The prolactin receptor: Diverse and emerging roles in pathophysiology

por Gorvin, Caroline M.
Publicado 2015

Genetic causes of neonatal and infantile hypercalcaemia

por Gorvin, Caroline M.
Publicado 2021

The Importance of Functionally Characterizing Calcium-Sensing Receptor Variants in Individuals With Hypercalcemia

por Gorvin, Caroline M
Publicado 2022

RISING STARS: Targeting G protein-coupled receptors to regulate energy homeostasis

por Jamaluddin, Aqfan, Gorvin, Caroline M
Publicado 2023

OR03-05 Cinacalcet Acts As A Spatially Biased Allosteric Modulator To Enhance CaSR Signaling From Endosomal Membranes

por Wyatt, Rachael, Gorvin, Caroline M
Publicado 2023

Heterogeneity of G protein activation by the calcium-sensing receptor

por Abid, Hasnat Ali, Inoue, Asuka, Gorvin, Caroline M
Publicado 2021

Identification of prolactin receptor variants with diverse effects on receptor signalling

por Gorvin, Caroline M, Newey, Paul J, Thakker, Rajesh V
Publicado 2022

The emerging role of heterodimerisation and interacting proteins in ghrelin receptor function

por Price, Maria L, Ley, Cameron D, Gorvin, Caroline M
Publicado 2021

Vascular wall regulator of G-protein signalling-1 (RGS-1) is required for angiotensin II–mediated blood pressure control

por Patel, Jyoti, Chuaiphichai, Surawee, Douglas, Gillian, Gorvin, Caroline M., Channon, Keith M.
Publicado 2018

The bromodomain inhibitor JQ1+ reduces calcium-sensing receptor activity in pituitary cell lines

por Lines, Kate E, Gluck, Anna K, Thongjuea, Supat, Bountra, Chas, Thakker, Rajesh V, Gorvin, Caroline M
Publicado 2021

A G‐protein Subunit‐α11 Loss‐of‐Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2)

por Gorvin, Caroline M, Cranston, Treena, Hannan, Fadil M, Rust, Nigel, Qureshi, Asjid, Nesbit, M Andrew, Thakker, Rajesh V
Publicado 2016

Cinacalcet Rectifies Hypercalcemia in a Patient With Familial Hypocalciuric Hypercalcemia Type 2 (FHH2) Caused by a Germline Loss‐of‐Function Gα(11) Mutation

por Gorvin, Caroline M, Hannan, Fadil M, Cranston, Treena, Valta, Helena, Makitie, Outi, Schalin‐Jantti, Camilla, Thakker, Rajesh V
Publicado 2017

Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation

por Piret, Sian E., Gorvin, Caroline M., Trinh, Anne, Taylor, John, Lise, Stefano, Taylor, Jenny C., Ebeling, Peter R., Thakker, Rajesh V.
Publicado 2016

OR07-06 The Roles of GNAQ and GNA11 in Calcium-Sensing Receptor (CaSR) Signalling

por Gluck, Anna K, Stevenson, Mark, Falcone, Sara, Inoue, Asuka, Breitwieser, Gerda E, Gorvin, Caroline M, Lines, Kate E, Thakker, Rajesh V
Publicado 2020

Calcium-sensing receptor residues with loss- and gain-of-function mutations are located in regions of conformational change and cause signalling bias

por Gorvin, Caroline M, Frost, Morten, Malinauskas, Tomas, Cranston, Treena, Boon, Hannah, Siebold, Christian, Jones, E Yvonne, Hannan, Fadil M, Thakker, Rajesh V
Publicado 2018

Whole genome sequence analysis identifies a PAX2 mutation to establish a correct diagnosis for a syndromic form of hyperuricemia

por Stevenson, Mark, Pagnamenta, Alistair T., Reichart, Silvia, Philpott, Charlotte, Lines, Kate E., Gorvin, Caroline M., Lhotta, Karl, Taylor, Jenny C., Thakker, Rajesh V.
Publicado 2020

Neonatal Hypocalcemic Seizures in Offspring of a Mother With Familial Hypocalciuric Hypercalcemia Type 1 (FHH1)

por Dharmaraj, Poonam, Gorvin, Caroline M, Soni, Astha, Nelhans, Nick D, Olesen, Mie K, Boon, Hannah, Cranston, Treena, Thakker, Rajesh V, Hannan, Fadil M
Publicado 2020

SAT-404 Neonatal Hypocalcemic Seizures in Offspring of a Mother with Familial Hypocalciuric Hypercalcemia Type 1 (FHH1)

por Hannan, Fadil M, Dharmaraj, Poonam, Gorvin, Caroline M, Soni, Astha, Nelhans, Nick D, Olesen, Mie Kronborg, Boon, Hannah, Cranston, Treena, Thakker, Rajesh V
Publicado 2020

N‐ethyl‐N‐nitrosourea–Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss‐of‐Function Mice

por Gorvin, Caroline M, Rogers, Angela, Stewart, Michelle, Paudyal, Anju, Hough, Tertius A, Teboul, Lydia, Wells, Sara, Brown, Steve DM, Cox, Roger D, Thakker, Rajesh V
Publicado 2017

Familial Hypocalciuric Hypercalcemia Type 1 and Autosomal-Dominant Hypocalcemia Type 1: Prevalence in a Large Healthcare Population

por Dershem, Ridge, Gorvin, Caroline M., Metpally, Raghu P.R., Krishnamurthy, Sarathbabu, Smelser, Diane T., Hannan, Fadil M., Carey, David J., Thakker, Rajesh V., Breitwieser, Gerda E.
Publicado 2020