Tatsuya Takizawa
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Tatsuya Takizawa has a total of 66 co-authors. Here are the top co-authors by number of shared publications:
Takehito Suzuki
Graduate School of Veterinary Medicine, Azabu University, Fuchinobe, Chuo-ku, Sagamihara, 252-5201, Japan
12 shared publicationsYoko Miyazaki
Graduate School of Veterinary Medicine, Azabu University, Fuchinobe, Chuo-ku, Sagamihara, 252-5201, Japan
11 shared publicationsKazuaki Tanaka
Graduate School of Veterinary Medicine, Azabu University, Fuchinobe, Chuo-ku, Sagamihara, 252-5201, Japan
8 shared publicationsMakoto Usami
Graduate School of Veterinary Medicine, Azabu University, Fuchinobe, Chuo-ku, Sagamihara, 252-5201, Japan
6 shared publications- Kazuaki Tanaka
School of Veterinary Medicine, Azabu University, Chuo-Ku, Sagamihara 252-5201, Japan
5 shared publications Hidetoshi Morita
Graduate School of Veterinary Medicine
3 shared publications
Latest Publications
- 19 February 2024
- Published by Elsevier in Nitric Oxide
- Vol. 145, 21-32
Protein S-nitrosylation is involved in valproic acid-promoted neuronal differentiation of adipose tissue-derived stem cells
- 19 February 2024
- Published by Elsevier in Nitric Oxide
- Vol. 145, 21-32
Protein S-nitrosylation is involved in valproic acid-promoted neuronal differentiation of adipose tissue-derived stem cells
- 4 January 2023
- Published by Wiley in Congenital Anomalies
- Vol. 63 (2) , 47-51
Complementary mRNA expression of enzymes producing nitric oxide and prostaglandin in ductus arteriosus with respect to their role in maintaining patency
MRNA expression of molecules related to the activity of nitric oxide or prostaglandin E2, the critical regulators maintaining the ductus arteriosus patency, was examined in rat ductus arteriosus at preterm (days 18.5 and 19.5 of pregnancy) and near term (days 20.5 and 21.5). The endothelial nitric oxide synthase mRNA level increased transiently at preterm and then decreased at near term. The cyclooxygenase 2 mRNA increased gradually from near-term to the term complementary to the reduced endothelial nitric oxide synthase mRNA. These results suggest that the role shift between nitric oxide and prostaglandin E2 in maintaining ductus arteriosus patency at preterm and near term may be due to complementary expression changes of endothelial nitric oxide synthase and cyclooxygenase 2 at the transcriptional level.
- 4 January 2023
- Published by Wiley in Congenital Anomalies
- Vol. 63 (2) , 47-51
Complementary mRNA expression of enzymes producing nitric oxide and prostaglandin in ductus arteriosus with respect to their role in maintaining patency
MRNA expression of molecules related to the activity of nitric oxide or prostaglandin E2, the critical regulators maintaining the ductus arteriosus patency, was examined in rat ductus arteriosus at preterm (days 18.5 and 19.5 of pregnancy) and near term (days 20.5 and 21.5). The endothelial nitric oxide synthase mRNA level increased transiently at preterm and then decreased at near term. The cyclooxygenase 2 mRNA increased gradually from near-term to the term complementary to the reduced endothelial nitric oxide synthase mRNA. These results suggest that the role shift between nitric oxide and prostaglandin E2 in maintaining ductus arteriosus patency at preterm and near term may be due to complementary expression changes of endothelial nitric oxide synthase and cyclooxygenase 2 at the transcriptional level.
