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Human Molecular Genetics|March 21, 2015
Cardiac deficiency of single cytochrome oxidase assembly factor scox induces p53-dependent apoptosis in a Drosophila cardiomyopathy modelLeticia Martínez-Morentin, Lidia Martínez, Sarah Piloto, et al.Revista Espanola De Enfermedades Digestivas|January 20, 2010
Peutz-Jeghers syndrome and duodeno-jejunal adenocarcinoma--therapeutic implicationsJ A Cienfuegos, J Baixauli, G Zozaya, et al.Transplantation Proceedings|July 31, 2012
Efficacy of laparoscopic approach in the management of early liver transplant complicationsN Pedano, F Rotellar, J Alvarez-Cienfuegos, et al.Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|August 7, 2016
Mid-term oncologic outcome of a novel approach for locally advanced colon cancer with neoadjuvant chemotherapy and surgeryJ Arredondo, J Baixauli, C Pastor, et al.Journal of Medical Genetics|March 3, 2009
Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndromeR A Maselli, J J Ng, J A Anderson, et al.Cells|January 22, 2024
A High-Protein Diet Promotes Atrial Arrhythmogenesis via Absent-in-Melanoma 2 InflammasomeJia Song, Jiao Wu, Dexter J Robichaux, et al.Journal of Cell Science|March 3, 2001
Programmed cell death of keratinocytes culminates in apoptotic secretion of a humectant upon secretagogue action of acetylcholineV T Nguyen, A Ndoye, L L Hall, et al.Clinical Genetics|December 24, 2010
Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNER A Maselli, J Arredondo, O Cagney, et al.Clinical Genetics|March 16, 2013
Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myastheniaR A Maselli, J Arredondo, J Nguyen, et al.Human Molecular Genetics|June 4, 2024
Extended haplotype with rs41524547-G defines the ancestral origin of SCA10Karen N McFarland, Anjana Tiwari, Vera Hashem, et al.Pageof 9