Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Munis Dündar"'
Autor:
Sura Hilal Ahmed Al-Sammarraie, Şerife Ayaz-Güner, Mustafa Burak Acar, Ahmet Şimşek, Betül Seyhan Sınıksaran, Habibe Damla Bozalan, Miray Özkan, Recep Saraymen, Munis Dündar, Servet Özcan
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Obesity is a health problem characterized by large expansion of adipose tissue. During this expansion, genotoxic stressors can be accumulated and negatively affect the mesenchymal stem cells (MSCs) of adipose tissue. Due to the oxidative str
Externí odkaz:
https://doaj.org/article/a1323561cdd247feb7f9eb2c0a99c52f
Publikováno v:
JCRPE, Vol 15, Iss 4, Pp 426-430 (2023)
Neonatal diabetes and congenital hypothyroidism (CH) syndrome is a rare condition caused by homozygous or compound heterozygous mutations in the GLIS3 gene. Small for gestational age, congenital glaucoma, polycystic kidney disease, cholestatic hepati
Externí odkaz:
https://doaj.org/article/df0e55a39b4b4e4cb8c98c31de1ace13
Publikováno v:
The Journal of Pediatric Academy, Vol 4, Iss 4, Pp 149-151 (2023)
Pentasomy X syndrome is a very rare sex chromosome numerical anomaly of unknown frequency. The karyotype consists of 49,XXXXX. Musculoskeletal, craniofacial, cardiac, and kidney anomalies accompany psychomotor developmental delays. This report descri
Externí odkaz:
https://doaj.org/article/c18773445fdf401297b58880608f6a0c
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 52, Iss 4, Pp 270-275 (2022)
Objectives:Hereditary retinal dystrophies are a rare group of diseases which are heterogeneous in genotype and phenotype and result in total blindness. One of the genetic defects that cause hereditary retinal dystrophy is mutation of the RPE65 gene.
Externí odkaz:
https://doaj.org/article/dad5e2e310ab48c2846b2c62327a7717
Autor:
Zahraa Alzaidi, Şule Menziletoğlu Yildiz, Çetin Saatçi, Hilal Ünlü Akalin, Iptisam Ipek Muderris, Buşra Aynekin, Izem Olcay Şahin, Munis Dündar
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-5 (2021)
Abstract Background Successful implantation of blastocysts is indeed an important path in mammalian reproduction that is governed by a complicated web of cytokines interactions. Leukemia inhibitory factor (LIF) and interleukin-11 (IL-11) part of the
Externí odkaz:
https://doaj.org/article/1a33ae907aaf4af3979d8d05909de4dc
Publikováno v:
Pathophysiology, Vol 28, Iss 2, Pp 238-249 (2021)
Limb girdle muscular dystrophy type R1 disease is a progressive disease that is caused by mutations in the CAPN3 gene and involves the extremity muscles of the hip and shoulder girdle. The CAPN3 protein has proteolytic and non-proteolytic properties.
Externí odkaz:
https://doaj.org/article/5c2b0550356a4973a334237ee52338e6
Autor:
Munis Dündar, Adam Mechler, Jean-pierre Alcaraz, Gary Henehan, Satya Prakash, Ratnesh Lal, Donald Martin
Publikováno v:
Erciyes Medical Journal, Vol 42, Iss 4, Pp 370-379 (2020)
Nanomedicine technologies seem to play an increasing role in modern medicine. Although there are many challenges, it is important to consider emerging technologies that may impact nanomedicine. To establish a rational basis for such consideration in
Externí odkaz:
https://doaj.org/article/41f309ef1bdf4f1881c28ba202704aeb
Autor:
Munis Dündar, Saide Betül Arslan
Publikováno v:
Erciyes Medical Journal, Vol 41, Iss 4, Pp 355-356 (2019)
Externí odkaz:
https://doaj.org/article/e1393ec06cea4d56a5df244693911e24
Autor:
Mehmet Serdar Kütük, Mehmet Dolanbay, Hilal Akalın, Mahmut Tuncay Özgün, Turhan Öktem, Munis Dündar, Ercan Aygen
Publikováno v:
Gynecology Obstetrics & Reproductive Medicine, Vol 21, Iss 3 (2016)
Partial hydatidiform mole with dichorionic twin fetuses is extremely rare condition, and only three cases have been reported before. Twenty- five years old primigravida having a trizygotic triplet pregnancy that has been conceived by ovulation induct
Externí odkaz:
https://doaj.org/article/958bf9cef697466ca1f5ee2183278c8e
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 35:845-850
Objectives Arthrogryposis multiplex congenita-5 (AMC5) is an autosomal recessive disease caused by homozygous or compound heterozygous mutations in the TOR1A gene on chromosome 9q34. Congenital multiple joint contractures with microcephaly, typical f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a50ea707114ed33c507d0cdda6c18c59
https://doi.org/10.1515/jpem-2021-0766
https://doi.org/10.1515/jpem-2021-0766