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1دورية أكاديمية
المؤلفون: Brooks, P. J., Miller, Timothy M., Revah, Frédéric, Suh, Junghae, Garrison, Bradley R., Starke, Lawrence C., MacLachlan, Timothy K., Neilan, Edward G., Raychaudhuri, Gopa, Kassim, Sadik H., Dehdashti, Jean, Rutter, Joni L.
المصدر: Nature Reviews Drug Discovery. 23(3):157-158
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2دورية أكاديمية
المؤلفون: Sen, Anando, Hedley, Victoria, Degraeuwe, Eva, Hirschfeld, Steven, Cornet, Ronald, Walls, Ramona, Owen, John, Robinson, Peter N., Neilan, Edward G., Liener, Thomas, Nisato, Giovanni, Modi, Neena, Woodworth, Simon, Palmeri, Avril, Gaentzsch, Ricarda, Walsh, Melissa, Berkery, Teresa, Lee, Joanne, Persijn, Laura, Baker, Kasey
المصدر: Data (2306-5729); Apr2024, Vol. 9 Issue 4, p55, 18p
مصطلحات موضوعية: EDUCATION conferences, CHILD patients, PEDIATRICS, DATA dictionaries, METADATA, HUMAN phenotype
الشركة/الكيان: NATIONAL Cancer Institute (U.S.)
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3كتاب إلكتروني
المؤلفون: Morton, Sarah U.Aff13, Aff14, Neilan, Edward G.Aff15, Peake, Roy W. A.Aff16, Shi, JiahaiAff17, Schmitz-Abe, KlausAff15, Towne, MeghanAff14, Aff15, Markianos, KyriacosAff13, Aff14, Prabhu, Sanjay P.Aff18, Agrawal, Pankaj B.Aff13, Aff14, Aff15
المساهمون: Baumgartner, Matthias R., Series editorAff1, Patterson, Marc, Series editorAff2, Aff9, Rahman, Shamima, Series editorAff3, Aff10, Peters, Verena, Series editorAff4, Aff12, Morava, Eva, Editor-in-chiefAff5, Aff7, Zschocke, Johannes, Series editorAff6, Aff11, Baumgartner, Matthias, editorAff8
المصدر: JIMD Reports, Volume 35. 35:7-15
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4دورية أكاديمية
المؤلفون: Kimonis, Virginia E, Mehta, Sarju G, Fulchiero, Erin C, Thomasova, Dana, Pasquali, Marzia, Boycott, Kym, Neilan, Edward G, Kartashov, Alex, Forman, Mark S, Tucker, Stuart, Kimonis, Katerina, Mumm, Steven, Whyte, Michael P, Smith, Charles D, Watts, Giles DJ
المصدر: American Journal of Medical Genetics Part A, vol 146A. (6)
مصطلحات موضوعية: Intellectual and Developmental Disabilities (IDD), Neurodegenerative, Muscular Dystrophy, Dementia, Brain Disorders, Neurosciences, Genetics, Rare Diseases, Aging, Acquired Cognitive Impairment, 2.1 Biological and endogenous factors, Aetiology, Neurological, Musculoskeletal, Adenosine Triphosphatases, Adult, Cell Cycle Proteins, Cross-Sectional Studies, Family, Female, Humans, Inclusion Bodies, Male, Middle Aged, Muscle, Skeletal, Muscular Diseases, Osteitis Deformans, Pedigree, Retrospective Studies, Valosin Containing Protein, autosomal dominant, hereditary inclusion body myopathy, limb-girdle muscular dystrophy, Paget disease of bone, frontotemporal dementia, chromosome 9p13.3-12, VCP, Clinical Sciences
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/3t13p9jp
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5دورية أكاديمية
المؤلفون: Neilan, Edward G., Barsh, Gregory S.
المصدر: Transgenic Research. December 1999 8(6):451-458
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6دورية أكاديمية
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7
المؤلفون: Deegan, Patrick, Murphy, Elaine, Rahman, Yusof, EZGÜ, FATİH SÜHEYL, Smolka, Vratislav, Quinn, Anthony G., Rojas-Caro, Sandra, Eckert, Stephen, Yang, Yijun, Balwani, Manisha, Burton, Barbara, Baric, Ivo, Bialer, Martin, Burrow, Thomas A., Camarena Grande, Carmen, ÇOKER, MAHMUT, Consuelo Sanchez, Alejandra, Di Rocco, Maja, Enns, Gregory M., Erbe, Richard W., Zeniya, Mikio, Wood, Marnie, Valayannopoulos, Vassili, Taybert, Joanna, Feillet, Francois, Ficicioglu, Can, Furuya, Katryn N., Bernardo Guelbert, Norberto, Kane, John, Kostyleva, Maria, Laukaitis, Christina M., Malinova, Vera, Mengel, Eugen, Neilan, Edward G., Nightingale, Scott, Pastor Rosado, Jose, Peters, Heidi, Scarpa, Maurizio, Schwab, Karl Otfried
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_____10046::fc98c8f4c4dd1ce86e9292ed97c0e4f1
https://avesis.gazi.edu.tr/publication/details/47252bbc-bade-46da-b83a-a75fe99520da/oai -
8دورية أكاديمية
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9
المؤلفون: Poduri, Annapurna, Chopra, Sameer S., Neilan, Edward G., Elhosary, P. Christina, Kurian, Manju A., Meyer, Esther, Barry, Brenda J., Khwaja, Omar S., Salih, Mustafa A. M., Sci, Dr Med, Stödberg, Tommy, Scheffer, Ingrid E., Maher, Eamonn R., Sahin, Mustafa, Wu, Bai-Lin, Med, M, Berry, Gerard T., Walsh, Christopher A., Picker, Jonathan, Kothare, Sanjeev V.
مصطلحات موضوعية: Male, Homozygote, Phospholipase C beta, Humans, Infant, Epilepsies, Partial, Article, Gene Deletion, Pedigree
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::cdc00f1e0e486d836c69d72c6f4f4599
https://europepmc.org/articles/PMC3851296/ -
10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.