Found: 19
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Cysteinyl Leukotrienes Pathway Genes, Atopic Asthma and Drug Response: From Population Isolates to Large Genome-Wide Association Studies.
- Published in:
- Frontiers in Pharmacology, 2016, v. 7, p. 1, doi. 10.3389/fphar.2016.00299
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- Article
G-Protein-Coupled Receptors and Asthma Endophenotypes.
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- Molecular Diagnosis & Therapy, 2006, v. 10, n. 6, p. 353, doi. 10.1007/BF03256212
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- Publication type:
- Article
Cysteinyl-leukotrienes and their receptors in asthma and other inflammatory diseases: Critical update and emerging trends.
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- Medicinal Research Reviews, 2007, v. 27, n. 4, p. 469, doi. 10.1002/med.20071
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- Publication type:
- Article
Innovations in Phenotyping and Diagnostics Create Opportunities for Improved Treatment and Genetic Counseling for Rare Diseases.
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- Genes, 2024, v. 15, n. 6, p. 715, doi. 10.3390/genes15060715
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- Publication type:
- Article
Rare Genetic Developmental Disabilities: Mabry Syndrome (MIM 239300) Index Cases and Glycophosphatidylinositol (GPI) Disorders.
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- Genes, 2024, v. 15, n. 5, p. 619, doi. 10.3390/genes15050619
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- Publication type:
- Article
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3).
- Published in:
- Genes, 2023, v. 14, n. 2, p. 359, doi. 10.3390/genes14020359
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- Publication type:
- Article
OX<sub>1</sub> and OX<sub>2</sub> orexin/hypocretin receptor pharmacogenetics.
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- Frontiers in Neuroscience, 2014, v. 8, p. 1, doi. 10.3389/fnins.2014.00057
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- Article
Variation in the Serotonin Transporter Gene and Alcoholism: Risk and Response to Pharmacotherapy.
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- Alcohol & Alcoholism. Supplement, 2016, v. 51, n. 2, p. 164, doi. 10.1093/alcalc/agv090
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- Publication type:
- Article
Variation in the Serotonin Transporter Gene and Alcoholism: Risk and Response to Pharmacotherapy.
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- Alcohol & Alcoholism, 2016, v. 51, n. 2, p. 164, doi. 10.1093/alcalc/agv090
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- Publication type:
- Article
PHENOTYPIC VARIABILITY IN MABRY SYNDROME: EVIDENCE FOR GENETIC HETEROGENEITY.
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- Bulletin du Girso, 2012, v. 51, n. 1, p. e31
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- Publication type:
- Article
Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome).
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 3, p. 553, doi. 10.1002/ajmg.a.35202
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- Publication type:
- Article
Corrigendum to 'Hyperphosphatasia With Seizures, Neurologic Deficit, and Characteristic Facial Features: Five New Patients With Mabry Syndrome' Am J Med Genet 152A: 1661-1669.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 5, p. 1215, doi. 10.1002/ajmg.a.33680
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- Publication type:
- Article
Metabolic Syndrome features and risk of neural tube defects.
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- BMC Pregnancy & Childbirth, 2007, v. 7, p. 21, doi. 10.1186/1471-2393-7-21
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- Publication type:
- Article
Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia with Mental Retardation Syndrome.
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- Human Mutation, 2016, v. 37, n. 8, p. 737, doi. 10.1002/humu.23006
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- Article
Recessive PIGN Mutations in Fryns Syndrome: Evidence for Genetic Heterogeneity.
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- 2016
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- Publication type:
- Other
Whole genome amplification of buccal cell DNA: genotyping concordance before and after multiple displacement amplification.
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- Clinical Chemistry & Laboratory Medicine, 2005, v. 43, n. 2, p. 157, doi. 10.1515/CCLM.2005.026
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- Publication type:
- Article
Significantly different clinical phenotypes associated with mutations in synthesis and transamidase+remodeling glycosylphosphatidylinositol (GPI)-anchor biosynthesis genes.
- Published in:
- 2020
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- Publication type:
- journal article
Antiseizure effects of the cannabinoids in the amygdala‐kindling model.
- Published in:
- Epilepsia (Series 4), 2021, v. 62, n. 9, p. 2274, doi. 10.1111/epi.16973
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- Publication type:
- Article
Orexin Receptor Multimerization versus Functional Interactions: Neuropharmacological Implications for Opioid and Cannabinoid Signalling and Pharmacogenetics.
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- Pharmaceuticals (14248247), 2017, v. 10, n. 4, p. 79, doi. 10.3390/ph10040079
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- Article