Works matching DE "GENETIC variation"
Results: 5000
Immunohistochemistry‐based molecular subtypes of urothelial carcinoma derive different survival benefit from platinum chemotherapy.
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- Journal of Pathology: Clinical Research, 2025, v. 11, n. 1, p. 1, doi. 10.1002/2056-4538.70017
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- Article
Insights into the genetics of body size in the Bull Terrier.
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.70000
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- Article
Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (Capra hircus).
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13509
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- Article
Unexpected recombination at the polled locus in a horned Holstein calf from the mating of a homozygous polled sire and a heterozygous polled cow.
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13507
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- Article
Assessing genomic diversity and signatures of selection in Qingyuan Wapiti.
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13505
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- Article
Comprehensive genomic analysis and selection signature detection in endangered Beigang pigs using whole‐genome sequencing data.
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13502
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- Article
Single‐step genome‐wide association study reveals candidate genes for body mass index trait in Yunong‐black pigs.
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13501
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- Article
Novel insights into sheep domestication in Southwest Asia based on genome‐wide sequencing.
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13500
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- Article
The genomic landscape of short tandem repeats in cattle.
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13498
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- Article
Genome sequencing and assembly of feral chickens in the wild of Sulawesi, Indonesia.
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13497
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- Article
A TYR‐iffic discovery: Identification of a second TYR variant associated with acromelanism in dogs.
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13496
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- Article
History and genetic diversity of African sheep: Contrasting phenotypic and genomic diversity.
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- Animal Genetics, 2025, v. 56, n. 1, p. 1, doi. 10.1111/age.13488
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- Article
Service evaluation of R90 bleeding and platelet disorders gene panel in thrombocytopenia cases.
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- British Journal of Haematology, 2025, v. 206, n. 3, p. 930, doi. 10.1111/bjh.19947
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- Article
Fibrinogen genotypes and their impact on recurrence of venous thromboembolism and family history: A prospective population‐based study.
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- British Journal of Haematology, 2025, v. 206, n. 2, p. 657, doi. 10.1111/bjh.19999
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- Article
Identification of a GFI1B variant associated with abnormal platelet function and normal platelet count.
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- British Journal of Haematology, 2025, v. 206, n. 2, p. 777, doi. 10.1111/bjh.19964
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- Article
Comparative study of the diversity of amino acids on human leucocyte antigen class II molecules in patients with acquired aplastic anaemia.
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- British Journal of Haematology, 2025, v. 206, n. 2, p. 735, doi. 10.1111/bjh.19899
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- Article
Relevance of the E756del common variant in the PIEZO1 gene for haemolytic anaemia and hepatic iron overload.
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- British Journal of Haematology, 2025, v. 206, n. 1, p. 337, doi. 10.1111/bjh.19886
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- Article
Novel POMT2 variants associated with limb-girdle muscular dystrophy R14: genetic, histological and functional studies.
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- Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03578-7
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- Article
Genome-Related Mechanisms Contributing to Differences in Alzheimer's Disease Incidence Between White and Black Older US Adults.
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- Journal of Racial & Ethnic Health Disparities, 2025, v. 12, n. 2, p. 674, doi. 10.1007/s40615-024-01907-3
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- Article
Associations of polygenic risk scores differentiating attention-deficit hyperactivity disorder from autism spectrum disorder with cognitive and cortical alterations in Schizophrenia patients.
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- European Child & Adolescent Psychiatry, 2025, v. 34, n. 3, p. 1149, doi. 10.1007/s00787-024-02549-w
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- Article
DNAJC13 influences responses of the extended reward system to conditioned stimuli: a genome-wide association study.
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- European Archives of Psychiatry & Clinical Neuroscience, 2025, v. 275, n. 2, p. 499, doi. 10.1007/s00406-024-01905-w
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- Article
Clinical and genetic aspects of Bardet–Biedl syndrome in adults in Norway.
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- Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03641-3
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- Article
Genotype Phenotype Correlation of Renal Tumors in the Cancer Genome Atlas Database.
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- International Journal of Surgical Pathology, 2025, v. 33, n. 2, p. 289, doi. 10.1177/10668969241260236
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- Article
Analysis of Common Alpha‐Globin Gene Abnormalities and Their Effects as Genetic Modifiers in Thai Children With β‐Globin Gene Abnormalities.
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- Anemia (20901267), 2025, v. 2025, n. 1, p. 1, doi. 10.1155/anem/9933808
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- Article
Reinforcements in the face of ongoing threats: a case study from a critically small carnivore population.
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- Animal Conservation, 2025, v. 28, n. 1, p. 49, doi. 10.1111/acv.12945
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- Article
Rare dysfunctional SCN2A variants are associated with malformation of cortical development.
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- Epilepsia (Series 4), 2025, v. 66, n. 3, p. 914, doi. 10.1111/epi.18234
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- Article
SYMPOSIUM: Biological Diversity and Evolution of the Tarweeds (Compositae—Madiinae).
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- American Journal of Botany, 1988, v. 75, n. 6, p. 151, doi. 10.1002/j.1537-2197.1988.tb11211.x
- Publication type:
- Article
CONTRIBUTED PAPERS.
