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Mitochondria-Endoplasmic Reticulum Crosstalk in Parkinson's Disease: The Role of Brain Renin Angiotensin System Components.

Biomolecules

Sunanda T, Ray B, Mahalakshmi AM, Bhat A, Rashan L, Rungratanawanich W, Song BJ, Essa MM, Sakharkar MK, Chidambaram SB.
PMID: 34827667
Biomolecules. 2021 Nov 10;11(11). doi: 10.3390/biom11111669.

The past few decades have seen an increased emphasis on the involvement of the mitochondrial-associated membrane (MAM) in various neurodegenerative diseases, particularly in Parkinson's disease (PD) and Alzheimer's disease (AD). In PD, alterations in mitochondria, endoplasmic reticulum (ER), and...

Cite
Sunanda T, Ray B, Mahalakshmi AM, et al. Mitochondria-Endoplasmic Reticulum Crosstalk in Parkinson's Disease: The Role of Brain Renin Angiotensin System Components. Biomolecules. 2021;11(11)doi: 10.3390/biom11111669.
Sunanda, T., Ray, B., Mahalakshmi, A. M., Bhat, A., Rashan, L., Rungratanawanich, W., Song, B. J., Essa, M. M., Sakharkar, M. K., & Chidambaram, S. B. (2021). Mitochondria-Endoplasmic Reticulum Crosstalk in Parkinson's Disease: The Role of Brain Renin Angiotensin System Components. Biomolecules, 11(11), . https://doi.org/10.3390/biom11111669
Sunanda, Tuladhar, et al. "Mitochondria-Endoplasmic Reticulum Crosstalk in Parkinson's Disease: The Role of Brain Renin Angiotensin System Components." Biomolecules vol. 11,11 (2021). doi: https://doi.org/10.3390/biom11111669
Sunanda T, Ray B, Mahalakshmi AM, Bhat A, Rashan L, Rungratanawanich W, Song BJ, Essa MM, Sakharkar MK, Chidambaram SB. Mitochondria-Endoplasmic Reticulum Crosstalk in Parkinson's Disease: The Role of Brain Renin Angiotensin System Components. Biomolecules. 2021 Nov 10;11(11). doi: 10.3390/biom11111669. PMID: 34827667; PMCID: PMC8615717.
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Changes of gene expressions in spontaneously hypertensive rat model after losartan treatment.

Korean circulation journal

Cha JH, Lee HR, Kim KC, Cho MS, Hong YM.
PMID: 23236328
Korean Circ J. 2012 Nov;42(11):761-8. doi: 10.4070/kcj.2012.42.11.761. Epub 2012 Nov 28.

BACKGROUND AND OBJECTIVES: The renin angiotensin system seems to play an important role in the development of cardiac and vascular hypertrophy in hypertension. The changes in pathology, and gene expressions of the angiotensin II receptor type 1A (ATIA) and...

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Cha JH, Lee HR, Kim KC, et al. Changes of gene expressions in spontaneously hypertensive rat model after losartan treatment. Korean Circ J. 2012;42(11):761-8doi: 10.4070/kcj.2012.42.11.761.
Cha, J. H., Lee, H. R., Kim, K. C., Cho, M. S., & Hong, Y. M. (2012). Changes of gene expressions in spontaneously hypertensive rat model after losartan treatment. Korean circulation journal, 42(11), 761-8. https://doi.org/10.4070/kcj.2012.42.11.761
Cha, Ji Hei, et al. "Changes of gene expressions in spontaneously hypertensive rat model after losartan treatment." Korean circulation journal vol. 42,11 (2012): 761-8. doi: https://doi.org/10.4070/kcj.2012.42.11.761
Cha JH, Lee HR, Kim KC, Cho MS, Hong YM. Changes of gene expressions in spontaneously hypertensive rat model after losartan treatment. Korean Circ J. 2012 Nov;42(11):761-8. doi: 10.4070/kcj.2012.42.11.761. Epub 2012 Nov 28. PMID: 23236328; PMCID: PMC3518710.
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The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147 receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease.

Clinical science (London, England : 1979)

Avolio E, Carrabba M, Milligan R, Kavanagh Williamson M, Beltrami AP, Gupta K, Elvers KT, Gamez M, Foster RR, Gillespie K, Hamilton F, Arnold D, Berger I, Davidson AD, Hill D, Caputo M, Madeddu P.
PMID: 34807265
Clin Sci (Lond). 2021 Dec 22;135(24):2667-2689. doi: 10.1042/CS20210735.

