| p53-induced ARVCF modulates the splicing landscape and supports the tumor suppressive function of p53. | p53-induced ARVCF modulates the splicing landscape and supports the tumor suppressive function of p53.
Suzuki N, Idogawa M, Tange S, Ohashi T, Sasaki Y, Nakase H, Tokino T. | 11/28/2020 |
| observed ARVCF-dependent changes in small GTPase (mainly RhoA) activity in lung cancer cells. We confirmed that ARVCF plays an important role in the malignant phenotype | ARVCF expression is significantly correlated with the malignant phenotype of non-small cell lung cancer.
Zhang D, Tang N, Liu Y, Wang EH. | 09/12/2015 |
| Carriage of the minor allele at rs2518824 in the armadillo repeat gene deleted in velocardiofacial syndrome (ARVCF) gene was associated with white matter abnormality. | Common genetic variants and risk of brain injury after preterm birth.
Boardman JP, Walley A, Ball G, Takousis P, Krishnan ML, Hughes-Carre L, Aljabar P, Serag A, King C, Merchant N, Srinivasan L, Froguel P, Hajnal J, Rueckert D, Counsell S, Edwards AD. | 08/9/2014 |
| Data indicate that armadillo repeat protein ARVCF interacts with the splicing factors the splicing factor SRSF1 (SF2/ASF), the RNA helicase p68 (DDX5), and the heterogeneous nuclear ribonucleoprotein hnRNP H2. | Nuclear ARVCF protein binds splicing factors and contributes to the regulation of alternative splicing.
Rappe U, Schlechter T, Aschoff M, Hotz-Wagenblatt A, Hofmann I., Free PMC Article | 08/9/2014 |
| Schizophrenic patients with more copies of the haplotype T-G-A-T-T-G-G-C-T-G-T (ARVCF-Hap1) have lower white matter integrity in caudate nucleus and greater perseverative errors. | ARVCF genetic influences on neurocognitive and neuroanatomical intermediate phenotypes in Chinese patients with schizophrenia.
Sim K, Chan WY, Woon PS, Low HQ, Lim L, Yang GL, Lee J, Chong SA, Sitoh YY, Chan YH, Liu J, Tan EC, Williams H, Nowinski WL. | 06/30/2012 |
| Five SNPs were validated as being significantly associated with prostate cancer mortality, one each in the LEPR, CRY1, RNASEL, IL4, and ARVCF genes. | Genetic variants in the LEPR, CRY1, RNASEL, IL4, and ARVCF genes are prognostic markers of prostate cancer-specific mortality.
Lin DW, FitzGerald LM, Fu R, Kwon EM, Zheng SL, Kolb S, Wiklund F, Stattin P, Isaacs WB, Xu J, Ostrander EA, Feng Z, Grönberg H, Stanford JL., Free PMC Article | 03/24/2012 |
| The functional variant rs165815, which affects a critical region of ARVCF, is a considerable source of the genetic variability associated with the risk of developing schizophrenia. | A functional variant provided further evidence for the association of ARVCF with schizophrenia.
Mas S, Bernardo M, Gassó P, Alvarez S, Garcia-Rizo C, Bioque M, Kirkpatrick B, Lafuente A, Mas S, Bernardo M, Gassó P, Alvarez S, Garcia-Rizo C, Bioque M, Kirkpatrick B, Lafuente A., Free PMC Articles: PMC4390130, PMC4390130 | 10/4/2010 |
| Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR., Free PMC Article | 06/30/2010 |
| Single nucleotide polymorphisms in the ARVGF gene are associated with the risk of schizophrenia. | ARVCF single marker and haplotypic association with schizophrenia.
Mas S, Bernardo M, Parellada E, Garcia-Rizo C, Gassó P, Alvarez S, Lafuente A. | 04/19/2010 |
| Over-expression of TXNRD2, COMT and ARVCF affects incentive learning and working memory in transgenic mice. | Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice.
