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Nature Communications|April 13, 2018
Somatic activating mutations in MAP2K1 cause melorheostosisHeeseog Kang, Smita Jha, Zuoming Deng, et al.
Nature Medicine|March 12, 2021
A targeted antisense therapeutic approach for Hutchinson-Gilford progeria syndromeMichael R Erdos, Wayne A Cabral, Urraca L Tavarez, et al.
The Journal of Rheumatology|January 6, 2006
Old challenges and new directions in pediatric rheumatologyDavid A Cabral, Ron M Laxer, John Schrader, et al.
Nature Genetics|February 6, 2007
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaWayne A Cabral, Weizhong Chang, Aileen M Barnes, et al.
The Journal of Experimental Medicine|April 2, 2020
Somatic SMAD3-activating mutations cause melorheostosis by up-regulating the TGF-β/SMAD pathwayHeeseog Kang, Smita Jha, Aleksandra Ivovic, et al.
Frontiers in Immunology|March 11, 2021
Different Disease Endotypes in Phenotypically Similar Vasculitides Affecting Small-to-Medium Sized Blood VesselsErin E Gill, Maren L Smith, Kristen M Gibson, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|February 14, 2006
The role of IFN-gamma and IL-4 in gastric mucosa inflammation associated with Helicobacter heilmannii type 1 infectionS M S Cinque, G A Rocha, R Correa-Oliveira, et al.
Arthritis Care & Research|March 31, 2021
Parent-Reported Medication Side Effects and Their Impact on Health-Related Quality of Life in Children With Juvenile Idiopathic ArthritisGaëlle Chédeville, Katherine McGuire, David A Cabral, et al.
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