Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hatice Asuman Ozkara"'
Autor:
Nesibe Gevher Eroglu-Ertugrul, Mohammadreza Yousefi, Faruk Pekgül, Tansu Doran, Ceren Günbey, Meral Topcu, Kader K. Oguz, Hatice Asuman Ozkara, Atay Vural, Banu Anlar
Publikováno v:
Journal of neuroimmunology. 369
Accumulation of intermediate metabolites due to enzyme deficiencies and demyelination can provoke inflammation in genetic leukodystrophies. Thirty patients with genetic leukodystrophy and 48 healthy control sera were tested for anti-myelin oligodendr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4f29c2f78011ef07061e6ec86e6e046
https://pubmed.ncbi.nlm.nih.gov/35752102
https://pubmed.ncbi.nlm.nih.gov/35752102
Publikováno v:
Advances in protein chemistry and structural biology. 114
Lysosome is the organelle responsible for breaking down macromolecules to maintain homeostasis and to fight infection. The disruption of normal lysosomal function due to mutations in the sphingolipid metabolism proteins leads to a class of lysosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5acbe32216e8307dfef566fa0360b1a8
https://pubmed.ncbi.nlm.nih.gov/30635081
https://pubmed.ncbi.nlm.nih.gov/30635081
Autor:
S Songül, Yalçin, Emel, Orün, Banu, Mutlu, Yusuf, Madendağ, Incilay, Sinici, Arzu, Dursun, Hatice Asuman, Ozkara, Zeynep, Ustünyurt, Sehnaz, Kutluk, Kadriye, Yurdakök
Publikováno v:
Paediatric and perinatal epidemiology. 24(6)
We aimed to analyse infant (birth characteristics, feeding type, faecal enzyme activities) and environmental (maternal smoking, nutrition and psychological status, mother-child bonding, family structure, support for the mother, familial atopy) risk f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2793cf49e4b7c27ca99f93f9270cf4c2
https://pubmed.ncbi.nlm.nih.gov/20955236
https://pubmed.ncbi.nlm.nih.gov/20955236
Autor:
Faruk Pekgül, Nesibe Gevher Eroğlu-Ertuğrul, Can Ebru Bekircan-Kurt, Sevim Erdem-Ozdamar, Arda Çetinkaya, Ersin Tan, Bahadır Konuşkan, Ergun Karaağaoğlu, Meral Topçu, Nurten Ayşe Akarsu, Kader K. Oguz, Banu Anlar, Hatice Asuman Özkara
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100688- (2020)
Metachromatic leukodystrophy (MLD) is a glycosphingolipid storage disease caused by deficiency of the lysosomal enzyme arylsulfatase A (ASA) or its activator protein saposin B. MLD can affect all age groups in severity varying from a severe fatal for
Externí odkaz:
https://doaj.org/article/04adf75434bf4fb083408a4e29032740