MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels

By Xiong Lan   Catoire Hlne   Dion Patrick   Gaspar Claudia   Lafrenire Ronald G.   Girard Simon L.   Levchenko Anastasia   Rivire Jean-Baptiste   Fiori Laura   St-Onge Judith   Bachand Isabelle   Thibodeau Pascale   Allen Richard   Earley Christopher   Turecki Gustavo   Montplaisir Jacques   Rouleau Guy A.  

Human Molecular Genetics, Vol. 18, Iss. 6, 2009-03 ,pp. : 1065-1074

Oxford University Press

Access to resources Recommend Favorite

Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency

By Friedrich Ulrike   Myers Connie A.   Fritsche Lars G.   Milenkovich Andrea   Wolf Armin   Corbo Joseph C.   Weber Bernhard H.F.  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1387-1399

Oxford University Press

Access to resources Recommend Favorite

Inner ear localization of mRNA and protein products of COCH , mutated in the sensorineural deafness and vestibular disorder, DFNA9

By Robertson N.G.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2493-2500

Oxford University Press

Access to resources Recommend Favorite

mRNA Expression and DNA Methylation Analysis of Serotonin Receptor 2A (HTR2A) in the Human Schizophrenic Brain

By Cheah Sern-Yih   Lawford Bruce R.   Young Ross McD.   Morris Charles P.   Voisey Joanne  

Genes, Vol. 8, Iss. 1, 2017-01 ,pp. : 14-14

MDPI

Access to resources Recommend Favorite

Sequence and mRNA expression of nonclassical SLA class I genes SLA-7 and SLA-8

By Crew Mark   Phanavanh Bounleut   Garcia-Borges Carmen  

Immunogenetics, Vol. 56, Iss. 2, 2004-05 ,pp. : 111-114

Springer Publishing Company

Access to resources Recommend Favorite