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Showing 13 to 24 of 44 entries
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Human Wharton's jelly-derived mesenchymal stem cells express oocyte developmental genes during co-culture with placental cells.

Iranian journal of basic medical sciences

Asgari HR, Akbari M, Abbasi M, Ai J, Korouji M, Aliakbari F, Babatunde KA, Aval FS, Joghataei MT.
PMID: 25810872
Iran J Basic Med Sci. 2015 Jan;18(1):22-9.

OBJECTIVES: The present day challenge is how to obtain germ cells from stem cells to treat patients with cancer and infertility. Much more efforts have been made to develop a procedure for attaining germ cells in vitro. Recently, human...

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Asgari HR, Akbari M, Abbasi M, et al. Human Wharton's jelly-derived mesenchymal stem cells express oocyte developmental genes during co-culture with placental cells. Iran J Basic Med Sci. 2015;18(1):22-9
Asgari, H. R., Akbari, M., Abbasi, M., Ai, J., Korouji, M., Aliakbari, F., Babatunde, K. A., Aval, F. S., & Joghataei, M. T. (2015). Human Wharton's jelly-derived mesenchymal stem cells express oocyte developmental genes during co-culture with placental cells. Iranian journal of basic medical sciences, 18(1), 22-9.
Asgari, Hamid Reza, et al. "Human Wharton's jelly-derived mesenchymal stem cells express oocyte developmental genes during co-culture with placental cells." Iranian journal of basic medical sciences vol. 18,1 (2015): 22-9.
Asgari HR, Akbari M, Abbasi M, Ai J, Korouji M, Aliakbari F, Babatunde KA, Aval FS, Joghataei MT. Human Wharton's jelly-derived mesenchymal stem cells express oocyte developmental genes during co-culture with placental cells. Iran J Basic Med Sci. 2015 Jan;18(1):22-9. PMID: 25810872; PMCID: PMC4366739.
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Biomolecular phases in transverse palatal distraction: A review.

Saudi journal of biological sciences

Alshahrani I.
PMID: 30505176
Saudi J Biol Sci. 2018 Nov;25(7):1322-1325. doi: 10.1016/j.sjbs.2018.05.009. Epub 2018 May 07.

Transverse palatal distraction is a biological process of regenerating new bone and enveloping soft tissues in the maxillary palate region. This technique is similar to Osteo-distraction (OD) procedure for bone lengthening in which gradual and controlled traction forces are...

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Alshahrani I. Biomolecular phases in transverse palatal distraction: A review. Saudi J Biol Sci. 2018;25(7):1322-1325doi: 10.1016/j.sjbs.2018.05.009.
Alshahrani, I. (2018). Biomolecular phases in transverse palatal distraction: A review. Saudi journal of biological sciences, 25(7), 1322-1325. https://doi.org/10.1016/j.sjbs.2018.05.009
Alshahrani, Ibrahim. "Biomolecular phases in transverse palatal distraction: A review." Saudi journal of biological sciences vol. 25,7 (2018): 1322-1325. doi: https://doi.org/10.1016/j.sjbs.2018.05.009
Alshahrani I. Biomolecular phases in transverse palatal distraction: A review. Saudi J Biol Sci. 2018 Nov;25(7):1322-1325. doi: 10.1016/j.sjbs.2018.05.009. Epub 2018 May 07. PMID: 30505176; PMCID: PMC6252022.
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Differentiation of adipose-derived stem cells to chondrocytes using electrospraying.

Scientific reports

Nosoudi N, Hart C, McKnight I, Esmaeilpour M, Ghomian T, Zadeh A, Raines R, Ramirez Vick JE.
PMID: 34934143
Sci Rep. 2021 Dec 21;11(1):24301. doi: 10.1038/s41598-021-03824-5.

An important challenge in the fabrication of tissue engineered constructs for regenerative medical applications is the development of processes capable of delivering cells and biomaterials to specific locations in a consistent manner. Electrospraying live cells has been introduced in...

