檢索結果 - Mohammad Hamid
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Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abn... 由 Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, Andrew Touati, Sara Pajouhanfar, Taghi Baghdadi, Azam Ahmadi Shadmehri, Cecilia Giunta, Marius Kraenzlin, Delfien Syx, Fransiska Malfait, Cristina Has, Su M. Lwin, Razieh Karamzadeh, Lu Liu, Alyson Guy, Mohammad Hamid, Ariana Kariminejad, Sirous Zeinali, John A. McGrath, Jouni Uitto
出版 2018Artigo
相關主題
Medicine
Pathology
Amino acid
Anatomy
Anchoring fibrils
Artificial intelligence
Basement membrane
Biology
Categorization
Computer science
Connective Tissue Disorder
Connective tissue
Convolutional neural network
Deep learning
Disease
Ehlers–Danlos syndrome
Epidermolysis bullosa
Gene
Genetics
Hydroxylysine
Internal medicine
Lamina densa
Lung cancer
Lysine
Missense mutation
Mutation
Phenotype
Pneumonia
Residual neural network