Works matching DE "GENETIC variation"
Results: 5000
Genetic instability of a single exposure to sevoflurane at different concentrations in monitored mice.
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- Environmental & Molecular Mutagenesis, 2025, v. 66, n. 1/2, p. 58, doi. 10.1002/em.22647
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Identification of Genetic Factors Related With Nonhereditary Colorectal Polyposis and Its Recurrence Through Genome‐Wide Association Study.
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- Journal of Gastroenterology & Hepatology, 2025, v. 40, n. 2, p. 482, doi. 10.1111/jgh.16840
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Causal Association Between Female Infertility and Circulating Immune Cells: A Bidirectional Mendelian Randomization Study.
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- American Journal of Reproductive Immunology, 2025, v. 93, n. 3, p. 1, doi. 10.1111/aji.70061
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Heterozygous PNPT1 Variants Cause a Sensory Ataxic Neuropathy.
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- European Journal of Neurology, 2025, v. 32, n. 2, p. 1, doi. 10.1111/ene.70064
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The novel p.A30G SNCA pathogenic variant in Greek patients with familial and sporadic Parkinson's disease.
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- European Journal of Neurology, 2025, v. 32, n. 2, p. 1, doi. 10.1111/ene.16562
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From spastic paraplegia to infantile neurodegenerative disorder: Expanding the phenotypic spectrum associated with biallelic SPAST variants.
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- European Journal of Neurology, 2025, v. 32, n. 1, p. 1, doi. 10.1111/ene.70025
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Cerebrotendinous xanthomatosis: A complex interplay between a clinically and genetically heterogeneous condition.
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- European Journal of Neurology, 2025, v. 32, n. 1, p. 1, doi. 10.1111/ene.70006
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Delineating the genetic landscape of Charcot–Marie–tooth disease in Türkiye: Distinct distribution, rare phenotypes, and novel variants.
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- European Journal of Neurology, 2025, v. 32, n. 1, p. 1, doi. 10.1111/ene.16572
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Phenotype–genotype correlation in X‐linked Charcot‐Marie‐Tooth disease: A French cohort study.
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- European Journal of Neurology, 2025, v. 32, n. 1, p. 1, doi. 10.1111/ene.16523
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Understanding Parkinson disease in Spain: Genetic and clinical insights.
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- European Journal of Neurology, 2025, v. 32, n. 1, p. 1, doi. 10.1111/ene.16499
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A founder variant in the RYR1 gene is associated with hyperCKemia, myalgia and muscle cramps.
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- European Journal of Neurology, 2025, v. 32, n. 1, p. 1, doi. 10.1111/ene.16471
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Genetic and Functional Characterization of DPYD Exon 4 Deletion Common in the Finnish Population.
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- Basic & Clinical Pharmacology & Toxicology, 2025, v. 136, n. 3, p. 1, doi. 10.1111/bcpt.70011
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Effective therapy with simvastatin compound ointment in palmoplantar keratoderma induced by lanosterol synthase (LSS) gene variants.
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- British Journal of Dermatology, 2025, v. 192, n. 4, p. 749, doi. 10.1093/bjd/ljae451
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Genetic Analysis and Reproductive Interventions for Two Rare Families Affected by Severe Haemophilia A.
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- Haemophilia, 2025, v. 31, n. 1, p. 148, doi. 10.1111/hae.15140
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Genetic parameters, genomic prediction, and identification of regulatory regions located on chromosome 14 for weight traits in Nellore cattle.
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- Journal of Animal Breeding & Genetics, 2025, v. 142, n. 2, p. 184, doi. 10.1111/jbg.12895
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Search for germline gene variants in colorectal cancer families presenting with multiple primary colorectal cancers.
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- International Journal of Cancer, 2025, v. 156, n. 7, p. 1393, doi. 10.1002/ijc.35283
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Latent class analysis‐derived classification improves the cancer‐specific death stratification of lymphomas: A large retrospective cohort study.
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- International Journal of Cancer, 2025, v. 156, n. 6, p. 1131, doi. 10.1002/ijc.35219
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Clinical benefit from palbociclib, letrozole and goserelin combination therapy for sweat gland carcinoma with neuroendocrine differentiation (SCAND).
