Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

VARIABLE PHENOTYPE IN FEMALES WITH HETEROZYGOUS GJB1 MUTATION

KURT C. E., ERGÜL ÜLGER Z., TEMUÇİN Ç. M., Kumtepe E. T., BALCI B., Tan E., et al.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM , 2024 (SCI-Expanded) identifier

Mitochondrial Dysfunction in Cyanotic Congenital Heart Disease: A Promising Therapeutic Approach for the Future.

Ucar Z., Akbaba T. H., Aydinoglu A. T., Onder S. C., Balci-Peynircioglu B., Demircin M., et al.
Pediatric cardiology , cilt.43, sa.8, ss.1870-1878, 2022 (SCI-Expanded) identifier identifier identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

MAP1B upregulation and its involvement of microtubule stability in spinal muscular atrophy.

Bora G., Hensel N., Rademacher S., Koyunoğlu D., Sunguroğlu M., Aksu Mengeş E., et al.
44th FEBS Congress, Krakow, Polonya, 6 - 11 Temmuz 2019, ss.2-18

In-Silico Methods to Identify Common MicroRNAs and Pathways of Neuromuscular Diseases

ÜNLÜ YAZICI M., AKSU MENGEŞ E., Ulum Y. Z. A., HAYTA B., Bakir-Gungor B.
27th Signal Processing and Communications Applications Conference (SIU), Sivas, Türkiye, 24 - 26 Nisan 2019 identifier identifier

Low SMN Level Causes Alterations in Alpha Tubulin Detyrosination and Microtubule-associated protein 1B in Spinal Muscular Atrophy

Bora G., Rademacher S., Hensel N., Yurter H., Hayta B., Aksu Mengeş E., et al.
FEBS Advanced Lecture Course and 33rd European Cytoskeletal Forum Meeting on “Biology and pathology of cytoskeleton: the crossroads of three cytoskeletal systems., Praha, Çek Cumhuriyeti, 20 - 24 Ekim 2018

Activation of the mitochondrial unfolded protein responce pathway in C2C12 myoblast cell lin

Aksu Mengeş E., Talim B., Dinçer P. R., Hayta B.
ESHG, Barcelona, İspanya, 21 Mayıs 2016, ss.15

A novel mutation in the desmin gene DES cause an autosomal recessive form of limb girdle muscular dystrophy type 2R without clear cut desminopathy pathology.

Hayta B., Puralı N., Tan M. E., Erdem Özdamar S., Talim B., Korkusuz P., et al.
ESHG, Barcelona, İspanya, 21 Mayıs 2016, ss.45

Histopathological characteristics of muscular dystrophy caused by mutation in the nuclear envelope protein LAP1B

Kayman Kürekçi G., Talim B., Korkusuz P., Hayta B., Puralı N., Dinçer P. R.
7th UK Conference on the Nuclear Envelope in Disease and Chromatin Organization, Sheffield, Birleşik Krallık, 22 Haziran 2015

Torsin A-interacting protein 1/Lamina-associated polypeptide 1B in a form of limb-girdle muscular dystrophy: a novel gene related to nuclear envelopathies

Kayman Kürekçi G., Hayta B., Talim B., Puralı N., Dinçer P. R.
18. International Meeting of the World Muscle Society, California, Amerika Birleşik Devletleri, 05 Ekim 2013, ss.64

Metrikler

Yayın

17

Atıf (WoS)

12

H-İndeks (WoS)

2

Atıf (Scopus)

32

H-İndeks (Scopus)

3

Proje

28

Tez Danışmanlığı

1

Açık Erişim

4
BM Sürdürülebilir Kalkınma Amaçları