Ara
Toplam kayıt 2357, listelenen: 731-740
Screening of the BRAF V600E mutation prevalance at papillary thyroid carcinomas (PTCs) in Turkish population
(Nature Publishing Group, 2018)
[No Abstract Available]
Thyroid Hormone Resistance Beta: Eighteen Pediatric Patient Experience
(Karger, 2018)
[No Abstract Available]
Does the mitochondrial genome much more stabile in the aggressive papillary thyroid cancers ('PTCs)? - the preliminary findings
(Wiley, 2018)
[No Abstract Available]
Saliva extract of Dermacentor marginatus (Acari: Ixodidae) leads to apoptotic cell death
(Wiley, 2018)
[No Abstract Available]
Development of waterproof breathable coatings and laminates
(Woodhead Publ Ltd, 2018)
[No Abstract Available]
Energy Harvesting Smart Textiles
(Springer International Publishing Ag, 2017)
The ever-increasing population of the world is putting a significant demand on the need for multifunctional electronic devices and electricity to power them. This growing demand has led to an enhanced focus on the development ...
Genetics and phenomics of inherited and sporadic non-autoimmune hyperthyroidism
(Elsevier Ireland Ltd, 2010)
TSH receptor (TSHR) germline mutations occur as activating mutations in familial non-autoimmune hyperthyroidism (FNAH) or sporadic non-autoimmune hyperthyroidism (SNAH). Up to date 17 constitutively activating TSHR mutations ...
Prophylactic feeding with immune-enhanced diet ameliorates chemoradiation-induced gastrointestinal injury in rats
(Taylor & Francis Ltd, 2010)
Materials and methods: Forty-eight Sprague-Dawley rats were divided into control (C, n = 6), irradiation (IR, n = 14), fluoropyrimidine (5-FU, n = 14)-treated, IR + 5-FU (n = 14)-treated groups. Half of each irradiated ...
Examination of Competitiveness of Irradiated (Caesium-137) Hyalomma marginatum Males in Copulation
(Kafkas Univ, Veteriner Fakultesi Dergisi, 2010)
We had previously reported in one of our studies that the irradiated males of Hyalomma anatolicum anatolicum were not able to compete with the normal males while mating with the females. In this study, it is aimed to ...
A Novel Mutation in the MC2R Gene Causing Familial Glucocorticoid Deficiency Type 1
(Karger, 2011)
Familial glucocorticoid deficiency (FGD) or hereditary unresponsiveness to adrenocorticotropin (ACTH) is an autosomal recessive disorder characterized by isolated glucocorticoid deficiency associated with normal mineralocorticoid ...