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- Journal of the European Academy of Dermatology & Venereology, 2025, v. 39, n. 3, p. e283, doi. 10.1111/jdv.20276
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Identification of Alzheimer's disease susceptibility genes by integrating eight human brain single‐cell transcriptomes with genome‐wide association studies.
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- Journal of Neurochemistry, 2025, v. 169, n. 1, p. 1, doi. 10.1111/jnc.16276
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NF2 mutation associated with accelerated time to recurrence for older patients with atypical meningiomas.
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- British Journal of Neurosurgery, 2025, v. 39, n. 2, p. 173, doi. 10.1080/02688697.2023.2204927
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Pathogen dynamism and variability of rice yellow mottle virus in Kenya.
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- Phytopathology Research, 2025, v. 7, n. 1, p. 1, doi. 10.1186/s42483-025-00329-1
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Unlocking the Power of Gene Banks: Diversity in Base Growth Temperature Provides Opportunities for Climate‐Smart Agriculture.
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- Food & Energy Security, 2025, v. 14, n. 1, p. 1, doi. 10.1002/fes3.70029
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Association of PADI4 Gene Polymorphisms With Susceptibility to Rheumatoid Arthritis: Evidence From 24 Case–Control Studies.
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- International Journal of Immunogenetics, 2025, v. 52, n. 1, p. 1, doi. 10.1111/iji.12701
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Assessment of genetic diversity, population structure, and gene flow in snow leopards across Ladakh region, India.
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- European Journal of Wildlife Research, 2025, v. 71, n. 2, p. 1, doi. 10.1007/s10344-025-01907-6
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Genetic Variants of the IL‐23/IL‐17 Axis and Its Association With Periodontal Disease: A Systematic Review.
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- Immunity, Inflammation & Disease, 2025, v. 13, n. 2, p. 1, doi. 10.1002/iid3.70147
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Sub‐ and supratherapeutic efavirenz plasma concentrations with risk for HIV therapy failure are mainly genetically explained in Ugandan children: The prospective GENEFA cohort study.
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- British Journal of Clinical Pharmacology, 2025, v. 91, n. 2, p. 464, doi. 10.1111/bcp.16272
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Exploring the contribution of genetic variants to high sunitinib exposure in patients with cancer.
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- British Journal of Clinical Pharmacology, 2025, v. 91, n. 2, p. 297, doi. 10.1111/bcp.16196
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Translating pharmacogenomic sequencing data into drug response predictions—How to interpret variants of unknown significance.
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- British Journal of Clinical Pharmacology, 2025, v. 91, n. 2, p. 252, doi. 10.1111/bcp.15915
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Rivers and spatial distance are drivers of genetic diversity in the South American dwarf caiman (Paleosuchus palpebrosus).
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- Journal of Zoology, 2025, v. 325, n. 1, p. 36, doi. 10.1111/jzo.13226
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The development of orofacial complex in bats: Implications for orofacial clefting.
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- Journal of Anatomy, 2025, v. 246, n. 3, p. 331, doi. 10.1111/joa.14173
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Still rethinking the J‐shaped curve: A commentary on Kember et al., 2024.
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- Alcohol, Clinical & Experimental Research, 2025, v. 49, n. 3, p. 503, doi. 10.1111/acer.15523
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Genetic variation in subpopulations of the European bark beetle Ips typographus L. from three mountains of the Inner Western Carpathians.
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- Sylwan, 2025, v. 169, n. 1, p. 1, doi. 10.26202/sylwan.2024051
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COMPARATIVE ANALYSIS OF GENETIC VARIABILITY AND DIVERSITY IN SPANISH AND VIRGINIA BUNCH PEANUT CULTIVARS.
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- Agricultural Research Journal, 2024, v. 10, n. 6, p. 962, doi. 10.5958/2395-146X.2024.00120.9
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GENETIC VARIABILITY, HERITABILITY AND GENETIC ADVANCE FOR YIELD AND YIELD COMPONENTS IN TEF RECOMBINANT INBRED LINES ACROSS DIVERSE ENVIRONMENTS.
