Publications & Works

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Journal articles indexed in SCI, SSCI, and AHCI

ERF-Related Craniosynostosis in a Patient With Hypochondroplasia: A Case Report

JUMAYEVA G., SOĞUKPINAR M., KARAOSMANOĞLU B., ÜREL DEMİR G., GÖÇMEN R., ÜTİNE G. E., et al.
CLEFT PALATE CRANIOFACIAL JOURNAL , 2025 (SCI-Expanded) identifier identifier

Hierarchical TiO<sub>2</sub> nanotube arrays enhance mesenchymal stem cell adhesion and regenerative potential through surface nanotopography

Tasdemir N. K., KILIÇARSLAN B., İMREN G., KARAOSMANOĞLU B., TAŞKIRAN Z. E., BAYRAM C.
JOURNAL OF THE ROYAL SOCIETY INTERFACE , no.223, 2025 (SCI-Expanded) identifier identifier

Microfluidic Fabrication of Gelatin-Nano Hydroxyapatite Scaffolds for Enhanced Control of Pore Size Distribution and Osteogenic Differentiation of Dental Pulp Stem Cells

BAYRAM C., ÖZTÜRK Ş., KARAOSMANOĞLU B., GÜLTEKİNOĞLU BAYRAM M., TAŞKIRAN Z. E., ULUBAYRAM K., et al.
MACROMOLECULAR BIOSCIENCE , vol.24, 2024 (SCI-Expanded) identifier identifier identifier

Allele-Specific Antisense Oligonucleotides for the Treatment of BEST1-Related Dominantly Inherited Retinal Diseases: An In Vitro Model

KARAOSMANOĞLU B., İMREN G., ÜTİNE G. E., TAYLAN ŞEKEROĞLU H., TAŞKIRAN Z. E.
EUROPEAN JOURNAL OF HUMAN GENETICS , pp.1795, 2024 (SCI-Expanded) identifier

ERF-related craniosynostosis in a patient with hypochondroplasia: a rare coincidence

Simsek-Kiper P., SOĞUKPINAR M., KARAOSMANOĞLU B., JUMAYEVA G., ÜREL DEMİR G., GÖÇMEN R., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS , pp.982-983, 2024 (SCI-Expanded) identifier

ERF-related craniosynostosis in a patient with hypochondroplasia: a rare coincidence

Simsek-Kiper P., SOĞUKPINAR M., KARAOSMANOĞLU B., JUMAYEVA G., ÜREL DEMİR G., GÖÇMEN R., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS , pp.982-983, 2024 (SCI-Expanded) identifier

Ex vivo disease modelling of Rett syndrome: the transcriptomic and metabolomic implications of direct neuronal conversion

KARAOSMANOĞLU B., İMREN G., Ozisin M. S., REÇBER T., ŞİMŞEK KİPER P. Ö., Haliloglu G., et al.
MOLECULAR BIOLOGY REPORTS , vol.51, no.1, 2024 (SCI-Expanded) identifier identifier identifier

Allele-Specific Antisense Oligonucleotides for the Treatment of BEST1-Related Dominantly Inherited Retinal Diseases: An In Vitro Model

KARAOSMANOĞLU B., İMREN G., ÜTİNE G. E., TAYLAN ŞEKEROĞLU H., TAŞKIRAN Z. E.
EUROPEAN JOURNAL OF HUMAN GENETICS , pp.1795, 2024 (SCI-Expanded) identifier

Two cases with undefined childhood interstitial lung disease: Can it be related to telomere variants?

Buyuksahin H. N., EMİRALİOĞLU ORDUKAYA N., Yalcin E., ÖZCAN H. N., OĞUZ B., ÜTİNE G. E., et al.
JOURNAL OF PAEDIATRICS AND CHILD HEALTH , vol.60, pp.754-756, 2024 (SCI-Expanded) identifier identifier identifier

A novel GRK2 variant in a patient with Jeune asphyxiating thoracic dysplasia accompanied by Morgagni hernia

Şimşek Kiper P. Ö., Karaosmanoğlu B., Taşkıran Z. E., Boybeyi Türer Ö., Ütine G. E., Soyer T.
AMERICAN JOURNAL OF MEDICAL GENETICS, PART A , vol.194, no.Apr22, pp.1-7, 2024 (SCI-Expanded) identifier identifier