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes a broad range of clinical responses including prominent microvascular damage. The capacity of SARS-CoV-2 to infect vascular cells is still debated. Additionally, the SARS-CoV-2 Spike (S) protein may act as...

Cite
Avolio E, Carrabba M, Milligan R, et al. The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147 receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease. Clin Sci (Lond). 2021;135(24):2667-2689doi: 10.1042/CS20210735.
Avolio, E., Carrabba, M., Milligan, R., Kavanagh Williamson, M., Beltrami, A. P., Gupta, K., Elvers, K. T., Gamez, M., Foster, R. R., Gillespie, K., Hamilton, F., Arnold, D., Berger, I., Davidson, A. D., Hill, D., Caputo, M., & Madeddu, P. (2021). The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147 receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease. Clinical science (London, England : 1979), 135(24), 2667-2689. https://doi.org/10.1042/CS20210735
Avolio, Elisa, et al. "The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147 receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease." Clinical science (London, England : 1979) vol. 135,24 (2021): 2667-2689. doi: https://doi.org/10.1042/CS20210735
Avolio E, Carrabba M, Milligan R, Kavanagh Williamson M, Beltrami AP, Gupta K, Elvers KT, Gamez M, Foster RR, Gillespie K, Hamilton F, Arnold D, Berger I, Davidson AD, Hill D, Caputo M, Madeddu P. The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147 receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease. Clin Sci (Lond). 2021 Dec 22;135(24):2667-2689. doi: 10.1042/CS20210735. PMID: 34807265.
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The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147 receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease.

Clinical science (London, England : 1979)

Avolio E, Carrabba M, Milligan R, Kavanagh Williamson M, Beltrami AP, Gupta K, Elvers KT, Gamez M, Foster RR, Gillespie K, Hamilton F, Arnold D, Berger I, Davidson AD, Hill D, Caputo M, Madeddu P.
PMID: 34807265
Clin Sci (Lond). 2021 Dec 22;135(24):2667-2689. doi: 10.1042/CS20210735.

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes a broad range of clinical responses including prominent microvascular damage. The capacity of SARS-CoV-2 to infect vascular cells is still debated. Additionally, the SARS-CoV-2 Spike (S) protein may act as...

Cite
Avolio E, Carrabba M, Milligan R, et al. The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147 receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease. Clin Sci (Lond). 2021;135(24):2667-2689doi: 10.1042/CS20210735.
Avolio, E., Carrabba, M., Milligan, R., Kavanagh Williamson, M., Beltrami, A. P., Gupta, K., Elvers, K. T., Gamez, M., Foster, R. R., Gillespie, K., Hamilton, F., Arnold, D., Berger, I., Davidson, A. D., Hill, D., Caputo, M., & Madeddu, P. (2021). The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147 receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease. Clinical science (London, England : 1979), 135(24), 2667-2689. https://doi.org/10.1042/CS20210735
Avolio, Elisa, et al. "The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147 receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease." Clinical science (London, England : 1979) vol. 135,24 (2021): 2667-2689. doi: https://doi.org/10.1042/CS20210735
Avolio E, Carrabba M, Milligan R, Kavanagh Williamson M, Beltrami AP, Gupta K, Elvers KT, Gamez M, Foster RR, Gillespie K, Hamilton F, Arnold D, Berger I, Davidson AD, Hill D, Caputo M, Madeddu P. The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147 receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease. Clin Sci (Lond). 2021 Dec 22;135(24):2667-2689. doi: 10.1042/CS20210735. PMID: 34807265.
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Human eggs, zygotes, and embryos express the receptor angiotensin 1-converting enzyme 2 and transmembrane serine protease 2 protein necessary for severe acute respiratory syndrome coronavirus 2 infection.

F&S science

Rajput SK, Logsdon DM, Kile B, Engelhorn HJ, Goheen B, Khan S, Swain J, McCormick S, Schoolcraft WB, Yuan Y, Krisher RL.
PMID: 33521687
F S Sci. 2021 Feb;2(1):33-42. doi: 10.1016/j.xfss.2020.12.005. Epub 2020 Dec 24.

