121 related articles for article (PubMed ID: 28474257)
1. A cumulative effect involving malfunction of the PTH1R and ATP4A genes explains a familial gastric neuroendocrine tumor with hypothyroidism and arthritis.
Calvete O; Herraiz M; Reyes J; Patiño A; Benitez J
Gastric Cancer; 2017 Nov; 20(6):998-1003. PubMed ID: 28474257
[TBL] [Abstract][Full Text] [Related]
2. Exome sequencing identifies ATP4A gene as responsible of an atypical familial type I gastric neuroendocrine tumour.
Calvete O; Reyes J; Zuñiga S; Paumard-Hernández B; Fernández V; Bujanda L; Rodriguez-Pinilla MS; Palacios J; Heine-Suñer D; Banka S; Newman WG; Cañamero M; Pritchard DM; Benítez J
Hum Mol Genet; 2015 May; 24(10):2914-22. PubMed ID: 25678551
[TBL] [Abstract][Full Text] [Related]
3. A genetic origin for acid-base imbalance triggers the mitochondrial damage that explains the autoimmune response and drives to gastric neuroendocrine tumours.
Benítez J; Marra R; Reyes J; Calvete O
Gastric Cancer; 2020 Jan; 23(1):52-63. PubMed ID: 31250150
[TBL] [Abstract][Full Text] [Related]
4. A knockin mouse model for human ATP4aR703C mutation identified in familial gastric neuroendocrine tumors recapitulates the premalignant condition of the human disease and suggests new therapeutic strategies.
Calvete O; Varro A; Pritchard DM; Barroso A; Oteo M; Morcillo MÁ; Vargiu P; Dodd S; Garcia M; Reyes J; Ortega S; Benitez J
Dis Model Mech; 2016 Sep; 9(9):975-84. PubMed ID: 27491072
[TBL] [Abstract][Full Text] [Related]
5. Alterations in SLC4A2, SLC26A7 and SLC26A9 Drive Acid-Base Imbalance in Gastric Neuroendocrine Tumors and Uncover a Novel Mechanism for a Co-Occurring Polyautoimmune Scenario.
Calvete O; Reyes J; Valdés-Socin H; Martin P; Marazuela M; Barroso A; Escalada J; Castells A; Torres-Ruiz R; Rodríguez-Perales S; Currás-Freixes M; Benítez J
Cells; 2021 Dec; 10(12):. PubMed ID: 34944008
[TBL] [Abstract][Full Text] [Related]
6. Dynamic characterization of intestinal metaplasia in the gastric corpus mucosa of Atp4a-deficient mice.
Liu W; Yang LJ; Liu YL; Yuan DS; Zhao ZM; Wang Q; Yan Y; Pan HF
Biosci Rep; 2020 Feb; 40(2):. PubMed ID: 31904088
[TBL] [Abstract][Full Text] [Related]
7. Gastric achlorhydria in H/K-ATPase-deficient (Atp4a(-/-)) mice causes severe hyperplasia, mucocystic metaplasia and upregulation of growth factors.
Judd LM; Andringa A; Rubio CA; Spicer Z; Shull GE; Miller ML
J Gastroenterol Hepatol; 2005 Aug; 20(8):1266-78. PubMed ID: 16048577
[TBL] [Abstract][Full Text] [Related]
8. Case Report: CMV Infection and Same Mechanism-Originated Intestinal Inflammation Compatible With Bowel/Crohn's Disease Is Suggested in ATP4A Mutated-Driven Gastric Neuroendocrine Tumors.
Calvete O; Reyes J; Benítez J
Front Med (Lausanne); 2021; 8():553110. PubMed ID: 33889580
[TBL] [Abstract][Full Text] [Related]
9. A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family.
Jelani M; Kang C; Mohamoud HS; Al-Rehaili R; Almramhi MM; Serafi R; Yang H; Al-Aama JY; Naeem M; Alkhiary YM
Arch Oral Biol; 2016 Jul; 67():28-33. PubMed ID: 27019138
[TBL] [Abstract][Full Text] [Related]
10. Enterochromaffin-like Cell Hyperplasia-Associated Gastric Neuroendocrine Tumors May Arise in the Setting of Proton Pump Inhibitor Use.