Etiology of Primary Spontaneous pneumothorax in Children and Adolescents

Tural D. A., Ozsezen B., ŞİMŞEK KİPER P. Ö., TAŞKIRAN Z. E., Buyuksahin H. N., GÜZELKAŞ İ., et al.
EUROPEAN RESPIRATORY JOURNAL , 2024 (SCI-Expanded) identifier

AP-1-Dependent Fibrosis: Exploring its Potential Role in the Pathogenesis of Placental Transmogrification of the Lung (PTL) via Tissue-Level Transcriptome Analysis

Karaosmanoğlu B., Imren G., Uner M., Orhan D., Gucer S., Turer O. B., et al.
PATHOLOGY RESEARCH AND PRACTICE , vol.258, no.Pre-proof, pp.1, 2024 (SCI-Expanded) identifier identifier

Allele-specific antisense oligonucleotides for the treatment of BEST1-Related dominantly inherited retinal diseases: An in vitro model

Karaosmanoğlu B., Imren G., Utine E., Sekeroglu H. T., Taskiran E.
EXPERIMENTAL EYE RESEARCH , vol.241, pp.1, 2024 (SCI-Expanded) identifier identifier

Acquired immune resistance is associated with interferon signature and modulation of KLF6/c-MYB transcription factors in myeloid leukemia

Parveen M., KARAOSMANOĞLU B., SUCULARLI C., ÜNER A., TAŞKIRAN Z. E., ESENDAĞLI G.
European Journal of Immunology , 2024 (SCI-Expanded) identifier identifier

A Novel ZBTB20 Variant in a Patient with Primrose Syndrome: A Rare Clinical Entity with Distinctive Features

Soǧukplnar M., KARAOSMANOĞLU B., ÜTİNE G. E., Boduroǧlu K., ŞİMŞEK KİPER P. Ö.
Molecular Syndromology , 2024 (SCI-Expanded) identifier identifier

Biomedical Efficacy of Garlic-Extract-Loaded Core-Sheath Plasters for Natural Antimicrobial Wound Care

Majd H., GÜLTEKİNOĞLU BAYRAM M., BAYRAM C., KARAOSMANOĞLU B., Taşkıran E. Z., KART D., et al.
Macromolecular Materials and Engineering , 2024 (SCI-Expanded) identifier

CHRND variant in a paternally inherited esophageal atresia and tracheoesophgageal fistula: Report of a case

SOYER T., BOYBEYİ TÜRER Ö., KARAOSMANOĞLU B., Taşkıran E., Şimşek Ö. P., ÜTİNE G. E.
Birth Defects Research , vol.116, no.1, 2024 (SCI-Expanded) identifier identifier

Further Expanding the Mutational Spectrum of Gorlin Syndrome in Three Unrelated Families

Kolkıran A., Şimşek Kiper P. Ö., Topaloğlu Yasan G., Karaosmanoğlu B., Taşklran E., Ütine G. E., et al.
Molecular Syndromology , 2024 (SCI-Expanded) identifier identifier

Mutated Transcripts of ZEB2 Do Not Undergo Nonsense-Mediated Decay in Mowat-Wilson Syndrome

Güleray Lafcl N., KARAOSMANOĞLU B., TAŞKIRAN Z. E., ŞİMŞEK KİPER P. Ö., ÜTİNE G. E.
Molecular Syndromology , vol.14, no.3, pp.258-265, 2023 (SCI-Expanded) identifier identifier identifier

A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features

AKALIN A., ŞİMŞEK KİPER P. Ö., Taşkıran E. Z., KARAOSMANOĞLU B., ÜTİNE G. E., BODUROĞLU O. K.
American Journal of Medical Genetics, Part A , vol.191, no.4, pp.1119-1127, 2023 (SCI-Expanded) identifier identifier identifier

Neonatal ichthyosis-sclerosing cholangitis syndrome: report of a novel mutation and a review of the literature

Demir E., TUNA KIRSAÇLIOĞLU C., SALTIK TEMİZEL İ. N., ÜREL DEMİR G., KARAOSMANOĞLU B., Taşkiran E. Z., et al.
Clinical Dysmorphology , vol.32, no.2, pp.88-91, 2023 (SCI-Expanded) identifier identifier identifier

Biallelic loss-of-function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo-epi-metaphyseal dysplasia with joint laxity type 3

ŞİMŞEK KİPER P. Ö., Jacob P., Upadhyai P., TAŞKIRAN Z. E., Guleria V. S., KARAOSMANOĞLU B., et al.
HUMAN MUTATION , vol.43, no.12, pp.2116-2129, 2022 (SCI-Expanded) identifier identifier identifier