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- Agricultural Research Journal, 2024, v. 10, n. 6, p. 904, doi. 10.5958/2395-146X.2024.00112.3
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The Levels of Serum Leptin and TNF-α in Patients with Alcoholic Liver Disease in the Alcoholic Indian Population.
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- Alcoholism Treatment Quarterly, 2024, v. 42, n. 2, p. 241, doi. 10.1080/07347324.2023.2298505
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Next-generation sequencing in pharmacogenomics – fit for clinical decision support?
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- Expert Review of Clinical Pharmacology, 2024, v. 17, n. 3, p. 213, doi. 10.1080/17512433.2024.2307418
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Causal association between insulin sensitivity index and Alzheimer's disease.
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- Journal of Neurochemistry, 2025, v. 169, n. 2, p. 1, doi. 10.1111/jnc.16254
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Association of serum lipidomic profiles with risk of intracranial aneurysm: A Mendelian randomization study.
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- Journal of Neurochemistry, 2025, v. 169, n. 2, p. 1, doi. 10.1111/jnc.16247
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Morphological and genetic diversity of Eichwald Toad, Bufo eichwaldi in marginal populations of the east and west Caspian Sea lowland.
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- Zoology in the Middle East, 2024, v. 70, n. 3, p. 210, doi. 10.1080/09397140.2024.2378515
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Genetic variability and population genetic structure in the Caucasian Parsley Frog, Pelodytes caucasicus (Boulenger, 1896) based on microsatellite markers.
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- Zoology in the Middle East, 2024, v. 70, n. 3, p. 226, doi. 10.1080/09397140.2024.2378516
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Distribution and genetic diversity of cobitid species in Iran (Teleostei: Cobitidae).
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- Zoology in the Middle East, 2024, v. 70, n. 2, p. 120, doi. 10.1080/09397140.2024.2353906
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New discoveries in the genetics and genomics of systemic juvenile idiopathic arthritis.
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- Expert Review of Clinical Immunology, 2024, v. 20, n. 9, p. 1053, doi. 10.1080/1744666X.2024.2345868
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Lack of host‐associated differentiation in Ixodes scapularis using population genetics.
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- Entomologia Experimentalis et Applicata, 2025, v. 173, n. 2, p. 183, doi. 10.1111/eea.13533
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Germplasm collection and ex situ conservation of Adansonia digitata in Ghana.
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- Biodiversity, 2025, v. 26, n. 1, p. 40, doi. 10.1080/14888386.2024.2442580
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Same, same but different! Exploring children's understandings of within-species variation.
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- Journal of Biological Education (Taylor & Francis Ltd), 2024, v. 58, n. 3, p. 530, doi. 10.1080/00219266.2022.2081244
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Phenotypic and genotyping spectrum of two Iranian cases with RBCK1‐associated polyglucosan body myopathy.
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- Neuropathology, 2025, v. 45, n. 1, p. 48, doi. 10.1111/neup.12993
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MFRP, PRSS56, and MYRF account for 60.5% of a Chinese cohort with nanophthalmos.
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- Clinical & Experimental Ophthalmology, 2025, v. 53, n. 2, p. 194, doi. 10.1111/ceo.14465
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Genetic Variation of Hypothalamic-Pituitary-Adrenal Axis Activity in Farm Animals and Beyond.
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- Neuroendocrinology, 2025, v. 115, n. 2, p. 128, doi. 10.1159/000542831
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Patients with detectable KIT p.D816V in peripheral blood are at high risk for adverse systemic events during venom immunotherapy and treatment failure.
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- Clinical & Translational Allergy, 2025, v. 15, n. 1, p. 1, doi. 10.1002/clt2.70019
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Insights Into Genetic Variations of the OCT1 Gene in Metformin Poor Responders Among Bangladeshi Type 2 Diabetic Patients.
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- Advances in Pharmacological & Pharmaceutical Sciences, 2025, v. 2025, p. 1, doi. 10.1155/adpp/8568658
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