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Nosoudi N, Hart C, McKnight I, et al. Differentiation of adipose-derived stem cells to chondrocytes using electrospraying. Sci Rep. 2021;11(1):24301doi: 10.1038/s41598-021-03824-5.
Nosoudi, N., Hart, C., McKnight, I., Esmaeilpour, M., Ghomian, T., Zadeh, A., Raines, R., & Ramirez Vick, J. E. (2021). Differentiation of adipose-derived stem cells to chondrocytes using electrospraying. Scientific reports, 11(1), 24301. https://doi.org/10.1038/s41598-021-03824-5
Nosoudi, Nasim, et al. "Differentiation of adipose-derived stem cells to chondrocytes using electrospraying." Scientific reports vol. 11,1 (2021): 24301. doi: https://doi.org/10.1038/s41598-021-03824-5
Nosoudi N, Hart C, McKnight I, Esmaeilpour M, Ghomian T, Zadeh A, Raines R, Ramirez Vick JE. Differentiation of adipose-derived stem cells to chondrocytes using electrospraying. Sci Rep. 2021 Dec 21;11(1):24301. doi: 10.1038/s41598-021-03824-5. PMID: 34934143.
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Hypermethylation at the CXCR5 gene locus limits trafficking potential of CD8+ T cells into B-cell follicles during HIV-1 infection.

Blood advances

Ogunshola FJ, Smidt W, Naidoo AF, Nkosi TP, Ngubane T, Khaba PT, Baiyegunhi OO, Mahlobo B, Rasehlo S, Ngema N, Jajbhay I, Dong KL, Ramsuran V, Pansegrouw J, Ndung'u T, Walker B, Oliveria T, Ndhlovu ZM.
PMID: 34991160
Blood Adv. 2022 Jan 06; doi: 10.1182/bloodadvances.2021006001. Epub 2022 Jan 06.

CD8+ T-cells play an important role in HIV control. However, in human lymph nodes (LNs), only a small subset of CD8+ T-cells expresses CXCR5, the chemokine receptor required for cell migration into B cell follicles, which are major sanctuaries...

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Ogunshola FJ, Smidt W, Naidoo AF, et al. Hypermethylation at the CXCR5 gene locus limits trafficking potential of CD8+ T cells into B-cell follicles during HIV-1 infection. Blood Adv. 2022;doi: 10.1182/bloodadvances.2021006001.
Ogunshola, F. J., Smidt, W., Naidoo, A. F., Nkosi, T. P., Ngubane, T., Khaba, P. T., Baiyegunhi, O. O., Mahlobo, B., Rasehlo, S., Ngema, N., Jajbhay, I., Dong, K. L., Ramsuran, V., Pansegrouw, J., Ndung'u, T., Walker, B., Oliveria, T., & Ndhlovu, Z. M. (2022). Hypermethylation at the CXCR5 gene locus limits trafficking potential of CD8+ T cells into B-cell follicles during HIV-1 infection. Blood advances, . https://doi.org/10.1182/bloodadvances.2021006001
Ogunshola, Funsho J, et al. "Hypermethylation at the CXCR5 gene locus limits trafficking potential of CD8+ T cells into B-cell follicles during HIV-1 infection." Blood advances vol. (2022). doi: https://doi.org/10.1182/bloodadvances.2021006001
Ogunshola FJ, Smidt W, Naidoo AF, Nkosi TP, Ngubane T, Khaba PT, Baiyegunhi OO, Mahlobo B, Rasehlo S, Ngema N, Jajbhay I, Dong KL, Ramsuran V, Pansegrouw J, Ndung'u T, Walker B, Oliveria T, Ndhlovu ZM. Hypermethylation at the CXCR5 gene locus limits trafficking potential of CD8+ T cells into B-cell follicles during HIV-1 infection. Blood Adv. 2022 Jan 06; doi: 10.1182/bloodadvances.2021006001. Epub 2022 Jan 06. PMID: 34991160.
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[Myostatin - a modern understanding of the physiological role and significance in the development of age-associated diseases.].

Advances in gerontology = Uspekhi gerontologii

Gazdanova AA, Kukes VG, Parfenova OK, Sidorov NG, Perkov AV, Solovieva SA, Ryazantceva OV, Lenkova NI.
PMID: 34998007
Adv Gerontol. 2021;34(5):701-706.

