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1كتاب إلكتروني
المؤلفون: Perrot, AndreasAff10, Rickert-Sperling, SilkeAff11
المساهمون: Crusio, Wim E., Series EditorAff1, Dong, Haidong, Series EditorAff2, Radeke, Heinfried H., Series EditorAff3, Rezaei, Nima, Series EditorAff4, Steinlein, Ortrud, Series EditorAff5, Xiao, Junjie, Series EditorAff6, Rickert-Sperling, Silke, editorAff7, Kelly, Robert G., editorAff8, Haas, Nikolaus, editorAff9
المصدر: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. 1441:505-534
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2دورية أكاديمية
المؤلفون: Fangfang Nie, Qinfang Zhang, WeiNa Ma, Jun Yan
المصدر: Discover Oncology, Vol 15, Iss 1, Pp 1-11 (2024)
مصطلحات موضوعية: Malignant phenotype, Epithelial-mesenchymal transition, Triple-negative breast cancer, CRKL, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2730-6011
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3دورية أكاديمية
المؤلفون: Liang, Yonggang, Zhang, Xiaoqiang, Peng, Jinhua, Liu, Jing, Chen, He, Guo, ShanxianAff4, Aff5, IDs00432023055861_cor6
المصدر: Journal of Cancer Research and Clinical Oncology. 150(2)
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4دورية أكاديمية
المؤلفون: Bingruo Wu, Brian Wu, Sonia Benkaci, Lijie Shi, Pengfei Lu, Taeju Park, Bernice E. Morrow, Yidong Wang, Bin Zhou
المصدر: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 18 (2023)
مصطلحات موضوعية: Crk, Crkl, endocardial cushion, endocardium, heart valve development, Diseases of the circulatory (Cardiovascular) system, RC666-701
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2047-9980
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5دورية أكاديمية
المؤلفون: Nie, Fangfang, Zhang, Qinfang, Ma, WeiNaAff2, IDs12672024010041_cor3, Yan, JunAff1, IDs12672024010041_cor4
المصدر: Discover Oncology. 15(1)
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6دورية أكاديمية
المؤلفون: Zhao, Yingjie, Diacou, Alexander, Johnston, H Richard, Musfee, Fadi I, McDonald-McGinn, Donna M, McGinn, Daniel, Crowley, T Blaine, Repetto, Gabriela M, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R, Kates, Wendy R, Digilio, M Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne, Moss, Hayley, Owen, Michael J, Murphy, Kieran C, Murphy, Clodagh M, Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J, Shprintzen, Robert J, Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Consortium, International 22q11 2 Brain and Behavior, Antonarakis, Stylianos E, Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P, Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S, Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther DA, Vergaelen, Elfi, Warren, Steve T, Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong, Zwick, Michael, Bearden, Carrie E, Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob AS, Gothelf, Doron, Zackai, Elaine, Agopian, AJ, Gur, Raquel E, Bassett, Anne S, Emanuel, Beverly S, Goldmuntz, Elizabeth, Mitchell, Laura E, Wang, Tao, Morrow, Bernice E
المصدر: American Journal of Human Genetics. 106(1)
مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Epidemiology, Health Sciences, Clinical Research, Human Genome, Heart Disease, Cardiovascular, Pediatric, Aetiology, 2.1 Biological and endogenous factors, Case-Control Studies, Chromosome Deletion, Chromosomes, Human, Pair 22, Cohort Studies, Female, Genome-Wide Association Study, Heart Defects, Congenital, Humans, Linkage Disequilibrium, Male, Phenotype, Polymorphism, Single Nucleotide, Proto-Oncogene Mas, Segmental Duplications, Genomic, International 22q11.2 Brain and Behavior Consortium, CRKL, DiGeorge syndrome, TBX1, chromosome 22q11.2 deletion syndrome, complex trait, congenital heart disease, conotruncal heart defects, copy number variation, genetic association, genetic modifier, haploinsufficiency, 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/38b9f8cx
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7دورية أكاديمية
المصدر: Cancers, Vol 15, Iss 20, p 5033 (2023)
مصطلحات موضوعية: triple-negative breast cancer, USP53, CRKL, deubiquitinase, epithelial–mesenchymal transition, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
وصف الملف: electronic resource
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8دورية أكاديمية
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9دورية أكاديمية
المؤلفون: Dongmei Wang, Limei Tian, Yan Wang, Xiaoli Gao, Hanbo Tang, Junbo Ge
المصدر: ESC Heart Failure, Vol 9, Iss 2, Pp 998-1007 (2022)
مصطلحات موضوعية: circ_0001206, miR‐665, CRKL, Myocardial infarction, Diseases of the circulatory (Cardiovascular) system, RC666-701
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2055-5822
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10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.