Small cell lung cancer stem cells display mesenchymal properties and exploit immune checkpoint pathways in activated cytotoxic T lymphocytes

KURŞUNEL M. A., Taskiran E. Z., Tavukcuoglu E., Yanik H., Demirag F., KARAOSMANOĞLU B., et al.
CANCER IMMUNOLOGY IMMUNOTHERAPY , vol.71, no.2, pp.445-459, 2022 (SCI-Expanded) Creative Commons License Sustainable Development identifier identifier identifier

Biallelic ITGB4 variants in familial pyloric atresia without epidermolysis bullosa: Report of two families with five siblings

SOYER T., KARAOSMANOĞLU B., TAŞKIRAN Z. E., ŞİMŞEK KİPER P. Ö., KARNAK İ., BODUROĞLU O. K., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.185, no.11, pp.3427-3432, 2021 (SCI-Expanded) identifier identifier identifier

Expanding the phenotypic spectrum of TNFRSF11A-associated dysosteosclerosis: a case with intracranial extramedullary hematopoiesis

Xue J., Simsek-Kiper P. O., ÜTİNE G. E., Yan L., Wang Z., Taskiran E. Z., et al.
JOURNAL OF HUMAN GENETICS , vol.66, no.6, pp.607-611, 2021 (SCI-Expanded) identifier identifier identifier

Proerythroblast Cells of Diamond-Blackfan Anemia Patients With RPS19 and CECR1 Mutations Have Similar Transcriptomic Signature

KARAOSMANOĞLU B., KURŞUNEL M. A., ÇETİNKAYA F. D., GÜMRÜK F., ESENDAĞLI G., ÜNAL Ş., et al.
FRONTIERS IN PHYSIOLOGY , vol.12, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier

Diagnostic yield of whole-exome sequencing in non-syndromic intellectual disability

Taşkıran Z. E., Karaosmanoglu B., Kosukcu C., Urel-Demir G., Akgun-Dogan O., Simsek-Kiper P. O., et al.
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH , vol.65, no.6, pp.577-588, 2021 (SSCI) identifier identifier identifier

Two Siblings with Kaufman Oculocerebrofacial Syndrome Resembling Oculoauriculovertebral Spectrum

ÜREL DEMİR G., Aydin B., KARAOSMANOĞLU B., AKGÜN DOĞAN Ö., Taskiran E. Z., ŞİMŞEK KİPER P. Ö., et al.
MOLECULAR SYNDROMOLOGY , vol.12, no.2, pp.106-111, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier

The rare reason of pain in hip girdle: Mucolipidosis type 3 gamma

KOLKIRAN A., KARAOSMANOĞLU B., TAŞKIRAN Z. E., Kiper P. Ö. Ş., ÜTİNE G. E.
Turkish Journal of Pediatrics , vol.63, no.6, pp.1091-1096, 2021 (SCI-Expanded) identifier identifier

Molecular etiology of isolated congenital cataract using next-generation sequencing: Single center exome sequencing data from Turkey

Taylan Şekeroğlu H., Karaosmanoğlu B., Taşkıran E. Z., Şimşek Kiper P. Ö., Alikaşifoğlu M., Boduroğlu O. K., et al.
Molecular Syndromology , vol.11, pp.302-308, 2020 (SCI-Expanded) Creative Commons License identifier identifier identifier

Novel insights into diabetes mellitus due toDNAJC3-defect: Evolution of neurological and endocrine phenotype in the pediatric age group

ÖZÖN Z. A., ALİKAŞİFOĞLU A., KANDEMİR N., Aydin B., GÖNÇ E. N., KARAOSMANOĞLU B., et al.
PEDIATRIC DIABETES , vol.21, no.7, pp.1176-1182, 2020 (SCI-Expanded) identifier identifier identifier

An immunological and transcriptomics approach on differential modulation of NK cells in multiple sclerosis patients under interferon-beta 1 and fingolimod therapy

Acar N. P., Tuncer A., Ozkazanc D., Ozbay F. G., KARAOSMANOĞLU B., Goksen S., et al.
JOURNAL OF NEUROIMMUNOLOGY , vol.347, 2020 (SCI-Expanded) identifier identifier identifier

Transcriptome and proteome profiles of human umbilical cord vein CD146+ stem cells.

