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1دورية أكاديمية
المؤلفون: Xin Lin, Xiaofan Ma, Xiaoting Yi, Chao Qu, Fuye Li
المصدر: Frontiers in Public Health, Vol 11 (2023)
مصطلحات موضوعية: job burnout, occupational stress, coping styles, NR3C2 gene, GMDR, Public aspects of medicine, RA1-1270
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fpubh.2023.1237843/fullTest; https://doaj.org/toc/2296-2565Test
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2دورية أكاديمية
المؤلفون: Rima Braukyliene, Ali Aldujeli, Ayman Haq, Laurynas Maciulevicius, Darija Jankauskaite, Martynas Jurenas, Ramunas Unikas, Vytautas Zabiela, Vaiva Lesauskaite, Sandrita Simonyte, Diana Zaliaduonytė
المصدر: International Journal of Environmental Research and Public Health; Volume 20; Issue 1; Pages: 12
مصطلحات موضوعية: NR3C2 gene, acute myocardial infarction, mineralocorticoid receptor, rs5522, rs4635799, rs2070950
جغرافية الموضوع: agris
وصف الملف: application/pdf
العلاقة: Global Health; https://dx.doi.org/10.3390/ijerph20010012Test
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3دورية أكاديمية
المؤلفون: Su Jin Kim, Dasom Park, Woori Jang, Juyoung Lee
المصدر: Children; Volume 8; Issue 12; Pages: 1090
مصطلحات موضوعية: pseudohypoaldosteronism, mineralocorticoid receptors, NR3C2 gene, dehydration, hyponatremia, hyperkalemia, neonate
وصف الملف: application/pdf
العلاقة: Pediatric Nephrology; https://dx.doi.org/10.3390/children8121090Test
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4دورية أكاديمية
المؤلفون: Jan Terock, Sandra Van der Auwera, Deborah Janowitz, Katharina Wittfeld, Alexander Teumer, Hans J. Grabe
المصدر: Molecular Genetics & Genomic Medicine, Vol 8, Iss 9, Pp n/a-n/a (2020)
مصطلحات موضوعية: cognitive decline, mineralocorticoid receptor, NR3C2 gene, rs2070951, rs5522, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2324-9269Test
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5دورية أكاديمية
المؤلفون: Hyun Ah Jeong, Yoon Kyoung Park, Yeong Sang Jung, Myung-Hyun Nam, Hyo-Kyoung Nam, Kee Hyoung Lee, Young-Jun Rhie
المصدر: Annals of Pediatric Endocrinology & Metabolism, Vol 20, Iss 4, Pp 230-234 (2015)
مصطلحات موضوعية: Pseudohypoaldosteronism, NR3C2 gene, Mineralocorticoid receptors, Hyponatremia, Hyperkalemia, Pediatrics, RJ1-570
وصف الملف: electronic resource
العلاقة: http://e-apem.org/upload/pdf/apem-20-230.pdfTest; https://doaj.org/toc/2287-1012Test; https://doaj.org/toc/2287-1292Test
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المؤلفون: Dasom Park, Juyoung Lee, Woori Jang, Su Jin Kim
المصدر: Children
Children, Vol 8, Iss 1090, p 1090 (2021)مصطلحات موضوعية: medicine.medical_specialty, Microarray, hyponatremia, Case Report, Pediatrics, RJ1-570, mineralocorticoid receptors, Mineralocorticoid receptor, Polyuria, Internal medicine, Medicine, Exome sequencing, business.industry, Pseudohypoaldosteronism, nutritional and metabolic diseases, pseudohypoaldosteronism, dehydration, NR3C2 gene, medicine.disease, hyperkalemia, Endocrinology, Pediatrics, Perinatology and Child Health, Failure to thrive, medicine.symptom, neonate, business, Hyponatremia, Rare disease
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40dcc7f7c00b37955a9748e5d95b3f70Test
http://europepmc.org/articles/PMC8700017Test -
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المؤلفون: Young Min Kim, Hae Il Cheong, Kim Chan Jong, In Su Choi, YangEunMi
المصدر: Childhood Kidney Diseases. 24:58-61
مصطلحات موضوعية: Genetics, Hyperkalemia, business.industry, medicine, General Earth and Planetary Sciences, NR3C2 Gene, Pseudohypoaldosteronism, medicine.symptom, Hyponatremia, medicine.disease, business, Novel mutation, General Environmental Science
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::1011e0bf797f4af8c4d719a75c56d27bTest
https://doi.org/10.3339/jkspn.2020.24.1.58Test -
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المؤلفون: Hans J. Grabe, Sandra Van der Auwera, Jan Terock, Katharina Wittfeld, Deborah Janowitz, Alexander Teumer
المصدر: Molecular Genetics & Genomic Medicine, Vol 8, Iss 9, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine
Molecular genetics & genomic medicine 8(9), e1345 (2020). doi:10.1002/mgg3.1345مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, lcsh:QH426-470, rs2070951, 030105 genetics & heredity, Verbal learning, Polymorphism, Single Nucleotide, 03 medical and health sciences, genetics [Receptors, Mineralocorticoid], Memory, Internal medicine, Genotype, Genetics, Humans, Medicine, Cognitive Dysfunction, ddc:610, Cognitive decline, Allele, Molecular Biology, Genetics (clinical), Aged, mineralocorticoid receptor, Recall, business.industry, Haplotype, genetics [Cognitive Dysfunction], rs5522, Original Articles, NR3C2 gene, Middle Aged, cognitive decline, lcsh:Genetics, Receptors, Mineralocorticoid, 030104 developmental biology, Endocrinology, Haplotypes, Study of Health in Pomerania, Population study, Original Article, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::142834cad776dffb658e00aa40052a81Test
https://doi.org/10.1002/mgg3.1345Test -
9
المؤلفون: Seniye Targen, Ozlen Konu
المصدر: Aldosterone-Mineralocorticoid Receptor-Cell Biology to Translational Medicine
مصطلحات موضوعية: Mutation, 30405 Molecular Medicine, aldosterone, Molecular medicine, InformationSystems_INFORMATIONSTORAGEANDRETRIEVAL, Cancer, The Cancer Genome Atlas, Genomics, FOS: Basic medicine, Computational biology, Biology, medicine.disease, medicine.disease_cause, Genome, Transcriptome, transcriptomics, Mineralocorticoid receptor, medicine, genomics, NR3C2 Gene, Copy-number variation, prognosis, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries), mineralocorticoid receptor, epithelial cancers
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09c3470d1dd881d0ca366a65a6fd5b05Test
http://www.intechopen.com/articles/show/title/investigating-the-role-of-mineralocorticoid-receptor-signaling-in-cancer-biology-in-the-genomic-eraTest -
10دورية أكاديمية
المؤلفون: Mohabati, D., Schellevis, R.L., Dijk, E.H.C. van, Altay, L., Fauser, S., Hoyng, C.B., Jong, E.K. de, Boon, C.J.F., Yzer, S.
المصدر: RETINA, The Journal of Retinal and Vitreous Diseases
مصطلحات موضوعية: acute central serous chorioretinopathy, ARMS2 gene, chronic central serous chorioretinopathy, complement factor H, complement component 4, CFH gene, C4B copy numbers, genetic association, NR3C2 gene
العلاقة: lumc-id: 84094676; https://hdl.handle.net/1887/122669Test