OBJECTIVE: To study messenger ribonucleic acid (mRNA) and protein expressions of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) entry receptors (angiotensin 1-converting enzyme 2 [ACE2] and CD147) and proteases (transmembrane serine protease 2 [TMPRSS2] and cathepsin L [CTSL]) in...

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Rajput SK, Logsdon DM, Kile B, et al. Human eggs, zygotes, and embryos express the receptor angiotensin 1-converting enzyme 2 and transmembrane serine protease 2 protein necessary for severe acute respiratory syndrome coronavirus 2 infection. F S Sci. 2020;2(1):33-42doi: 10.1016/j.xfss.2020.12.005.
Rajput, S. K., Logsdon, D. M., Kile, B., Engelhorn, H. J., Goheen, B., Khan, S., Swain, J., McCormick, S., Schoolcraft, W. B., Yuan, Y., & Krisher, R. L. (2021). Human eggs, zygotes, and embryos express the receptor angiotensin 1-converting enzyme 2 and transmembrane serine protease 2 protein necessary for severe acute respiratory syndrome coronavirus 2 infection. F&S science, 2(1), 33-42. https://doi.org/10.1016/j.xfss.2020.12.005
Rajput, Sandeep K, et al. "Human eggs, zygotes, and embryos express the receptor angiotensin 1-converting enzyme 2 and transmembrane serine protease 2 protein necessary for severe acute respiratory syndrome coronavirus 2 infection." F&S science vol. 2,1 (2021): 33-42. doi: https://doi.org/10.1016/j.xfss.2020.12.005
Rajput SK, Logsdon DM, Kile B, Engelhorn HJ, Goheen B, Khan S, Swain J, McCormick S, Schoolcraft WB, Yuan Y, Krisher RL. Human eggs, zygotes, and embryos express the receptor angiotensin 1-converting enzyme 2 and transmembrane serine protease 2 protein necessary for severe acute respiratory syndrome coronavirus 2 infection. F S Sci. 2021 Feb;2(1):33-42. doi: 10.1016/j.xfss.2020.12.005. Epub 2020 Dec 24. PMID: 33521687; PMCID: PMC7831752.
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The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147-receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease.

Clinical science (London, England : 1979)

Avolio E, Carrabba M, Milligan R, Kavanagh Williamson M, Beltrami A, Gupta K, Elvers KT, Gamez M, Foster R, Gillespie K, Hamilton F, Arnold D, Berger I, Davidson A, Hill DJ, Caputo M, Madeddu P.
PMID: 34807265
Clin Sci (Lond). 2021 Nov 22; doi: 10.1042/CS20210735. Epub 2021 Nov 22.

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes a broad range of clinical responses including prominent microvascular damage. The capacity of SARS-CoV-2 to infect vascular cells is still debated. Additionally, the SARS-CoV-2 Spike (S) protein may act as...

Cite
Avolio E, Carrabba M, Milligan R, et al. The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147-receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease. Clin Sci (Lond). 2021;doi: 10.1042/CS20210735.
Avolio, E., Carrabba, M., Milligan, R., Kavanagh Williamson, M., Beltrami, A., Gupta, K., Elvers, K. T., Gamez, M., Foster, R., Gillespie, K., Hamilton, F., Arnold, D., Berger, I., Davidson, A., Hill, D. J., Caputo, M., & Madeddu, P. (2021). The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147-receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease. Clinical science (London, England : 1979), . https://doi.org/10.1042/CS20210735
Avolio, Elisa, et al. "The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147-receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease." Clinical science (London, England : 1979) vol. (2021). doi: https://doi.org/10.1042/CS20210735
Avolio E, Carrabba M, Milligan R, Kavanagh Williamson M, Beltrami A, Gupta K, Elvers KT, Gamez M, Foster R, Gillespie K, Hamilton F, Arnold D, Berger I, Davidson A, Hill DJ, Caputo M, Madeddu P. The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147-receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease. Clin Sci (Lond). 2021 Nov 22; doi: 10.1042/CS20210735. Epub 2021 Nov 22. PMID: 34807265.
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Renin angiotensin system and gender differences in dopaminergic degeneration.

