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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 1
1984 1
1988 1
1990 1
1991 3
1992 1
1993 6
1994 6
1995 5
1996 3
1997 6
1998 7
1999 3
2000 5
2001 2
2002 6
2003 8
2004 4
2005 4
2006 8
2007 5
2008 10
2009 7
2010 11
2011 16
2012 14
2013 8
2014 15
2015 9
2016 19
2017 18
2018 22
2019 28
2020 27
2021 18
2022 33
2023 37
2024 10

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347 results

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Page 1
The Potential of ANK1 to Predict Parkinson's Disease.
Xue J, Li F, Dai P. Xue J, et al. Genes (Basel). 2023 Jan 15;14(1):226. doi: 10.3390/genes14010226. Genes (Basel). 2023. PMID: 36672967 Free PMC article.
Additionally, DEGs between high ANK1 and low ANK1 in GSE99039 were picked out and then uploaded to the Database for Annotation, Visualization and Integrated Discovery (DAVID) for gene ontology (GO) functional annotation analysis. ...Thus, ANK1 may serve as a …
Additionally, DEGs between high ANK1 and low ANK1 in GSE99039 were picked out and then uploaded to the Database for Annotation …
Molecular Genetic Mechanisms of Hereditary Spherocytosis: Current Perspectives.
He BJ, Liao L, Deng ZF, Tao YF, Xu YC, Lin FQ. He BJ, et al. Acta Haematol. 2018;139(1):60-66. doi: 10.1159/000486229. Epub 2018 Jan 22. Acta Haematol. 2018. PMID: 29402830 Free article. Review.
With the widespread use of genetic diagnostic technologies, many novel mutations have been identified in hereditary spherocytosis (HS)-related genes, including SPTA1, SPTB, ANK1, SLC4A1, and EPB42. However, mutations in HS-related genes are dispersed and nonspecific in the …
With the widespread use of genetic diagnostic technologies, many novel mutations have been identified in hereditary spherocytosis (HS)-relat …
Genotype-phenotype correlation in children with hereditary spherocytosis.
Tole S, Dhir P, Pugi J, Drury LJ, Butchart S, Fantauzzi M, Langer JC, Baker JM, Blanchette VS, Kirby-Allen M, Carcao MD. Tole S, et al. Br J Haematol. 2020 Nov;191(3):486-496. doi: 10.1111/bjh.16750. Epub 2020 May 20. Br J Haematol. 2020. PMID: 32436265 Free article.
In 160/166 (97%) children with HS a disease-causing mutation was identified. Pathogenic variants in ANK1, SPTB, SLC4A1 and SPTA1 were found in 49%, 33%, 13% and 5% of patients. ...Conversely, children with autosomal recessive SPTA1-HS had the most severe clinical phenotype …
In 160/166 (97%) children with HS a disease-causing mutation was identified. Pathogenic variants in ANK1, SPTB, SLC4A1 and SPTA1 were …
Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis.
Hao L, Li S, Ma D, Chen S, Zhang B, Xiao D, Zhang J, Jiang N, Jiang S, Ma J. Hao L, et al. J Cell Mol Med. 2019 Jun;23(6):4454-4463. doi: 10.1111/jcmm.14343. Epub 2019 Apr 23. J Cell Mol Med. 2019. PMID: 31016877 Free PMC article.
Two novel heterozygous mutations (c.C841T, p.R281X and c.T290G, p.L97R) of the ANK1 gene were identified in the two families respectively. Then, the pathogenicity of the two new mutations and two previously reported ANK1 mutations (c.C648G, p.Y216X and c.G424T, p.E1 …
Two novel heterozygous mutations (c.C841T, p.R281X and c.T290G, p.L97R) of the ANK1 gene were identified in the two families respecti …
Malignant clonal evolution drives multiple myeloma cellular ecological diversity and microenvironment reprogramming.
Liang Y, He H, Wang W, Wang H, Mo S, Fu R, Liu X, Song Q, Xia Z, Wang L. Liang Y, et al. Mol Cancer. 2022 Sep 22;21(1):182. doi: 10.1186/s12943-022-01648-z. Mol Cancer. 2022. PMID: 36131282 Free PMC article.
RESULTS: The malignant mutation event was localized to the tumor cell clusters with shared mutation of ANK1 and IFITM2 in all malignant subpopulations of all MM patients. ...
RESULTS: The malignant mutation event was localized to the tumor cell clusters with shared mutation of ANK1 and IFITM2 in all maligna …
Identification of type 2 diabetes loci in 433,540 East Asian individuals.
