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Acta Diabetologica|March 22, 2015
Glycemic control and clinic attendance of emerging adults with type 1 diabetes at a transition care clinicY Levy-Shraga, N Elisha, M Ben-Ami, et al.The Journal of Biological Chemistry|December 30, 1994
A novel C-terminal domain in the thyroid hormone receptor selectively mediates thyroid hormone inhibitionT R Flynn, A N Hollenberg, O Cohen, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1983
Analysis of HLA class I genes with restriction endonuclease fragments: implications for polymorphism of the human major histocompatibility complexD Cohen, P Paul, M P Font, et al.Diabetes|February 1, 1994
Prevalence of mutations in the insulin receptor gene in subjects with features of the type A syndrome of insulin resistanceD E Moller, O Cohen, Y Yamaguchi, et al.Human Gene Therapy|February 24, 1998
Efficient transduction of hemopoietic CD34+ progenitors of human origin using an original retroviral vector derived from Fr-MuLV-FB29: in vitro assessmentO Cohen-Haguenauer, L M Restrepo, M Masset, et al.The Journal of Biological Chemistry|March 12, 2005
Biochemical and biophysical characterization of photosystem I from phytoene desaturase and zeta-carotene desaturase deletion mutants of Synechocystis Sp. PCC 6803: evidence for PsaA- and PsaB-side electron transport in cyanobacteriaJames A Bautista, Fabrice Rappaport, Mariana Guergova-Kuras, et al.Gene Therapy|May 13, 2011
CTF/NF1 transcription factors act as potent genetic insulators for integrating gene transfer vectorsA Gaussin, U Modlich, C Bauche, et al.AIDS Research and Human Retroviruses|January 1, 1987
Antibodies to HIV in Israeli hemophiliacs: relationship between serological profile and disease developmentS Orgad, G Malone, R Zaizov, et al.Presse Medicale (Paris, France : 1983)|March 27, 1993
[Gallium-67 scintigraphy in malignant lymphoma]O Cohen-Haguenauer, P Brice, M Gaci, et al.Journal of Intellectual Disability Research : JIDR|May 22, 2009
The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorderA Holland, J Whittington, O Cohen, et al.Pageof 31