Molecular neurodegeneration

Rodriguez-Perez AI, Valenzuela R, Joglar B, Garrido-Gil P, Guerra MJ, Labandeira-Garcia JL.
PMID: 21846363
Mol Neurodegener. 2011 Aug 16;6(1):58. doi: 10.1186/1750-1326-6-58.

BACKGROUND: There are sex differences in dopaminergic degeneration. Men are approximately two times as likely as premenopausal women of the same age to develop Parkinson's disease (PD). It has been shown that the local renin angiotensin system (RAS) plays...

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Rodriguez-Perez AI, Valenzuela R, Joglar B, et al. Renin angiotensin system and gender differences in dopaminergic degeneration. Mol Neurodegener. 2011;6(1):58doi: 10.1186/1750-1326-6-58.
Rodriguez-Perez, A. I., Valenzuela, R., Joglar, B., Garrido-Gil, P., Guerra, M. J., & Labandeira-Garcia, J. L. (2011). Renin angiotensin system and gender differences in dopaminergic degeneration. Molecular neurodegeneration, 6(1), 58. https://doi.org/10.1186/1750-1326-6-58
Rodriguez-Perez, Ana I, et al. "Renin angiotensin system and gender differences in dopaminergic degeneration." Molecular neurodegeneration vol. 6,1 (2011): 58. doi: https://doi.org/10.1186/1750-1326-6-58
Rodriguez-Perez AI, Valenzuela R, Joglar B, Garrido-Gil P, Guerra MJ, Labandeira-Garcia JL. Renin angiotensin system and gender differences in dopaminergic degeneration. Mol Neurodegener. 2011 Aug 16;6(1):58. doi: 10.1186/1750-1326-6-58. PMID: 21846363; PMCID: PMC3169490.
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Molecular Profiling of Coronavirus Disease 2019 (COVID-19) Autopsies Uncovers Novel Disease Mechanisms.

The American journal of pathology

Pujadas E, Beaumont M, Shah H, Schrode N, Francoeur N, Shroff S, Bryce C, Grimes Z, Gregory J, Donnelly R, Fowkes ME, Beaumont KG, Sebra R, Cordon-Cardo C.
PMID: 34506752
Am J Pathol. 2021 Dec;191(12):2064-2071. doi: 10.1016/j.ajpath.2021.08.009. Epub 2021 Sep 08.

Current understanding of coronavirus disease 2019 (COVID-19) pathophysiology is limited by disease heterogeneity, complexity, and a paucity of studies assessing patient tissues with advanced molecular tools. Rapid autopsy tissues were evaluated using multiscale, next-generation RNA-sequencing methods (bulk, single-nuclei, and...

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Pujadas E, Beaumont M, Shah H, et al. Molecular Profiling of Coronavirus Disease 2019 (COVID-19) Autopsies Uncovers Novel Disease Mechanisms. Am J Pathol. 2021;191(12):2064-2071doi: 10.1016/j.ajpath.2021.08.009.
Pujadas, E., Beaumont, M., Shah, H., Schrode, N., Francoeur, N., Shroff, S., Bryce, C., Grimes, Z., Gregory, J., Donnelly, R., Fowkes, M. E., Beaumont, K. G., Sebra, R., & Cordon-Cardo, C. (2021). Molecular Profiling of Coronavirus Disease 2019 (COVID-19) Autopsies Uncovers Novel Disease Mechanisms. The American journal of pathology, 191(12), 2064-2071. https://doi.org/10.1016/j.ajpath.2021.08.009
Pujadas, Elisabet, et al. "Molecular Profiling of Coronavirus Disease 2019 (COVID-19) Autopsies Uncovers Novel Disease Mechanisms." The American journal of pathology vol. 191,12 (2021): 2064-2071. doi: https://doi.org/10.1016/j.ajpath.2021.08.009
Pujadas E, Beaumont M, Shah H, Schrode N, Francoeur N, Shroff S, Bryce C, Grimes Z, Gregory J, Donnelly R, Fowkes ME, Beaumont KG, Sebra R, Cordon-Cardo C. Molecular Profiling of Coronavirus Disease 2019 (COVID-19) Autopsies Uncovers Novel Disease Mechanisms. Am J Pathol. 2021 Dec;191(12):2064-2071. doi: 10.1016/j.ajpath.2021.08.009. Epub 2021 Sep 08. PMID: 34506752; PMCID: PMC8423774.
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Non-HLA antibodies targeting angiotensin II type 1 receptors and endothelin-1 type A receptors impair endothelial repair via a β2-arrestin link to the mTOR pathway.