Gökçinar-Yagci B., Karaosmanoglu B., Taskiran E., Çelebi-Saltik B.
Molecular biology reports , vol.47, pp.3833-3856, 2020 (SCI-Expanded) identifier identifier identifier

The Effect of Boron-Containing Nano-Hydroxyapatite on Bone Cells

Gizer M., Köse S., Karaosmanoglu B., Taskiran E., Berkkan A., Timuçin M., et al.
BIOLOGICAL TRACE ELEMENT RESEARCH , vol.193, no.2, pp.364-376, 2020 (SCI-Expanded) identifier identifier identifier

Development, characterization and research of efficacy on in vitro cell culture of glucosamine carrying hyaluronic acid nanoparticles

Şahin Ş., BİLGİÇ E., Salimi K., Tuncel A., KARAOSMANOĞLU B., Taşkıran E. Z., et al.
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY , vol.52, pp.393-402, 2019 (SCI-Expanded) identifier identifier

Transcriptome analysis reveals differentially expressed genes between human primary bone marrow mesenchymal stem cells and human primary dermal fibroblasts

TASKIRAN E. Z., KARAOSMANOĞLU B.
TURKISH JOURNAL OF BIOLOGY , vol.43, no.1, pp.21-27, 2019 (SCI-Expanded) Sustainable Development identifier identifier identifier

Heightened CXCR4 and CXCL12 expression in NF1-associated neurofibromas

KARAOSMANOĞLU B., Kocaefe C. Y., Soylemezoglu F., Anlar B., VARAN A., VARGEL İ., et al.
CHILDS NERVOUS SYSTEM , vol.34, no.5, pp.877-882, 2018 (SCI-Expanded) Sustainable Development identifier identifier identifier

Human bone marrow mesenchymal stem cells secrete endocannabinoids that stimulate in vitro hematopoietic stem cell migration effectively comparable to beta-adrenergic stimulation

KOSE S., AERTS-KAYA F. S. F., Kopru C. Z., NEMUTLU E., Koskonmaz B., KARAOSMANOĞLU B., et al.
EXPERIMENTAL HEMATOLOGY , vol.57, pp.30-41, 2018 (SCI-Expanded) Creative Commons License Sustainable Development identifier identifier identifier

Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome

Taşkıran Z. E., Karaosmanoğlu B., Koşukcu C., Akgün Doğan Ö., Taylan Şekeroğlu H., Şimşek Kiper P. Ö., et al.
American Journal Of Medical Genetics Part A , vol.173, no.12, pp.3143-3152, 2017 (SCI-Expanded)

HERC1 mutations in idiopathic intellectual disability

ÜTİNE G. E., Taskiran E. Z., KOŞUKCU C., KARAOSMANOĞLU B., GÜLERAY N., Dogan O. A., et al.
European Journal of Medical Genetics , vol.60, no.5, pp.279-283, 2017 (SCI-Expanded) identifier identifier identifier
Articles Published in Other Journals

Investigating the potential impact of ELF3-associated SNPs on chondrocyte inflammation

KARAOSMANOĞLU B., AYDIN B., İMREN G., SAĞ E.
Acta Medica , vol.55, no.3, pp.162-170, 2024 (Peer-Reviewed Journal) identifier

The Effect of Erythropoietin Treatment on Gene Expression Profile of Mesenchymal Stem Cells

Dalkiran D., KARAOSMANOĞLU B., TAŞKIRAN Z. E.
Acta Medica , vol.50, no.2, pp.16-24, 2019 (Peer-Reviewed Journal) Creative Commons License

Neuronal Conversion of Dermal Fibroblasts as a Disease Model

TAŞKIRAN Z. E., KARAOSMANOĞLU B.
Cumhuriyet Medical Journal , vol.40, no.4, pp.392-399, 2018 (Peer-Reviewed Journal) Creative Commons License
Papers Presented at Peer-Reviewed Scientific Conferences

A Novel ZBTB20 Variant In A Patient With Primrose syndrome: A rare clinical entity

SOĞUKPINAR M., KARAOSMANOĞLU B., ÜTİNE G. E., Boduroglu K., Simsek-Kiper P.
56th Annual Conference of the European-Society-of-Human-Genetics (ESHG), Glasgow, England, 10 - 13 June 2023, pp.185, (Summary Text) identifier

Osteojenik Matriks Olgunlaşmasında La-ilişkili Protein 7 ‘nin Rolü

Özışın M. Ş., İMREN G., KARAOSMANOĞLU B., TAŞKIRAN Z. E.
18. Tıbbi Biyoloji ve Genetik Kongresi, 26 October 2023, (Full Text)

