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

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.)

المؤلفون: Morton, Sarah U.^{Aff13, Aff14}, Neilan, Edward G.^Aff15, Peake, Roy W. A.^Aff16, Shi, Jiahai^Aff17, Schmitz-Abe, Klaus^Aff15, Towne, Meghan^{Aff14, Aff15}, Markianos, Kyriacos^{Aff13, Aff14}, Prabhu, Sanjay P.^Aff18, Agrawal, Pankaj B.^{Aff13, Aff14, Aff15}

المساهمون: Baumgartner, Matthias R., Series editor^Aff1, Patterson, Marc, Series editor^{Aff2, Aff9}, Rahman, Shamima, Series editor^{Aff3, Aff10}, Peters, Verena, Series editor^{Aff4, Aff12}, Morava, Eva, Editor-in-chief^{Aff5, Aff7}, Zschocke, Johannes, Series editor^{Aff6, Aff11}, Baumgartner, Matthias, editor^Aff8

المصدر: JIMD Reports, Volume 35. 35:7-15

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

المؤلفون: Neilan, Edward G., Barsh, Gregory S.

المصدر: Transgenic Research. December 1999 8(6):451-458

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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

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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/

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