Aina S. O, Iranloye B.O. Oladele Adebayo, Evangelshane, Atoyebi Kayode, Igbayilola Y. D
Purpose: Clomiphene citrate (CC) is used in the management of infertile females. Estrus Cycle indices are good parameters for evaluating reproductive changes, while actual ova shed represents evidence of ovulation. This study is aimed at investigating how different doses of CC can affect the Estrus Cycle (EC), Estrus Cycle Ratio, (ECR), and ova shed (OS) in adult female rats.
Methodology: Twenty-five (50) female Sprague Dawley (SD) rats were divided into 5 groups. Group A was controlled while groups B, C, D, and E were treated groups. Group A received 0.5 ml of sterile water. Groups B, C, and D were given 0.2 mg/kg, 2 mg/kg, and 4 mg/kg respectively at diestrus. Group E was given 6mg/kg/day of CC dissolved in sterile water. The administration was done orally. A vaginal smear was evaluated for various estrus phases. ECR was calculated, and ova shed at the estrus phase was evaluated at autopsy. All data were presented as mean ± standard error of the mean (SEM). Statistical significance was taken at P < 0.05
Findings: There was a significant decrease (p<0.05) in the number of proestrus, estrus, metestrus, and diestrus in treated groups compared with control. ECR value in all treated groups also decreased significantly (p<0.05) when compared with control. This study further shows that all the animal groups (A-E) released ova but there was a significant decrease (p<0.05) in the number of ova released in groups B, C, D, and E against the control group.
Conclusion: CC decreases EC. It reduced ECR, hence prolonging luteogenesis. It decreases the number of eggs released. With a large dose and prolonged use, eggs were still released even when the ova released and counted were fewer compared with when this drug was not in use.
Recommendation: Infertile couples should copulate more at the luteal phase of the menstrual cycle when on CC to increase their chances of pregnancy. CC decreases the number of eggs released but makes the few eggs released stay longer for fertilization.
{"title":"Effect of Clomiphene Citrate on Estrus Cycle and The Ova Shed in the Ovary of Female Sprague Dawley Rats","authors":"Aina S. O, Iranloye B.O. Oladele Adebayo, Evangelshane, Atoyebi Kayode, Igbayilola Y. D","doi":"10.47672/ejb.1628","DOIUrl":"https://doi.org/10.47672/ejb.1628","url":null,"abstract":"Purpose: Clomiphene citrate (CC) is used in the management of infertile females. Estrus Cycle indices are good parameters for evaluating reproductive changes, while actual ova shed represents evidence of ovulation. This study is aimed at investigating how different doses of CC can affect the Estrus Cycle (EC), Estrus Cycle Ratio, (ECR), and ova shed (OS) in adult female rats. 
 Methodology: Twenty-five (50) female Sprague Dawley (SD) rats were divided into 5 groups. Group A was controlled while groups B, C, D, and E were treated groups. Group A received 0.5 ml of sterile water. Groups B, C, and D were given 0.2 mg/kg, 2 mg/kg, and 4 mg/kg respectively at diestrus. Group E was given 6mg/kg/day of CC dissolved in sterile water. The administration was done orally. A vaginal smear was evaluated for various estrus phases. ECR was calculated, and ova shed at the estrus phase was evaluated at autopsy. All data were presented as mean ± standard error of the mean (SEM). Statistical significance was taken at P < 0.05
 Findings: There was a significant decrease (p<0.05) in the number of proestrus, estrus, metestrus, and diestrus in treated groups compared with control. ECR value in all treated groups also decreased significantly (p<0.05) when compared with control. This study further shows that all the animal groups (A-E) released ova but there was a significant decrease (p<0.05) in the number of ova released in groups B, C, D, and E against the control group.
 Conclusion: CC decreases EC. It reduced ECR, hence prolonging luteogenesis. It decreases the number of eggs released. With a large dose and prolonged use, eggs were still released even when the ova released and counted were fewer compared with when this drug was not in use. 
