Výsledky vyhľadávania - "MOLECULAR genetics"

Genetic Polymorphisms of Chicken Antiviral Mx1 and TVB Genes in Indigenous and Giriraja Chicken.

Autori: Nihar, S. Kumar, S. Naveen Ruban, Wilfred a ďalší

Zdroj: Indian Journal of Animal Research. Dec2024, Vol. 58 Issue 12, p2052-2056. 5p.

Predmet: Molecular genetics, Genetic polymorphisms, Gene frequency, Poultry diseases, Chickens

Molecular Genetics of Primary Congenital Hypothyroidism: Established and Emerging Contributors to Thyroid Dysgenesis.

Autori: Dermitzaki, Niki Serbis, Anastasios Baltogianni, Maria a ďalší

Zdroj: International Journal of Molecular Sciences. Nov2025, Vol. 26 Issue 22, p10849. 19p.

Predmety: *CONGENITAL hypothyroidism, *MOLECULAR genetics, *GENETIC mutation, *GENES, *ENDOCRINE diseases, *GENETIC disorders, *EMBRYOLOGY

Bioacoustics and molecular genetics reveal a new species of glassfrog, genus Chimerella (Anura: Centrolenidae), from white sand outcrops in the Yungas ecoregion of northeastern Peru.

Autori: VENEGAS, PABLO J. GARCÍA-AYACHI, LUIS A. KÖHLER, JÖRN a ďalší

Zdroj: Salamandra. 10/30/2025, Vol. 61 Issue 4, p407-422. 16p.

Predmety: *BIOACOUSTICS, *MOLECULAR genetics, *AMPHIBIANS, *TAXONOMY, *HERPETOFAUNA, *MOUNTAIN forests, *ANURA

Geografický termín: PERU (Viceroyalty), ANDES

Answer to the letter to the editor of T.T. Aduri, et al. concerning "CALM1 polymorphism in degenerative cervical myelopathy of the Indian cohort" by Maheshwari S, et al. (Eur spine J [2025]; doi:10.1007/s00586-025-09090-7).

Autori: Maheshwari, Shivam Kumar, Vishal

Zdroj: European Spine Journal. Oct2025, Vol. 34 Issue 10, p4805-4808. 4p.

Predmety: *MOLECULAR genetics, *GENETIC polymorphisms, *MATHEMATICAL statistics, *CERVICAL spondylotic myelopathy, *PILOT projects, *SPINAL cord compression, *SAMPLE size (Statistics), *COHORT analysis

Estructura de proteínas mitocondriales y complejos DNA-proteína

Autori: Illanes Vicioso, Ramiro

Prispievatelia: University/Department: Universitat de Barcelona. Facultat de Farmàcia i Ciències de l'Alimentació

Thesis Advisors: Solà Vilarrubias, Maria, Badía Palacín, Josefa

Zdroj: TDX (Tesis Doctorals en Xarxa)

Predmety: Bioquímica, Biochemistry, Genètica molecular, Genética molecular, Molecular genetics, Proteïnes, Proteínas, Proteins, ADN, DNA, Ciències de la Salut

Popis súboru: application/pdf

Prístupová URL adresa: http://hdl.handle.net/10803/690758

Molecular characteristics and antimicrobial susceptibility profiles of bovine mastitis agents in western Türkiye.

Autori: Yalcin, Semiha Ozgen, Arzu Simsir, Metehan

Zdroj: Journal of Veterinary Science. Sep2024, Vol. 25 Issue 5, p1-14. 14p.

Predmet: Bovine mastitis, Molecular genetics, Dairy farms, Polymerase chain reaction, Dairy cattle

Reinterpretació de les variants genètiques identificades en una unitat especialitzada en cardiopaties familiars

Autori: Fernandez Falgueras, Anna

Prispievatelia: University/Department: Universitat de Girona. Departament de Ciències Mèdiques

Thesis Advisors: Brugada, Ramon, Campuzano Larrea, Oscar, Sarquella Brugada, Georgia

Zdroj: TDX (Tesis Doctorals en Xarxa)

Predmety: Mort sobtada, Sudden death, Muerte súbita, Genética molecular, Molecular genetics, Cardiopatia congènita, Congenital heart disease, Cardiopatía congénita, Canalopatia cardíaca, Heart channelopathy, Canalopatía cardíaca, Cromosomes humans, Anomalies, Diagnòstic, Human cromosome abnormalities, Diagnosis, Cromosomas humanos, Anomalías, Diagnóstico, Variants genètiques, Classificació, Reinterpretació, Genetic variant, Classification, Reinterpretation, Variantes genéticas, Classificación, Reinterpretación

Time: 616.1

Popis súboru: application/pdf

Prístupová URL adresa: http://hdl.handle.net/10803/687653

Genetic Factors Contributing to the Development of Polymorphic Teratozoospermia in Humans.