Kidney international

Catar RA, Wischnewski O, Chen L, Heidecke H, Rutz C, Schülein R, Dragun D, Philippe A, Kusch A.
PMID: 34757123
Kidney Int. 2021 Oct 29; doi: 10.1016/j.kint.2021.09.029. Epub 2021 Oct 29.

Functional non-HLA antibodies (antibodies to non-human leukocyte antigens) targeting the G protein-coupled receptors angiotensin II type 1 receptor (AT1R) and endothelin-1 type A receptor (ETAR) are implicated in the pathogenesis of transplant vasculopathy. While ERK signaling (a regulator of...

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Catar RA, Wischnewski O, Chen L, et al. Non-HLA antibodies targeting angiotensin II type 1 receptors and endothelin-1 type A receptors impair endothelial repair via a β2-arrestin link to the mTOR pathway. Kidney Int. 2021;doi: 10.1016/j.kint.2021.09.029.
Catar, R. A., Wischnewski, O., Chen, L., Heidecke, H., Rutz, C., Schülein, R., Dragun, D., Philippe, A., & Kusch, A. (2021). Non-HLA antibodies targeting angiotensin II type 1 receptors and endothelin-1 type A receptors impair endothelial repair via a β2-arrestin link to the mTOR pathway. Kidney international, . https://doi.org/10.1016/j.kint.2021.09.029
Catar, Rusan Ali, et al. "Non-HLA antibodies targeting angiotensin II type 1 receptors and endothelin-1 type A receptors impair endothelial repair via a β2-arrestin link to the mTOR pathway." Kidney international vol. (2021). doi: https://doi.org/10.1016/j.kint.2021.09.029
Catar RA, Wischnewski O, Chen L, Heidecke H, Rutz C, Schülein R, Dragun D, Philippe A, Kusch A. Non-HLA antibodies targeting angiotensin II type 1 receptors and endothelin-1 type A receptors impair endothelial repair via a β2-arrestin link to the mTOR pathway. Kidney Int. 2021 Oct 29; doi: 10.1016/j.kint.2021.09.029. Epub 2021 Oct 29. PMID: 34757123.
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Neonatal hyperoxia enhances age-dependent expression of SARS-CoV-2 receptors in mice.

bioRxiv : the preprint server for biology

Yee M, Cohen ED, Haak J, Dylag AM, O'Reilly MA.
PMID: 32743585
bioRxiv. 2020 Jul 22; doi: 10.1101/2020.07.22.215962.

The severity of COVID-19 lung disease is higher in the elderly and people with pre-existing co-morbidities. People who were born preterm may be at greater risk for COVID-19 because their early exposure to oxygen at birth increases their risk...

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Yee M, Cohen ED, Haak J, et al. Neonatal hyperoxia enhances age-dependent expression of SARS-CoV-2 receptors in mice. bioRxiv. 2020;doi: 10.1101/2020.07.22.215962.
Yee, M., Cohen, E. D., Haak, J., Dylag, A. M., & O'Reilly, M. A. (2020). Neonatal hyperoxia enhances age-dependent expression of SARS-CoV-2 receptors in mice. bioRxiv : the preprint server for biology, . https://doi.org/10.1101/2020.07.22.215962
Yee, Min, et al. "Neonatal hyperoxia enhances age-dependent expression of SARS-CoV-2 receptors in mice." bioRxiv : the preprint server for biology vol. (2020). doi: https://doi.org/10.1101/2020.07.22.215962
Yee M, Cohen ED, Haak J, Dylag AM, O'Reilly MA. Neonatal hyperoxia enhances age-dependent expression of SARS-CoV-2 receptors in mice. bioRxiv. 2020 Jul 22; doi: 10.1101/2020.07.22.215962. PMID: 32743585; PMCID: PMC7386505.
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Roles of G Protein-Coupled Receptors (GPCRs) in Gastrointestinal Cancers: Focus on Sphingosine 1-Shosphate Receptors, Angiotensin II Receptors, and Estrogen-Related GPCRs.

