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Genome-wide association study identifies novel susceptible loci and evaluation of polygenic risk score for chronic obstructive pulmonary disease in a Taiwanese population.
- Published in:
- BMC Genomics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12864-024-10526-5
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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
Acupuncture Decreases Risk of Hypertension in Patients with Chronic Spontaneous Urticaria in Taiwan: A Nationwide Study.
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- Healthcare (2227-9032), 2023, v. 11, n. 10, p. 1510, doi. 10.3390/healthcare11101510
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- Article
Genetic Testing in Children with Developmental and Epileptic Encephalopathies: A Review of Advances in Epilepsy Genomics.
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- Children, 2023, v. 10, n. 3, p. 556, doi. 10.3390/children10030556
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- Article
CD3+CD56+ T Lymphocytes Are Associated With ER Stress and Inflammasome Activation in Type 1 Diabetes.
- Published in:
- In Vivo, 2022, v. 36, n. 5, p. 2083, doi. 10.21873/invivo.12934
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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
Genetic factors of idiopathic central precocious puberty and their polygenic risk in early puberty.
- Published in:
- European Journal of Endocrinology, 2021, v. 185, n. 4, p. 441, doi. 10.1530/EJE-21-0424
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- Article
Genetic Analysis of Acid β-Glucosidase in Patients with Multiple Myeloma from Central Taiwan: A Small-Cohort Case-Control Study.
- Published in:
- Biomedicine Hub, 2021, v. 6, n. 3, p. 1, doi. 10.1159/000519704
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- Article
Is Preterm Birth a Risk Factor for Subsequent Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder in Children with Febrile Seizure?—A Retrospective Study.
- Published in:
- Life (2075-1729), 2021, v. 11, n. 8, p. 854, doi. 10.3390/life11080854
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- Article
Effects of Acrylamide-Induced Vasorelaxation and Neuromuscular Blockage: A Rodent Study.
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- Toxics, 2021, v. 9, n. 6, p. 117, doi. 10.3390/toxics9060117
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- Article
Association Between Kawasaki Disease and Childhood Epilepsy: A Nationwide Cohort Study in Taiwan.
- Published in:
- Frontiers in Neurology, 2021, v. 11, p. N.PAG, doi. 10.3389/fneur.2021.627712
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- Article
Author Correction: NT5C2 methylation regulatory interplay between DNMT1 and insulin receptor in type 2 diabetes.
- Published in:
- 2021
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- Publication type:
- Correction Notice
NT5C2 methylation regulatory interplay between DNMT1 and insulin receptor in type 2 diabetes.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-71336-9
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- Publication type:
- Article
Effects of Multi-Strain Probiotics on Immune Responses and Metabolic Balance in Helicobacter pylori-Infected Mice.
- Published in:
- Nutrients, 2020, v. 12, n. 8, p. 2476, doi. 10.3390/nu12082476
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- Article
Heterogeneous neurodevelopmental disorders in children with Kawasaki disease: what is new today?
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- 2019
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- Publication type:
- journal article
Impact of Active Surface Area on Performance and Reliability of Tri-gate FinFET.
- Published in:
- Sensors & Materials, 2019, v. 31, n. 7, Part 1, p. 2237, doi. 10.18494/SAM.2019.2209
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- Publication type:
- Article
Epilepsy and Neurodevelopmental Outcomes in Children With Etiologically Diagnosed Central Nervous System Infections: A Retrospective Cohort Study.
- Published in:
- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00528
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- Publication type:
- Article
Epileptic spasms in PPP1CB-associated Noonan-like syndrome: a case report with clinical and therapeutic implications.
- Published in:
- 2018
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- Publication type:
- journal article
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
- Published in:
- Human Mutation, 2017, v. 38, n. 5, p. 540, doi. 10.1002/humu.23186
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- Publication type:
- Article
Modification of Mechanical Properties, Polymerization Temperature, and Handling Time of Polymethylmethacrylate Cement for Enhancing Applicability in Vertebroplasty.
- Published in:
- BioMed Research International, 2016, v. 2016, p. 1, doi. 10.1155/2016/7901562
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- Publication type:
- 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
Genetic screening of the makorin ring finger 3 gene in girls with idiopathic central precocious puberty.
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- Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 3, p. e93, doi. 10.1515/cclm-2015-0408
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- Publication type:
- Article
Deletion of Exon 4 in the N-Acetylgalactosamine-4-Sulfatase Gene in a Taiwanese Patient with Mucopolysaccharidosis Type VI.
- Published in:
- Tohoku Journal of Experimental Medicine, 2015, v. 235, n. 4, p. 267, doi. 10.1620/tjem.235.267
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- Publication type:
- 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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- Publication type:
- Article
Association study in Taiwanese girls with precocious puberty.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 1/2, p. 103, doi. 10.1515/JPEM.2011.084
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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
FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndrome.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2010, v. 48, n. 4, p. 485, doi. 10.1515/CCLM.2010.100
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- Publication type:
- Article
Lysine racemase: a novel non-antibiotic selectable marker for plant transformation.
- Published in:
- Plant Molecular Biology, 2010, v. 72, n. 1-2, p. 1, doi. 10.1007/s11103-009-9558-y
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- Publication type:
- Article
Asymmetrically simultaneous synthesis of L-homophenylalanine and N<sup>6</sup>-protected-2-oxo-6-amino-hexanoic acid by engineered Escherichia coli aspartate aminotransferase.
- Published in:
- Biotechnology Progress, 2009, v. 25, n. 6, p. 1637, doi. 10.1002/btpr.272
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- Publication type:
- Article
Analysis of urinary nucleosides as helper tumor markers in hepatocellular carcinoma diagnosis.
- Published in:
- Rapid Communications in Mass Spectrometry: RCM, 2009, v. 23, n. 11, p. 1543, doi. 10.1002/rcm.4034
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- Publication type:
- Article
Rapid screening assay of trimethylaminuria in urine with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
- Published in:
- Rapid Communications in Mass Spectrometry: RCM, 2007, v. 21, n. 12, p. 1915, doi. 10.1002/rcm.3043
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- Publication type:
- Article
Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots.
- Published in:
- 2002
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- Publication type:
- journal article
Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots.
- Published in:
- Rapid Communications in Mass Spectrometry: RCM, 2001, v. 15, n. 22, p. 2145, doi. 10.1002/rcm.493
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- Publication type:
- Article
Identification of a polymorphism (D168N) in the XRP2 gene in Chinese.
- Published in:
- Human Mutation, 2001, v. 17, n. 4, p. 354, doi. 10.1002/humu.43
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- Publication type:
- Article
Identification of a polymorphism (G83S) in the TWIST gene in Taiwanese.
- Published in:
- Human Mutation, 2000, v. 16, n. 5, p. 448, doi. 10.1002/1098-1004(200011)16:5<448::AID-HUMU21>3.0.CO;2-#
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- Publication type:
- Article
Identification of a polymorphism (D366H) in the endoglin gene in Chinese.
- Published in:
- Human Mutation, 2000, v. 15, n. 6, p. 583, doi. 10.1002/1098-1004(200006)15:6<583::AID-HUMU23>3.0.CO;2-#
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- Publication type:
- Article