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S Beken

Showing results (11-20 of 21) with videos related to

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Toxicology in Vitro : an International Journal Published in Association with BIBRA|July 27, 2010
Effect of Extracellular Matrix Composition on the Expression of Glutathione S-transferase Isoenzymes in Organotypical Hepatocyte CulturesS Beken, K Slaus, K De Smet, et al.
Genetic Counseling (Geneva, Switzerland)|September 10, 2015
UHL'S ANOMALY AS A PART OF VACTERL ASSOCIATIONI Ertugrul, V Dogan, S Beken, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
Crisponi syndrome: a new mutation in CRLF1 gene associated with moderate outcomeN Uzunalic, A Zenciroglu, S Beken, et al.
Genetic Counseling (Geneva, Switzerland)|August 19, 2011
A neonatal case of left ventricular noncompaction associated with trisomy 18S Beken, A Cevik, O Turan, et al.
Annals of the New York Academy of Sciences|December 27, 1996
Peroxisome mosaics in the liver of patients and the regulation of peroxisome expression in rat hepatocyte culturesF Roels, T Tytgat, S Beken, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
Papillorenal syndrome with de novo reciprocal translocation t(2;15) (q31; q26)B Aydin, D Dilli, S Beken, et al.
Archives of Toxicology|February 24, 2001
Glutathione transferase activities in renal carcinomas and adjacent normal renal tissues: factors influencing renal carcinogenesis induced by xenobioticsE H Delbanco, H M Bolt, W W Huber, et al.
Reproductive Toxicology (Elmsford, N.Y.)|December 18, 2014
Toward a comparative retrospective analysis of rat and rabbit developmental toxicity studies for pharmaceutical compoundsP T Theunissen, S Beken, G D Cappon, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|May 22, 2012
Prevalence of iron deficiency at the first age of the infants hospitalized in neonatal periodN Altuntas, S Beken, F Kulali, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
A novel mutation of laminin β-2 gene in Pierson syndrome manifested with nephrotic syndrome in the early neonatal periodB Aydin, M S Ipek, F Ozaltin, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Toxicology in Vitro : an International Journal Published in Association with BIBRA|July 27, 2010
Effect of Extracellular Matrix Composition on the Expression of Glutathione S-transferase Isoenzymes in Organotypical Hepatocyte CulturesS Beken, K Slaus, K De Smet, et al.
Genetic Counseling (Geneva, Switzerland)|September 10, 2015
UHL'S ANOMALY AS A PART OF VACTERL ASSOCIATIONI Ertugrul, V Dogan, S Beken, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
Crisponi syndrome: a new mutation in CRLF1 gene associated with moderate outcomeN Uzunalic, A Zenciroglu, S Beken, et al.
Genetic Counseling (Geneva, Switzerland)|August 19, 2011
A neonatal case of left ventricular noncompaction associated with trisomy 18S Beken, A Cevik, O Turan, et al.
Annals of the New York Academy of Sciences|December 27, 1996
Peroxisome mosaics in the liver of patients and the regulation of peroxisome expression in rat hepatocyte culturesF Roels, T Tytgat, S Beken, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
Papillorenal syndrome with de novo reciprocal translocation t(2;15) (q31; q26)B Aydin, D Dilli, S Beken, et al.
Archives of Toxicology|February 24, 2001
Glutathione transferase activities in renal carcinomas and adjacent normal renal tissues: factors influencing renal carcinogenesis induced by xenobioticsE H Delbanco, H M Bolt, W W Huber, et al.
Reproductive Toxicology (Elmsford, N.Y.)|December 18, 2014
Toward a comparative retrospective analysis of rat and rabbit developmental toxicity studies for pharmaceutical compoundsP T Theunissen, S Beken, G D Cappon, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|May 22, 2012
Prevalence of iron deficiency at the first age of the infants hospitalized in neonatal periodN Altuntas, S Beken, F Kulali, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
A novel mutation of laminin β-2 gene in Pierson syndrome manifested with nephrotic syndrome in the early neonatal periodB Aydin, M S Ipek, F Ozaltin, et al.
Pageof 3