 Recommendation: Infertile couples should copulate more at the luteal phase of the menstrual cycle when on CC to increase their chances of pregnancy. CC decreases the number of eggs released but makes the few eggs released stay longer for fertilization.","PeriodicalId":9711,"journal":{"name":"Central European Journal of Biology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136232764","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: Crimean-Congo hemorrhagic fever virus (CCHFV), a single-stranded RNA (ssRNA) virus that spreads via tick bites. For the treatment of CCHFV, there is still a lack of vaccine or any antiviral medicine. For this purpose, a study was performed to design a multiepitope based subunit vaccine (MESV) for effective prevention against CCHFV infection.
Methodology: The study contains immunoinformatic and docking methodologies to obtain a MESV by choosing highly antigenic and overlapping epitopes comprising of 8 epitopes of both MHC class I and II from viral proteins. Epitopes were chosen which were conserved within the epitopes of IFN- gamma, T-cell and B-cell. Then these epitopes were joined to final peptide by GPGPG and AAY linkers. An adjuvant was added at N terminal of vaccine via EAAAK linker for the improvement of vaccine’s immunogenicity.
Findings: Our final construct was comprised of 278 amino acids. To validate the vaccine’s immunogenicity and safety, its physiochemical properties, allergenicity as well as antigenicity were checked and it was predicted to be non-allergenic and antigenic. The construct was further analyzed by molecular docking within vaccine and TLR3 receptor to assure its molecular interaction and binding affinity. In the end, In-silico cloning was also carried out for ensuring its expression efficiency.
Recommendations: Nonetheless, the designed construct is proposed to be tested in laboratory settings to confirm its immunogenicity and safety.
{"title":"Exploring Proteome of Crimean-Congo Hemorrhagic Fever Virus to Construct Multiepitope Based Subunit Vaccine: Molecular Docking with Immunoinformatic Framework","authors":"Hira Shafique, Iqra Shafique, Farah Shahid, Nimra Asif, Usman Ali Ashfaq Ashfaq","doi":"10.47672/ejb.1622","DOIUrl":"https://doi.org/10.47672/ejb.1622","url":null,"abstract":"Purpose: Crimean-Congo hemorrhagic fever virus (CCHFV), a single-stranded RNA (ssRNA) virus that spreads via tick bites. For the treatment of CCHFV, there is still a lack of vaccine or any antiviral medicine. For this purpose, a study was performed to design a multiepitope based subunit vaccine (MESV) for effective prevention against CCHFV infection.
 Methodology: The study contains immunoinformatic and docking methodologies to obtain a MESV by choosing highly antigenic and overlapping epitopes comprising of 8 epitopes of both MHC class I and II from viral proteins. Epitopes were chosen which were conserved within the epitopes of IFN- gamma, T-cell and B-cell. Then these epitopes were joined to final peptide by GPGPG and AAY linkers. An adjuvant was added at N terminal of vaccine via EAAAK linker for the improvement of vaccine’s immunogenicity.
 Findings: Our final construct was comprised of 278 amino acids. To validate the vaccine’s immunogenicity and safety, its physiochemical properties, allergenicity as well as antigenicity were checked and it was predicted to be non-allergenic and antigenic. The construct was further analyzed by molecular docking within vaccine and TLR3 receptor to assure its molecular interaction and binding affinity. In the end, In-silico cloning was also carried out for ensuring its expression efficiency.
