Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Ana Karin Kusnetzow"'
Autor:
Jian Zhao, Shimiao Wang, Stacy Markison, Sun Hee Kim, Sangdon Han, Mi Chen, Ana Karin Kusnetzow, Elizabeth Rico-Bautista, Michael Johns, Rosa Luo, R. Scott Struthers, Ajay Madan, Yunfei Zhu, Stephen F. Betz
Publikováno v:
ACS Medicinal Chemistry Letters. 14:66-74
Autor:
Jian Zhao, Shimiao Wang, Sun Hee Kim, Sangdon Han, Elizabeth Rico-Bautista, Emmanuel Sturchler, Julie Nguyen, Hannah Tan, Christine Staley, Ana Karin Kusnetzow, Stephen F. Betz, Michael Johns, Lance Goulet, Rosa Luo, Melissa Fowler, Jon Athanacio, Stacy Markison, R. Scott Struthers, Yunfei Zhu
Publikováno v:
Bioorganicmedicinal chemistry letters. 71
SST5 receptor activation potently inhibits insulin secretion from pancreatic β-cells, and an orally available nonpeptide selective SST5 agonist may be used to effectively manage the blood glucose levels of congenital HI patients to avoid severe hypo
Autor:
R. Scott Struthers, Stephen F. Betz, Taylor Kredel, Shirley Cruz, Melissa Fowler, Michael Johns, Jon Athanacio, Agnes Antwan, Stacy Markison, Ajay Madan, Greg J. Reinhart, Oleg Tsivkovski, Ana Karin Kusnetzow, Rosa Luo
Publikováno v:
Endocrine Abstracts.
Autor:
Sun Hee Kim, Taylor Kredel, Rosa Luo, Christine Staley, Ana Karin Kusnetzow, Jon Athanacio, Yun Fei Zhu, Stephen F. Betz, Melissa Fowler, Elizabeth Rico, Ajay Madan, Stacy Markison, Greg J. Reinhart, Agnes Antwan, Oleg Tsivkovski, Hannah Tan, Sangdon Han, Scott Struthers, Michael Johns, Julie Nguyen
Publikováno v:
Journal of the Endocrine Society
Adrenocorticotropic hormone (ACTH) is an important modulator of steroidal hormone synthesis and secretion from the adrenal gland and its selective activity at the melanocortin type 2 receptor (MC2) dictates the synthesis and secretion of cortisol (co
Autor:
Melissa Fowler, Taylor Kredel, Rosa Luo, Stacy Markison, Shirley Cruz, Ana Karin Kusnetzow, Stephen F. Betz, Scott Struthers, Oleg Tsivkovski, Michael Johns, Agnes Antwan, Greg J. Reinhart, Jon Athanacio, Ajay Madan
Publikováno v:
Journal of the Endocrine Society
Cushing’s disease (CD) and Ectopic ACTH syndrome (EAS) stem from excess circulating adrenocorticotropic hormone (ACTH) and resulting hypercortisolemia. In CD, excess ACTH is secreted from pituitary tumors, whereas excess ACTH in EAS arises from non
Autor:
Rosa Luo, Ana Karin Kusnetzow, Stacy Markison, Stephen F. Betz, Agnes Antwan, Michael Johns, Oleg Tsivkovski, Rosalia de Necochea-Campion, Yun Fei Zhu, Scott Struthers, Melissa Fowler, Shmiao Wang, Jon Athanacio, Ajay Madan, Elizabeth Rico, Emmanuel Sturchler, Taylor Kredel, Jian Zhao
Publikováno v:
Journal of the Endocrine Society
Congenital hyperinsulinism (CHI) results from mutations within the insulin secretion pathway and is characterized by excessive and/or inappropriate insulin secretion by pancreatic islet β-cells. CHI is the most common cause of persistent hypoglycemi
Autor:
Taylor Kredel, Melissa Fowler, Ana Karin Kusnetzow, Jian Zhao, Elizabeth Rico-Bautista, Yun Fei Zhu, Shimiao Wang, Stephen F. Betz, Stacy Markison, Jon Athanacio, Scott Struthers
Publikováno v:
Journal of the Endocrine Society
Hyperinsulinemia is a heterogeneous condition in which dangerously low blood sugar levels are caused by improperly regulated insulin secretion from pancreatic ß-cells. The most severe form of hyperinsulinemia arises from congenital hyperinsulinism (
Autor:
Ana Karin Kusnetzow, Scott Struthers, Michael Johns, Julie Nguyen, Elizabeth Rico-Bautista, Taylor Kredel, Rosa Luo, Yun Fei Zhu, Stacy Markison, Melissa Fowler, Stephen F. Betz, Greg J. Reinhart, Sun Hee Kim, Christine Staley, Sangdon Han, Hannah Tan, Jon Athanacio, Ajay Madan
Publikováno v:
Journal of the Endocrine Society
Cushing’s disease is most commonly the result of a microadenoma derived from pituitary corticotrophic cells that secretes excess adrenocorticotropic hormone (ACTH). ACTH is an important modulator of steroidal hormone synthesis and secretion from th
Autor:
Ana Karin Kusnetzow, Michael Johns, Stacy Markison, Stephen F. Betz, Shimiao Wang, Yun Fei Zhu, Melissa Fowler, Jon Athanacio, Ajay Madan, Scott Struthers, Taylor Kredel, Jian Zhao, Rosa Luo, Emmanuel Sturchler
Publikováno v:
Journal of the Endocrine Society
Congenital hyperinsulinism (CHI) results from mutations within the insulin secretion pathway and is characterized by excessive and/or inappropriate insulin secretion by pancreatic islet β-cells. CHI is the most common cause of persistent hypoglycemi
Publikováno v:
Journal of the Endocrine Society
Congenital hyperinsulinism (HI) is the most common cause of persistent hypoglycemia in newborns and infants and arises from dysregulated insulin secretion. Rapid recognition and treatment are vital to prevent seizures, permanent developmental delays,