Myostatin is a protein belonging to the myokine class, the family of transforming growth factors β (TGF-β). The review article, based on the analysis of literature data, shows the key role of myostatin in the development of senile sarcopenia...

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Gazdanova AA, Kukes VG, Parfenova OK, et al. [Myostatin - a modern understanding of the physiological role and significance in the development of age-associated diseases.]. Adv Gerontol. 2021;34(5):701-706
Gazdanova, A. A., Kukes, V. G., Parfenova, O. K., Sidorov, N. G., Perkov, A. V., Solovieva, S. A., Ryazantceva, O. V., & Lenkova, N. I. (2021). [Myostatin - a modern understanding of the physiological role and significance in the development of age-associated diseases.]. Advances in gerontology = Uspekhi gerontologii, 34(5), 701-706.
Gazdanova, A A, et al. "[Myostatin - a modern understanding of the physiological role and significance in the development of age-associated diseases.]." Advances in gerontology = Uspekhi gerontologii vol. 34,5 (2021): 701-706.
Gazdanova AA, Kukes VG, Parfenova OK, Sidorov NG, Perkov AV, Solovieva SA, Ryazantceva OV, Lenkova NI. [Myostatin - a modern understanding of the physiological role and significance in the development of age-associated diseases.]. Adv Gerontol. 2021;34(5):701-706. Russian. PMID: 34998007.
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Bioactive molecules for regenerative pulp capping.

European cells & materials

Whitehouse LL, Thomson NH, Do T, Feichtinger GA.
PMID: 34842279
Eur Cell Mater. 2021 Nov 29;41:415-437. doi: 10.22203/eCM.v042a26.

Since the discovery of bioactive molecules sequestered in dentine, researchers have been exploring ways to harness their activities for dental regeneration. One specific area, discussed in this review, is that of dental-pulp capping. Dental-pulp caps are placed when the...

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Whitehouse LL, Thomson NH, Do T, et al. Bioactive molecules for regenerative pulp capping. Eur Cell Mater. 2021;41:415-437doi: 10.22203/eCM.v042a26.
Whitehouse, L. L., Thomson, N. H., Do, T., & Feichtinger, G. A. (2021). Bioactive molecules for regenerative pulp capping. European cells & materials, 41415-437. https://doi.org/10.22203/eCM.v042a26
Whitehouse, L L, et al. "Bioactive molecules for regenerative pulp capping." European cells & materials vol. 41 (2021): 415-437. doi: https://doi.org/10.22203/eCM.v042a26
Whitehouse LL, Thomson NH, Do T, Feichtinger GA. Bioactive molecules for regenerative pulp capping. Eur Cell Mater. 2021 Nov 29;41:415-437. doi: 10.22203/eCM.v042a26. PMID: 34842279.
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Bioactive molecules for regenerative pulp capping.

European cells & materials

Whitehouse LL, Thomson NH, Do T, Feichtinger GA.
PMID: 34842279
Eur Cell Mater. 2021 Nov 29;42:415-437. doi: 10.22203/eCM.v042a26.

Since the discovery of bioactive molecules sequestered in dentine, researchers have been exploring ways to harness their activities for dental regeneration. One specific area, discussed in this review, is that of dental-pulp capping. Dental-pulp caps are placed when the...

Cite
Whitehouse LL, Thomson NH, Do T, et al. Bioactive molecules for regenerative pulp capping. Eur Cell Mater. 2021;42:415-437doi: 10.22203/eCM.v042a26.
Whitehouse, L. L., Thomson, N. H., Do, T., & Feichtinger, G. A. (2021). Bioactive molecules for regenerative pulp capping. European cells & materials, 42415-437. https://doi.org/10.22203/eCM.v042a26
Whitehouse, L L, et al. "Bioactive molecules for regenerative pulp capping." European cells & materials vol. 42 (2021): 415-437. doi: https://doi.org/10.22203/eCM.v042a26
Whitehouse LL, Thomson NH, Do T, Feichtinger GA. Bioactive molecules for regenerative pulp capping. Eur Cell Mater. 2021 Nov 29;42:415-437. doi: 10.22203/eCM.v042a26. PMID: 34842279.
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Suture biology: Lessons from molecular genetics of craniosynostosis syndromes.

