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Toplam kayıt 24, listelenen: 1-10
Hacettepe Üniversitesi Hastaneleri Kan Bankası Aferez Ünitesi'nde Gerçekleştirilen Tedavi Amaçlı Aferez İşlemlerinin Değerlendirilmesi
(Tıp Fakültesi, 2002)
Apheresis is the process of separation and collection of blood components. A study was carried out to evaluate the safety and efficacy of therapeutic apheresis procedures performed in Hacettepe University Hospitals Blood ...
Disruption Of A Long-Range Cis-Acting Regulator For Shh Causes Preaxial Polydactyly
(Natl Acad Sciences, 2002)
Preaxial polydactyly (PPD) is a common limb malformation in human. A number of polydactylous mouse mutants indicate that misexpression of Shh is a common requirement for generating extra digits. Here we identify a translocation ...
Comparison Of The Effects Of Patellar Tendon Bearing And Total Surface Bearing Sockets On Prosthetic Fitting And Rehabilitation
(Int Soc Prosthet Orthotics, 2002)
Patellar tendon bearing (PTB) and total surface bearing (TSB) sockets have been used respectively in the prosthetic treatment of 20 trans-tibial amputees to investigate the effectiveness of both sockets on prosthetic fitting ...
Lipoxygenase-3 (Aloxe3) and 12(R)-Lipoxygenase (Alox12B) Are Mutated in Non-Bullous Congenital Ichthyosiform Erythroderma (Ncie) Linked to Chromosome 17P13.1
(Oxford Univ Press, 2002)
We report the identification of mutations in lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) genes in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17. Linkage disequilibrium analysis ...
5,7,7,8,10-Pentabromo-7,8-Dihydrobenzocyclooctene
(Blackwell Munksgaard, 2002)
Tumour Necrosis Factor Alpha G -> A-238 And G -> A-308 Polymorphisms In Juvenile Idiopathic Arthritis
(Oxford Univ Press, 2002)
Objectives. To study G-->A -238 and G-->A -308 polymorphisms in the promoter region of the tumour necrosis factor (TNF) alpha gene in patients with juvenile idiopathic arthritis (JIA). We analysed whether there were any ...
Mutations In Col6A3 Cause Severe And Mild Phenotypes Of Ullrich Congenital Muscular Dystrophy
(Univ Chicago Press, 2002)
Ullrich congenital muscular dystrophy (UCMD) is an autosomal recessive disorder characterized by generalized muscular weakness, contractures of multiple joints, and distal hyperextensibility. Homozygous and compound ...
The Position Of The Polycystic Kidney Disease 1 (Pkd1) Gene Mutation Correlates With The Severity Of Renal Disease
(Amer Soc Nephrology, 2002)
The severity of renal cystic disease in the major form of autosomal dominant polycystic kidney disease (PKD1) is highly variable. Clinical data was analyzed from 324 mutation-characterized PKD1 patients (80 families) to ...