المؤلفون: Coll Martínez, Bernat

المساهمون: University/Department: Universitat Ramon Llull. Departament de Bioenginyeria

مرشدي الرسالة: Crosas Navarro, Bernat, Faijes Simona, Magda

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Proteasome, SUMO, Protac, Lid, Rpn5, PSMD12, IMPDH2, Targeted, Protein, Degradation, Ciències naturals, químiques, físiques i matemàtiques

Time: 616.9

وصف الملف: application/pdf

URL الوصول: http://hdl.handle.net/10803/674248

المؤلفون: Lv, Junqi^{Aff1, IDs13258023014845_cor1}, Ma, Shengmao, Wang, Xiaowen, Dang, Jifang, Ma, Fuchun

المصدر: Genes & Genomics. 46(3):263-277

المؤلفون: Xi Lv, Ran Chen, Taizhen Liang, Haojie Peng, Qiannan Fang, Shiqi Xiao, Sen Liu, Meilin Hu, Fei Yu, Lixue Cao, Yiwen Zhang, Ting Pan, Zhihui Xi, Yao Ding, Linyuan Feng, Tao Zeng, Wenjing Huang, Hui Zhang, Xiancai Ma

المصدر: mBio, Vol 15, Iss 3 (2024)

مصطلحات موضوعية: NSP6, ACE2, exosomes, SARS-CoV-2, CD63, PSMD12, Microbiology, QR1-502

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2150-7511

URL الوصول: https://doaj.org/article/219a4ca67a7843a7bb6fab61ad524902

المؤلفون: ZHANG Xuelei, HE Qinyu, ZHANG Xiwen, CHEN Lifen, DONG Zhiya

المصدر: Zhenduanxue lilun yu shijian, Vol 22, Iss 01, Pp 58-63 (2023)

مصطلحات موضوعية: stankiewicz-isidor syndrome, psmd12 gene, genotype, clinical phenotype, Medicine

وصف الملف: electronic resource

Relation: https://www.qk.sjtu.edu.cn/jdcp/fileup/1671-2870/PDF/1688631606057-1746152657.pdf; https://doaj.org/toc/1671-2870

URL الوصول: https://doaj.org/article/d4b3e51e83dd469983cd78c376c78643

المؤلفون: Li, Xiaocheng, Qiao, Ming, Zhou, Yan, Peng, Yan, Wen, Gang, Xie, Chenchen, Zhang, Yamei^{Aff5, IDs10020024008703_cor7}

المصدر: Molecular Medicine. 30(1)

المؤلفون: Hanpu Zhang, Chenyuan Li, Shichong Liao, Yi Tu, Shengrong Sun, Feng Yao, Zhiyu Li, Zhong Wang

المصدر: Cancer Biology & Therapy, Vol 23, Iss 1, Pp 1-11 (2022)

مصطلحات موضوعية: psmd12, kif15, mek, erk, hepatocellular carcinoma, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1538-4047; https://doaj.org/toc/1555-8576

URL الوصول: https://doaj.org/article/4818dd66f2db46008a876e186a5932ab

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Küry, Sébastien, Besnard, Thomas, Ebstein, Frédéric, Khan, Tahir N, Gambin, Tomasz, Douglas, Jessica, Bacino, Carlos A, Craigen, William J, Sanders, Stephan J, Lehmann, Andrea, Latypova, Xénia, Khan, Kamal, Pacault, Mathilde, Sacharow, Stephanie, Glaser, Kimberly, Bieth, Eric, Perrin-Sabourin, Laurence, Jacquemont, Marie-Line, Cho, Megan T, Roeder, Elizabeth, Denommé-Pichon, Anne-Sophie, Monaghan, Kristin G, Yuan, Bo, Xia, Fan, Simon, Sylvain, Bonneau, Dominique, Parent, Philippe, Gilbert-Dussardier, Brigitte, Odent, Sylvie, Toutain, Annick, Pasquier, Laurent, Barbouth, Deborah, Shaw, Chad A, Patel, Ankita, Smith, Janice L, Bi, Weimin, Schmitt, Sébastien, Deb, Wallid, Nizon, Mathilde, Mercier, Sandra, Vincent, Marie, Rooryck, Caroline, Malan, Valérie, Briceño, Ignacio, Gómez, Alberto, Nugent, Kimberly M, Gibson, James B, Cogné, Benjamin, Lupski, James R, Stessman, Holly AF, Eichler, Evan E, Retterer, Kyle, Yang, Yaping, Redon, Richard, Katsanis, Nicholas, Rosenfeld, Jill A, Kloetzel, Peter-Michael, Golzio, Christelle, Bézieau, Stéphane, Stankiewicz, Paweł, Isidor, Bertrand

المصدر: American Journal of Human Genetics. 100(2)

مصطلحات موضوعية: Biochemistry and Cell Biology, Bioinformatics and Computational Biology, Biological Sciences, Neurosciences, Congenital Structural Anomalies, Dental/Oral and Craniofacial Disease, Biotechnology, Genetics, Intellectual and Developmental Disabilities (IDD), Human Genome, Pediatric, Brain Disorders, 2.1 Biological and endogenous factors, Aetiology, Adolescent, Animals, Child, Child, Preschool, DNA Copy Number Variations, Disease Models, Animal, Down-Regulation, Female, Gene Deletion, Humans, Infant, Intellectual Disability, Male, Microcephaly, Neurodevelopmental Disorders, Polymorphism, Single Nucleotide, Proteasome Endopeptidase Complex, Zebrafish, PSMD12, RPN5, intellectual disability, proteasome 26S, syndromic neurodevelopmental disorder, ubiquitin, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/4s2493nh

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.