Tag Archives: Genotype

Early renal abnormalities in autosomal dominant polycystic kidney disease

Meijer E, Rook M, Tent H, Navis G, van der Jagt EJ, de Jong PE, Gansevoort RT. Early renal abnormalities in autosomal dominant polycystic kidney disease. Clin J Am Soc Nephrol. June 2010;5(6):1091-1098. Full Text – Open Access Publication Date June 2010 How Analyze was Used “Renal volume was measured on T2 weighted coronal images….

Childhood stress, serotonin transporter gene and brain structures in major depression

Frodl T, Reinhold E, Koutsouleris N, Donohoe G, Bondy B, Reiser M, Möller HJ, Meisenzahl EM. Childhood stress, serotonin transporter gene and brain structures in major depression. Neuropsychopharmacology. May 2010;35(6):1383-1390. Full Text – Open Access Publication Date May 2010 How Analyze was Used “The commercial software package Analyze was used (ANALYZE …) for further image…

Genetic influences on hippocampal structure and function in recombinant inbred mice

Martin MV, Churchill JD, Dong H, Wozniak DF, Cheverud JM, Csernansky JG. Genetic influences on hippocampal structure and function in recombinant inbred mice. Behav Brain Res. January 2009;196(1):78-83. Full Text – Open Access Publication Date January 2009 How Analyze was Used “Every fifth section was mounted on 2% porcine skin coated slides and Nissl-stained. Slides…

Increased GABA levels in medial prefrontal cortex of young adults with narcolepsy

Kim SJ, Lyoo IK, Lee YS, Sung YH, Kim HJ, Kim JH, Kim KH, Jeong DU. Increased GABA levels in medial prefrontal cortex of young adults with narcolepsy. Sleep. March 2008;31(3):342-347. Full Text – Open Access Publication Date March 2008 How Analyze was Used “In the axial slice, which showed the most anterior boundary of…

Genetic variation in endocannabinoid metabolism, gastrointestinal motility, and sensation

Camilleri M, Carlson P, McKinzie S, Grudell A, Busciglio I, Burton D, Baxter K, Ryks M, Zinsmeister AR. Genetic variation in endocannabinoid metabolism, gastrointestinal motility, and sensation. Am J Physiol Gastrointest Liver Physiol. January 2008;294(1):G13-19. Full Text – Open Access Publication Date January 2008 How Analyze was Used “The stomach was identified in the transaxial…

Association of the brain-derived neurotrophic factor Val66Met polymorphism with reduced hippocampal volumes in major depression

Frodl T, Schüle C, Schmitt G, Born C, Baghai T, Zill P, Bottlender R, Rupprecht R, Bondy B, Reiser M, Möller HJ, Meisenzahl EM. Association of the brain-derived neurotrophic factor Val66Met polymorphism with reduced hippocampal volumes in major depression. Arch Gen Psychiatry. April 2007;64(4):410-416. Full Text – Open Access Publication Date April 2007 How Analyze…

YPI1 and SDS22 proteins regulate the nuclear localization and function of yeast type 1 phosphatase Glc7

Pedelini L, Marquina M, Arino J, Casamayor A, Sanz L, Bollen M, Sanz P, Garcia-Gimeno MA. YPI1 and SDS22 proteins regulate the nuclear localization and function of yeast type 1 phosphatase Glc7. J Biol Chem. February 2007;282(5):3282-3292. Full Text – Open Access Publication Date February 2007 How Analyze was Used “A Color View 12 CCD…

The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT

Perlyn CA, DeLeon VB, Babbs C, Govier D, Burell L, Darvann T, Kreiborg S, Morriss-Kay G. The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT. Cleft Palate Craniofac J. November 2006;43(6):740-748. Full Text – Open Access Publication Date November 2006 How Analyze was Used “We used ANALYZE…

Magnetic resonance imaging study in older fragile X premutation male carriers

Loesch DZ, Litewka L, Brotchie P, Huggins RM, Tassone F, Cook M. Magnetic resonance imaging study in older fragile X premutation male carriers. Ann Neurol. August 2005;58(2):326-330. Publication Date August 2005 How Analyze was Used “Volumetric analysis was performed on a UNIX workstation using ANALYZE AVW.” Keywords Adult Aged Aged, 80 and over Brain/pathology Case-Control…

Loss of the serine/threonine kinase fused results in postnatal growth defects and lethality due to progressive hydrocephalus

Merchant M, Evangelista M, Luoh SM, Frantz GD, Chalasani S, Carano RAD, van Hoy M, Ramirez J, Ogasawara AK, McFarland LM, Filvaroff EH, French DM, de Sauvage FJ. Loss of the serine/threonine kinase fused results in postnatal growth defects and lethality due to progressive hydrocephalus. Mol Cell Biol. August 2005;25(16):7054-7068. Full Text – Open Access…