Mutant prolactin receptor and familial hyperprolactinemia.
about
Prolactin induces apoptosis of lactotropes in female rodents.Pituitary Medicine From Discovery to Patient-Focused Outcomes.Allosteric Modulation of the Calcium-sensing Receptor Rectifies Signaling Abnormalities Associated with G-protein α-11 Mutations Causing Hypercalcemic and Hypocalcemic Disorders.Identification of a G-Protein Subunit-α11 Gain-of-Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2)A G-protein Subunit-α11 Loss-of-Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2)Knockin mouse with mutant Gα11 mimics human inherited hypocalcemia and is rescued by pharmacologic inhibitors.Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy.New insights in prolactin: pathological implications.The prolactin receptor as a therapeutic target in human diseases: browsing new potential indications.The role of prolactin in andrology: what is new?Biological underpinnings of breastfeeding challenges: the role of genetics, diet, and environment on lactation physiology.Interactions between prolactin and kisspeptin to control reproduction.Gestational Diabetes Mellitus From Inactivation of Prolactin Receptor and MafB in Islet β-Cells.The prolactin receptor: Diverse and emerging roles in pathophysiology.Cinacalcet Rectifies Hypercalcemia in a Patient With Familial Hypocalciuric Hypercalcemia Type 2 (FHH2) Caused by a Germline Loss-of-Function Gα11 Mutation.Natural and molecular history of prolactinoma: insights from a Prlr-/- mouse model.AP2? Mutations Impair Calcium-Sensing Receptor Trafficking and Signaling, and Show an Endosomal Pathway to Spatially Direct G-Protein Selectivity.Natural and molecular history of prolactinoma: insights from a Prlr –/– mouse model.Large-scale exome datasets reveal a new class of adaptor-related protein complex 2 sigma subunit (AP2σ) mutations, located at the interface with the AP2 alpha subunit, that impair calcium-sensing receptor signalling.N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss-of-Function Mice.
P2860
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P2860
Mutant prolactin receptor and familial hyperprolactinemia.
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Mutant prolactin receptor and familial hyperprolactinemia.
@ast
Mutant prolactin receptor and familial hyperprolactinemia.
@en
Mutant prolactin receptor and familial hyperprolactinemia.
@nl
type
label
Mutant prolactin receptor and familial hyperprolactinemia.
@ast
Mutant prolactin receptor and familial hyperprolactinemia.
@en
Mutant prolactin receptor and familial hyperprolactinemia.
@nl
prefLabel
Mutant prolactin receptor and familial hyperprolactinemia.
@ast
Mutant prolactin receptor and familial hyperprolactinemia.
@en
Mutant prolactin receptor and familial hyperprolactinemia.
@nl
P2093
P2860
P50
P356
P1476
Mutant prolactin receptor and familial hyperprolactinemia.
@en
P2093
Chas Bountra
Marcus Bridge
Mohammed Azharuddin
Paul J Newey
Russell S Drummond
Stephen J Cleland
P2860
P304
P356
10.1056/NEJMOA1307557
P407
P577
2013-11-06T00:00:00Z