المؤلفون: Manjula Gorre, Pranavchand Rayabarapu, Sriteja Reddy Battini, Kumuda Irgam, Mohan Reddy Battini

المصدر: BMC Cardiovascular Disorders, Vol 22, Iss 1, Pp 1-12 (2022)

مصطلحات موضوعية: Coronary artery disease, GWAS, 11q23.3, 9p21.3, SNPs, Indian population, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2261

URL الوصول: https://doaj.org/article/6442d2d0693b45af9bb07abea013a401

المؤلفون: Gorre, Manjula, Rayabarapu, Pranavchand, Battini, Sriteja Reddy, Irgam, Kumuda, Battini, Mohan Reddy^{Aff1, Aff2, IDs12872022025624_cor5}

المصدر: BMC Cardiovascular Disorders. 22(1)

المؤلفون: Shi, Min^Aff4, Reichard, Kaaren K.^Aff4

المساهمون: Cheng, Liang, Series editor^Aff1, George, Tracy I., editor^Aff2, Arber, Daniel A., editor^Aff3

المصدر: Atlas of Bone Marrow Pathology. :199-209

المؤلفون: Tomasz Iwanicki, Joanna Iwanicka, Anna Balcerzyk-Matić, Tomasz Nowak, Katarzyna Mizia-Stec, Paweł Bańka, Artur Filipecki, Jolanta Krauze, Alicja Jarosz, Sylwia Górczyńska-Kosiorz, Anna Ochalska-Tyka, Iwona Żak, Paweł Niemiec

المصدر: Journal of Clinical Medicine, Vol 11, Iss 15, p 4532 (2022)

مصطلحات موضوعية: biological interactions, coronary artery disease, lipid abnormalities, 11q23.3 region, single nucleotide polymorphism, mortality, Medicine

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2077-0383/11/15/4532; https://doaj.org/toc/2077-0383

URL الوصول: https://doaj.org/article/9c351ac284df4e3296187aaf8af2dbdf

المؤلفون: Sanghoon Moon, Young Lee, Sungho Won, Juyoung Lee

المصدر: Human Genomics, Vol 12, Iss 1, Pp 1-10 (2018)

مصطلحات موضوعية: Multiple variants, Multiple traits, Metabolic syndrome, 11q23.3, SIDT2, Medicine, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s40246-018-0180-4; https://doaj.org/toc/1479-7364

URL الوصول: https://doaj.org/article/24bb1f9a964f4f2a99f165189fd55320

المؤلفون: Moon, Sanghoon^Aff1, Lee, Young^{Aff1, Aff2}, Won, Sungho^Aff3, Lee, Juyoung^Aff1

المصدر: Human Genomics. 12(1)

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Sungho Won, Young Ho Lee, Sanghoon Moon, Juyoung Lee

المصدر: Human Genomics, Vol 12, Iss 1, Pp 1-10 (2018)
Human Genomics

مصطلحات موضوعية: Male, 0301 basic medicine, Muscle Proteins, lcsh:Medicine, Type 2 diabetes, Cohort Studies, 0302 clinical medicine, Polymorphism (computer science), Drug Discovery, Genetics, Microfilament Proteins, Middle Aged, Metabolic syndrome, Cardiovascular Diseases, 030220 oncology & carcinogenesis, Nucleotide Transport Proteins, Intronic SNP, Molecular Medicine, Female, Primary Research, Adult, SIDT2, Genotype, lcsh:QH426-470, Multiple traits, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Republic of Korea, medicine, Humans, SNP, Genetic Predisposition to Disease, Molecular Biology, Genetic Association Studies, Aged, Genetic association, lcsh:R, Genetic Variation, Multiple variants, medicine.disease, Introns, Human genetics, lcsh:Genetics, 030104 developmental biology, Diabetes Mellitus, Type 2, 11q23.3

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b15e4266d1cc98ac537602b39e2c3d4c
http://link.springer.com/article/10.1186/s40246-018-0180-4

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المساهمون: Rédei, George P.^Aff1

المصدر: Encyclopedia of Genetics, Genomics, Proteomics and Informatics. :945-945