Titanyum Bazlı Nanotopografik Yüzeylerle Mezenkimal Kök Hücre Modifikasyonu

Taşdemir N. K., Kılıçarslan B., İMREN G., KARAOSMANOĞLU B., BAYRAM C., TAŞKIRAN Z. E.
18. Tıbbi Biyoloji ve Genetik Kongresi, 26 October 2023, (Full Text)

Kondrositlerde ELF3 Hedefli Anti-Sense Oligonükleotidlerin Kullanımı: Osteoartrit Tedavisine Yeni Bir In Vitro Yaklaşım

Aydın B., İMREN G., TAŞKIRAN Z. E., KARAOSMANOĞLU B.
18. Tıbbi Biyoloji ve Genetik Kongresi, 26 October 2023, (Full Text)

Zihinsel Yetersizlik ve Dismorfik Bulgular ile Başvuran Yeni Nesil Dizi Analizi ile Tanı Alan 5 Nadir Sendrom

Soğukpınar M., KARAOSMANOĞLU B., TAŞKIRAN Z. E., ÜREL DEMİR G., ŞİMŞEK KİPER P. Ö., ÜTİNE G. E., et al.
6. Ulusal Çocuk Genetik Kongresi, 09 November 2023, (Full Text)

ScRNA Veri Analizi Ile Hematopoetik Yolculuk: Ribozomal Proteinlerin İfadesi

KARAOSMANOĞLU B., İMREN G., TAŞKIRAN Z. E.
2. Ulusal HematoOnkoGenetik Kongresi, 04 May 2023, (Summary Text)

Allel-Spesifik Anti-Sense Oligonükleotidler: Kalıtsal Retina Hastalıklarında ‘’Ince Ayar’’ Tedavi Mümkün Olabilir Mi?

Karaosmanoğlu B., İmren G., Ütine G. E., Taylan-Şekeroğlu H., Taşkıran Z. E.
15. Ulusal Tıbbi Genetik Kongresi, Muğla, Turkey, 9 - 13 November 2022, (Full Text)

RSPRY1 İlişkili Spondiloepimetafizyel Displazide Transkriptomik Yaklaşım

Karaosmanoğlu B., Taşkıran Z. E., Kiper Şimşek P. Ö., Ütine G. E.
XXIV. Ulusal Pediatrik Endokrinoloji &amp; Diyabet Kongresi, Ankara, Turkey, 30 October 2020, (Full Text)

Fonksiyondan Hastalığa: Hastalığı Nasıl Modelliyorum?

KARAOSMANOĞLU B.
4. Ulusal Çocuk Genetik Kongresi, Turkey, 25 - 27 September 2019, (Full Text)

Çok Merkezli Diamond Blackfan Anemisi Moleküler İnceleme Sonuçları: EURODBA Türkiye

ÜNAL CANGÜL Ş., CELKAN T. T., YARALI H. N., ÖREN H., ALBAYRAK C., KARAKAŞ Z., et al.
45. Ulusal Hematoloji Kongresi, Antalya, Turkey, 30 October - 02 November 2019, (Summary Text)

Büyük veriden hücre karakterizasyonuna: Transkripsiyon faktörü kataloglarınınoluşturulması

İMREN G., KARAOSMANOĞLU B., ÇELEBİ SALTIK B., ESENDAĞLI G., TAŞKIRAN Z. E.
Tıbbi Biyoloji ve Genetik Kongresi, Turkey, 27 - 30 October 2019

Sendromik olmayan zihinsel yetersizlikte tüm ekzom dizilemenin tanısal verimi

TAŞKIRAN Z. E., KARAOSMANOĞLU B., KOŞUKCU C., ÜREL DEMİR G., akgün doğan ö., Kiper şimşek P. Ö., et al.
16. Tıbbi Biyoloji ve Genetik Kongresi, Turkey, 25 - 27 October 2019, (Full Text)

Boron-Containing Nano-Hydroxyapatite Composites Alters Mesenchymal Stem Cell Proliferation and Osteogenic Differentiation

GİZER M., KÖSE S., KARAOSMANOĞLU B., TAŞKIRAN Z. E., BERKKAN A., TİMUÇİN M., et al.
European Orthopedic Research Society 27th Annual Anniversary Meeting, 2 - 05 October 2019, (Summary Text)

Development of a new antiproliferative arachydonoylcyclopropilamide (ACPA) releasing nanoparticle-based drug for endometrial cancers by targeting cannabinoid 1 receptors

