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The Journal of Steroid Biochemistry and Molecular Biology|December 1, 1992
Inducibility of the avidin gene by progesterone is suppressed during estrogen-induced cytodifferentiationT Joensuu, A Niemelä, T Kunnas, et al.The International Journal of Developmental Biology|March 1, 1989
Development of progestin-specific response in the chicken oviductP Tuohimaa, T Joensuu, J Isola, et al.Audiology & Neuro-Otology|January 15, 2005
Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patientsR F Plantinga, L Kleemola, P L M Huygen, et al.Scandinavian Journal of Rheumatology|December 10, 2016
Drug survival on tumour necrosis factor inhibitors in patients with rheumatoid arthritis in FinlandK J Aaltonen, J T Joensuu, L Pirilä, et al.Rheumatology (Oxford, England)|June 30, 2016
Cost-effectiveness of biologic compared with conventional synthetic disease-modifying anti-rheumatic drugs in patients with rheumatoid arthritis: a Register studyJaana T Joensuu, Kalle J Aaltonen, Pasi Aronen, et al.Scandinavian Journal of Gastroenterology|January 31, 2004
IL-1 RN 2/2 genotype and simultaneous carriage of genotypes IL-1 RN 2/2 and IL-1beta-511 T/T associated with oesophagitis in Helicobacter pylori-negative patientsO P Koivurova, J M J Karhukorpi, E T Joensuu, et al.Nature Genetics|May 10, 2000
Mutations in KERA, encoding keratocan, cause cornea planaN S Pellegata, J L Dieguez-Lucena, T Joensuu, et al.American Journal of Human Genetics|August 29, 2001
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3T Joensuu, R Hämäläinen, B Yuan, et al.The Journal of Rheumatology|October 17, 2015
Effectiveness and Drug Survival of TNF Inhibitors in the Treatment of Ankylosing Spondylitis: A Prospective Cohort StudyArto V Heinonen, Kalle J Aaltonen, Jaana T Joensuu, et al.Journal of Neurology|December 10, 2015
Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxiaN Schwarz, A Hahn, T Bast, et al.Pageof 4