PubMed (GeneRIF) for id: 2235

Year	Number of Results
2002	2
2003	1
2004	4
2005	3
2006	4
2007	10
2008	4
2009	9
2010	9
2011	1
2012	1
2013	3
2014	2
2015	3
2016	2
2017	3
2018	4
2019	5
2020	2
2021	2
2024	0

1

Nkx3-1 and Fech genes might be switch genes involved in pituitary non-functioning adenoma invasiveness.

Khayer N, Jalessi M, Jahanbakhshi A, Tabib Khooei A, Mirzaie M. Khayer N, et al. Sci Rep. 2021 Oct 22;11(1):20943. doi: 10.1038/s41598-021-00431-2. Sci Rep. 2021. PMID: 34686726 Free PMC article.

2

Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiation.

Lanzafame M, Branca G, Landi C, Qiang M, Vaz B, Nardo T, Ferri D, Mura M, Iben S, Stefanini M, Peverali FA, Bini L, Orioli D. Lanzafame M, et al. Nucleic Acids Res. 2021 Nov 8;49(19):10911-10930. doi: 10.1093/nar/gkab819. Nucleic Acids Res. 2021. PMID: 34581821 Free PMC article.

3

Novel mutation of the ferrochelatase gene in a Japanese family with erythropoietic protoporphyria.

Saito A, Okiyama N, Inoue S, Kubota N, Nakamura Y, Ishitsuka Y, Watanabe R, Nakano H, Fujisawa Y. Saito A, et al. J Dermatol. 2020 Apr;47(4):e114-e116. doi: 10.1111/1346-8138.15258. Epub 2020 Feb 13. J Dermatol. 2020. PMID: 32056258 No abstract available.

4

Targeted resequencing of FECH locus reveals that a novel deep intronic pathogenic variant and eQTLs may cause erythropoietic protoporphyria (EPP) through a methylation-dependent mechanism.

Chiara M, Primon I, Tarantini L, Agnelli L, Brancaleoni V, Granata F, Bollati V, Di Pierro E. Chiara M, et al. Genet Med. 2020 Jan;22(1):35-43. doi: 10.1038/s41436-019-0584-0. Epub 2019 Jul 5. Genet Med. 2020. PMID: 31273344 Free article.

5

Ferrochelatase Deficiency Abrogated the Enhancement of Aminolevulinic Acid-mediated Protoporphyrin IX by Iron Chelator Deferoxamine.

Palasuberniam P, Kraus D, Mansi M, Braun A, Howley R, Myers KA, Chen B. Palasuberniam P, et al. Photochem Photobiol. 2019 Jul;95(4):1052-1059. doi: 10.1111/php.13091. Epub 2019 Mar 15. Photochem Photobiol. 2019. PMID: 30767226 Free PMC article.

6

Congenital erythropoietic porphyria and erythropoietic protoporphyria: Identification of 7 uroporphyrinogen III synthase and 20 ferrochelatase novel mutations.

Weiss Y, Balwani M, Chen B, Yasuda M, Nazarenko I, Desnick RJ. Weiss Y, et al. Mol Genet Metab. 2019 Nov;128(3):358-362. doi: 10.1016/j.ymgme.2018.08.015. Epub 2018 Aug 31. Mol Genet Metab. 2019. PMID: 30454868

7

Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans.

Wang H, Cade BE, Sofer T, Sands SA, Chen H, Browning SR, Stilp AM, Louie TL, Thornton TA, Johnson WC, Below JE, Conomos MP, Evans DS, Gharib SA, Guo X, Wood AC, Mei H, Yaffe K, Loredo JS, Ramos AR, Barrett-Connor E, Ancoli-Israel S, Zee PC, Arens R, Shah NA, Taylor KD, Tranah GJ, Stone KL, Hanis CL, Wilson JG, Gottlieb DJ, Patel SR, Rice K, Post WS, Rotter JI, Sunyaev SR, Cai J, Lin X, Purcell SM, Laurie CC, Saxena R, Redline S, Zhu X. Wang H, et al. Hum Mol Genet. 2019 Feb 15;28(4):675-687. doi: 10.1093/hmg/ddy387. Hum Mol Genet. 2019. PMID: 30403821 Free PMC article.

8

Strong correlation of ferrochelatase enzymatic activity with Mitoferrin-1 mRNA in lymphoblasts of patients with protoporphyria.

Phillips J, Farrell C, Wang Y, Singal AK, Anderson K, Balwani M, Bissell M, Bonkovsky H, Seay T, Paw B, Desnick R, Bloomer J. Phillips J, et al. Mol Genet Metab. 2019 Nov;128(3):391-395. doi: 10.1016/j.ymgme.2018.10.005. Epub 2018 Oct 22. Mol Genet Metab. 2019. PMID: 30391163 Free PMC article.

9

FAM210B is an erythropoietin target and regulates erythroid heme synthesis by controlling mitochondrial iron import and ferrochelatase activity.

Yien YY, Shi J, Chen C, Cheung JTM, Grillo AS, Shrestha R, Li L, Zhang X, Kafina MD, Kingsley PD, King MJ, Ablain J, Li H, Zon LI, Palis J, Burke MD, Bauer DE, Orkin SH, Koehler CM, Phillips JD, Kaplan J, Ward DM, Lodish HF, Paw BH. Yien YY, et al. J Biol Chem. 2018 Dec 21;293(51):19797-19811. doi: 10.1074/jbc.RA118.002742. Epub 2018 Oct 26. J Biol Chem. 2018. PMID: 30366982 Free PMC article.

10

Digital PCR (dPCR) analysis reveals that the homozygous c.315-48T>C variant in the FECH gene might cause erythropoietic protoporphyria (EPP).

Brancaleoni V, Granata F, Missineo P, Fustinoni S, Graziadei G, Di Pierro E. Brancaleoni V, et al. Mol Genet Metab. 2018 Aug;124(4):287-296. doi: 10.1016/j.ymgme.2018.06.005. Epub 2018 Jun 13. Mol Genet Metab. 2018. PMID: 29941360

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