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المؤلفون: Fiona Macdonald, Colin E. Willoughby, E Forsythe, Gudrun E. Moore, Marielle Alders, Derek Lim, Jan Maarten Cobben, S Abu Amero, Emma Wakeling, Rebecca L. Poole, Deborah J G Mackay, Sandeep Kumar, Eamonn R. Maher, M. M. van Haelst, I K Temple, Cls Turner, T Tangeraas, SM Price, Jet Bliek
المساهمون: ACS - Amsterdam Cardiovascular Sciences, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Other Research, Human Genetics, ANS - Amsterdam Neuroscience, Paediatric Genetics, Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D), Pediatric surgery
المصدر: Journal of medical genetics, 47(11), 760-768. BMJ Publishing Group
JOURNAL OF MEDICAL GENETICS, 47(11), 760-768. BMJ PUBLISHING GROUP
Wakeling, E L, Amero, S A, Alders, M, Bliek, J, Forsythe, E, Kumar, S, Lim, D H, MacDonald, F, Mackay, D J, Maher, E R, Moore, G E, Poole, R L, Price, S M, Tangeraas, T, Turner, C L S, Van Haelst, M M, Willoughby, C, Temple, I K & Cobben, J M 2010, ' Epigenotype-phenotype correlations in Silver-Russell syndrome ', Journal of Medical Genetics, vol. 47, no. 11, pp. 760-8 . https://doi.org/10.1136/jmg.2010.079111
Journal of Medical Genetics
Journal of Medical Genetics, 47(11), 760-8. BMJ Publishing Groupمصطلحات موضوعية: Male, Pediatrics, RNA, Untranslated, Movement disorders, mUPD7, HYPOMETHYLATION, 11p15 hypomethylation, Intrauterine growth restriction, PHENOTYPE, Epigenesis, Genetic, Prospective Studies, Child, Prospective cohort study, Genetics (clinical), Chromosome 7 (human), Genetics, education.field_of_study, Silver Russell syndrome, CHROMOSOME 11P15, METHYLATION, Uniparental disomy, Potassium Channels, Voltage-Gated, Child, Preschool, IMPRINTING CENTER REGION, Medical genetics, Female, RNA, Long Noncoding, Original Article, imprinting, medicine.symptom, MATERNAL UNIPARENTAL DISOMY, Chromosomes, Human, Pair 7, Adult, medicine.medical_specialty, Adolescent, DYSTONIA, Population, Biology, Genomic Imprinting, Young Adult, ASSISTED REPRODUCTIVE TECHNOLOGY, medicine, Humans, education, Genetic Association Studies, SPECTRUM, Chromosomes, Human, Pair 11, Silver–Russell syndrome, Infant, DNA Methylation, Uniparental Disomy, medicine.disease, Silver-Russell Syndrome, clinical genetics, GROWTH-RETARDATION
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المؤلفون: J.-M. Elalouf, J.R. Mann, S.C. Barton, A.S. Garfield, C. Rasberry, K. Okumura, M.S. Gross, T. Yokomine, Barbara Hutter, C.M. Williamson, A. Ogura, Timothy Bestor, M. Kimura, C. Gallou-Kabani, S. Khosla, G. Cathala, C. Jacquet, P. Stanier, Y. Hayashizaki, H. Soejima, P. Hajkova, J.P. Jais, W. Mills, A. Ward, C. Junien, F. Ishino, R. Ono, N. Wake, C. Ciaudo, G. Mendiratta, J.R. Chaillet, S. Abu-Amero, N. Maeda, T.H. Vu, A. Fabre, L. Estabrooks, L. Steele, C. Shuman, R. Nasser, Y. Sekita, H. Seitz, Colin V. Beechey, M. Irie, Kenichiro Hata, A.C. Smith, M. Tsudzuki, T. Ochiya, T. Kaneko-Ishino, David Monk, Paul D. Soloway, T. Rubin, M.