The Short Synacthen Test and Its Utility in Assessing Recovery of Adrenal Function in Patients With Central Adrenal Insufficiency

Por Sherlock, Mark, Stewart, Paul M
Publicado no J Clin Endocrinol Metab (2018)

Hyponatraemia – presentations and management

Por Dineen, Rosemary, Thompson, Christopher J, Sherlock, Mark
Publicado no Clin Med (Lond) (2017)

Cellular and genetic models of H6PDH and 11β‐HSD1 function in skeletal muscle

Por Zielinska, Agnieszka E., Fletcher, Rachel S., Sherlock, Mark, Doig, Craig L., Lavery, Gareth G.
Publicado no Cell Biochem Funct (2017)

A Modified Experimental Hut Design for Studying Responses of Disease-Transmitting Mosquitoes to Indoor Interventions: The Ifakara Experimental Huts

Por Okumu, Fredros O., Moore, Jason, Mbeyela, Edgar, Sherlock, Mark, Sangusangu, Robert, Ligamba, Godfrey, Russell, Tanya, Moore, Sarah J.
Publicado em 2012

Glucocorticoids and 11β-HSD1 are major regulators of intramyocellular protein metabolism

Por Morgan, Stuart A, Hassan-Smith, Zaki K, Doig, Craig L, Sherlock, Mark, Stewart, Paul M, Lavery, Gareth G
Publicado no J Endocrinol (2016)

Hexose-6-Phosphate Dehydrogenase Contributes to Skeletal Muscle Homeostasis Independent of 11β-Hydroxysteroid Dehydrogenase Type 1

Por Semjonous, Nina M., Sherlock, Mark, Jeyasuria, Pancharatnam, Parker, Keith L., Walker, Elizabeth A., Stewart, Paul M., Lavery, Gareth G.
Publicado em 2011

Lack of Significant Metabolic Abnormalities in Mice with Liver-Specific Disruption of 11β-Hydroxysteroid Dehydrogenase Type 1

Por Lavery, Gareth G., Zielinska, Agnieszka E., Gathercole, Laura L., Hughes, Beverly, Semjonous, Nina, Guest, Phillip, Saqib, Khalid, Sherlock, Mark, Reynolds, Gary, Morgan, Stuart A., Tomlinson, Jeremy W., Walker, Elizabeth A., Rabbitt, Elizabeth H., Stewart, Paul M.
Publicado em 2012

11β-Hydroxysteroid Dehydrogenase Type 1 Regulates Glucocorticoid-Induced Insulin Resistance in Skeletal Muscle

Por Morgan, Stuart A., Sherlock, Mark, Gathercole, Laura L., Lavery, Gareth G., Lenaghan, Carol, Bujalska, Iwona J., Laber, David, Yu, Alice, Convey, Gemma, Mayers, Rachel, Hegyi, Krisztina, Sethi, Jaswinder K., Stewart, Paul M., Smith, David M., Tomlinson, Jeremy W.
Publicado em 2009

DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency

Por Logan, Clare V., Murray, Jennie E., Parry, David A., Robertson, Andrea, Bellelli, Roberto, Tarnauskaitė, Žygimantė, Challis, Rachel, Cleal, Louise, Borel, Valerie, Fluteau, Adeline, Santoyo-Lopez, Javier, Aitman, Tim, Barroso, Inês, Basel, Donald, Bicknell, Louise S., Goel, Himanshu, Hu, Hao, Huff, Chad, Hutchison, Michele, Joyce, Caroline, Knox, Rachel, Lacroix, Amy E., Langlois, Sylvie, McCandless, Shawn, McCarrier, Julie, Metcalfe, Kay A., Morrissey, Rose, Murphy, Nuala, Netchine, Irène, O’Connell, Susan M., Olney, Ann Haskins, Paria, Nandina, Rosenfeld, Jill A., Sherlock, Mark, Syverson, Erin, White, Perrin C., Wise, Carol, Yu, Yao, Zacharin, Margaret, Banerjee, Indraneel, Reijns, Martin, Bober, Michael B., Semple, Robert K., Boulton, Simon J., Rios, Jonathan J., Jackson, Andrew P.
Publicado no Am J Hum Genet (2018)