Showing results (31-40 of 56) with videos related to
Sort By:
Pageof 6
Journal of Oral Rehabilitation|August 28, 2024
Genetic susceptibility to temporomandibular joint involvement in juvenile idiopathic arthritisP Niibo, T Nikopensius, T Jagomägi, et al.Hernia : the Journal of Hernias and Abdominal Wall Surgery|April 27, 2016
Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal herniaE Mihailov, T Nikopensius, A Reigo, et al.The Journal of Cell Biology|March 1, 1988
A 5S rRNA/L5 complex is a precursor to ribosome assembly in mammalian cellsJ A Steitz, C Berg, J P Hendrick, et al.International Journal of Andrology|July 27, 2007
Androgen receptor gene haplotype is associated with male infertilityM Saare, A Belousova, M Punab, et al.Psychological Medicine|September 26, 2017
Genetic risk scores and family history as predictors of schizophrenia in Nordic registersY Lu, J G Pouget, O A Andreassen, et al.Biomarkers in Medicine|March 15, 2018
Genome-wide analysis of nuclear magnetic resonance metabolites revealed parent-of-origin effect on triglycerides in medium very low-density lipoprotein in PTPRD geneN Pervjakova, V Kukushkina, T Haller, et al.Gene Therapy|May 9, 2008
Correction of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapyJ Kong, S-R Kim, K Binley, et al.European Journal of Human Genetics : EJHG|March 14, 2000
High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delGP Gasparini, R Rabionet, G Barbujani, et al.Journal of Dental Research|April 23, 2013
Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA)T Nikopensius, T Annilo, T Jagomägi, et al.Scientific Reports|June 3, 2015
Comparative study reveals better far-red fluorescent protein for whole body imagingK E Luker, P Pata, I I Shemiakina, et al.Pageof 6