Search Results - "Kempton, Amber"

Systemic γ-sarcoglycan AAV gene transfer results in dose-dependent correction of muscle deficits in the LGMD 2C/R5 mouse model by Seo, Young-Eun, Baine, Stephen H., Kempton, Amber N., Rogers, Oliver C., Lewis, Sarah, Adegboye, Kaitlin, Haile, Alex, Griffin, Danielle A., Peterson, Ellyn L., Pozsgai, Eric R., Potter, Rachael A., Rodino-Klapac, Louise R.

“…Limb-girdle muscular dystrophy (LGMD) type 2C/R5 results from mutations in the γ-sarcoglycan (SGCG) gene and is characterized by muscle weakness and…”
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Dysfunction of the β2-spectrin-based pathway in human heart failure by Smith, Sakima A, Hughes, Langston D, Kline, Crystal F, Kempton, Amber N, Dorn, Lisa E, Curran, Jerry, Makara, Michael, Webb, Tyler R, Wright, Patrick, Voigt, Niels, Binkley, Philip F, Janssen, Paul M L, Kilic, Ahmet, Carnes, Cynthia A, Dobrev, Dobromir, Rasband, Matthew N, Hund, Thomas J, Mohler, Peter J

“…β2-Spectrin is critical for integrating membrane and cytoskeletal domains in excitable and nonexcitable cells. The role of β2-spectrin for vertebrate function…”
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Pazopanib for renal cell carcinoma leads to elevated mean arterial pressures in a murine model by Kempton, Amber, Justice, Cody, Guo, Aaron, Cefalu, Matthew, Makara, Michael, Janssen, Paul, Ho, Thai H, Smith, Sakima A

“…Background: In the setting of metastatic RCC (mRCC), pazopanib is approved as first line therapy. Unfortunately treatment may lead to cardiotoxicity such as…”
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Altered regulation of cardiac ankyrin repeat protein in heart failure by Kempton, Amber, Cefalu, Matt, Justice, Cody, Baich, Tesla, Derbala, Mohamed, Canan, Benjamin, Janssen, Paul M.L., Mohler, Peter J., Smith, Sakima A.

“…Left ventricular assist devices (LVADs) have revolutionized and improved the care of the sickest heart failure (HF) patients, and it is imperative that they…”
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Evaluating Pharmacology and Efficacy of Delandistrogene Moxeparvovec in Young and Aged DMDmdx Rats (P3-8.008) by Potter, Rachael, Wier, Chris, Cooper-Olson, Grace, Wheeler, Esther, Anderbery, Emily, Kempton, Amber, Clements, Leah, Adegboye, Kaitlin, Haile, Alex, Peterson, Ellyn, Rodino-Klapac, Louise

“…Abstract only…”
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Neonatal apneic phenotype in a murine congenital central hypoventilation syndrome model is induced through non‐cell autonomous developmental mechanisms by Alzate‐Correa, Diego, Mei‐ling Liu, Jillian, Jones, Mikayla, Silva, Talita M., Alves, Michele Joana, Burke, Elizabeth, Zuñiga, Jessica, Kaya, Behiye, Zaza, Giuliana, Aslan, Mehmet Tahir, Blackburn, Jessica, Shimada, Marina Y., Fernandes‐Junior, Silvio A., Baer, Lisa A., Stanford, Kristin I., Kempton, Amber, Smith, Sakima, Szujewski, Caroline C., Silbaugh, Abby, Viemari, Jean‐Charles, Takakura, Ana C., Garcia, Alfredo J., Moreira, Thiago S., Czeisler, Catherine M., Otero, José J.

“…Congenital central hypoventilation syndrome (CCHS) represents a rare genetic disorder usually caused by mutations in the homeodomain transcription factor…”
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Abstract 20284: Cardiac Ankyrin Repeat Protein Expression Is Impacted By Ventricular Loading Conditions In Chronic Heart Failure by Kempton, Amber, Canan, Ben, Kline, Faith, Janssen, Paul, Mohler, Peter J, Smith, Sakima A

“…IntroductionAnkyrin repeat domain 1 (ANKRD1), the gene encoding CARP, a transcription co-factor that translocates to the nucleus in response to mechanical…”
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