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Items: 1 to 20 of 66

1.
The association of TMPRSS6 gene polymorphism with iron status in Egyptian children (a pilot study)
Hanan M. Hamed, Eman El Bostany, Ayat A. Motawie, Amany M. Abd Al-Aziz, Abbass A. Mourad, Hassan M. Salama, Solaf Kamel, Eman M. Hassan, Neveen A. Helmy, Gamila S. El-saeed, Eman A. Elghoroury
BMC Pediatr. 2024; 24: 105. Published online 2024 Feb 10. doi: 10.1186/s12887-024-04573-w
PMCID:
PMC10858485
AbstractArticlePDF–1.4M
2.
Race, Interleukin‐6, TMPRSS6 Genotype, and Cardiovascular Disease in Patients With Chronic Kidney Disease
Ian R. Barrows, Matt Devalaraja, Rahul Kakkar, Jing Chen, Jayanta Gupta, Sylvia E. Rosas, Santosh Saraf, Jiang He, Alan Go, Dominic S. Raj, Richard L. Amdur, the CRIC Study Investigators
J Am Heart Assoc. 2022 Sep 20; 11(18): e025627. Published online 2022 Sep 14. doi: 10.1161/JAHA.122.025627
PMCID:
PMC9683639
AbstractArticlePDF–998K
3.
Common Single Nucleotide Polymorphism of TMPRSS6, an Iron Regulation Gene, Associated with Variable Red Blood Cell Indices in Deletional α-Globin Genotypes
Thidarat Suksangpleng, Waraporn Glomglao, Vip Viprakasit
Genes (Basel) 2022 Sep; 13(9): 1502. Published online 2022 Aug 23. doi: 10.3390/genes13091502
PMCID:
PMC9498602
AbstractArticlePDF–2.0M
4.
Functionally impaired isoforms regulate TMPRSS6 proteolytic activity
Sébastien P. Dion, Antoine Désilets, Gabriel Lemieux, Richard Leduc
PLoS One. 2022; 17(8): e0273825. Published online 2022 Aug 31. doi: 10.1371/journal.pone.0273825
PMCID:
PMC9432768
AbstractArticlePDF–1.7M
5.
IRIDA Phenotype in TMPRSS6 Monoallelic-Affected Patients: Toward a Better Understanding of the Pathophysiology
Vera Hoving, Scott E. Korman, Petros Antonopoulos, Albertine E. Donker, Saskia E. M. Schols, Dorine W. Swinkels
Genes (Basel) 2022 Aug; 13(8): 1309. Published online 2022 Jul 23. doi: 10.3390/genes13081309
PMCID:
PMC9331965
AbstractArticlePDF–832K
6.
CFTR interactome mapping using the mammalian membrane two‐hybrid high‐throughput screening system
Sang Hyun Lim, Jamie Snider, Liron Birimberg‐Schwartz, Wan Ip, Joana C Serralha, Hugo M Botelho, Miquéias Lopes‐Pacheco, Madalena C Pinto, Mohamed Taha Moutaoufik, Mara Zilocchi, Onofrio Laselva, Mohsen Esmaeili, Max Kotlyar, Anna Lyakisheva, Priscilla Tang, Lucía López Vázquez, Indira Akula, Farzaneh Aboualizadeh, Victoria Wong, Ingrid Grozavu, Teuta Opacak‐Bernardi, Zhong Yao, Meg Mendoza, Mohan Babu, Igor Jurisica, Tanja Gonska, Christine E Bear, Margarida D Amaral, Igor Stagljar
Mol Syst Biol. 2022 Feb; 18(2): e10629. Published online 2022 Feb 14. doi: 10.15252/msb.202110629
PMCID:
PMC8842165
AbstractArticlePDF–3.0M
7.
Transferrin Saturation/Hepcidin Ratio Discriminates TMPRSS6-Related Iron Refractory Iron Deficiency Anemia from Patients with Multi-Causal Iron Deficiency Anemia
Hilde van der Staaij, Albertine E. Donker, Dirk L. Bakkeren, Jan M. J. I. Salemans, Lisette A. A. Mignot-Evers, Marlies Y. Bongers, Jeanne P. Dieleman, Tessel E. Galesloot, Coby M. Laarakkers, Siem M. Klaver, Dorine W. Swinkels
Int J Mol Sci. 2022 Feb; 23(3): 1917. Published online 2022 Feb 8. doi: 10.3390/ijms23031917
PMCID:
PMC8836508
AbstractArticlePDF–966K
8.
Association of SNPs within TMPRSS6 and BMP2 genes with iron deficiency status in Saudi Arabia
Osama M. Al-Amer, Atif Abdulwahab A. Oyouni, Mohammed Ali Alshehri, Abdulrahman Alasmari, Othman R. Alzahrani, Saad Ali S. Aljohani, Noura Alasmael, Abdulrahman Theyab, Mohammad Algahtani, Hadeel Al Sadoun, Khalaf F. Alsharif, Abdullah Hamad, Wed A. Abdali, Yousef MohammedRabaa Hawasawi
PLoS One. 2021; 16(11): e0257895. Published online 2021 Nov 15. doi: 10.1371/journal.pone.0257895
Correction in:
PLoS One. 2024; 19(7): e0306683.
PMCID:
PMC8592490
AbstractArticlePDF–831K
9.
The TMPRSS6 variant (SNP rs855791) affects iron metabolism and oral iron absorption – a stable iron isotope study in Taiwanese women
Simone Buerkli, Sung-Nan Pei, Shu-Chen Hsiao, Chien-Te Lee, Christophe Zeder, Michael B. Zimmermann, Diego Moretti
Haematologica. 2021 Nov 1; 106(11): 2897–2905. Published online 2020 Oct 5. doi: 10.3324/haematol.2020.264556
PMCID:
PMC8561285
AbstractArticlePDF–1.8M
10.
