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Publication date
2019 04
Authors
Grigelioniene, G Suzuki, HI Taylan, F Mirzamohammadi, F Borochowitz, ZU Ayturk, UM Tzur, S Horemuzova, E Lindstrand, A Weis, MA Grigelionis, G Hammarsjo, A Marsk, E Nordgren, A Nordenskjold, M Eyre, DR Warman, ML Nishimura, G Sharp, PA Kobayashi, T
Author KI Usernames
Grigelioniene, G|giegri Hammarsjo, A|annaha3 Hammarsjö, A|annaha3 Horemuzova, E|evahor Lindstrand, A|alindst Marsk, E|elipet Nordenskjold, M|magnor Nordenskjöld, M|magnor Nordgren, A|annord Taylan, F|fultay
Pubmed ID
30804514
Journal
Nature medicine
Doctype
Article
KI Connection
Hög
Mesh SV
Bassekvens Broskceller Djur Fenotyp Homozygot Kvinnlig Manlig MikroRNA Människa Möss, inavlade C57BL Möss, mutanta stammar Skelettsjukdomar, utvecklingsbetingade Stamtavla Transkripton
Mesh EN
Base Sequence Bone Diseases, Developmental Chondrocytes Gain of Function Mutation Homozygote Mice, Inbred C57BL Mice, Mutant Strains MicroRNAs Pedigree Phenotype Transcriptome
First date
2019-04-21T07:33:37.658Z