Cells

Zeng Z, Ma C, Chen K, Jiang M, Vasu R, Liu R, Zhao Y, Zhang H.
PMID: 34831211
Cells. 2021 Nov 03;10(11). doi: 10.3390/cells10112988.

It is well established that gastrointestinal (GI) cancers are common and devastating diseases around the world. Despite the significant progress that has been made in the treatment of GI cancers, the mortality rates remain high, indicating a real need...

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Zeng Z, Ma C, Chen K, et al. Roles of G Protein-Coupled Receptors (GPCRs) in Gastrointestinal Cancers: Focus on Sphingosine 1-Shosphate Receptors, Angiotensin II Receptors, and Estrogen-Related GPCRs. Cells. 2021;10(11)doi: 10.3390/cells10112988.
Zeng, Z., Ma, C., Chen, K., Jiang, M., Vasu, R., Liu, R., Zhao, Y., & Zhang, H. (2021). Roles of G Protein-Coupled Receptors (GPCRs) in Gastrointestinal Cancers: Focus on Sphingosine 1-Shosphate Receptors, Angiotensin II Receptors, and Estrogen-Related GPCRs. Cells, 10(11), . https://doi.org/10.3390/cells10112988
Zeng, Zhen, et al. "Roles of G Protein-Coupled Receptors (GPCRs) in Gastrointestinal Cancers: Focus on Sphingosine 1-Shosphate Receptors, Angiotensin II Receptors, and Estrogen-Related GPCRs." Cells vol. 10,11 (2021). doi: https://doi.org/10.3390/cells10112988
Zeng Z, Ma C, Chen K, Jiang M, Vasu R, Liu R, Zhao Y, Zhang H. Roles of G Protein-Coupled Receptors (GPCRs) in Gastrointestinal Cancers: Focus on Sphingosine 1-Shosphate Receptors, Angiotensin II Receptors, and Estrogen-Related GPCRs. Cells. 2021 Nov 03;10(11). doi: 10.3390/cells10112988. PMID: 34831211; PMCID: PMC8616429.
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Mitochondria-Endoplasmic Reticulum Crosstalk in Parkinson's Disease: The Role of Brain Renin Angiotensin System Components.

Biomolecules

Sunanda T, Ray B, Mahalakshmi AM, Bhat A, Rashan L, Rungratanawanich W, Song BJ, Essa MM, Sakharkar MK, Chidambaram SB.
PMID: 34827667
Biomolecules. 2021 Nov 10;11(11). doi: 10.3390/biom11111669.

The past few decades have seen an increased emphasis on the involvement of the mitochondrial-associated membrane (MAM) in various neurodegenerative diseases, particularly in Parkinson's disease (PD) and Alzheimer's disease (AD). In PD, alterations in mitochondria, endoplasmic reticulum (ER), and...

Cite
Sunanda T, Ray B, Mahalakshmi AM, et al. Mitochondria-Endoplasmic Reticulum Crosstalk in Parkinson's Disease: The Role of Brain Renin Angiotensin System Components. Biomolecules. 2021;11(11)doi: 10.3390/biom11111669.
Sunanda, T., Ray, B., Mahalakshmi, A. M., Bhat, A., Rashan, L., Rungratanawanich, W., Song, B. J., Essa, M. M., Sakharkar, M. K., & Chidambaram, S. B. (2021). Mitochondria-Endoplasmic Reticulum Crosstalk in Parkinson's Disease: The Role of Brain Renin Angiotensin System Components. Biomolecules, 11(11), . https://doi.org/10.3390/biom11111669
Sunanda, Tuladhar, et al. "Mitochondria-Endoplasmic Reticulum Crosstalk in Parkinson's Disease: The Role of Brain Renin Angiotensin System Components." Biomolecules vol. 11,11 (2021). doi: https://doi.org/10.3390/biom11111669
Sunanda T, Ray B, Mahalakshmi AM, Bhat A, Rashan L, Rungratanawanich W, Song BJ, Essa MM, Sakharkar MK, Chidambaram SB. Mitochondria-Endoplasmic Reticulum Crosstalk in Parkinson's Disease: The Role of Brain Renin Angiotensin System Components. Biomolecules. 2021 Nov 10;11(11). doi: 10.3390/biom11111669. PMID: 34827667; PMCID: PMC8615717.
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Showing 1 to 12 of 12 entries