-L. Bortolin, I. Hatada, B. Horsthemke, A. Gossler, N. Miyoshi, R.L. Jirtle, L. Dandolo, N. Aptel, T. Ohhata, M. Tevendale, A. Paoloni-Giacobino, T. Ito, H. Sasaki, B. Cattanach, T. Saito, Yuko Hoki, L. Milligan, D. Haig, B. Tycko, Anne C. Ferguson-Smith, M. Yokoyama, T. Mukai, Takashi Sado, Gavin Kelsey, P.A. Latos, L. Han, T. Forné, A.S. Aylsworth, P.E. Szabó, M.A. Surani, T. Kono, L. Zakin, Jörn Walter, T. Abe, J. Hyo-Jung, G.E. Moore, A. Bourdet, M. Fukasawa, K. Buiting, B.M. Cattanach, Takahiro Arima, M. Spielman, K. Okamura, A. Vigé, J. Cavaillé, T. Kishino, R. Shemer, Tarang Khare, K. Regha, A. Razin, W. Reik, M. Watkins, Robert Feil, K. Higashimoto, E. Heard, A.R. Hoffman, K. Schuster-Gossler, M.T. McDonald, T. Horii, S. Kobayashi, I. Okamoto, Gary F. Moore, R.A. Drewell, Marisa S. Bartolomei, Michael Weber, S. Apostolidou, H. Kobayashi, F.M. Smith, C. Rusniok, M.-A. Ripoche, M. Kaneda, R. Weksberg, S. Morita, H. Wagatsuma, Thomas A. Moore, A. Plagge, P.N. Ray, T. Ikemura, Jo Peters, V. Brahmachari, P. Avner, K.J. Reese, H. Hagège, H. Royo, J. Weissenbach, J. Matsuda, L. Spahn, D. Solter, R.J. Scott, Martina Paulsen, B. Kantor, Y. Kohara, Déborah Bourc'his, C. Suda, A. Gabory, Rebecca J. Holmes, A. Lewis, T. Kohda, Alexandre Wagschal, T. Yoshimizu
المصدر: Cytogenetic and Genome Research. 113:351-352
مصطلحات موضوعية: Botany, Genetics, Zoology, Biology, Molecular Biology, Genetics (clinical)
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3دورية أكاديمية
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4دورية أكاديمية
المؤلفون: Oni, Morohuntodun O., Brito, Miguel, Rotman, Chloe, Archer, Natasha M.
المصدر: International Journal of Molecular Sciences; Jun2024, Vol. 25 Issue 12, p6317, 17p
مصطلحات موضوعية: SICKLE cell anemia, STROKE patients, STROKE, WHITE matter (Nerve tissue), CONSORTIA
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5دورية أكاديمية
المصدر: Biomedicines; Apr2024, Vol. 12 Issue 4, p817, 23p
مصطلحات موضوعية: BLOOD vessels, RETINAL blood vessels, OXIDATIVE stress, AGING, CELLULAR aging
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6دورية أكاديمية
المؤلفون: Velmurugan, Saranya, Pauline, Rashmi, Chandrashekar, Gurudeva, Kulanthaivel, Langeswaran, Subbaraj, Gowtham Kumar
المصدر: Nigerian Postgraduate Medical Journal; Apr-Jun2024, Vol. 31 Issue 2, p93-101, 9p
مصطلحات موضوعية: MACULAR degeneration, AGE factors in disease, SIRTUINS, DISEASE prevalence, BIOMARKERS
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7دورية أكاديمية
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8دورية أكاديمية
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9دورية أكاديمية
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10دورية أكاديمية
المؤلفون: Kumar, Anika, Han, Ying, Oatts, Julius T.
المصدر: PLoS ONE; 2/22/2024, Vol. 19 Issue 2, p1-23, 23p
مصطلحات موضوعية: GENETIC testing, OPEN-angle glaucoma, CONGENITAL glaucoma, GLAUCOMA, GENETIC variation