 Recommendations: Nonetheless, the designed construct is proposed to be tested in laboratory settings to confirm its immunogenicity and safety.","PeriodicalId":9711,"journal":{"name":"Central European Journal of Biology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135512711","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-20DOI: 10.26650/eurjbiol.2023.1239827
Tülin Aşkun
{"title":"Investigation of Anti-Mycobacterial Activity of Orientin and Vitexin on the Six Mycobacterium tuberculosis Strains","authors":"Tülin Aşkun","doi":"10.26650/eurjbiol.2023.1239827","DOIUrl":"https://doi.org/10.26650/eurjbiol.2023.1239827","url":null,"abstract":"","PeriodicalId":9711,"journal":{"name":"Central European Journal of Biology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135617076","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-13DOI: 10.26650/eurjbiol.2023.1307239
Mehmet Gül, Fatma Özgeriş, Nezahat Kurt, Burcu Volkan, Ali İşlek, Atilla Çayır
Objective: Celiac disease (CD) is an inflammatory condition of the small intestine triggered by the consumption of gluten. A strict gluten-free diet (GFD) is the only treatment that can eliminate CD complications. It was aimed to evaluate the effect of a gluten-free diet on serum total glutathione (tGSH) level, superoxide dismutase (SOD), myeloperoxida (MPO), paroxanase (PON-1) and aryl esterase (ARE) activity in patients with celiac disease, an autoimmune disease. Materials and Methods: The study was conducted with 68 participants, 39 of whom were celiac and 29 were healthy. Two groups were formed in patients with celiac disease as newly diagnosed and previously diagnosed and following a gluten-free diet. Blood samples were taken from all participants and tGSH, SOD, MPO, PON-1, and ARE measurements were made spectrophotometrically from serum samples. Results: While no significant change was observed in tGSH, SOD, and ARE levels, MPO activity was observed to be significantly lower in celiac patients compared to healthy controls, while this decrease was found to be higher in the newly diagnosed group. While PON-1 activity was significantly lower in newly diagnosed patients compared to the control group, it was higher in the gluten-compatible diet group. Conclusion: Low MPO values in celiac patients may be insufficient to function by creating oxidative stress in inflammation. While PON-1 values are significantly lower in newly diagnosed celiacs, it can be said that they reach normal values with adherence to a gluten-free diet.
{"title":"Effect of Gluten-Free Diet on Serum Antioxidant Levels in Children with Celiac","authors":"Mehmet Gül, Fatma Özgeriş, Nezahat Kurt, Burcu Volkan, Ali İşlek, Atilla Çayır","doi":"10.26650/eurjbiol.2023.1307239","DOIUrl":"https://doi.org/10.26650/eurjbiol.2023.1307239","url":null,"abstract":"Objective: Celiac disease (CD) is an inflammatory condition of the small intestine triggered by the consumption of gluten. A strict gluten-free diet (GFD) is the only treatment that can eliminate CD complications. It was aimed to evaluate the effect of a gluten-free diet on serum total glutathione (tGSH) level, superoxide dismutase (SOD), myeloperoxida (MPO), paroxanase (PON-1) and aryl esterase (ARE) activity in patients with celiac disease, an autoimmune disease. Materials and Methods: The study was conducted with 68 participants, 39 of whom were celiac and 29 were healthy. Two groups were formed in patients with celiac disease as newly diagnosed and previously diagnosed and following a gluten-free diet. Blood samples were taken from all participants and tGSH, SOD, MPO, PON-1, and ARE measurements were made spectrophotometrically from serum samples. Results: While no significant change was observed in tGSH, SOD, and ARE levels, MPO activity was observed to be significantly lower in celiac patients compared to healthy controls, while this decrease was found to be higher in the newly diagnosed group. While PON-1 activity was significantly lower in newly diagnosed patients compared to the control group, it was higher in the gluten-compatible diet group. Conclusion: Low MPO values in celiac patients may be insufficient to function by creating oxidative stress in inflammation. While PON-1 values are significantly lower in newly diagnosed celiacs, it can be said that they reach normal values with adherence to a gluten-free diet.","PeriodicalId":9711,"journal":{"name":"Central European Journal of Biology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135918825","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: Dysentery is a severe form of diarrhea and caused by four bacteria include Shigella, Campylobacter, E.coli and Salmonella. They are responsible for higher morbidity and mortality rates resulting from dysentery every year across the world. Antibiotic therapy of this disease plays a critical role in decreasing the prevalence as well as the fatality rate of this infection. However, the management of this disease remains challenging, owing to the overall increase in resistance against many antimicrobials. Hence, it has become important to identify as well as develop therapeutic methods presenting novel avenues for infections. In the current study, proteome based mapping was utilized to find the potential drug targets for dysentery. There is need to identify novel drug and vaccine targets to control this disease. This study is designed to identify new drug targets to develop drug and vaccines to battle bacillary dysentery. Subtractive genomics approach was used in this study to find novel drug targets.
