Pregnancy and parenthood in surgical training: a cross-sectional survey in the UK

por Whitburn, Jessica, Miah, Saiful, Howles, Sarah A
Publicado 2023

ApoA-IV improves insulin sensitivity and glucose uptake in mouse adipocytes via PI3K-Akt Signaling

por Li, Xiaoming, Wang, Fei, Xu, Min, Howles, Philip, Tso, Patrick
Publicado 2017

Impact of an Orthopedic-Delivered ‘One-Stop’ Clinic for Ambulatory Trauma on Emergency Department and Fracture Clinic Pressures During the COVID-19 Pandemic

por Howles, Sophie M, Mahmood, Tariq, Lala, Sadiah, Pearse, Andrew, Docker, Charles
Publicado 2021

Biological versus chronological ovarian age: implications for assisted reproductive technology

por Alviggi, Carlo, Humaidan, Peter, Howles, Colin M, Tredway, Donald, Hillier, Stephen G
Publicado 2009

A CESA from Griffithsia monilis (Rhodophyta, Florideophyceae) has a family 48 carbohydrate-binding module

por Matthews, Peter R., Schindler, Michael, Howles, Paul, Arioli, Tony, Williamson, Richard E.
Publicado 2010

Safety of Ovaleap® (Follitropin Alfa) in Infertile Women Undergoing Superovulation for Assisted Reproductive Technologies: A Multinational Comparative, Prospective Cohort Study

por Kaplan, Sigal, Levy-Toledano, Rachel, Davies, Miranda, Roy, Debabrata, Howles, Colin M., Lass, Amir
Publicado 2021

Apolipoprotein E content of VLDL limits LPL-mediated triglyceride hydrolysis

por Whitacre, Brynne E., Howles, Philip, Street, Scott, Morris, Jamie, Swertfeger, Debi, Davidson, W. Sean
Publicado 2021

Label-free Quantitative Proteomics Reveals Differentially Regulated Proteins Influencing Urolithiasis

por Wright, C. A., Howles, S., Trudgian, D. C., Kessler, B. M., Reynard, J. M., Noble, J. G., Hamdy, F. C., Turney, B. W.
Publicado 2011

Exome sequencing identifies a disease variant of the mitochondrial ATP‐Mg/Pi carrier SLC25A25 in two families with kidney stones

por Jabalameli, M. Reza, Fitzpatrick, Fiona M., Colombo, Roberto, Howles, Sarah A., Leggatt, Gary, Walker, Valerie, Wiberg, Akira, Kunji, Edmund R. S., Ennis, Sarah
Publicado 2021

Contemporary genetic technologies and female reproduction

por Fauser, B.C.J.M., Diedrich, K., Bouchard, P., Domínguez, F., Matzuk, M., Franks, S., Hamamah, S., Simón, C., Devroey, P., Ezcurra, D., Howles, C.M.
Publicado 2011

Bariatric surgery emphasizes biological sex differences in rodent hepatic lipid handling

por Grayson, Bernadette E., Gutierrez-Aguilar, Ruth, Sorrell, Joyce E., Matter, Emily K., Adams, Michelle R., Howles, Philip, Karns, Rebekah, Seeley, Randy J., Sandoval, Darleen A.
Publicado 2017

Allosteric Modulation of the Calcium-sensing Receptor Rectifies Signaling Abnormalities Associated with G-protein α-11 Mutations Causing Hypercalcemic and Hypocalcemic Disorders

por Babinsky, Valerie N., Hannan, Fadil M., Gorvin, Caroline M., Howles, Sarah A., Nesbit, M. Andrew, Rust, Nigel, Hanyaloglu, Aylin C., Hu, Jianxin, Spiegel, Allen M., Thakker, Rajesh V.
Publicado 2016

Impact of COVID-19 on the management of ureteric stones in the UK: The COVID Stones study

por Byrne, M.H.V., Georgiades, F., Lovegrove, C.E., Klatte, T., Saeb-Parsy, K., Kumar, R., Light, A., Josephine, R., Dominic, C., Kathiravelupillai, S., Howles, S., Stewart, G.D., Turney, B., Wiseman, O.
Publicado 2022

