يعرض 1 - 20 نتائج من 230 نتيجة بحث عن '"Alison, M R"', وقت الاستعلام: 0.71s تنقيح النتائج
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    المساهمون: Passman, A M, Haughey, M J, Carlotti, E, Williams, M J, Cereser, B, Lin, M L, Devkumar, S, Gabriel, J P, Gringeri, E, Cillo, U, Russo, F P, Hoare, M, Chinaleong, J, Jansen, M, Wright, N A, Kocher, H M, Huang, W, Alison, M R, Mcdonald, S A C

    مصطلحات موضوعية: Stem cell, clonal expansion, mitochondria

    Relation: info:eu-repo/semantics/altIdentifier/pmid/37088309; info:eu-repo/semantics/altIdentifier/wos/WOS:001044537300001; journal:JOURNAL OF HEPATOLOGY; https://hdl.handle.net/11577/3479370; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85161644875

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    المساهمون: Children's Hospital of Eastern Ontario, CHU Sainte Justine Montréal, Tel Aviv University (TAU), University of California (UC), IRCCS Ospedale Pediatrico Bambino Gesù = Bambino Gesù Children’s Hospital, CHU Pitié-Salpêtrière AP-HP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Medizinische Hochschule Hannover = Hannover Medical School (MHH), BC Children's Hospital Research Institute Vancouver, BC, Canada (BCCHR), University of British Columbia (UBC), The Greenwood Genetic Center, Università degli Studi di Pavia Italia = University of Pavia Italy = Université de Pavie Italie (UNIPV), IRCCS Mondino Foundation

    المصدر: EISSN: 2376-7839 ; Neurology Genetics ; https://hal.sorbonne-universite.fr/hal-03409007 ; Neurology Genetics, 2021, 7 (6), pp.e631. ⟨10.1212/NXG.0000000000000631⟩

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    Academic Journal

    المؤلفون: Radio, Francesca Clementina, Pang, Kaifang, Ciolfi, Andrea, Levy, Michael A., Hernández-García, Andrés, Pedace, Lucia, Pantaleoni, Francesca, Liu, Zhandong, de Boer, Elke, Jackson, Adam, Bruselles, Alessandro, McConkey, Haley, Stellacci, Emilia, Lo Cicero, Stefania, Motta, Marialetizia, Carrozzo, Rosalba, Dentici, Maria Lisa, McWalter, Kirsty, Desai, Megha, Monaghan, Kristin G., Telegrafi, Aida, Philippe, Christophe, Vitobello, Antonio, Au, Margaret, Grand, Katheryn, Sanchez-Lara, Pedro A., Baez, Joanne, Lindstrom, Kristin, Kulch, Peggy, Sebastian, Jessica, Madan-Khetarpal, Suneeta, Roadhouse, Chelsea, MacKenzie, Jennifer J., Monteleone, Berrin, Saunders, Carol J., Jean Cuevas, July K., Cross, Laura, Zhou, Dihong, Hartley, Taila, Sawyer, Sarah L., Monteiro, Fabíola Paoli, Secches, Tania Vertemati, Kok, Fernando, Schultz-Rogers, Laura E., Macke, Erica L., Morava, Eva, Klee, Eric W., Kemppainen, Jennifer, Iascone, Maria, Selicorni, Angelo, Tenconi, Romano, Amor, David J., Pais, Lynn, Gallacher, Lyndon, Turnpenny, Peter D., Stals, Karen, Ellard, Sian, Cabet, Sara, Lesca, Gaetan, Pascal, Joset, Steindl, Katharina, Ravid, Sarit, Weiss, Karin, Castle, Alison M. R., Carter, Melissa T., Kalsner, Louisa, de Vries, Bert B. A., van Bon, Bregje W., Wevers, Marijke R., Pfundt, Rolph, Stegmann, Alexander P. A., Kerr, Bronwyn, Kingston, Helen M., Chandler, Kate E., Sheehan, Willow, Elias, Abdallah F., Shinde, Deepali N., Towne, Meghan C., Robin, Nathaniel H., Goodloe, Dana, Vanderver, Adeline, Sherbini, Omar, Bluske, Krista, Hagelstrom, R. Tanner, Zanus, Caterina, Faletra, Flavio, Musante, Luciana, Kurtz-Nelson, Evangeline C., Earl, Rachel K., Anderlid, Britt-Marie, Morin, Gilles, van Slegtenhorst, Marjon, Diderich, Karin E. M., Brooks, Alice S., Gribnau, Joost, Boers, Ruben G., Finestra, Teresa Robert, Carter, Lauren B., Rauch, Anita, Gasparini, Paolo, Boycott, Kym M., Barakat, Tahsin Stefan, Graham, John M. Jr, Faivre, Laurence, Banka, Siddharth, Wang, Tianyun, Eichler, Evan E., Priolo, Manuela, Dallapiccola, Bruno, Vissers, Lisenka E. L. M., Sadikovic, Bekim, Scott, Daryl A., Holder, Jimmy Lloyd Jr, Tartaglia, Marco

    Relation: https://linkinghub.elsevier.com/retrieve/pii/S0002-9297(21)00015-X; Radio, F. C. et al. (2021) ‘SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.’, American journal of human genetics, 108(3), pp. 502–516. doi:10.1016/j.ajhg.2021.01.015.; https://rde.dspace-express.com/handle/11287/622098; American journal of human genetics; PMC8008487

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    Book

    المؤلفون: Ferrie, Alison M. R.

    المصدر: Methods in Molecular Biology ; Doubled Haploid Technology ; page 103-111 ; ISSN 1064-3745 1940-6029 ; ISBN 9781071613344 9781071613351

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    Book

    المؤلفون: Ferrie, Alison M. R., Ehlert, Zoë

    المصدر: Methods in Molecular Biology ; Doubled Haploid Technology ; page 263-270 ; ISSN 1064-3745 1940-6029 ; ISBN 9781071613306 9781071613313

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    المؤلفون: Davies, Alison M. R.

    المصدر: Taxon, 2005 Aug 01. 54(3), 838-839.

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