Methodology: The proteomes of Shigella, E. coli, Campylobacter and Salmonella were retrieved from Uniprot. Paralogs in these proteomes were removed by CD-HIT. Gene essentiality was screened by Geptop server 2.0. Host-pathogen interaction was analyzed through HPIDB database. To identify non-homologous proteins, the essential proteins were analyzed in Blastp against Homo sapiens (H. sapiens). The unique metabolic pathways were recognized by comparison of metabolic pathways of selected strains of bacteria and H. sapiens using the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway. Subcellular localization and functional classification of proteins involved in unique metabolic pathways were analyzed through PSORTb and SVMProt. Druggability potential of unique essential proteins was investigated using the DrugBank database.
Findings: Over all analysis showed 7 proteins that were common in all four bacteria. These proteins were essential to pathogens. Out of 7 proteins 6 proteins MURA, MURG, DAPA, MURB, DAPE, DnaA are reported as a drug target in different bacteria and one protein DAPD is novel. The study will enable the development of natural and cost-effective drugs against dysentery infections.
Recommendation: However, further validations are necessary to confirm their drug effectiveness and biocompatibility.
目的:痢疾是一种严重的腹泻，由志贺氏菌、弯曲杆菌、大肠杆菌和沙门氏菌四种细菌引起。它们每年在世界各地造成较高的痢疾发病率和死亡率。这种疾病的抗生素治疗在降低这种感染的患病率和死亡率方面起着至关重要的作用。然而，由于对许多抗微生物药物的耐药性总体上有所增加，该病的管理仍然具有挑战性。因此，重要的是确定并发展治疗方法，提出新的感染途径。在目前的研究中，基于蛋白质组的定位被用于寻找潜在的药物靶点痢疾。有必要确定新的药物和疫苗靶点来控制这种疾病。本研究旨在确定新的药物靶点，开发对抗细菌性痢疾的药物和疫苗。本研究采用减法基因组学方法寻找新的药物靶点。
方法:从Uniprot中提取志贺氏菌、大肠杆菌、弯曲杆菌和沙门氏菌的蛋白质组。通过CD-HIT去除这些蛋白质组中的相似物。基因重要性通过Geptop server 2.0进行筛选。通过HPIDB数据库分析宿主-病原体相互作用。为了鉴定非同源蛋白，我们分析了Blastp对智人(Homo sapiens)的必需蛋白。利用京都基因与基因组百科全书(KEGG)途径对所选细菌和智人的代谢途径进行比较，发现了独特的代谢途径。通过PSORTb和SVMProt分析了参与独特代谢途径的蛋白质的亚细胞定位和功能分类。使用DrugBank数据库研究独特必需蛋白的药物潜力。
结果:总体分析显示，在所有四种细菌中，共有7种蛋白质。这些蛋白质对病原体至关重要。在7种蛋白中，有6种蛋白MURA、MURG、DAPA、MURB、DAPE、DnaA被报道为不同细菌的药物靶点，其中一种蛋白DAPD是新发现的。这项研究将有助于开发抗痢疾感染的天然且具有成本效益的药物。建议:然而，需要进一步验证以确认其药物有效性和生物相容性。
{"title":"The Identification of Common Druggable Targets For Acute Dysentery in Four Pathogenic Bacteria, Shigella, Salmonella, Campylobacter and E.Coli","authors":"Iqra Shafique, Hira Shafique, Nimra Asif, Sadia Liaquat, Husnain Shahbaz","doi":"10.47672/ejb.1610","DOIUrl":"https://doi.org/10.47672/ejb.1610","url":null,"abstract":"Purpose: Dysentery is a severe form of diarrhea and caused by four bacteria include Shigella, Campylobacter, E.coli and Salmonella. They are responsible for higher morbidity and mortality rates resulting from dysentery every year across the world. Antibiotic therapy of this disease plays a critical role in decreasing the prevalence as well as the fatality rate of this infection. However, the management of this disease remains challenging, owing to the overall increase in resistance against many antimicrobials. Hence, it has become important to identify as well as develop therapeutic methods presenting novel avenues for infections. In the current study, proteome based mapping was utilized to find the potential drug targets for dysentery. There is need to identify novel drug and vaccine targets to control this disease. This study is designed to identify new drug targets to develop drug and vaccines to battle bacillary dysentery. Subtractive genomics approach was used in this study to find novel drug targets.