Identification of a G‐Protein Subunit‐α11 Gain‐of‐Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2)

por Piret, Sian E, Gorvin, Caroline M, Pagnamenta, Alistair T, Howles, Sarah A, Cranston, Treena, Rust, Nigel, Nesbit, M Andrew, Glaser, Ben, Taylor, Jenny C, Buchs, Andreas E, Hannan, Fadil M, Thakker, Rajesh V
Publicado 2016

Cinacalcet corrects hypercalcemia in mice with an inactivating Gα(11) mutation

por Howles, Sarah A., Hannan, Fadil M., Gorvin, Caroline M., Piret, Sian E., Paudyal, Anju, Stewart, Michelle, Hough, Tertius A., Nesbit, M. Andrew, Wells, Sara, Brown, Stephen D.M., Cox, Roger D., Thakker, Rajesh V.
Publicado 2017

Genetic variants of calcium and vitamin D metabolism in kidney stone disease

por Howles, Sarah A., Wiberg, Akira, Goldsworthy, Michelle, Bayliss, Asha L., Gluck, Anna K., Ng, Michael, Grout, Emily, Tanikawa, Chizu, Kamatani, Yoichiro, Terao, Chikashi, Takahashi, Atsushi, Kubo, Michiaki, Matsuda, Koichi, Thakker, Rajesh V., Turney, Benjamin W., Furniss, Dominic
Publicado 2019

Author Correction: Genetic variants of calcium and vitamin D metabolism in kidney stone disease

por Howles, Sarah A., Wiberg, Akira, Goldsworthy, Michelle, Bayliss, Asha L., Gluck, Anna K., Ng, Michael, Grout, Emily, Tanikawa, Chizu, Kamatani, Yoichiro, Terao, Chikashi, Takahashi, Atsushi, Kubo, Michiaki, Matsuda, Koichi, Thakker, Rajesh V., Turney, Benjamin W., Furniss, Dominic
Publicado 2022

Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3

por Nesbit, M. Andrew, Hannan, Fadil M., Howles, Sarah A., Reed, Anita A.C., Cranston, Treena, Thakker, Clare E., Gregory, Lorna, Rimmer, Andrew J., Rust, Nigel, Graham, Una, Morrison, Patrick J., Hunter, Steven J., Whyte, Michael P., McVean, Gil, Buck, David, Thakker, Rajesh V.
Publicado 2012

Gα(11) mutation in mice causes hypocalcemia rectifiable by calcilytic therapy

por Gorvin, Caroline M., Hannan, Fadil M., Howles, Sarah A., Babinsky, Valerie N., Piret, Sian E., Rogers, Angela, Freidin, Andrew J., Stewart, Michelle, Paudyal, Anju, Hough, Tertius A., Nesbit, M. Andrew, Wells, Sara, Vincent, Tonia L., Brown, Stephen D.M., Cox, Roger D., Thakker, Rajesh V.
Publicado 2017

Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype–phenotype correlations, codon bias and dominant-negative...

por Hannan, Fadil M., Howles, Sarah A., Rogers, Angela, Cranston, Treena, Gorvin, Caroline M., Babinsky, Valerie N., Reed, Anita A., Thakker, Clare E., Bockenhauer, Detlef, Brown, Rosalind S., Connell, John M., Cook, Jacqueline, Darzy, Ken, Ehtisham, Sarah, Graham, Una, Hulse, Tony, Hunter, Steven J., Izatt, Louise, Kumar, Dhavendra, McKenna, Malachi J., McKnight, John A., Morrison, Patrick J., Mughal, M. Zulf, O'Halloran, Domhnall, Pearce, Simon H., Porteous, Mary E., Rahman, Mushtaqur, Richardson, Tristan, Robinson, Robert, Scheers, Isabelle, Siddique, Haroon, van't Hoff, William G., Wang, Timothy, Whyte, Michael P., Nesbit, M. Andrew, Thakker, Rajesh V.
Publicado 2015