathy: A Case Report.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 16, p. 9261, doi. 10.3390/ijms23169261
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- Article
Chromosomal aberrations in nasopharyngeal carcinoma analyzed by comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1999, v. 25, n. 2, p. 169, doi. 10.1002/(SICI)1098-2264(199906)25:2<169::AID-GCC13>3.0.CO;2-I
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- Article
Complex Movement Disorders in a Boy with PURA Syndrome.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 7, p. 1137, doi. 10.1002/mdc3.13272
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- Article
The signaling role of feedback in the repeated public goods game: Experimental evidence from the laboratory.
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- PLoS ONE, 2024, v. 19, n. 2, p. 1, doi. 10.1371/journal.pone.0299196
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- Article
Genetic Heterogeneity of Familial Primary Cutaneous Amyloidosis: Lack of Evidence for Linkage with the Chromosome 10 Pericentromeric Region in Chinese Families.
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- Journal of Investigative Dermatology, 1996, v. 107, n. 1, p. 30, doi. 10.1111/1523-1747.ep12297840
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- Article
ARD1 Stabilization of TSC2 Suppresses Tumorigenesis Through the mTOR Signaling Pathway.
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- Science Signaling, 2010, v. 3, n. 108, p. 1, doi. 10.1126/scisignal.2000590
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- Article
Generation and Analysis of the Expressed Sequence Tags from the Mycelium of <i>Ganoderma lucidum</i>
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- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0061127
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- Article
Copy Number Change of the NDM-1 Sequence in a Multidrug-Resistant <i>Klebsiella pneumoniae</i> Clinical Isolate.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0062774
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- Article
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.
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- Nature Genetics, 2001, v. 28, n. 3, p. 232, doi. 10.1038/90067
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- Article
Qualitative and comparative proteomic analysis of Xanthomonas campestris pv. campestris 17.
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- Proteomics, 2007, v. 7, n. 12, p. 2047, doi. 10.1002/pmic.200600647
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- Article
Epigenetic Enhancement of the Post-replicative DNA Mismatch Repair of Mammalian Genomes by a Hemi-<sup>m</sup>CpG-Np95-Dnmt1 Axis.
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- Scientific Reports, 2016, p. 37490, doi. 10.1038/srep37490
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- Article
Network Signatures of IgG Immune Repertoires in Hepatitis B Associated Chronic Infection and Vaccination Responses.
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- Scientific Reports, 2016, p. 26556, doi. 10.1038/srep26556
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- Article
Identification of the common regulators for hepatocellular carcinoma induced by hepatitis B virus X antigen in a mouse model.
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- Carcinogenesis, 2012, v. 33, n. 1, p. 209, doi. 10.1093/carcin/bgr224
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- Article
Mutation of epidermal growth factor receptor is associated with MIG6 expression.
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- FEBS Journal, 2009, v. 276, n. 18, p. 5239, doi. 10.1111/j.1742-4658.2009.07220.x
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- Article
Resonance assignments of a CoA binding protein from Klebsiella pneumoniae.
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- 2006
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- Publication type:
- Letter
Integration of genome-wide association study and expression quantitative trait locus mapping for identification of endometriosis-associated genes.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-020-79515-4
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- Article
Clinical Relevance of Plasma DNA Methylation in Colorectal Cancer Patients Identified by Using a Genome-Wide High-Resolution Array.
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- Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2015, v. 22, p. 1419, doi. 10.1245/s10434-014-4277-2
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- Article
Artificial-Intelligence-Assisted Discovery of Genetic Factors for Precision Medicine of Antiplatelet Therapy in Diabetic Peripheral Artery Disease.
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- Biomedicines, 2022, v. 10, n. 1, p. 116, doi. 10.3390/biomedicines10010116
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- Article
IL-10 promoter genetic polymorphisms and risk of Kawasaki disease in Taiwan.
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- Disease Markers, 2011, v. 30, n. 1, p. 51, doi. 10.1155/2011/909407
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- Article
ALPK1 genetic regulation and risk in relation to gout.
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- International Journal of Epidemiology, 2013, v. 42, n. 2, p. 466, doi. 10.1093/ije/dyt028
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- Article
TPMD: a database and resources of microsatellite marker genotyped in Taiwanese populations.
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- Nucleic Acids Research, 2005, v. 33, n. suppl 1, p. d174
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- Article
Genomic shotgun array: a procedure linking large‐scale DNA sequencing with regional transcript mapping.
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- Nucleic Acids Research, 2004, v. 32, n. 3, p. e27
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- Article
EGFR Mutation-Harboring Lung Cancer Cells Produce CLEC11A with Endothelial Trophic and Tumor-Promoting Activities.
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- Cancers, 2022, v. 14, n. 5, p. 1356, doi. 10.3390/cancers14051356
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- Article
MCP-1 as an Effector of IL-31 Signaling in Familial Primary Cutaneous Amyloidosis.
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- Journal of Investigative Dermatology, 2013, v. 133, n. 5, p. 1375, doi. 10.1038/jid.2012.484
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- Article
Genomic profiling with whole‐exome sequencing revealed distinct mutations and novel pathways in Asian melanoma.
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- Journal of Dermatology, 2022, v. 49, n. 12, p. 1299, doi. 10.1111/1346-8138.16579
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- Article
High-Throughput Sequencing of Complementarity Determining Region 3 in the Heavy Chain of B-Cell Receptor in Renal Transplant Recipients: A Preliminary Report.
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- Journal of Clinical Medicine, 2022, v. 11, n. 11, p. 2980, doi. 10.3390/jcm11112980
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- Article
A Novel BTK Gene Mutation in a Child With Atypical X-Linked Agammaglobulinemia and Recurrent Hemophagocytosis: A Case Report.
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- Frontiers in Immunology, 2019, p. 1, doi. 10.3389/fimmu.2019.01953
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- Article
Protein O-fucosyltransferase-1 mutation in familial Dowling-Degos Disease concomitant with atopic dermatitis.
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- Dermatologica Sinica, 2022, v. 40, n. 4, p. 251, doi. 10.4103/1027-8117.359341
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- Article
Selective Retention of an Inactive Allele of the DKK2 Tumor Suppressor Gene in Hepatocellular Carcinoma.
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- PLoS Genetics, 2016, v. 12, n. 5, p. 1, doi. 10.1371/journal.pgen.1006051
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- Article