BİLGİÇ E., BOYACIOĞLU Ö., VARAN C., BİLENSOY E., NEMUTLU E., KARAOSMANOĞLU B., et al.
EACR Conference Nanotechnology in Cancer: Engineering for Oncology, 12 - 14 September 2019, (Summary Text) Sustainable Development

Cannabinoid Receptor 1-Mediated Antiproliferative Effect of ACPA and ACPA-PCL Controlled Release System on Non-Small Cell Lung Cancer Lines

BOYACIOĞLU Ö., BİLGİÇ E., VARAN C., BİLENSOY E., NEMUTLU E., KARAOSMANOĞLU B., et al.
EACR Conference Nanotechnology in Cancer: Engineering for Oncology, Cambridge, Canada, 12 - 14 September 2019, (Summary Text) Sustainable Development

Transcriptomic and immunophenotypic analyses on natural killer cells in RRMS patients under fingolimod therapy

Acar-Ozen N. P., TUNCER A., Ozkazanc D., Ozbay F. G., KARAOSMANOĞLU B., Goksen S., et al.
35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS, Stockholm, Sweden, 11 - 13 September 2019, vol.25, pp.664-665, (Summary Text) identifier

Kemik hücrelerine bor içeren nano-hidroksiapatit kompozitlerin moleküler etki mekanizması

Gizer M., KÖSE S., KARAOSMANOĞLU B., TAŞKIRAN Z. E., BERKKAN A., TİMUÇİN M., et al.
24. Ulusal Elektron Mikroskopi Kongresi, Edirne, Turkey, 24 - 26 April 2019, (Summary Text)

Endometriyum kanserinde araşidonilsiklopropilamid (ACPA)’in kannabinoid 1 reseptörü aracılı antiproliferatif etkisinin gösterilmesi

BİLGİÇ E., BOYACIOĞLU Ö., KARAOSMANOĞLU B., TAŞKIRAN Z. E., KORKUSUZ P.
24. Ulusal Elektron Mikroskopi Kongresi, Edirne, Turkey, 24 - 26 April 2019, pp.112-113, (Summary Text) Sustainable Development

Mezenkimal Kök Hücreler Endokannabinoidler Aracılığı ile Hematopoietik Kök Hücre Mobilizasyonunu Düzenlemektedir

KÖSE S., KÖPRÜ Ç. Z., KARAOSMANOĞLU B., TAŞKIRAN Z. E., AERTS KAYA F. S. F., NEMUTLU E., et al.
Elektron Mikroskobu Kongresi, Turkey, 24 - 26 April 2019, (Full Text)

Mesenchymal stem cells regulate the hematopoietic stem cell mobilization through the endocannabinoids

KOSE S., KOPRU Z. C., KARAOSMANOĞLU B., Taskiran E. Z., Kaya F. A., NEMUTLU E., et al.
Conference on Changing the Face of Modern Medicine - Stem Cells and Gene Therapy, Florence, Italy, 18 - 21 October 2016, vol.27, (Summary Text) identifier

Mesenchymal stem cells regulate the hematopoietic stem cell mobilization through the endocannabinoids.

KÖSE S., KÖPRÜ Ç. Z., KARAOSMANOĞLU B., Taşkıran E. Z., AERTS KAYA F. S. F., NEMUTLU E., et al.
ESGCT annual meeting 2016, 18 - 21 October 2016, vol.27, pp.1-185, (Summary Text)

Determination of properties of bone marrow and tissue-derived mesenchymal stromal/stem cell population in neurofibromatosis type 1 patients

Soycan I. A., KARAOSMANOĞLU B., Cetinkaya D. U., Ayter S., Taskiran E., ÇETİN M., et al.
41st FEBS Congress on Molecular and Systems Biology for a Better Life, Kusadasi, Turkey, 3 - 08 September 2016, vol.283, pp.271-272, (Summary Text) identifier

Mezenkimal Kök Hücreler Hematopoetik Kök Hücrelerin mobilizasyonunu Endokannabinoidler aracılığı ile düzenlemektedir.

KÖSE S., KÖPRÜ Ç. Z., KARAOSMANOĞLU B., TAŞKIRAN Z. E., AERTS KAYA F. S. F., NEMUTLU E., et al.
XIII. Ulusal Histol ve Embriyol Kongresi, İzmir, Turkey, 30 April - 03 May 2016, pp.89-90, (Summary Text)
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Publication

66

Citation (WoS)

66

H-Index (WoS)

5

Citation (Scopus)

218

H-Index (Scopus)

7

Citation (Scholar)

169

H-Index (Scholar)

6

Project

11

Open Access

7
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