Diseases associated with calcium-sensing receptor

C Vahe, K Benomar, S Espiard, L Coppin… - Orphanet journal of rare …, 2017 - Springer
The calcium-sensing receptor (CaSR) plays a pivotal role in systemic calcium metabolism by
regulating parathyroid hormone secretion and urinary calcium excretion. The diseases …

Association between polymorphisms in vitamin d pathway-related genes, vitamin d status, muscle mass and function: A systematic review

E Krasniqi, A Boshnjaku, KH Wagner, B Wessner - Nutrients, 2021 - mdpi.com
An association between vitamin D level and muscle-related traits has been frequently
reported. Vitamin D level is dependent on various factors such as sunlight exposure and …

Polymorphisms contributing to calcium status: A systematic review

K da Silva Lopes, SK Abe - Nutrients, 2021 - mdpi.com
This systematic review assessed genotypes and changes in calcium homeostasis. A
literature search was performed in EMBASE, Medline and CENTRAL on 7 August 2020 …

Vitamin D deficiency and diseases: a review from Pakistan

Y Mahmood, N Waris, A Fawwad, A Basit - Journal of Diabetology, 2021 - journals.lww.com
Objective: Vitamin D deficiency is claimed to be associated with many diseases in the world
population. Many studies reported that vitamin D deficiency is quite prevalent in Pakistan …

Molecular assessment of calcium-sensing receptor gene polymorphism rs1801725 in Iraqi women with osteoporosis

AF Al-Azzawie - Asian Journal of Agriculture and Biology, 2021 - classical.goforpromo.com
Calcium-sensing receptor (CaSR) gene polymorphism A986S (rs1801725) is a genetic
factor of the calcium homeostasis and susceptibility of osteoporosis. Although, its role in …

Association between calcium-sensing receptor gene polymorphism A986S and some calcium-related parameters in pregnant women

WM Mahmood, AF AL-Azzawie - AIP Conference Proceedings, 2022 - pubs.aip.org
There are a few studies about the relationship between genetic polymorphism with
metabolic and hormonal changes that occur during pregnancy. Therefore, the study aimed …

[PDF][PDF] Case Reports of Patients Diagnosed with Familial Hypocalciuric Hypercalcemia, A Disorder That Should be Kept in Mind in Hypercalcemia Cases

AD Buluş, Y Yaşartekin, AC Ceylan - Trends in Pediatrics, 2022 - jag.journalagent.com
Familial hypocalciuric hypercalcemia (FHH) causes hypercalcemia by three genetic
mechanisms: Inactivating mutations in the calcium-sensing receptor (CaSR), G-protein …

Molecular genetic predictors of the development of urolithiasis

DN Khotko, NV Polukonova, AI Khotko, NA Navolokin… - Urologiia, 2022 - innoscience.ru
Urolithiasis is one of the most urgent problems of clinical urology. Currently, there is no
consensus on the causes of stone formation, as well as the role of various factors in the …

[PDF][PDF] Seven Decades of Vitamin D research in Pakistan: Too little, too much or just right!

AH Khan - 2018 - ecommons.aku.edu
Pakistan has one of the highest reported incidence of vitamin D deficiency (VDD) in studies
conducted worldwide and within Pakistan. Data mining of vitamin D (VD) testing and small …

МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЕ ПРЕДИКТОРЫ РАЗВИТИЯ МОЧЕКАМЕННОЙ БОЛЕЗНИ

ДН ХОТЬКО, НВ ПОЛУКОНОВА, АИ ХОТЬКО… - elibrary.ru
Мочекаменная болезнь представляет собой одну из наиболее актуальных проблем
клинической урологии. В настоящее время нет единого мнения о причинах …