Rais R; Trikalinos NA; Liu J; Chatterjee D
Arch Pathol Lab Med; 2022 Mar; 146(3):366-371. PubMed ID: 34283890
[TBL] [Abstract][Full Text] [Related]
11. ECL-cell carcinoids and carcinoma in patients homozygous for an inactivating mutation in the gastric H(+) K(+) ATPase alpha subunit.
Fossmark R; Calvete O; Mjønes P; Benitez J; Waldum HL
APMIS; 2016 Jul; 124(7):561-6. PubMed ID: 27150581
[TBL] [Abstract][Full Text] [Related]
12. Classification, clinicopathologic features and treatment of gastric neuroendocrine tumors.
Li TT; Qiu F; Qian ZR; Wan J; Qi XK; Wu BY
World J Gastroenterol; 2014 Jan; 20(1):118-25. PubMed ID: 24415864
[TBL] [Abstract][Full Text] [Related]
13. Functional Analysis of PTH1R Variants Found in Primary Failure of Eruption.
Izumida E; Suzawa T; Miyamoto Y; Yamada A; Otsu M; Saito T; Yamaguchi T; Nishimura K; Ohtaka M; Nakanishi M; Yoshimura K; Sasa K; Takimoto R; Uyama R; Shirota T; Maki K; Kamijo R
J Dent Res; 2020 Apr; 99(4):429-436. PubMed ID: 31986066
[TBL] [Abstract][Full Text] [Related]
14. PTH1R Mutants Found in Patients with Primary Failure of Tooth Eruption Disrupt G-Protein Signaling.
Subramanian H; Döring F; Kollert S; Rukoyatkina N; Sturm J; Gambaryan S; Stellzig-Eisenhauer A; Meyer-Marcotty P; Eigenthaler M; Wischmeyer E
PLoS One; 2016; 11(11):e0167033. PubMed ID: 27898723
[TBL] [Abstract][Full Text] [Related]
15. Disruption of β-catenin binding to parathyroid hormone (PTH) receptor inhibits PTH-stimulated ERK1/2 activation.
Yang Y; Wang B
Biochem Biophys Res Commun; 2015 Aug; 464(1):27-32. PubMed ID: 26047699
[TBL] [Abstract][Full Text] [Related]
16. A Novel Heterozygous Missense Variant in
Yang D; Zhou Z; Wang S; Ying H; Wang S; Ma Q; Wu J; Jiao Q; Fan L; Chen M; Wang Y; Zhao L
Genet Test Mol Biomarkers; 2023 Mar; 27(3):74-80. PubMed ID: 36989525
[No Abstract] [Full Text] [Related]
17. Novel mutations in PTH1R associated with primary failure of eruption and osteoarthritis.
Frazier-Bowers SA; Hendricks HM; Wright JT; Lee J; Long K; Dibble CF; Bencharit S
J Dent Res; 2014 Feb; 93(2):134-9. PubMed ID: 24300310
[TBL] [Abstract][Full Text] [Related]
18. Characterization of a PTH1R missense mutation responsible for Jansen type metaphyseal chondrodysplasia.
Shimomura-Kuroki J; Farooq M; Sekimoto T; Amizuka N; Shimomura Y
Odontology; 2017 Apr; 105(2):150-154. PubMed ID: 27160269
[TBL] [Abstract][Full Text] [Related]
19. Identification of six novel PTH1R mutations in families with a history of primary failure of tooth eruption.
Risom L; Christoffersen L; Daugaard-Jensen J; Hove HD; Andersen HS; Andresen BS; Kreiborg S; Duno M
PLoS One; 2013; 8(9):e74601. PubMed ID: 24058597
[TBL] [Abstract][Full Text] [Related]
20. Primary failure of eruption: Clinical and genetic findings in the mixed dentition.
Grippaudo C; Cafiero C; D'Apolito I; Ricci B; Frazier-Bowers SA
Angle Orthod; 2018 May; 88(3):275-282. PubMed ID: 29376733
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]