Search Results - "Uyanık, Gökhan"
-
1
Effect of post-mating GnRH or TAK-683 (Kisspeptin analog) treatment on the reproductive performance and serum progesterone concentration in ewes during the non-breeding season
Published in Small ruminant research (01-09-2024)“…This study was designed to evaluate the effect of post-mating GnRH or TAK-683 (kisspeptin analog) treatment on serum progesterone (P4) concentrations and…”
Get full text
Journal Article -
2
How Did SARS-CoV-2 Pandemic Affect the Cats’ Health in Hatay Province? A retrospective study
Published in Topics in companion animal medicine (01-09-2022)“…The SARS-CoV-2 pandemic affected not only the physical and emotional health of human beings but also cats. Restrictions put into effect during the pandemic…”
Get full text
Journal Article -
3
The effects of the “Predict-Observe-Explain (POE)” strategy on academic achievement, attitude and retention in science learning
Published in Journal of pedagogical research (01-06-2022)“…This paper employed a quasi-experimental design with pretest-posttest control group to investigate the effects of the predict-observe-explain (POE) strategy on…”
Get full text
Journal Article -
4
Protective Effect of Tyrosol on Cisplatin–Induced Ovarian Inflammation and Oxidative Stress in Rats
Published in Revista científica (Universidad del Zulia. Facultad de Ciencias Veterinarias. División de Investigación) (19-09-2024)“…Ovarian cancer is a widespread type of cancer among gynecologic cancers and has a very high mortality rate. For this reason, the search for new treatments…”
Get full text
Journal Article -
5
Identifying adult hypophosphatasia in the rheumatology unit
Published in Orphanet journal of rare diseases (14-12-2022)“…The most frequent manifestation in adult hypophosphatasia (HPP) is musculoskeletal pain. The unspecific nature of its clinical presentation may prevent correct…”
Get full text
Journal Article -
6
Alterations of bone material properties in adult patients with X-linked hypophosphatemia (XLH)
Published in Journal of structural biology (01-09-2020)“…[Display omitted] •Altered bone material in adult XLH patients at micro- and submicroscopic scales.•Decreased area of hypomineralized periosteocytic lesions…”
Get full text
Journal Article -
7
Effects of carvacrol on hormonal, inflammatory, antioxidant changes, and ovarian reserve in polycystic ovary syndrome in Wistar rats
Published in Naunyn-Schmiedeberg's archives of pharmacology (07-11-2024)“…The study, which explored the effects of carvacrol on female reproductive health, particularly in terms of hormonal, inflammatory, antioxidant, and ovarian…”
Get full text
Journal Article -
8
Investigation of the attitudes towards environmental issues and knowledge levels of prospective teachers
Published in Eægitim Fakèultesi dergisi (Samsun, Samsun çIli, Turkey) (01-01-2017)“…The aim of this study is to investigate the knowledge levels and attitudes towards environmental issues of prospective teachers. The study was conducted at…”
Get full text
Journal Article -
9
Genetic Landscape of Congenital Myasthenic Syndromes From Turkey: Novel Mutations and Clinical Insights
Published in Journal of child neurology (01-07-2017)“…Congenital myasthenic syndromes are clinically and genetically heterogeneous disorders of neuromuscular transmission. Most are treatable, but certain subtypes…”
Get full text
Journal Article -
10
Birleştirme tekniğine dayalı öğretimin çevre sorunlarına yönelik tutum akademik başarı ve kalıcılığa etkisi
Published in Turkish journal of education (11-05-2016)Get full text
Journal Article -
11
Clinical, Radiological, and Genetic Survey of Patients With Muscle-Eye-Brain Disease Caused by Mutations in POMGNT1
Published in Pediatric neurology (01-05-2014)“…Abstract Background To evaluate clinical, genetic, and radiologic features of our patients with muscle-eye-brain disease. Methods The data of patients who were…”
Get full text
Journal Article -
12
Pontocerebellar hypoplasia type 2 and TSEN2 : Review of the literature and two novel mutations
Published in European journal of medical genetics (01-06-2013)“…Abstract Pontocerebellar hypoplasias (PCH) represent a heterogeneous group of autosomal recessive neurodegenerative disorders characterized by hypoplasia of…”
Get full text
Journal Article -
13
Birleştirme tekniğine dayalı öğretimin çevre sorunlarına yönelik tutum akademik başarı ve kalıcılığa etkisi
Published in Turkish journal of education (15-02-2016)Get full text
Journal Article -
14
Overlapping cortical malformations and mutations in TUBB2B and TUBA1A
Published in Brain (London, England : 1878) (01-02-2013)“…Polymicrogyria and lissencephaly are causally heterogeneous disorders of cortical brain development, with distinct neuropathological and neuroimaging patterns…”
Get full text
Journal Article -
15
HFE hemochromatosis screening in patients with severe hip osteoarthritis: A prospective cross-sectional study
Published in PloS one (14-11-2018)“…Despite the high frequency of HFE gene mutations in Western Europe, widespread screening for HFE hemochromatosis is not recommended due to its variable…”
Get full text
Journal Article -
16
Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum
Published in Nature genetics (01-09-2008)“…CASK is a multi-domain scaffolding protein that interacts with the transcription factor TBR1 and regulates expression of genes involved in cortical development…”
Get full text
Journal Article -
17
Reference energy system analysis of a warship
Published in Journal of Naval Sciences and Engineering (2021)“…Considering the growing maritime sector in today's conditions, it is of great importance to use the energy used in ship systems in the most efficient and…”
Get full text
Journal Article -
18
Corrigendum: Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum
Published in Nature genetics (01-11-2008)Get full text
Journal Article -
19
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Published in Journal of medical genetics (01-06-2011)“…Submicroscopic deletions in 14q12 spanning FOXG1 or intragenic mutations have been reported in patients with a developmental disorder described as a congenital…”
Get more information
Journal Article -
20
A case of Walker–Warburg syndrome resulting from a homozygous POMT1 mutation
Published in European journal of paediatric neurology (01-01-2007)“…Abstract Walker––Warburg syndrome (WWS), the most severe α-dystroglycanopathy, is characterized by brain and eye anomalies, and congenital muscular dystrophy…”
Get full text
Journal Article