Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Loss of the Nuclear Envelope Protein LAP1B Disrupts the Myogenic Differentiation of Patient-Derived Fibroblasts

KAYMAN KÜREKÇİ G., ACAR A. C., Dincer P. R.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , cilt.23, sa.21, 2022 (SCI-Expanded) Creative Commons License identifier identifier identifier

Mutation in TOR1ALP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies

Sewry C. A., Goebel H. H., Kayman-Kurekci G., KORKUSUZ P., DİNÇER P.
NEUROMUSCULAR DISORDERS , cilt.24, sa.12, ss.1122, 2014 (SCI-Expanded) identifier identifier identifier

Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies

Kayman-Kurekci G., TALİM B., KORKUSUZ P., Sayar N., Sarioglu T., Oncel I., et al.
NEUROMUSCULAR DISORDERS , cilt.24, sa.7, ss.624-633, 2014 (SCI-Expanded) Creative Commons License identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

Exome Sequencing for The Identification of Mendelian Disease Genes

KAYMAN KÜREKÇİ G., Dincer P.
ERCIYES MEDICAL JOURNAL , cilt.36, sa.4, ss.139-143, 2014 (ESCI) Creative Commons License identifier identifier

Next-Generation DNA Sequencing Technologies

KAYMAN KÜREKÇİ G., Dincer P.
ERCIYES MEDICAL JOURNAL , cilt.36, sa.3, ss.99-103, 2014 (ESCI) Creative Commons License identifier identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Limb-Girdle Muscular Dystrophy 2R modelling in zebrafishto determine a novel mechanism related to desmin-lamin B interaction

KAYMAN KÜREKÇİ G., KURAL MANGIT E., ÜNSAL Ş., YERSAL N., ERGİN B., SAĞLAM B., et al.
Keystone Symposia, 11 - 15 Kasım 2018

Analysing the expression profiles of human DES orthologous desma and desmb by using knockout zebrafish models

Koyunlar C., Kayman-Kurekci G., Kural E., Talim B., Purali N., Dincer P. R.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.618 identifier

Disease Modeling in Zebrafish: Limb-Girdle MuscularDystrophy 2R

ÜNSAL Ş., KAYMAN KÜREKÇİ G., KURAL MANGIT E., TALİM B., YERSAL N., ERGİN B., et al.
6th International Congress of the Molecular Biology Association of Turkey, Türkiye, 5 - 08 Eylül 2018, ss.5-6

Desmin Mutation with an ultra rare and unique phenotype: Genome editing for a patient specific zebrafish model

Kayman Kürekçi G., Koyunlar C., Kural Mangıt E., Talim B., Korkusuz P., Erdem Özdamar S., et al.
keystone symposia Rare and Undiagnosed Diseases, Massachusetts, Amerika Birleşik Devletleri, 3 - 05 Ağustos 2017

Modeling of a unique desmin mutaion in zebrafish by using genome editing brings new insights into desmin function

KAYMAN KÜREKÇİ G., Koyunlar C., KURAL MANGIT E., TALİM B., ERGİN B., ÜNSAL İ., et al.
European Human Genetics Conference, 27 - 30 Mayıs 2017

Hacettepe University Zebrafish Research Laboratory: zebrafish disease modeling by genome editing tools

KURAL E., KAYMAN-KUREKCI G., KOYUNLAR C., DİNÇER P. R.
41st FEBS Congress on Molecular and Systems Biology for a Better Life, Kusadasi, Türkiye, 3 - 08 Eylül 2016, cilt.283, ss.116 identifier

Metrikler

Yayın

34

Atıf (WoS)

51

H-İndeks (WoS)

1

Atıf (Scopus)

50

H-İndeks (Scopus)

1

Proje

3

Açık Erişim

4
BM Sürdürülebilir Kalkınma Amaçları