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Scientific Reports|April 21, 2016
Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 functionClaudio R Cortés, Aideen M McInerney-Leo, Ida Vogel, et al.Spinal Cord|February 11, 2015
Common data elements for spinal cord injury clinical research: a National Institute for Neurological Disorders and Stroke projectF Biering-Sørensen, S Alai, K Anderson, et al.Nucleic Acids Research|December 22, 2022
Interfering with nucleotide excision by the coronavirus 3'-to-5' exoribonucleaseRukesh Chinthapatla, Mohamad Sotoudegan, Pankaj Srivastava, et al.Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians, Inc|September 13, 2019
Comparison of multilocus sequence types found among North American isolates of Mycoplasma bovis from cattle, bison, and deer, 2007-2017Karen B Register, Murray D Jelinski, Matthew Waldner, et al.Journal of Neurotrauma|July 1, 1996
MASCIS evaluation of open field locomotor scores: effects of experience and teamwork on reliability. Multicenter Animal Spinal Cord Injury StudyD M Basso, M S Beattie, J C Bresnahan, et al.JCI Insight|August 25, 2022
In vivo base editing by a single i.v. vector injection for treatment of hemoglobinopathiesChang Li, Aphrodite Georgakopoulou, Gregory A Newby, et al.BMJ Open|May 17, 2020
Geographic variation in preventable hospitalisations across Canada: a cross-sectional studyPiotr Wilk, Shehzad Ali, Kelly K Anderson, et al.European Journal of Haematology|October 1, 1996
The bone-marrow infiltration pattern in B-cell chronic lymphocytic leukemia is not an important prognostic factor. Danish CLL Study GroupC H Geisler, K Hou-Jensen, O M Jensen, et al.The Journal of Allergy and Clinical Immunology|December 2, 2019
Upadacitinib in adults with moderate to severe atopic dermatitis: 16-week results from a randomized, placebo-controlled trialEmma Guttman-Yassky, Diamant Thaçi, Aileen L Pangan, et al.Human Mutation|April 3, 2016
Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate FamiliesAideen M McInerney-Leo, Jessica E Harris, Michael Gattas, et al.Pageof 195