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Genome-wide association study of BNT162b2 vaccine-related myocarditis identifies potential predisposing functional areas in Hong Kong adolescents.
- Published in:
- BMC Genomic Data, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12863-024-01238-6
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- Publication type:
- Article
Genetics of Hirschsprung's disease.
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- Pediatric Surgery International, 2023, v. 39, n. 1, p. 1, doi. 10.1007/s00383-022-05358-x
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- Publication type:
- Article
Assessing the safety of lipid-modifying medications among Chinese adolescents: a drug-target Mendelian randomization study.
- Published in:
- BMC Medicine, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12916-023-03115-y
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- Publication type:
- Article
DANIEL LIE: In Relation to Rot.
- Published in:
- ArtAsiaPacific, 2023, n. 134, p. 28
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- Publication type:
- Article
Indigo Waves and Other Stories.
- Published in:
- 2023
- By:
- Publication type:
- Exhibition Review
Malicious Mischief.
- Published in:
- 2023
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- Publication type:
- Exhibition Review
COMING ON STRONG.
- Published in:
- ArtAsiaPacific, 2023, p. 82
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- Publication type:
- Article
Isogenic Human-Induced Pluripotent Stem-Cell-Derived Cardiomyocytes Reveal Activation of Wnt Signaling Pathways Underlying Intrinsic Cardiac Abnormalities in Rett Syndrome.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 24, p. 15609, doi. 10.3390/ijms232415609
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- Publication type:
- Article
Whole genome sequencing reveals epistasis effects within RET for Hirschsprung disease.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-24077-w
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- Publication type:
- Article
Forming Communities: Berliner Wege.
- Published in:
- 2022
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- Publication type:
- Exhibition Review
Current Understanding in the Clinical Characteristics and Molecular Mechanisms in Different Subtypes of Biliary Atresia.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 9, p. 4841, doi. 10.3390/ijms23094841
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- Publication type:
- Article
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases.
- Published in:
- Nucleic Acids Research, 2022, v. 50, n. 6, p. e34, doi. 10.1093/nar/gkab1234
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- Publication type:
- Article
Differential vulnerability of hippocampal CA3-CA1 synapses to Aβ.
- Published in:
- Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-022-01350-7
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- Publication type:
- Article
Mendelian randomization analysis of vitamin D in the secondary prevention of hypertensive-diabetic subjects: role of facilitating blood pressure control.
- Published in:
- Genes & Nutrition, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s12263-022-00704-z
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- Publication type:
- Article
Roles of Enteric Neural Stem Cell Niche and Enteric Nervous System Development in Hirschsprung Disease.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 18, p. 9659, doi. 10.3390/ijms22189659
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- Publication type:
- Article
Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system development.
- Published in:
- PLoS Genetics, 2021, v. 17, n. 8, p. 1, doi. 10.1371/journal.pgen.1009698
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- Publication type:
- Article
OWNED BY OTHERS.
- Published in:
- ArtAsiaPacific, 2021, n. 124, p. 32
- By:
- Publication type:
- Article
The functional role of sequentially neuromodulated synaptic plasticity in behavioural learning.
- Published in:
- PLoS Computational Biology, 2021, v. 17, n. 6, p. 1, doi. 10.1371/journal.pcbi.1009017
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- Publication type:
- Article
An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 9, p. 836, doi. 10.1093/hmg/ddab062
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- Publication type:
- Article
Impaired spatial learning and suppression of sharp wave ripples by cholinergic activation at the goal location.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.65998
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- Publication type:
- Article
Animal Welfare and Production Challenges Associated with Pasture Pig Systems: A Review.
- Published in:
- Agriculture; Basel, 2020, v. 10, n. 6, p. 223, doi. 10.3390/agriculture10060223
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- Publication type:
- Article
Berlin.
- Published in:
- 2020
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- Publication type:
- Exhibition Review
High-sensitivity troponin I and B-type natriuretic peptide biomarkers for prediction of cardiovascular events in patients with coronary artery disease with and without diabetes mellitus.