TMPRSS6 rs855791 Polymorphism Status in Children with Celiac Disease and Anemia
Klaudia Urbaszek, Natalia Drabińska, Anna Szaflarska-Popławska, Elżbieta Jarocka-Cyrta
Nutrients. 2021 Aug; 13(8): 2782. Published online 2021 Aug 13. doi: 10.3390/nu13082782
PMCID:
PMC8398390
AbstractArticlePDF–1.3M
11.
Molecular analysis of homeostatic iron regulator, transmembrane protease serine-6, and BTB domain-containing protein-9 variants and iron parameters in blood donors
Manal S. Fawzy, Abeer Fakhr-Eldeen, Baraah T. Abu AlSel, Eman A. Toraih
Biosci Rep. 2021 Jan 29; 41(1): BSR20202584. Published online 2021 Jan 14. doi: 10.1042/BSR20202584
PMCID:
PMC7809544
AbstractArticlePDF–988K
12.
Associations of common variants in HFE and TMPRSS6 with iron parameters are independent of serum hepcidin in a general population: a replication study
Tessel E Galesloot, Anneke J Geurts-Moespot, Martin den Heijer, Fred C G J Sweep, Robert E Fleming, Lambertus A L M Kiemeney, Sita H Vermeulen, Dorine W Swinkels
J Med Genet. Author manuscript; available in PMC 2021 Jan 5.
Published in final edited form as: J Med Genet. 2013 Sep; 50(9): 593–598. Published online 2013 Jun 21. doi: 10.1136/jmedgenet-2013-101673
PMCID:
PMC7784039
AbstractArticlePDF–538K
13.
FokI rs2228570和TMPRSS6 rs855791多态性与儿童牛奶蛋白过敏的相关性
张 也, 郭 勇, 马 健, 吕 栩再, 罗 先琼
Zhongguo Dang Dai Er Ke Za Zhi. 2018 Aug 25; 20(8): 641–646. Chinese. doi: 10.7499/j.issn.1008-8830.2018.08.008
PMCID:
PMC7389751
AbstractArticlePDF–1.3M
14.
The Association of TMPRSS6 Gene Polymorphism and Iron Intake with Iron Status among Under-Two-Year-Old Children in Lombok, Indonesia
Dewi Shinta, Asmarinah, Chris Adhiyanto, Min Kyaw Htet, Umi Fahmida
Nutrients. 2019 Apr; 11(4): 878. Published online 2019 Apr 19. doi: 10.3390/nu11040878
PMCID:
PMC6521251
AbstractArticlePDF–1.0M
15.
Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease
Violeta Dopsaj, Aleksandra Topić, Miljan Savković, Neda Milinković, Ivana Novaković, Danica Ćujić, Sanja Simić-Ogrizović
Dis Markers. 2019; 2019: 4864370. Published online 2019 Mar 7. doi: 10.1155/2019/4864370
PMCID:
PMC6431474
AbstractArticlePDF–1.0M
16.
Functional diversity of TMPRSS6 isoforms and variants expressed in hepatocellular carcinoma cell lines
Sébastien P. Dion, François Béliveau, Louis-Philippe Morency, Antoine Désilets, Rafaël Najmanovich, Richard Leduc
Sci Rep. 2018; 8: 12562. Published online 2018 Aug 22. doi: 10.1038/s41598-018-30618-z
PMCID:
PMC6105633
AbstractArticlePDF–1.6M
17.
Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?
Laura M. Raffield, Tin Louie, Tamar Sofer, Deepti Jain, Eli Ipp, Kent D. Taylor, George J. Papanicolaou, Larissa Avilés-Santa, Leslie A. Lange, Cathy C. Laurie, Matthew P. Conomos, Timothy A. Thornton, Yii-Der Ida Chen, Qibin Qi, Scott Cotler, Bharat Thyagarajan, Neil Schneiderman, Jerome I. Rotter, Alex P. Reiner, Henry J. Lin
Hum Mol Genet. 2017 May 15; 26(10): 1966–1978. Published online 2017 Mar 7. doi: 10.1093/hmg/ddx082
PMCID:
PMC6075359
AbstractArticlePDF–191K
18.
Transcriptome analysis reveals TMPRSS6 isoforms with distinct functionalities
Sébastien P. Dion, François Béliveau, Antoine Désilets, Mariana Gabriela Ghinet, Richard Leduc
J Cell Mol Med. 2018 Apr; 22(4): 2498–2509. Published online 2018 Feb 14. doi: 10.1111/jcmm.13562
PMCID:
PMC5867103
AbstractArticlePDF–1.9M
19.
Matriptase-2 suppresses hepcidin expression by cleaving multiple components of the hepcidin induction pathway
Mastura Wahedi, Aaron M. Wortham, Mark D. Kleven, Ningning Zhao, Shall Jue, Caroline A. Enns, An-Sheng Zhang
J Biol Chem. 2017 Nov 3; 292(44): 18354–18371. Published online 2017 Sep 18. doi: 10.1074/jbc.M117.801795
PMCID:
PMC5672056
AbstractArticlePDF–3.3M
20.
A new form of IRIDA due to combined heterozygous mutations of TMPRSS6 and ACVR1A encoding the BMP receptor ALK2
Alessia Pagani, Silvia Colucci, Renata Bocciardi, Marta Bertamino, Carlo Dufour, Roberto Ravazzolo, Laura Silvestri, Clara Camaschella
Blood. 2017 Jun 22; 129(25): 3392–3395. doi: 10.1182/blood-2017-03-773481
PMCID:
PMC5659816
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