- 3 January 2023
- Published by Elsevier in Reproductive Biology
- Vol. 23 (1) , 100726
Differential expression of desmin in the uterine myometrium and cervix as a possible mechanism for successful parturition in rats
- 3 January 2023
- Published by Elsevier in Reproductive Biology
- Vol. 23 (1) , 100726
Differential expression of desmin in the uterine myometrium and cervix as a possible mechanism for successful parturition in rats
- 20 April 2021
- Published by Wiley in Congenital Anomalies
- Vol. 61 (5) , 183-187
L‐NAME, a nitric oxide synthase inhibitor, increases the protein expression of both executioner and inhibitor of apoptosis in the placental bed of mid‐to‐late pregnant rats
The involvement of nitric oxide (NO) signaling in apoptosis was examined in the placental bed of mid‐to‐late pregnant rats. Pregnant rats were treated with l‐NAME, a nitric oxide synthase inhibitor, by subcutaneous infusion for 48 hours before the examination at day 13.5, 17.5, or 21.5. l‐NAME induced apoptosis in the placental bed to a limited extent at days 13.5 and 17.5, but not at day 21.5. When the placental bed was examined at day 17.5, the protein expression of both executioner (C‐Cas3) and inhibitor (XIAP) of apoptosis was increased by l‐NAME, but they did not co‐localized with apoptosis. It was presumed that placental bed apoptosis induced by l‐NAME is regulated through the expression of both executioner and inhibitor, possibly involving protein S‐nitrosylation.
- 20 April 2021
- Published by Wiley in Congenital Anomalies
- Vol. 61 (5) , 183-187
L‐NAME, a nitric oxide synthase inhibitor, increases the protein expression of both executioner and inhibitor of apoptosis in the placental bed of mid‐to‐late pregnant rats
The involvement of nitric oxide (NO) signaling in apoptosis was examined in the placental bed of mid‐to‐late pregnant rats. Pregnant rats were treated with l‐NAME, a nitric oxide synthase inhibitor, by subcutaneous infusion for 48 hours before the examination at day 13.5, 17.5, or 21.5. l‐NAME induced apoptosis in the placental bed to a limited extent at days 13.5 and 17.5, but not at day 21.5. When the placental bed was examined at day 17.5, the protein expression of both executioner (C‐Cas3) and inhibitor (XIAP) of apoptosis was increased by l‐NAME, but they did not co‐localized with apoptosis. It was presumed that placental bed apoptosis induced by l‐NAME is regulated through the expression of both executioner and inhibitor, possibly involving protein S‐nitrosylation.
- 1 January 2021
- Published by Elsevier in Nitric Oxide
- Vol. 106, 35-44
Valproic acid up-regulates the whole NO-citrulline cycle for potent iNOS-NO signaling to promote neuronal differentiation of adipose tissue-derived stem cells
- 1 January 2021
- Published by Elsevier in Nitric Oxide
- Vol. 106, 35-44
Valproic acid up-regulates the whole NO-citrulline cycle for potent iNOS-NO signaling to promote neuronal differentiation of adipose tissue-derived stem cells
- 1 December 2019
- Published by Elsevier in Nitric Oxide
- Vol. 93, 1-5
Valproic acid promotes mature neuronal differentiation of adipose tissue-derived stem cells through iNOS–NO–sGC signaling pathway
- 1 December 2019
- Published by Elsevier in Nitric Oxide
- Vol. 93, 1-5
Valproic acid promotes mature neuronal differentiation of adipose tissue-derived stem cells through iNOS–NO–sGC signaling pathway
- 7 October 2016
- Published by Oxford University Press (OUP) in Microscopy
- Vol. 66 (2) , 136-142
A convenient technique for live-cell observation on the surface of polytetrafluoroethylene with a phase-contrast microscope
Phase-contrast microscopy is a convenient technique for live-cell observation on the surface of materials with high optical transmittance. Here, we demonstrate a novel technique to observe living cells on the surface of materials with low optical transmittance, such as polytetrafluoroethylene (PTFE), which are widely used in biomaterials for blood-contacting devices. The surface of a cover glass was coated with a thin PTFE layer with sufficient transmittance, thereby enabling the observation of living cells on the PTFE surface with a phase-contrast microscope.
- 7 October 2016
- Published by Oxford University Press (OUP) in Microscopy
- Vol. 66 (2) , 136-142
A convenient technique for live-cell observation on the surface of polytetrafluoroethylene with a phase-contrast microscope
Phase-contrast microscopy is a convenient technique for live-cell observation on the surface of materials with high optical transmittance. Here, we demonstrate a novel technique to observe living cells on the surface of materials with low optical transmittance, such as polytetrafluoroethylene (PTFE), which are widely used in biomaterials for blood-contacting devices. The surface of a cover glass was coated with a thin PTFE layer with sufficient transmittance, thereby enabling the observation of living cells on the PTFE surface with a phase-contrast microscope.