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2019 2
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Examination of the associations between m6A-associated single-nucleotide polymorphisms and blood pressure.
Mo XB, Lei SF, Zhang YH, Zhang H. Mo XB, et al. Hypertens Res. 2019 Oct;42(10):1582-1589. doi: 10.1038/s41440-019-0277-8. Epub 2019 Jun 7. Hypertens Res. 2019. PMID: 31175347
We showed that rs56001051, rs9847953, rs197922, and rs740406 were associated with C1orf167 (P = 0.019), ZNF589 (P = 0.013), GOSR2 (P = 0.001), and DOT1L (P = 0.032) expression levels in peripheral blood mononuclear cells of 40 Chinese individuals, respectively. ...
We showed that rs56001051, rs9847953, rs197922, and rs740406 were associated with C1orf167 (P = 0.019), ZNF589 (P = 0.013), GOSR2 (P …
Impact of natriuretic peptide polymorphisms on diastolic and metabolic function in a populational cohort: insights from the STANISLAS cohort.
Xhaard C, Rouget R, Vodovar N, Le Floch E, Dandine-Roulland C, Wagner S, Bacq-Daian D, Thuillier Q, Boivin JM, Branlant C, Deleuze JF, Behm-Ansmant I, Zannad F, Rossignol P, Girerd N. Xhaard C, et al. ESC Heart Fail. 2022 Feb;9(1):729-739. doi: 10.1002/ehf2.13674. Epub 2021 Nov 3. ESC Heart Fail. 2022. PMID: 34734498 Free PMC article.
All above SNPs were located on the same gene cluster constituted of MTHFR, CLCN6, NPPA, NPPB, and C1orf167. NPPA gene expression was also associated with NT-proBNP levels. ...CONCLUSIONS: The heritability of natriuretic peptides appears relatively low (15%) and mainly base …
All above SNPs were located on the same gene cluster constituted of MTHFR, CLCN6, NPPA, NPPB, and C1orf167. NPPA gene expression was …
Focal facial dermal dysplasias type III: Two families with Setleis syndrome in China.
Cao Q, Zhang S, Wang J, Wang Y, Pan C, Wang X, Zhao A, Chen X, Qin P, Zhang S, Yao Z, Lv D, Yang Y, Li M. Cao Q, et al. J Dermatol. 2022 Oct;49(10):1057-1061. doi: 10.1111/1346-8138.16488. Epub 2022 Jun 17. J Dermatol. 2022. PMID: 35713327
The region contains eight genes, including FBXO2, FBXO44, FBXO6, MAD2L2, DRAXIN, AK125437, AGTRAP, and C1orf167. There were no candidate gene mutations of the second family with SS. ...
The region contains eight genes, including FBXO2, FBXO44, FBXO6, MAD2L2, DRAXIN, AK125437, AGTRAP, and C1orf167. There were no candid …
Three novel genes tied to mandibular prognathism in eastern Mediterranean families.
Genno PG, Nemer GM, Zein Eddine SB, Macari AT, Ghafari JG. Genno PG, et al. Am J Orthod Dentofacial Orthop. 2019 Jul;156(1):104-112.e3. doi: 10.1016/j.ajodo.2018.08.020. Am J Orthod Dentofacial Orthop. 2019. PMID: 31256822
Genetic screening did not correspond with previously reported MP-linked genes, but yielded 3 novel genes (C1orf167, NBPF8, NBPF9) on chromosome 1 potentially responsible for mandibular development and macrognathism. CONCLUSIONS: In this first genetic study with the use of …
Genetic screening did not correspond with previously reported MP-linked genes, but yielded 3 novel genes (C1orf167, NBPF8, NBPF9) on …
Cerebral venous thrombosis with hyperhomocysteinemia due to loss of heterozygosity at methylenetetrahydrofolate reductase (MTHFR) locus: a case report.
Zhang M, Shi B, Zhao M. Zhang M, et al. BMC Neurol. 2023 Apr 19;23(1):154. doi: 10.1186/s12883-023-03200-y. BMC Neurol. 2023. PMID: 37076800 Free PMC article.
Whole-exome sequencing revealed LOH at Chr1:11836597-11,867,232 affects exons 10-21 of C1orf167, the entire MTHFR, and exons 1-2 of the CLCN6 gene. The normal allele was the c.665 C > T/677 C > T variant in MTHFR. ...
Whole-exome sequencing revealed LOH at Chr1:11836597-11,867,232 affects exons 10-21 of C1orf167, the entire MTHFR, and exons 1-2 of t …