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

Year Number of Results
1994 1
1995 4
1996 1
1997 1
2001 2
2002 3
2005 2
2008 1
2010 2
2011 1
2012 1
2020 1
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2023 1
2024 0

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22 results

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Page 1
Bidirectional transcription from human LRRTM2/CTNNA1 and LRRTM1/CTNNA2 gene loci leads to expression of N-terminally truncated CTNNA1 and CTNNA2 isoforms.
Kask M, Pruunsild P, Timmusk T. Kask M, et al. Biochem Biophys Res Commun. 2011 Jul 22;411(1):56-61. doi: 10.1016/j.bbrc.2011.06.085. Epub 2011 Jun 17. Biochem Biophys Res Commun. 2011. PMID: 21708131
We demonstrate that bidirectional activity of these promoters results in alternative CTNNA1 and CTNNA2 transcripts that are expressed at high levels in the nervous system and show that N-terminally truncated CTNNA1 and CTNNA2 proteins lacking the beta-catenin intera …
We demonstrate that bidirectional activity of these promoters results in alternative CTNNA1 and CTNNA2 transcripts that are expressed …
Expression of Catenin family members CTNNA1, CTNNA2, CTNNB1 and JUP in the primate prefrontal cortex and hippocampus.
Smith A, Bourdeau I, Wang J, Bondy CA. Smith A, et al. Brain Res Mol Brain Res. 2005 Apr 27;135(1-2):225-31. doi: 10.1016/j.molbrainres.2004.12.025. Brain Res Mol Brain Res. 2005. PMID: 15857685
These studies demonstrate a distinct neuronal pattern of gene expression for catenin family members in primate brain structures characterized by high degrees of folding and strong lamination. The high level expression of these transcripts supports the notion of a major rol …
These studies demonstrate a distinct neuronal pattern of gene expression for catenin family members in primate brain structures chara …
Mechanisms Underlying Rare Inherited Pediatric Retinal Vascular Diseases: FEVR, Norrie Disease, Persistent Fetal Vascular Syndrome.
Le V, Abdelmessih G, Dailey WA, Pinnock C, Jobczyk V, Rashingkar R, Drenser KA, Mitton KP. Le V, et al. Cells. 2023 Nov 5;12(21):2579. doi: 10.3390/cells12212579. Cells. 2023. PMID: 37947657 Free PMC article. Review.
Recent discoveries of FEVR-linked variants in two other Catenin genes (CTNND1, CTNNA1) and the Endoplasmic Reticulum Membrane Complex Subunit-1 gene (EMC1) suggest that we will continue to find additional genes that impact the neural retinal vasculature, especially in mult …
Recent discoveries of FEVR-linked variants in two other Catenin genes (CTNND1, CTNNA1) and the Endoplasmic Reticulum Membrane Complex …
Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling.
Zhu X, Yang M, Zhao P, Li S, Zhang L, Huang L, Huang Y, Fei P, Yang Y, Zhang S, Xu H, Yuan Y, Zhang X, Zhu X, Ma S, Hao F, Sundaresan P, Zhu W, Yang Z. Zhu X, et al. J Clin Invest. 2021 Mar 15;131(6):e139869. doi: 10.1172/JCI139869. J Clin Invest. 2021. PMID: 33497368 Free PMC article.
In isolated mouse lung ECs, both CTNNA1-P893L and F72S mutants failed to rescue either the disrupted F-actin arrangement or the VE-cadherin and CTNNB1 distribution. Moreover, we discovered that compound heterozygous Ctnna1 F72S and a deletion allele could cause a si …
In isolated mouse lung ECs, both CTNNA1-P893L and F72S mutants failed to rescue either the disrupted F-actin arrangement or the VE-ca …
Development of a Genotype Assay for Age-Related Macular Degeneration: The EYE-RISK Consortium.
de Breuk A, Acar IE, Kersten E, Schijvenaars MMVAP, Colijn JM, Haer-Wigman L, Bakker B, de Jong S, Meester-Smoor MA, Verzijden T, Missotten TOAR, Monés J, Biarnés M, Pauleikhoff D, Hense HW, Silva R, Nunes S, Melo JB, Fauser S, Hoyng CB, Ueffing M, Coenen MJH, Klaver CCW, den Hollander AI; EYE-RISK Consortium. de Breuk A, et al. Ophthalmology. 2021 Nov;128(11):1604-1617. doi: 10.1016/j.ophtha.2020.07.037. Epub 2020 Jul 25. Ophthalmology. 2021. PMID: 32717343 Free article.