Clinical orthodontics and research

Nah H.
PMID: 11168283
Clin Orthod Res. 2000 Feb;3(1):37-45. doi: 10.1034/j.1600-0544.2000.030107.x.

Sutures are critical growth sites in the developing craniofacial skeleton, and equally importantly, they are the target tissues for certain orthodontic therapeutic modalities. For these reasons, suture biology has long been an area of significant interest in orthodontics. In...

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Nah H. Suture biology: Lessons from molecular genetics of craniosynostosis syndromes. Clin Orthod Res. 2000;3(1):37-45doi: 10.1034/j.1600-0544.2000.030107.x.
Nah, H. (2000). Suture biology: Lessons from molecular genetics of craniosynostosis syndromes. Clinical orthodontics and research, 3(1), 37-45. https://doi.org/10.1034/j.1600-0544.2000.030107.x
Nah, H. "Suture biology: Lessons from molecular genetics of craniosynostosis syndromes." Clinical orthodontics and research vol. 3,1 (2000): 37-45. doi: https://doi.org/10.1034/j.1600-0544.2000.030107.x
Nah H. Suture biology: Lessons from molecular genetics of craniosynostosis syndromes. Clin Orthod Res. 2000 Feb;3(1):37-45. doi: 10.1034/j.1600-0544.2000.030107.x. PMID: 11168283.
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[No title available]

Animals : an open access journal from MDPI

Ramirez G, Palomino J, Aspee K, De Los Reyes M.
PMID: 32164341
Animals (Basel). 2020 Mar 10;10(3). doi: 10.3390/ani10030462.

The competence to undergo expansion is a characteristic of cumulus cells (CCs). The aim was to investigate the expression of

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Ramirez G, Palomino J, Aspee K, et al. . Animals (Basel). 2020;10(3)doi: 10.3390/ani10030462.
Ramirez, G., Palomino, J., Aspee, K., & De Los Reyes, M. (2020). . Animals : an open access journal from MDPI, 10(3), . https://doi.org/10.3390/ani10030462
Ramirez, George, et al. "." Animals : an open access journal from MDPI vol. 10,3 (2020). doi: https://doi.org/10.3390/ani10030462
Ramirez G, Palomino J, Aspee K, De Los Reyes M. . Animals (Basel). 2020 Mar 10;10(3). doi: 10.3390/ani10030462. PMID: 32164341; PMCID: PMC7143337.
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Ineffective levels of transforming growth factors and their receptor account for old age being a risk factor for Alzheimer's disease.

Alzheimer's & dementia (New York, N. Y.)

Fessel J.
PMID: 31890854
Alzheimers Dement (N Y). 2019 Dec 09;5:899-905. doi: 10.1016/j.trci.2019.11.007. eCollection 2019.

After the midninth decade of age, the incidence rates of Alzheimer's disease (AD) and the presence of active TGF-β1 show comparable increases. The hypothesis is proposed that the reason why advanced age is a major risk factor for AD...

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Fessel J. Ineffective levels of transforming growth factors and their receptor account for old age being a risk factor for Alzheimer's disease. Alzheimers Dement (N Y). 2019;5:899-905doi: 10.1016/j.trci.2019.11.007.
Fessel, J. (2019). Ineffective levels of transforming growth factors and their receptor account for old age being a risk factor for Alzheimer's disease. Alzheimer's & dementia (New York, N. Y.), 5899-905. https://doi.org/10.1016/j.trci.2019.11.007
Fessel, Jeffrey. "Ineffective levels of transforming growth factors and their receptor account for old age being a risk factor for Alzheimer's disease." Alzheimer's & dementia (New York, N. Y.) vol. 5 (2019): 899-905. doi: https://doi.org/10.1016/j.trci.2019.11.007
Fessel J. Ineffective levels of transforming growth factors and their receptor account for old age being a risk factor for Alzheimer's disease. Alzheimers Dement (N Y). 2019 Dec 09;5:899-905. doi: 10.1016/j.trci.2019.11.007. eCollection 2019. PMID: 31890854; PMCID: PMC6926356.
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Exogenous transforming growth factor-beta(2) enhances connective tissue formation in transforming growth factor-beta(1)-deficient, healing-impaired dermal wounds in mice.

Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society

Ksander GA, Gerhardt CO, Olsen DR.
PMID: 17163882
Wound Repair Regen. 1993 Jul;1(3):137-48. doi: 10.1046/j.1524-475X.1993.10303.x.

Connective tissue formation is markedly reduced in full-thickness mouse dermal wounds that are covered with synthetic, adherent, moisture vapor-permeable membrane when compared with formation in similar but nonoccluded wounds. The transforming growth factors-beta (TGF-beta) are a family of multifunctional...

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Ksander GA, Gerhardt CO, Olsen DR. Exogenous transforming growth factor-beta(2) enhances connective tissue formation in transforming growth factor-beta(1)-deficient, healing-impaired dermal wounds in mice. Wound Repair Regen. 1993;1(3):137-48doi: 10.1046/j.1524-475X.1993.10303.x.
Ksander, G. A., Gerhardt, C. O., & Olsen, D. R. (1993). Exogenous transforming growth factor-beta(2) enhances connective tissue formation in transforming growth factor-beta(1)-deficient, healing-impaired dermal wounds in mice. Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society, 1(3), 137-48. https://doi.org/10.1046/j.1524-475X.1993.10303.x
Ksander, G A, et al. "Exogenous transforming growth factor-beta(2) enhances connective tissue formation in transforming growth factor-beta(1)-deficient, healing-impaired dermal wounds in mice." Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society vol. 1,3 (1993): 137-48. doi: https://doi.org/10.1046/j.1524-475X.1993.10303.x
Ksander GA, Gerhardt CO, Olsen DR. Exogenous transforming growth factor-beta(2) enhances connective tissue formation in transforming growth factor-beta(1)-deficient, healing-impaired dermal wounds in mice. Wound Repair Regen. 1993 Jul;1(3):137-48. doi: 10.1046/j.1524-475X.1993.10303.x. PMID: 17163882.
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Correction for Echeverría et al., Endotoxin-Induced Endothelial Fibrosis Is Dependent on Expression of Transforming Growth Factors β1 and β2.

Infection and immunity

Echeverría C, Montorfano I, Tapia P, Riedel C, Cabello-Verrugio C, Simon F.
PMID: 26810751
Infect Immun. 2016 Jan 25;84(2):609-10. doi: 10.1128/IAI.01314-15. Print 2016 Feb.

No abstract available.

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Echeverría C, Montorfano I, Tapia P, et al. Correction for Echeverría et al., Endotoxin-Induced Endothelial Fibrosis Is Dependent on Expression of Transforming Growth Factors β1 and β2. Infect Immun. 2016;84(2):609-10doi: 10.1128/IAI.01314-15.
Echeverría, C., Montorfano, I., Tapia, P., Riedel, C., Cabello-Verrugio, C., & Simon, F. (2016). Correction for Echeverría et al., Endotoxin-Induced Endothelial Fibrosis Is Dependent on Expression of Transforming Growth Factors β1 and β2. Infection and immunity, 84(2), 609-10. https://doi.org/10.1128/IAI.01314-15
Echeverría, César, et al. "Correction for Echeverría et al., Endotoxin-Induced Endothelial Fibrosis Is Dependent on Expression of Transforming Growth Factors β1 and β2." Infection and immunity vol. 84,2 (2016): 609-10. doi: https://doi.org/10.1128/IAI.01314-15
Echeverría C, Montorfano I, Tapia P, Riedel C, Cabello-Verrugio C, Simon F. Correction for Echeverría et al., Endotoxin-Induced Endothelial Fibrosis Is Dependent on Expression of Transforming Growth Factors β1 and β2. Infect Immun. 2016 Jan 25;84(2):609-10. doi: 10.1128/IAI.01314-15. Print 2016 Feb. PMID: 26810751; PMCID: PMC4730565.
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Showing 13 to 24 of 44 entries