Spracklen CN, Horikoshi M, Kim YJ, Lin K, Bragg F, Moon S, Suzuki K, Tam CHT, Tabara Y, Kwak SH, Takeuchi F, Long J, Lim VJY, Chai JF, Chen CH, Nakatochi M, Yao J, Choi HS, Iyengar AK, Perrin HJ, Brotman SM, van de Bunt M, Gloyn AL, Below JE, Boehnke M, Bowden DW, Chambers JC, Mahajan A, McCarthy MI, Ng MCY, Petty LE, Zhang W, Morris AP, Adair LS, Akiyama M, Bian Z, Chan JCN, Chang LC, Chee ML, Chen YI, Chen YT, Chen Z, Chuang LM, Du S, Gordon-Larsen P, Gross M, Guo X, Guo Y, Han S, Howard AG, Huang W, Hung YJ, Hwang MY, Hwu CM, Ichihara S, Isono M, Jang HM, Jiang G, Jonas JB, Kamatani Y, Katsuya T, Kawaguchi T, Khor CC, Kohara K, Lee MS, Lee NR, Li L, Liu J, Luk AO, Lv J, Okada Y, Pereira MA, Sabanayagam C, Shi J, Shin DM, So WY, Takahashi A, Tomlinson B, Tsai FJ, van Dam RM, Xiang YB, Yamamoto K, Yamauchi T, Yoon K, Yu C, Yuan JM, Zhang L, Zheng W, Igase M, Cho YS, Rotter JI, Wang YX, Sheu WHH, Yokota M, Wu JY, Cheng CY, Wong TY, Shu XO, Kato N, Park KS, Tai ES, Matsuda F, Koh WP, Ma RCW, Maeda S, Millwood IY, Lee J, Kadowaki T, Walters RG, Kim BJ, Mohlke KL, Sim X. Spracklen CN, et al. Nature. 2020 Jun;582(7811):240-245. doi: 10.1038/s41586-020-2263-3. Epub 2020 May 6. Nature. 2020. PMID: 32499647 Free PMC article.
At another locus, expression quantitative trait loci at two overlapping T2D signals affect two genes-NKX6-3 and ANK1-in different tissues(4-6). Association studies in diverse populations identify additional loci and elucidate disease-associated genes, biology, and pathways …
At another locus, expression quantitative trait loci at two overlapping T2D signals affect two genes-NKX6-3 and ANK1-in different tis …
Identification of a novel ANK1 mutation in hereditary spherocytosis co-existing with BWS.
Zhang Q, Zhang C, Wang Y, Hao S, Shi J, Feng X, Zheng L, Wang X, Xue C, Zhou B, Liu F, Zhao F, Li X, Deng L, Hou J, Meng Z. Zhang Q, et al. Mol Genet Genomic Med. 2022 Apr;10(4):e1903. doi: 10.1002/mgg3.1903. Epub 2022 Feb 25. Mol Genet Genomic Med. 2022. PMID: 35218326 Free PMC article.
Nevertheless, to scrutinize molecular causes of other symptoms of the patient, including anemia, hyperbilirubinemia, and jaundice, a whole exome sequencing (WES) was performed. We identified a novel and de novo mutation in ANK1 gene (c.520delC). This frameshift mutation of …
Nevertheless, to scrutinize molecular causes of other symptoms of the patient, including anemia, hyperbilirubinemia, and jaundice, a whole e …
A cross-brain regions study of ANK1 DNA methylation in different neurodegenerative diseases.
Smith AR, Smith RG, Burrage J, Troakes C, Al-Sarraj S, Kalaria RN, Sloan C, Robinson AC, Mill J, Lunnon K. Smith AR, et al. Neurobiol Aging. 2019 Feb;74:70-76. doi: 10.1016/j.neurobiolaging.2018.09.024. Epub 2018 Oct 13. Neurobiol Aging. 2019. PMID: 30439595
Recent epigenome-wide association studies in Alzheimer's disease have highlighted consistent robust neuropathology-associated DNA hypermethylation of the ankyrin 1 (ANK1) gene in the cortex. The extent to which altered ANK1 DNA methylation is also associated with ot …
Recent epigenome-wide association studies in Alzheimer's disease have highlighted consistent robust neuropathology-associated DNA hypermethy …
A Novel ANK1 Mutation in a Neonatal Hereditary Spherocytosis Case: Diagnostic Challenges and Familial Genetic Analysis.
Li J, Guo H, Zhu Z, Sun J. Li J, et al. Acta Haematol. 2022;145(6):575-581. doi: 10.1159/000525054. Epub 2022 Jul 11. Acta Haematol. 2022. PMID: 35817016
Hereditary spherocytosis (HS) is a congenital disease in which erythrocyte membranes are abnormal, with ANK1 defects as the main cause. The diagnosis of neonatal HS is difficult due to poor phenotypic specificity. ...The disease was caused by a frameshift mutation (c.3392d …
Hereditary spherocytosis (HS) is a congenital disease in which erythrocyte membranes are abnormal, with ANK1 defects as the main caus …
ANK1 Methylation regulates expression of MicroRNA-486-5p and discriminates lung tumors by histology and smoking status.
Tessema M, Yingling CM, Picchi MA, Wu G, Ryba T, Lin Y, Bungum AO, Edell ES, Spira A, Belinsky SA. Tessema M, et al. Cancer Lett. 2017 Dec 1;410:191-200. doi: 10.1016/j.canlet.2017.09.038. Epub 2017 Sep 29. Cancer Lett. 2017. PMID: 28965852 Free PMC article.

This study investigated epigenetic co-regulation of miR-486-5p and its host gene ANK1. MiR-486-5p expression in lung tumors and cell lines was significantly reduced compared to normal lung (p < 0.001) and is strongly correlated with ANK1 expression. ...ANK1

This study investigated epigenetic co-regulation of miR-486-5p and its host gene ANK1. MiR-486-5p expression in lung tumors and cell …
347 results