Autori: Kleshchev, M. A. Osadchuk, A. V. Osadchuk, L. V.

Zdroj: Russian Journal of Genetics. Sep2025, Vol. 61 Issue 9, p1041-1057. 17p.

Predmety: *MOLECULAR genetics, *SPERMATOZOA, *MALE infertility, *OXIDATIVE stress, *DIAGNOSIS, *GENETIC risk score, *SEMEN analysis

Transcriptome Analysis Reveals the Mechanism of Early Branching of Balsa (Ochroma lagopus Swartz).

Autori: Qian, Yiwen Bai, Xue Huang, Ping a ďalší

Zdroj: Physiologia Plantarum. Sep/Oct2025, Vol. 177 Issue 5, p1-15. 15p.

Predmety: *PLANT molecular genetics, *PLANT growth regulation, *RNA sequencing, *TREES, *TROPICAL crops, *ANGIOSPERM genetics

Geografický termín: INDONESIA

RAF1‐rearranged spindle cell neoplasm: a clinicopathological and molecular genetic study of six cases with review of the literature.

Autori: Zhu, Peipei Zeng, Xueying Yang, Lirui a ďalší

Zdroj: Histopathology. Sep2025, Vol. 87 Issue 3, p388-396. 9p.

Predmety: *MOLECULAR genetics, *GENE rearrangement, *TUMORS, *SARCOMA, *SCIENTIFIC observation, *MUSCLE tumors, *CLINICAL pathology, *IMMUNOHISTOCHEMISTRY

Special Issue: "Molecular Genetics and Plant Breeding, 5th Edition".

Autori: Du, Hai^1,2 (AUTHOR)

Zdroj: International Journal of Molecular Sciences. Sep2025, Vol. 26 Issue 17, p8439. 4p.

Predmety: *MOLECULAR genetics, *PLANT breeding, *GENETIC variation, *BIOINFORMATICS, *MULTIOMICS, *DROUGHT tolerance, *QUANTITATIVE genetics

BrCER4 Plays a Critical Role in Cuticular Wax Biosynthesis in Purple Cai-Tai (Brassica campestris L. ssp. chinensis var. purpurea).

Autori: Wu, Yifei Liu, Zhiquan Zhou, Xiaobo a ďalší

Zdroj: Plant Molecular Biology Reporter. Sep2025, Vol. 43 Issue 3, p1076-1085. 10p.

Predmety: *MOLECULAR genetics, *GENETIC markers, *GENES, *ANIMAL breeding, *WAXES, *EPIDERMIS, *CHINESE cabbage, *BOK choy

From genes to therapy: navigating the complex landscape of neurofibromatosis management in Canada through advanced diagnostic, targeted therapies, and holistic care.

Autori: Zhao, Victor Shu Cheng¹ (AUTHOR) victorsczhao@yahoo.com

Zdroj: Orphanet Journal of Rare Diseases. 8/5/2025, Vol. 20 Issue 1, p1-8. 8p.

Predmety: *NEUROFIBROMATOSIS, *MOLECULAR genetics, *PATIENT advocacy, *HOLISTIC medicine, *MENTAL health, *INDIVIDUALIZED medicine, *RAPID diagnostic tests

Geografický termín: CANADA

Global spatiotemporal distribution characteristics and regional risk stratification model of acute myeloid leukaemia based on molecular genetics and cytogenetic features.

Autori: Xiao, Jilong Xia, Yuan Yin, Fangjing a ďalší

Zdroj: British Journal of Haematology. Aug2025, Vol. 207 Issue 2, p395-406. 12p.

Predmety: *ACUTE myeloid leukemia, *MOLECULAR genetics, *HUMAN abnormality genetics, *SPATIOTEMPORAL processes, *PROGNOSTIC models, *CYTOGENETICS, *RISK assessment

Geografický termín: EUROPE, ASIA

Milestone Review: The History of Molecular Genetics Analysis of Alzheimer's Disease.

