Publications by authors named "Gozde Imren"

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Transcriptome analysis of unmedicated heterozygous familial Mediterranean fever patients reveals a type I interferon signature driving increasing Pyrin expression.
Erdal Sag, Gozde Imren, Lieselotte Vande Walle, Elif Arslanoglu Aydin, Yagmur Bayindir

Ann Rheum Dis· November 2025

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Recognizing multiple epiphyseal dysplasia in children presenting with joint pain: a commonly overlooked skeletal dysplasia.
Tuğba Daşar, Gözde İmren, Adalet Elçin Yıldız, Gizem Ürel Demir, Gülen Eda Utine

Eur J Pediatr· May 2025

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From Desbuquois Dysplasia to Multiple Epiphyseal Dysplasia: The Clinical Impact of a CANT1 Variant Across Five Unrelated Families.
Tuğba Daşar, Gizem Ürel Demir, Gözde İmren, Gülen Eda Utine, Güney Yilmaz

Am J Med Genet A· April 2025

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Hierarchical TiO nanotube arrays enhance mesenchymal stem cell adhesion and regenerative potential through surface nanotopography.
Nur Kubra Tasdemir, Bogac Kilicarslan, Gozde Imren, Beren Karaosmanoglu, Ekim Z Taskiran

J R Soc Interface· February 2025

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The effect of LARP7 on gene expression during osteogenesis.
M Samil Ozisin, Gozde Imren, Busra Aydin, Beren Karaosmanoglu, Ekim Z Taskiran

Mol Biol Rep· January 2025

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Unraveling the Role of RSPRY1 in TGF-β Pathway Dysregulation: Insights into the Pathogenesis of Spondyloepimetaphyseal Dysplasia.
Gozde Imren, Beren Karaosmanoglu, Bihter Muratoglu, Cansu Ozdemir, Gulen Eda Utine

Int J Mol Sci· January 2025

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Ex vivo disease modelling of Rett syndrome: the transcriptomic and metabolomic implications of direct neuronal conversion.
Beren Karaosmanoglu, Gozde Imren, M Samil Ozisin, Tuba Reçber, Pelin Ozlem Simsek Kiper

Mol Biol Rep· September 2024

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AP-1-dependent fibrosis: Exploring its potential role in the pathogenesis of placental transmogrification of the lung (PTL) via tissue-level transcriptome analysis.
Beren Karaosmanoglu, Gozde Imren, Meral Uner, Diclehan Orhan, Safak Gucer

Pathol Res Pract· June 2024

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Allele-specific antisense oligonucleotides for the treatment of BEST1-related dominantly inherited retinal diseases: An in vitro model.
Beren Karaosmanoglu, Gozde Imren, Eda Utine, Hande Taylan Sekeroglu, Ekim Z Taskiran

Exp Eye Res· April 2024

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Biallelic loss-of-function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo-epi-metaphyseal dysplasia with joint laxity type 3.
Pelin Ozlem Simsek-Kiper, Prince Jacob, Priyanka Upadhyai, Zihni Ekim Taşkıran, Vishal S Guleria, Gozde Imren

Hum Mutat· December 2022

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Expanding the phenotypic spectrum of TNFRSF11A-associated dysosteosclerosis: a case with intracranial extramedullary hematopoiesis.
Jing-Yi Xue, Pelin O Simsek-Kiper, Gulen Eda Utine, Li Yan, Zheng Wang, Gozde Imren

J Hum Genet· June 2021

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