Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Louis S, Premkumar"'
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 17, p 10016 (2022)
The most common medicinal claims for cannabis are relief from chronic pain, stimulation of appetite, and as an antiemetic. However, the mechanisms by which cannabis reduces pain and prevents nausea and vomiting are not fully understood. Among more th
Externí odkaz:
https://doaj.org/article/a20da811a7194a0ca6a57caf9c21f7ec
Supplementary Figure 3 from hCLCA2 Is a p53-Inducible Inhibitor of Breast Cancer Cell Proliferation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6175de36bc1c5f705a29791c344f563f
https://doi.org/10.1158/0008-5472.22378163
https://doi.org/10.1158/0008-5472.22378163
Supplementary Figure 4 from hCLCA2 Is a p53-Inducible Inhibitor of Breast Cancer Cell Proliferation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb83e3118305e2d36504d90d783dcec9
https://doi.org/10.1158/0008-5472.22378160
https://doi.org/10.1158/0008-5472.22378160
Supplementary Figure 1 from hCLCA2 Is a p53-Inducible Inhibitor of Breast Cancer Cell Proliferation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83560e998025f9a2d4b17bf9d8831a0b
https://doi.org/10.1158/0008-5472.22378172
https://doi.org/10.1158/0008-5472.22378172
Supplementary Figure 5 from hCLCA2 Is a p53-Inducible Inhibitor of Breast Cancer Cell Proliferation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::015f47db35cb9070145196b05fadf045
https://doi.org/10.1158/0008-5472.22378157.v1
https://doi.org/10.1158/0008-5472.22378157.v1
Autor:
Padmamalini Baskaran, Adithya Mohandass, Noah Gustafson, Jane Bennis, Somaja Louis, Brenda Alexander, Mikhail I. Nemenov, Baskaran Thyagarajan, Louis S. Premkumar
Publikováno v:
Pain.
Painful Diabetic Peripheral Neuropathy (PDPN) is one of the major complications of diabetes. Currently, centrally acting drugs and topical analgesics are used for treating PDPN. These drugs have adverse effects, some are ineffective and treatment wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa3393f005df4befdb6068cb876f562a
https://pubmed.ncbi.nlm.nih.gov/36001079
https://pubmed.ncbi.nlm.nih.gov/36001079
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 9, p 2065 (2019)
The nucleus of the solitary tract (NTS) receives visceral information via the solitary tract (ST) that comprises the sensory components of the cranial nerves VII, IX and X. The Transient Receptor Potential Ankyrin 1 (TRPA1) ion channels are non-selec
Externí odkaz:
https://doaj.org/article/ef7929b9ae2948a48209eacf54088929
Publikováno v:
Current diabetes reviews. 18(5)
The cutaneous mechanisms that trigger spontaneous neuropathic pain in diabetic peripheral neuropathy (PDPN) are far from clear. Two types of nociceptors are found within the epidermal and dermal skin layers. Small-diameter lightly myelinated Aδ and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13b319a75df28473590d0bacf6bfba6a
https://pubmed.ncbi.nlm.nih.gov/34879806
https://pubmed.ncbi.nlm.nih.gov/34879806
Autor:
De-Shou Cao, Linlin Zhong, Tsung-Han Hsieh, Mruvil Abooj, Mahendra Bishnoi, Lauren Hughes, Louis S Premkumar
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e38005 (2012)
Several transient receptor potential (TRP) channels are expressed in pancreatic beta cells and have been proposed to be involved in insulin secretion. However, the endogenous ligands for these channels are far from clear. Here, we demonstrate the exp
Externí odkaz:
https://doaj.org/article/2fb5e0741a5f414da17b944aa806a24e
Autor:
Joseph A Jeffry, Shuang-Quan Yu, Parul Sikand, Arti Parihar, M Steven Evans, Louis S Premkumar
Publikováno v:
PLoS ONE, Vol 4, Iss 9, p e7021 (2009)
Chronic pain is a major clinical problem and opiates are often the only treatment, but they cause significant problems ranging from sedation to deadly respiratory depression. Resiniferatoxin (RTX), a potent agonist of Transient Receptor Potential Van
Externí odkaz:
https://doaj.org/article/75ab4ff3f81a480597e2260f060e0214