Autori: Hardy, John¹ (AUTHOR) j.hardy@ucl.ac.uk

Zdroj: Journal of Neurochemistry. Jul2025, Vol. 169 Issue 7, p1-4. 4p.

Predmety: *ALZHEIMER'S disease, *MOLECULAR genetics, *PREDICTION models, *MICROGLIA, *AMYLOID, *PATHOGENESIS, *GENETIC profile, *GENOME-wide association studies

The Immunopathogenesis of Adamantiades-Behçet Uveitis: Advances in Understanding of Genetics and Molecular Mechanisms.

Autori: Kozek, Lindsay Klofas Vavvas, Demetrios G.

Zdroj: International Ophthalmology Clinics. Summer2025, Vol. 65 Issue 3, p114-124. 11p.

Predmety: *MOLECULAR genetics, *ANTIGEN processing, *IMMUNOGENETICS, *IMMUNE system, *UVEITIS

Elucidating the clinical and genetic spectrum of inositol polyphosphate phosphatase INPP4A-related neurodevelopmental disorder

Autori: Rawlins, Lettie E. Tajsharghi, Homa Crosby, Andrew H.

Zdroj: Genetics in Medicine. 27(2)

Predmety: Endocytosis, INPP4A, Neurodevelopmental disorder, Phosphoinositide phosphatase, Translation reinitiation, adolescent, adult, amino terminal sequence, Article, biological model, brain size, cell migration, cerebellum disease, cerebellum hypoplasia, child, clinical article, clinical assessment, computer model, contracture, developmental delay, disease severity, exon, female, fibroblast, gene, genetic analysis, genetic variability, genotype phenotype correlation, human, infant, INPP4A gene, intellectual impairment, limb weakness, male, mental disease, microcephaly, molecular genetics, protein function, refractory epilepsy, short stature, visual impairment, Translationell medicin TRIM, Translational Medicine TRIM

Popis súboru: electronic

Prístupová URL adresa: https://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-24847
https://doi.org/10.1016/j.gim.2024.101278

Combining exome sequencing and functional studies to identify causal genes of ultra-rare neurodevelopmental disorders

Autori: Castilla-Vallmanya, Laura

Prispievatelia: University/Department: Universitat de Barcelona. Departament de Genètica, Microbiologia i Estadística

Thesis Advisors: Balcells Comas, Susanna, Urreizti, Roser, Balcells, Susanna

Zdroj: TDX (Tesis Doctorals en Xarxa)

Predmety: Genètica molecular humana, Genética molecular humana, Human molecular genetics, Neurobiologia del desenvolupament, Neurobiología del desarrollo, Developmental neurobiology, Malalties rares, Enfermedades raras, Rare diseases, Diagnòstic, Diagnóstico, Diagnosis, Ciències Experimentals i Matemàtiques

Popis súboru: application/pdf

Prístupová URL adresa: http://hdl.handle.net/10803/674338

Duplicaciones génicas y virulencia en Escherichia coli

Autori: Bernabeu Lorenzo, Manuel

Prispievatelia: University/Department: Universitat de Barcelona. Departament de Genètica, Microbiologia i Estadística

Thesis Advisors: Juárez Giménez, Antonio, Hüttener Queiroz, Màrio

Zdroj: TDX (Tesis Doctorals en Xarxa)

Predmety: Bacteriologia, Bacteriología, Bacteriology, Escheríchia coli, Escherichia coli, Etiologia, Etiología, Etiology, Genètica molecular, Genética molecular, Molecular genetics, Duplicació de l'ADN, Replicación del ADN, DNA replication, Ciències Experimentals i Matemàtiques

Popis súboru: application/pdf

Prístupová URL adresa: http://hdl.handle.net/10803/673720

THE FAULT IN OUR STARS: MOLECULAR GENETICS AND INFORMATION TECHNOLOGY USE.

Autori: Brown, Susan A. Sias, Richard W.

Zdroj: MIS Quarterly. Jun2023, Vol. 47 Issue 2, p483-510. 28p. 2 Diagrams, 7 Charts, 1 Graph.

Predmety: *INFORMATION technology, MOLECULAR genetics, GENOME-wide association studies, EDUCATIONAL attainment, COGNITION, NEUROTICISM, MYOCARDIAL infarction, CORONARY artery disease