METHODS: We designed single-molecule molecular inversion probes for target selection and used next generation sequencing to sequence 87 single nucleotide polymorphisms (SNPs), coding and splice-site regions of 10 AMD-(related) genes (ARMS2, C3, C9, CD46, CFB, CFH, CFI, HTRA1, TIM …
METHODS: We designed single-molecule molecular inversion probes for target selection and used next generation sequencing to sequence 87 sing …
Wnt-1-dependent regulation of local E-cadherin and alpha N-catenin expression in the embryonic mouse brain.
Shimamura K, Hirano S, McMahon AP, Takeichi M. Shimamura K, et al. Development. 1994 Aug;120(8):2225-34. doi: 10.1242/dev.120.8.2225. Development. 1994. PMID: 7925023
E-cadherin is transiently expressed in local regions of the embryonic mouse brain, which include several patchy areas on the mesencephalon and diencephalon and their roof plate and part of cerebellar rudiments. ...These results suggest that the Wnt-1 signal is, either dire …
E-cadherin is transiently expressed in local regions of the embryonic mouse brain, which include several patchy areas on the mesencep …
Evaluating the Occurrence of Rare Variants in the Complement Factor H Gene in Patients With Early-Onset Drusen Maculopathy.
de Breuk A, Heesterbeek TJ, Bakker B, Verzijden T, Lechanteur YTE, Klaver CCW, den Hollander AI, Hoyng CB. de Breuk A, et al. JAMA Ophthalmol. 2021 Nov 1;139(11):1218-1226. doi: 10.1001/jamaophthalmol.2021.4102. JAMA Ophthalmol. 2021. PMID: 34647987 Free PMC article.
EXPOSURES: Coding regions of CFH, CFI, C3, C9, CFB, ABCA4, PRPH2, TIMP3, and CTNNA1 genes were sequenced, genetic risk scores (GRS) were calculated based on 52 AMD-associated variants, and phenotypic characteristics on color fundus photographs were analyzed comparing patie …
EXPOSURES: Coding regions of CFH, CFI, C3, C9, CFB, ABCA4, PRPH2, TIMP3, and CTNNA1 genes were sequenced, genetic risk scores (GRS) w …
Genome remodelling in a basal-like breast cancer metastasis and xenograft.
Ding L, Ellis MJ, Li S, Larson DE, Chen K, Wallis JW, Harris CC, McLellan MD, Fulton RS, Fulton LL, Abbott RM, Hoog J, Dooling DJ, Koboldt DC, Schmidt H, Kalicki J, Zhang Q, Chen L, Lin L, Wendl MC, McMichael JF, Magrini VJ, Cook L, McGrath SD, Vickery TL, Appelbaum E, Deschryver K, Davies S, Guintoli T, Lin L, Crowder R, Tao Y, Snider JE, Smith SM, Dukes AF, Sanderson GE, Pohl CS, Delehaunty KD, Fronick CC, Pape KA, Reed JS, Robinson JS, Hodges JS, Schierding W, Dees ND, Shen D, Locke DP, Wiechert ME, Eldred JM, Peck JB, Oberkfell BJ, Lolofie JT, Du F, Hawkins AE, O'Laughlin MD, Bernard KE, Cunningham M, Elliott G, Mason MD, Thompson DM Jr, Ivanovich JL, Goodfellow PJ, Perou CM, Weinstock GM, Aft R, Watson M, Ley TJ, Wilson RK, Mardis ER. Ding L, et al. Nature. 2010 Apr 15;464(7291):999-1005. doi: 10.1038/nature08989. Nature. 2010. PMID: 20393555 Free PMC article.
Here we describe the genomic analyses of four DNA samples from an African-American patient with basal-like breast cancer: peripheral blood, the primary tumour, a brain metastasis and a xenograft derived from the primary tumour. ...The xenograft retained all primary tumour …
Here we describe the genomic analyses of four DNA samples from an African-American patient with basal-like breast cancer: peripheral blood, …
Cancer: Genomics of metastasis.
Gray J. Gray J. Nature. 2010 Apr 15;464(7291):989-90. doi: 10.1038/464989a. Nature. 2010. PMID: 20393550 No abstract available.
22 results