- Published in:
- Cardiovascular Diabetology, 2019, v. 18, n. 1, p. 1, doi. 10.1186/s12933-019-0974-2
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- Publication type:
- Article
Alia Farid: In Lieu of What Was.
- Published in:
- 2019
- By:
- Publication type:
- Exhibition Review
Bani Abidi: They Died Laughing.
- Published in:
- 2019
- By:
- Publication type:
- Exhibition Review
SONG-MING ANG: Prelude to Venice.
- Published in:
- ArtAsiaPacific, 2019, n. 113, p. 68
- By:
- Publication type:
- Article
THE D-TALE, VIDEO ART FROM THE PEARL RIVER DELTA.
- Published in:
- 2019
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- Publication type:
- Exhibition Review
Genetic Regulation of Pigment Epithelium-Derived Factor (PEDF): An Exome-Chip Association Analysis in Chinese Subjects With Type 2 Diabetes.
- Published in:
- 2019
- By:
- Publication type:
- journal article
EKO NUGROHO.
- Published in:
- 2018
- By:
- Publication type:
- Exhibition Review
RASHEED ARAEEN: A RETROSPECTIVE.
- Published in:
- 2018
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- Publication type:
- Exhibition Review
De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 2, p. 351, doi. 10.1093/hmg/ddx406
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- Publication type:
- Article
Actionable secondary findings from whole-genome sequencing of 954 East Asians.
- Published in:
- Human Genetics, 2018, v. 137, n. 1, p. 31, doi. 10.1007/s00439-017-1852-1
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- Publication type:
- Article
2 OR 3 TIGERS.
- Published in:
- 2017
- By:
- Publication type:
- Exhibition Review
An Exome-Chip Association Analysis in Chinese Subjects Reveals a Functional Missense Variant of That Regulates FGF21 Levels.
- Published in:
- 2017
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- Publication type:
- journal article
Exome-chip association analysis reveals an Asian-specific missense variant in PAX4 associated with type 2 diabetes in Chinese individuals.
- Published in:
- Diabetologia, 2017, v. 60, n. 1, p. 107, doi. 10.1007/s00125-016-4132-z
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- Publication type:
- Article
Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes.
- Published in:
- BMC Medical Genomics, 2016, v. 9, p. 1, doi. 10.1186/s12920-016-0236-z
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- Publication type:
- Article
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 23, p. 5265, doi. 10.1093/hmg/ddw333
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- Publication type:
- Article
AYŞE ERKMEN.
- Published in:
- 2016
- By:
- Publication type:
- Exhibition Review
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.
- Published in:
- Nature Communications, 2015, v. 6, n. 12, p. 10206, doi. 10.1038/ncomms10206
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- Publication type:
- Article
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
- Published in:
- Scientific Reports, 2015, p. 16473, doi. 10.1038/srep16473
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- Publication type:
- Article
NEZAKET EKICI.
- Published in:
- 2015
- By:
- Publication type:
- Exhibition Review
Manipulating the Mundane.
- Published in:
- ArtAsiaPacific, 2015, n. 95, p. 57
- By:
- Publication type:
- Article
WORKS IN PROGRESS: PHOTOGRAPHY FROM CHINA.
- Published in:
- 2015
- By:
- Publication type:
- Exhibition Review
Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism
- Published in:
- BMC Medical Genetics, 2015, v. 16, n. 1, p. 49, doi. 10.1186/s12881-015-0189-7
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- Publication type:
- Article
Targeted Next-Generation Sequencing on Hirschsprung Disease: A Pilot Study Exploits DNA Pooling.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 5, p. 381, doi. 10.1111/ahg.12076
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- Publication type:
- Article
Genome-wide copy number variation study in anorectal malformations.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 3, p. 621, doi. 10.1093/hmg/dds451
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- Publication type:
- Article
Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 5, p. 1, doi. 10.1371/journal.pgen.1002687
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- Publication type:
- Article
A gene-based test of association using canonical correlation analysis.
- Published in:
- Bioinformatics, 2012, v. 28, n. 6, p. 845, doi. 10.1093/bioinformatics/bts051
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- Publication type:
- Article
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1184, doi. 10.1093/hmg/ddr550
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- Publication type:
- Article