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Oncogene
|
July 8, 2014
Autophagy mediates HIF2α degradation and suppresses renal tumorigenesis
X-D Liu, J Yao, D N Tripathi, et al.
Experimental Dermatology
|
January 8, 2016
Identification of two rare and novel large deletions in ITGB4 gene causing epidermolysis bullosa with pyloric atresia
Ángeles Mencía, Marta García, Eva García, et al.
The Journal of Investigative Dermatology
|
August 20, 2015
Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
Carlos J Perez, Lars Mecklenburg, Jean Jaubert, et al.
The British Journal of Dermatology
|
January 30, 2019
Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses
E Chacón-Solano, C León, F Díaz, et al.
American Journal of Human Genetics
|
February 14, 2017
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy
Daniel P S Osborn, Heather L Pond, Neda Mazaheri, et al.
Genome Biology
|
July 18, 2018
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Bram P Prins, Timothy J Mead, Jennifer A Brody, et al.
Page
of 38
Search research articles
Search
Showing results (371-380 of 376) with videos related to
Sort By:
Page
of 38
You have reached the last page of results.
This site can display upto 376 results.
Oncogene
|
July 8, 2014
Autophagy mediates HIF2α degradation and suppresses renal tumorigenesis
X-D Liu, J Yao, D N Tripathi, et al.
Experimental Dermatology
|
January 8, 2016
Identification of two rare and novel large deletions in ITGB4 gene causing epidermolysis bullosa with pyloric atresia
Ángeles Mencía, Marta García, Eva García, et al.
The Journal of Investigative Dermatology
|
August 20, 2015
Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
Carlos J Perez, Lars Mecklenburg, Jean Jaubert, et al.
The British Journal of Dermatology
|
January 30, 2019
Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses
E Chacón-Solano, C León, F Díaz, et al.
American Journal of Human Genetics
|
February 14, 2017
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy
Daniel P S Osborn, Heather L Pond, Neda Mazaheri, et al.
Genome Biology
|
July 18, 2018
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Bram P Prins, Timothy J Mead, Jennifer A Brody, et al.
Page
of 38