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Light And Scanning Electron Microscopic Examination Of Late Changes In Hair With Hereditary Trichodysplasia (Marie Unna Hypotrichosis)
(Saudi Med J, 2004)
Objective: Our aim was to investigate the microscopic structural alteration in hair with hereditary trichodysplasia. This article presents the results of light and scanning electron microscopy (SEM) examination of cases ...
Eğitim ve Bilgi Hizmetlerinde Toplam Kalite Uygulamaları
(TKD, 2004)
Total quality management is one of the key elements to improving the effective ness of education and information services. By applying total quality management it is possible to judge what the libraries are doing well; to ...
Assessing the Severity of the Small Inframe Deletion Mutation in the Alpha-Subunit of Beta-Hexosaminidase A Found in the Turkish Population By Reproducing It in the More Stable Beta-Subunit
(Springer, 2004)
GM(2) gangliosidoses are a group of panethnic lysosomal storage diseases in which GM(2) ganglioside accumulates in the lysosome due to a defect in one of three genes, two of which encode the alpha- or beta-subunits of ...
Effect of Combined Treatment With Melatonin and Methylprednisolone on Neurological Recovery After Experimental Spinal Cord Injury
(Springer, 2004)
Spinal cord injury (SCI) results in the loss of function below the lesion. Secondary injury following the primary impact includes a number of biochemical and cellular alterations leading to tissue necrosis and cell death. ...
Neisseria Meningitidis W135, Turkey
(2004)
We describe the first case of Neisseria meningitidis W135 meningitis in Turkey. The strain was genotypically unrelated to the clone (W)ET-37, isolated from Hajj pilgrims in 2000.
A Role for Endothelin-2 and Its Receptors in Breast Tumor Cell Invasion
(Amer Assoc Cancer Research, 2004)
We have studied the role of endothelins (ET-1, ET-2 and ET-3) and ET receptors (ET-RA and ET-RB) in the invasive capacity of breast tumor cells, which express ET-I and ET-2 as well as ET-RA and ET-RB. Of five human breast ...
Meta-Analysis Of 13 Genome Scans Reveals Multiple Cleft Lip/Palate Genes With Novel Loci On 9Q21 And 2Q32-35
(Univ Chicago Press, 2004)
Isolated or nonsyndromic cleft lip with or without cleft palate (CL/P) is a common birth defect with a complex etiology. A 10-cM genome scan of 388 extended multiplex families with CL/P from seven diverse populations (2,551 ...