نتائج البحث

Dietary acid load adopts the effect of ApoB ins/del genetic variant (rs11279109) on obesity trait, cardiovascular markers, lipid profile, and serum leptin level among patients with diabetes: a cross-sectional study.

• Authors : Esmaeily Z; Department of Nutrition, School of Public Health, Iran University of Medical Sciences, Tehran, Iran.; Abaj F

Subjects: Leptin*/Leptin*/Leptin*/blood ; Leptin*/Leptin*/Leptin*/genetics ; Obesity*/Obesity*/Obesity*/genetics

• Source: Scientific reports [Sci Rep] 2024 Oct 27; Vol. 14 (1), pp. 25650. Date of Electronic Publication: 2024 Oct 27.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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FADS1 Genetic Variant and Omega-3 Supplementation Are Associated with Changes in Fatty Acid Composition in Red Blood Cells of Subjects with Obesity.

• Authors : Reyes-Pérez SD; Doctorado en Ciencias en Biología Molecular en Medicina, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Sierra Mojada 950, Guadalajara 44340, Jalisco, Mexico.; Instituto de Nutrigenética y Nutrigenómica Traslacional, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Sierra Mojada 950, Guadalajara 44340, Jalisco, Mexico.

Subjects: Delta-5 Fatty Acid Desaturase* ; Fatty Acid Desaturases*/Fatty Acid Desaturases*/Fatty Acid Desaturases*/genetics ; Fatty Acids, Omega-3*/Fatty Acids, Omega-3*/Fatty Acids, Omega-3*/administration & dosage

• Source: Nutrients [Nutrients] 2024 Oct 17; Vol. 16 (20). Date of Electronic Publication: 2024 Oct 17.Publisher: MDPI Publishing Country of Publication: Switzerland NLM ID: 101521595 Publication Model: Electronic Cited Medium: Internet ISSN:

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Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes.

• Authors : Mianesaz H; Department of Human Genetics, Medical School, University of Debrecen, Debrecen, Hungary.; Department of Genetics and Molecular Biology, Isfahan University of Medical Sciences, Isfahan, Iran.

Subjects: Diabetes Mellitus*/Diabetes Mellitus*/Diabetes Mellitus*/genetics ; Diabetes Mellitus*/Diabetes Mellitus*/Diabetes Mellitus*/epidemiology; Humans

• Source: Journal of diabetes investigation [J Diabetes Investig] 2024 Oct; Vol. 15 (10), pp. 1390-1402. Date of Electronic Publication: 2024 Jul 06.Publisher: Asian Association for the Study of Diabetes and Blackwell Pub. Asia Country of Publication: Japan NLM ID: 101520702 Publication Model:

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KCNG4 Genetic Variant Linked to Migraine Prevents Expression of KCNB1.

• Authors : Lacroix G; Department of Physics, Université de Montréal, Montréal, QC H3T 1J4, Canada.; Bhat S

Subjects: Migraine Disorders*/Migraine Disorders*/Migraine Disorders*/genetics ; Migraine Disorders*/Migraine Disorders*/Migraine Disorders*/metabolism ; Potassium Channels, Voltage-Gated*/Potassium Channels, Voltage-Gated*/Potassium Channels, Voltage-Gated*/genetics

• Source: International journal of molecular sciences [Int J Mol Sci] 2024 Aug 17; Vol. 25 (16). Date of Electronic Publication: 2024 Aug 17.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Deep learning approaches for non-coding genetic variant effect prediction: current progress and future prospects.

• Authors : Wang X; Monash Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC 3800, Australia.; Monash Data Futures Institute, Monash University, Melbourne, VIC 3800, Australia.

Subjects: Deep Learning* ; Genetic Variation*; Humans

• Source: Briefings in bioinformatics [Brief Bioinform] 2024 Jul 25; Vol. 25 (5).Publisher: Oxford University Press Country of Publication: England NLM ID: 100912837 Publication Model: Print Cited Medium: Internet ISSN:

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Woodhouse-Sakati Syndrome: The New Genetic Variant of DCAF17 In 2 Adult Sisters.

• Authors : Amosova M; Endocrinology Department, Sechenov University, 119991 Moscow, Russia.; Poluboyarinova I

• Source: JCEM case reports [JCEM Case Rep] 2024 Jul 24; Vol. 2 (8), pp. luae130. Date of Electronic Publication: 2024 Jul 24 (Print Publication: 2024).Publisher: Oxford University Press on behalf of the Endocrine Society Country of Publication: England NLM ID: 9918609886906676 Publication Model: eCollection

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Identification and development of Tetra-ARMS PCR-based screening test for a genetic variant of OLA1 (Tyr254Cys) in the human failing heart.

• Authors : Dubey PK; Department of Biomedical Engineering, Schools of Medicine and Engineering, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.; Dubey S

Subjects: Heart Failure*/Heart Failure*/Heart Failure*/genetics ; Polymorphism, Single Nucleotide*; Humans

• Source: PloS one [PLoS One] 2024 Jun 18; Vol. 19 (6), pp. e0293105. Date of Electronic Publication: 2024 Jun 18 (Print Publication: 2024).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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EPHA4 Genetic Variant in a Patient with Epilepsy, Ophthalmological Anomalies, and Neurodevelopmental Delay.

• Authors : Sleptsova M; Genetic Medico-Diagnostic Laboratory 'Genica', Sofia, Bulgaria.; Department of Medical Chemistry and Biochemistry, Medical University Sofia, Sofia, Bulgaria.

• Source: Balkan journal of medical genetics : BJMG [Balkan J Med Genet] 2024 Mar 12; Vol. 26 (2), pp. 65-68. Date of Electronic Publication: 2024 Mar 12 (Print Publication: 2023).Publisher: Sciendo Country of Publication: Poland NLM ID: 9806959 Publication Model: eCollection Cited Medium: Print ISSN: 1311-0160 (Print)

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The Influence of a Genetic Variant in CCDC78 on LMNA -Associated Skeletal Muscle Disease.

• Authors : Mohar NP; Interdisciplinary Graduate Program in Genetics, University of Iowa, Iowa City, IA 52242, USA.; Department of Biochemistry and Molecular Biology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.

Subjects: Lamin Type A*/Lamin Type A*/Lamin Type A*/genetics ; Muscle Proteins*/Muscle Proteins*/Muscle Proteins*/genetics ; Muscle, Skeletal*/Muscle, Skeletal*/Muscle, Skeletal*/pathology

• Source: International journal of molecular sciences [Int J Mol Sci] 2024 Apr 30; Vol. 25 (9). Date of Electronic Publication: 2024 Apr 30.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Genetic variant rs1205 is associated with COVID-19 outcomes: The Strong Heart Study and Strong Heart Family Study.

• Authors : Best LG; Epidemiology Division, Missouri Breaks Industries Research, Inc. Eagle Butte, SD, United States of America.; Pathology Department, University of North Dakota, Grand Forks, ND, United States of America.

Subjects: COVID-19*/COVID-19*/COVID-19*/genetics ; COVID-19*/COVID-19*/COVID-19*/epidemiology ; COVID-19*/COVID-19*/COVID-19*/mortality

• Source: PloS one [PLoS One] 2024 Apr 25; Vol. 19 (4), pp. e0302464. Date of Electronic Publication: 2024 Apr 25 (Print Publication: 2024).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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