Suzuki G, Harper KM, Hiramoto T, Funke B, Lee M, Kang G, Buell M, Geyer MA, Kucherlapati R, Morrow B, Männistö PT, Agatsuma S, Hiroi N., Free PMC Article | 01/21/2010 |
| Differential expression pattern of protein ARVCF in nephron segments of human kidney. | Differential expression pattern of protein ARVCF in nephron segments of human and mouse kidney.
Walter B, Schlechter T, Hergt M, Berger I, Hofmann I. | 01/21/2010 |
| Observational study of gene-disease association. (HuGE Navigator) | See all PubMed (8) articlesMaternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.
Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Nguyen TT, Christiansen L, Lidral AC, Murray JC. A functional variant provided further evidence for the association of ARVCF with schizophrenia.
Mas S, Bernardo M, Gassó P, Alvarez S, Garcia-Rizo C, Bioque M, Kirkpatrick B, Lafuente A, Mas S, Bernardo M, Gassó P, Alvarez S, Garcia-Rizo C, Bioque M, Kirkpatrick B, Lafuente A. Association of genetic variants with hemorrhagic stroke in Japanese individuals.
Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y. Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals.
Oguri M, Kato K, Yokoi K, Yoshida T, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y. Association of gene polymorphisms with chronic kidney disease in Japanese individuals.
Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y. Genetic susceptibility to distinct bladder cancer subphenotypes.
Guey LT, García-Closas M, Murta-Nascimento C, Lloreta J, Palencia L, Kogevinas M, Rothman N, Vellalta G, Calle ML, Marenne G, Tardón A, Carrato A, García-Closas R, Serra C, Silverman DT, Chanock S, Real FX, Malats N, EPICURO/Spanish Bladder Cancer Study investigators. No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics.
Sanders AR, Duan J, Levinson DF, Shi J, He D, Hou C, Burrell GJ, Rice JP, Nertney DA, Olincy A, Rozic P, Vinogradov S, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Crowe RR, Cloninger CR, Martinez M, Gejman PV. Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family trios.
Michaelovsky E, Frisch A, Leor S, Stein D, Danziger Y, Carel C, Fennig S, Mimouni M, Klauck SM, Benner A, Poustka A, Apter A, Weizman A, Michaelovsky E, Frisch A, Leor S, Stein D, Danziger Y, Carel C, Fennig S, Mimouni M, Klauck SM, Benner A, Poustka A, Apter A, Weizman A. | 03/13/2008 |
| Evidence was found for association of illness to rs165849 in ARVCF, and a stronger signal from three-marker haplotypes spanning the 3' portions of COMT and ARVCF. Val(108/158)Met was in linkage disequilibrium with the markers in ARVCF. | Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.
Sanders AR, Rusu I, Duan J, Vander Molen JE, Hou C, Schwab SG, Wildenauer DB, Martinez M, Gejman PV. | 01/21/2010 |
| Two haplotypes covering the catechol-O-methyltransferase-ARVCF region show significant transmission disequilibrium in anorexia nervosa-restricting Israeli-Jewish families | Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family trios.
Michaelovsky E, Frisch A, Leor S, Stein D, Danziger Y, Carel C, Fennig S, Mimouni M, Klauck SM, Benner A, Poustka A, Apter A, Weizman A, Michaelovsky E, Frisch A, Leor S, Stein D, Danziger Y, Carel C, Fennig S, Mimouni M, Klauck SM, Benner A, Poustka A, Apter A, Weizman A. | 01/21/2010 |
| Results implicate a very close association of ARVCF with migrating neurons from the ganglionic eminence. | Expression of ARVCF in the human ganglionic eminence during fetal development.
Ulfig N, Chan WY. | 01/21/2010 |
| Interactions with zona occludens-1 and zona occludens-2, in particular, may mediate recruitment of ARVCF to the plasma membrane and the nucleus | Association of ARVCF with zonula occludens (ZO)-1 and ZO-2: binding to PDZ-domain proteins and cell-cell adhesion regulate plasma membrane and nuclear localization of ARVCF.
Kausalya PJ, Phua DC, Hunziker W., Free PMC Article | 01/21/2010 |