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1دورية أكاديمية
المساهمون: Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Moleküler Biyoloji ve Genetik Bölümü., orcid:0000-0002-1459-5485, Uz, Elif, 13807893000
مصطلحات موضوعية: Genetics & heredity, Integrin-linked kinase, Craniofacial region, Sequencing data, Cell-migration, Angiogenesis, Mechanism, Complex, Lesions, Growth, Bone, Adaptor proteins, signal transducing, Adult, Alleles, Animals, Bone and bones, Cell movement, Cytoskeletal proteins, Evolution, molecular, Female, Homozygote, Humans, Male, Mutation, Phenotype, Phylogeny, Rac GTP-binding proteins, Rac1 GTP-binding protein
وصف الملف: application/pdf
العلاقة: 108S420; K030-T439; 2011K120020; Makale - Uluslararası Hakemli Dergi; American Journal of Human Genetics; Yurt içi; Yurt dışı; Sanayi; Çetinkaya, A. vd. (2016). "Loss-of-function mutations in ELMO2 cause intraosseous vascular malformation by impeding RAC1 signaling". American Journal of Human Genetics, 99(2), 299-317.; https://doi.org/10.1016/j.ajhg.2016.06.008Test; https://www.sciencedirect.com/science/article/pii/S0002929716302105Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974086Test/; http://hdl.handle.net/11452/29550Test; 000381617200004; 2-s2.0-84979752469; 299; 317; 99
الإتاحة: https://doi.org/10.1016/j.ajhg.2016.06.008Test
http://hdl.handle.net/11452/29550Test
https://www.sciencedirect.com/science/article/pii/S0002929716302105Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974086Test/ -
2دورية أكاديمية
المساهمون: Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Moleküler Biyoloji ve Genetik Bölümü., orcid:0000-0002-1459-5485, Uz, Elif, 13807893000
مصطلحات موضوعية: Genetics & heredity, Integrin-linked kinase, Craniofacial region, Sequencing data, Cell-migration, Angiogenesis, Mechanism, Complex, Lesions, Growth, Bone, Adaptor proteins, signal transducing, Adult, Alleles, Animals, Bone and bones, Cell movement, Cytoskeletal proteins, Evolution, molecular, Female, Homozygote, Humans, Male, Mutation, Phenotype, Phylogeny, Rac GTP-binding proteins, Rac1 GTP-binding protein
وصف الملف: application/pdf
العلاقة: 108S420; K030-T439; 2011K120020; Makale - Uluslararası Hakemli Dergi; American Journal of Human Genetics; Yurt içi; Yurt dışı; Sanayi; Çetinkaya, A. vd. (2016). "Loss-of-function mutations in ELMO2 cause intraosseous vascular malformation by impeding RAC1 signaling". American Journal of Human Genetics, 99(2), 299-317.; https://doi.org/10.1016/j.ajhg.2016.06.008Test; https://www.sciencedirect.com/science/article/pii/S0002929716302105Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974086Test/; http://hdl.handle.net/11452/29550Test; 000381617200004; 2-s2.0-84979752469; 299; 317; 99
الإتاحة: https://doi.org/10.1016/j.ajhg.2016.06.008Test
http://hdl.handle.net/11452/29550Test
https://www.sciencedirect.com/science/article/pii/S0002929716302105Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974086Test/
النص الكامل