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- American Journal of Botany, 1988, v. 75, n. 6, p. 136, doi. 10.1002/j.1537-2197.1988.tb11208.x
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- Article
SYMPOSIUM: Population Biology of Ferns.
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- American Journal of Botany, 1988, v. 75, n. 6, p. 134, doi. 10.1002/j.1537-2197.1988.tb11207.x
- Publication type:
- Article
SYMPOSIUM: Molecular and Genetic Organization of Plant Chromosomes.
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- American Journal of Botany, 1988, v. 75, n. 6, p. 95, doi. 10.1002/j.1537-2197.1988.tb11200.x
- Publication type:
- Article
Six Chinese patients with propionic acidemia: from asymptomatic to death in the neonatal period.
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- Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03622-6
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- Article
DNAH9 variants in children with post-infectious bronchiolitis/bronchitis obliterans.
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- Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03616-4
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- Article
A novel c.59 C > T variant of the HSD17B10 gene as a possible cause of the neonatal form of HSD10 mitochondrial disease with hepatic dysfunction: a case report and review of the literature.
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- Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-024-03513-2
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- Article
Comprehensive analysis of TMEM9 in human tumors.
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- Discover Oncology, 2025, v. 16, n. 1, p. 1, doi. 10.1007/s12672-025-02040-1
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- Article
A study on dopaminergic and serotonergic genes that have a role in smoking addiction at the DNA level.
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- Experimental Biomedical Research, 2024, v. 7, n. 4, p. 208, doi. 10.30714/j-ebr.2024.225
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- Article
Variability in spruce beetle (Coleoptera: Curculionidae, Scolytinae) adult diapause and evidence for oocyte development prior to winter in a Colorado population.
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- Environmental Entomology, 2025, v. 54, n. 1, p. 154, doi. 10.1093/ee/nvae104
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- Article
Genetic diversity and population structure of Ethiopian Sweet Sorghum [Sorghum bicolor (L.) Moench] germplasms using SSR markers.
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- PLoS ONE, 2025, v. 20, n. 3, p. 1, doi. 10.1371/journal.pone.0316549
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- Article
Genetic diversity and correlation analysis of Indian date palm (Phoenix sylvestris Roxb.): Insights into an underutilized native fruit crop.
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- Journal of Applied Horticulture, 2024, v. 26, n. 4, p. 480, doi. 10.37855/jah.2024.v26i04.91
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- Article
Chromosome-level genome of the brown lacewing Micromus angulatus (Stephens, 1836) (Neuroptera: Hemerobiidae).
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- Scientific Data, 2025, v. 12, n. 1, p. 1, doi. 10.1038/s41597-025-04739-w
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- Article
SHBG Gene Polymorphisms and Their Influence on Serum SHBG, Total and Free Testosterone Concentrations in Men.
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- Journal of Clinical Endocrinology & Metabolism, 2025, v. 110, n. 3, p. e641, doi. 10.1210/clinem/dgae280
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- Article
Characterization of 35 Novel NR5A1/SF-1 Variants Identified in Individuals With Atypical Sexual Development: The SF1next Study.
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- Journal of Clinical Endocrinology & Metabolism, 2025, v. 110, n. 3, p. e675, doi. 10.1210/clinem/dgae251
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- Article
Lessons From Prospective Longitudinal Follow-up of a French APECED Cohort.
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- Journal of Clinical Endocrinology & Metabolism, 2025, v. 110, n. 3, p. e757, doi. 10.1210/clinem/dgae211
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- Article
Molecular epidemiology of Escherichia coli in bloodstream infections from a general hospital in Ningxia, China, 2022–2023.
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- BMC Infectious Diseases, 2025, v. 25, n. 1, p. 1, doi. 10.1186/s12879-025-10658-3
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- Article
Mammalian Species-Specific Resistance to Mammary Cancer.
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- Journal of Mammary Gland Biology & Neoplasia, 2025, v. 30, n. 1, p. 1, doi. 10.1007/s10911-025-09578-4
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- Article
Multiplexed assays of human disease-relevant mutations reveal UTR dinucleotide composition as a major determinant of RNA stability.
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- eLife, 2025, p. 1, doi. 10.7554/eLife.97682
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- Article
Identification of potential susceptibility loci for non-small cell lung cancer through whole genome sequencing in circadian rhythm genes.
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- Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-92083-9
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- Article
Introgression among subgroups is an important driving force for genetic improvement and evolution of the Asian cultivated rice Oryza sativa L.
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- Frontiers in Plant Science, 2025, p. 1, doi. 10.3389/fpls.2025.1535880
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- Article
Biliary, Renal, Neurological, and Skeletal syndrome in a Chinese boy.
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- Pediatric Nephrology, 2025, v. 40, n. 4, p. 947, doi. 10.1007/s00467-024-06591-3
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- Article
Molecular characterization of the heterogeneity of satellite cell populations isolated from an individual Turkey pectoralis major muscle.
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- Frontiers in Physiology, 2025, p. 1, doi. 10.3389/fphys.2025.1547188
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- Article
The novel SERPINC1 missense mutation c.1148 T > A (p.L383H) causes hereditary antithrombin deficiency and thromboembolism in a Chinese family: a case report.
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- 2025
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- Publication type:
- Case Study