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RNA-seq of peripheral blood mononuclear cells of congenital generalized lipodystrophy type 2 patients.
- Published in:
- Scientific Data, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41597-021-01040-4
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- Article
Genetic Architecture Associated With Familial Short Stature.
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- 2020
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- Publication type:
- journal article
Long, Noncoding RNA SRA Induces Apoptosis of β-Cells by Promoting the IRAK1/LDHA/Lactate Pathway.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 4, p. 1720, doi. 10.3390/ijms22041720
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- Article
FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndrome.
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- Clinical Chemistry & Laboratory Medicine, 2010, v. 48, n. 4, p. 485, doi. 10.1515/CCLM.2010.100
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- Article
The Association of Caveolin-1 Genotypes with Oral Cancer Susceptibility in Taiwan.
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- Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2011, v. 18, n. 5, p. 1431, doi. 10.1245/s10434-010-1483-4
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- Article
A Novel Single Nucleotide Polymorphism in XRCC4 Gene is Associated with Gastric Cancer Susceptibility in Taiwan.
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- Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2008, v. 15, n. 2, p. 514, doi. 10.1245/s10434-007-9674-3
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- Article
Genetic and clinical profiles of spondylocostal dysostosis patients in Taiwan.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 12, p. 3132, doi. 10.1002/ajmg.a.34301
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- Article
Risk of epilepsy in type 1 diabetes mellitus: a population-based cohort study.
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- Diabetologia, 2016, v. 59, n. 6, p. 1196, doi. 10.1007/s00125-016-3929-0
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- Article
Enterovirus infection is associated with an increased risk of childhood type 1 diabetes in Taiwan: a nationwide population-based cohort study.
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- Diabetologia, 2015, v. 58, n. 1, p. 79, doi. 10.1007/s00125-014-3400-z
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- Article
Long‐term safety and efficacy of glucagon‐like peptide‐1 receptor agonists in individuals with obesity and without type 2 diabetes: A global retrospective cohort study.
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- Diabetes, Obesity & Metabolism, 2024, v. 26, n. 11, p. 5222, doi. 10.1111/dom.15869
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- Article
Combining polygenic risk scores and human leukocyte antigen variants for personalized risk assessment of type 1 diabetes in the Taiwanese population.
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- Diabetes, Obesity & Metabolism, 2023, v. 25, n. 10, p. 2928, doi. 10.1111/dom.15187
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- Article
Two Frequent Mutations Associated with the Classic Form of Propionic Acidemia in Taiwan.
- Published in:
- Biochemical Genetics, 2014, v. 52, n. 9/10, p. 415, doi. 10.1007/s10528-014-9657-6
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- Article
Effects of cyproheptadine on body weight gain in children with nonorganic failure to thrive in Taiwan: A hospital-based retrospective study.
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- PLoS ONE, 2021, v. 16, n. 10, p. 1, doi. 10.1371/journal.pone.0258731
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- Article
GBA1 as a risk gene for osteoporosis in the specific populations and its role in the development of Gaucher disease.
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- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03132-x
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- Article
Changing clinical manifestations of Gaucher disease in Taiwan.
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- Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02895-z
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- Article
Your height affects your health: genetic determinants and health-related outcomes in Taiwan.
- Published in:
- 2022
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- Publication type:
- journal article
Genome-wide causal mediation analysis identifies genetic loci associated with uterine fibroids mediated by age at menarche.
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- Human Reproduction, 2022, v. 37, n. 10, p. 2197, doi. 10.1093/humrep/deac136
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- Article
Genome-wide causal mediation analysis identifies genetic loci associated with uterine fibroids mediated by age at menarche.
- Published in:
- 2022
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- Publication type:
- journal article
Nrf2 Activation as a Protective Feedback to Limit Cell Death in High Glucose-Exposed Cardiomyocytes.
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- Journal of Cellular Biochemistry, 2017, v. 118, n. 7, p. 1659, doi. 10.1002/jcb.25785
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- Article
Long-Term Non-Congenital Cardiac and Renal Complications in Down Syndrome: A Study of 32,936 Patients.
- Published in:
- Children, 2023, v. 10, n. 8, p. 1351, doi. 10.3390/children10081351
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- Article
Syndromic ciliopathy: a taiwanese single-center study.
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- BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-024-01880-0
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- Publication type:
- Article
Interleukin (IL)-1beta, IL-1 receptor antagonist, IL-6, IL-8, IL-10, and tumor necrosis factor alpha gene polymorphisms in patients with febrile seizures.
- Published in:
- 2010
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- Publication type:
- journal article
Interleukin (IL)-1β, IL-1 receptor antagonist, IL-6, IL-8, IL-10, and tumor necrosis factor α gene polymorphisms in patients with febrile seizures.
- Published in:
- Journal of Clinical Laboratory Analysis, 2010, v. 24, n. 3, p. 154, doi. 10.1002/jcla.20374
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- Publication type:
- Article
A novel one-base insertion mutation in the retinitis pigmentosa 2 gene in a large X-linked Taiwanese family.
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- Acta Ophthalmologica (1755375X), 2014, v. 92, n. 2, p. e161, doi. 10.1111/aos.12226
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- Publication type:
- Article
Effects of antiepileptic drugs on lipogenic gene regulation and hyperlipidemia risk in Taiwan: a nationwide population-based cohort study and supporting in vitro studies.
- Published in:
- Archives of Toxicology, 2018, v. 92, n. 9, p. 2829, doi. 10.1007/s00204-018-2263-3
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- Article
Adjuvant Probiotics of Lactobacillus salivarius subsp. salicinius AP-32, L. johnsonii MH-68, and Bifidobacterium animalis subsp. lactis CP-9 Attenuate Glycemic Levels and Inflammatory Cytokines in Patients With Type 1 Diabetes Mellitus.
- Published in:
- Frontiers in Endocrinology, 2022, v. 13, p. 1, doi. 10.3389/fendo.2022.754401
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- Article
Dasatinib plus chemotherapy to achieve full donor chimerism and complete molecular remission in a child with relapsed philadelphia chromosome-positive acute lymphoblastic leukemia.
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- Pediatric Blood & Cancer, 2013, v. 60, n. 10, p. 1727, doi. 10.1002/pbc.24618
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- Article
Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
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- Prenatal Diagnosis, 2006, v. 26, n. 10, p. 898, doi. 10.1002/pd.1520
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- Publication type:
- Article
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
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- Human Mutation, 2017, v. 38, n. 5, p. 540, doi. 10.1002/humu.23186
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- Article
A Novel Nonsense Mutation of the Sedlin Gene in a Family with Spondyloepiphyseal Dysplasia Tarda.
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- Human Heredity, 2002, v. 54, n. 1, p. 54, doi. 10.1159/000066694
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- Article
Restrictive dermopathy in a Taiwanese newborn.
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- Dermatologica Sinica, 2016, v. 34, n. 2, p. 112, doi. 10.1016/j.dsi.2015.10.003
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- Article
Improved final predicted height with the injection of leuprolide in children with earlier puberty: A retrospective cohort study.
- Published in:
- PLoS ONE, 2017, v. 12, n. 10, p. 1, doi. 10.1371/journal.pone.0185080
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- Publication type:
- Article