 Methodology: The proteomes of Shigella, E. coli, Campylobacter and Salmonella were retrieved from Uniprot. Paralogs in these proteomes were removed by CD-HIT. Gene essentiality was screened by Geptop server 2.0. Host-pathogen interaction was analyzed through HPIDB database. To identify non-homologous proteins, the essential proteins were analyzed in Blastp against Homo sapiens (H. sapiens). The unique metabolic pathways were recognized by comparison of metabolic pathways of selected strains of bacteria and H. sapiens using the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway. Subcellular localization and functional classification of proteins involved in unique metabolic pathways were analyzed through PSORTb and SVMProt. Druggability potential of unique essential proteins was investigated using the DrugBank database.
 Findings: Over all analysis showed 7 proteins that were common in all four bacteria. These proteins were essential to pathogens. Out of 7 proteins 6 proteins MURA, MURG, DAPA, MURB, DAPE, DnaA are reported as a drug target in different bacteria and one protein DAPD is novel. The study will enable the development of natural and cost-effective drugs against dysentery infections.
 Recommendation: However, further validations are necessary to confirm their drug effectiveness and biocompatibility.","PeriodicalId":9711,"journal":{"name":"Central European Journal of Biology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135251043","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-04DOI: 10.26650/eurjbiol.2023.1304325
Doruk Akdoğan, Ayşegül Peksel
{"title":"The Effectiveness of Ultrasound-Assisted Extraction on Antioxidative Properties of Bract Leaves of Globe Artichoke","authors":"Doruk Akdoğan, Ayşegül Peksel","doi":"10.26650/eurjbiol.2023.1304325","DOIUrl":"https://doi.org/10.26650/eurjbiol.2023.1304325","url":null,"abstract":"","PeriodicalId":9711,"journal":{"name":"Central European Journal of Biology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135644927","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-03DOI: 10.26650/eurjbiol.2023.01cn
Author Name Author Last Name
{"title":"Correction Note","authors":"Author Name Author Last Name","doi":"10.26650/eurjbiol.2023.01cn","DOIUrl":"https://doi.org/10.26650/eurjbiol.2023.01cn","url":null,"abstract":"","PeriodicalId":9711,"journal":{"name":"Central European Journal of Biology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135744884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-09-27DOI: 10.26650/eurjbiol.2023.1306497
Sehkar Oktay, Şükriye Çalışkan
{"title":"Potential Therapeutic Effect of Lipoic Acid on Methotrexate-Induced Oxidative Stress in Rat Heart","authors":"Sehkar Oktay, Şükriye Çalışkan","doi":"10.26650/eurjbiol.2023.1306497","DOIUrl":"https://doi.org/10.26650/eurjbiol.2023.1306497","url":null,"abstract":"","PeriodicalId":9711,"journal":{"name":"Central European Journal of Biology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135536563","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-09-21DOI: 10.26650/eurjbiol.2023.1328517
Eda Dağsuyu, Umar Magaji, Özlem Saçan, Refiye Yanardağ
{"title":"Moringa oleifera Ethanolic Extract Prevents Oxidative Damage on Lens Caused by Sodium Valproate Used in Epilepsy Treatment","authors":"Eda Dağsuyu, Umar Magaji, Özlem Saçan, Refiye Yanardağ","doi":"10.26650/eurjbiol.2023.1328517","DOIUrl":"https://doi.org/10.26650/eurjbiol.2023.1328517","url":null,"abstract":"","PeriodicalId":9711,"journal":{"name":"Central European Journal of Biology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136154335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-09-15DOI: 10.26650/eurjbiol.2023.1317681
Duygu Turan Sorhun, Ece Özturk
{"title":"The Effect of Culture Dimensionality and Brain Extracellular Matrix in Neuronal Differentiation","authors":"Duygu Turan Sorhun, Ece Özturk","doi":"10.26650/eurjbiol.2023.1317681","DOIUrl":"https://doi.org/10.26650/eurjbiol.2023.1317681","url":null,"abstract":"","PeriodicalId":9711,"journal":{"name":"Central European Journal of Biology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135395559","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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