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Nuclear β-catenin localization and mutation of the CTNNB1 gene: a context-dependent association
Author / Creator:Kim, Grace ; Kurnit, Katherine C. ; Djordjevic, Bojana ; Singh, Charanjeet ; Munsell, Mark F. ; Wang, Wei-Lien ; Lazar, Alexander J. ; Zhang, Wei ; Broaddus, Russell
Publisher:New York: Elsevier Inc
Journal title:Modern pathology, 2018-10, Vol.31 (10), p.1553-1559
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Prognostic Value of CTNNB1 Gene Mutation in Primary Sporadic Aggressive Fibromatosis
Author / Creator:van Broekhoven, Danique L. M. ; Verhoef, Cornelis ; Grünhagen, Dirk J. ; van Gorp, Joost M. H. H. ; den Bakker, Michael A. ; Hinrichs, John W. J. ; de Voijs, Carmen M. A. ; van Dalen, Thijs
Publisher:Boston: Springer US
Journal title:Annals of surgical oncology, 2015-05, Vol.22 (5), p.1464-1470
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Familial exudative vitreoretinopathy caused by CTNNB1 gene de novo mutation in a Chinese family: a case report
Author / Creator:Wang, Yanan ; Chang, Yujie ; Lei, Hongtao ; Yan, Weiyan ; Chai, Yuqiong ; Zang, Weiwei
Publisher:England: BioMed Central Ltd
Journal title:BMC pediatrics, 2025-02, Vol.25 (1), p.146-8, Article 146
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Investigation of CTNNB1 gene mutations and expression in hepatocellular carcinoma and cirrhosis in association with hepatitis B virus infection
Author / Creator:Javanmard, Davod ; Najafi, Mohammad ; Babaei, Mohammad Reza ; Karbalaie Niya, Mohammad Hadi ; Esghaei, Maryam ; Panahi, Mahshid ; Safarnezhad Tameshkel, Fahimeh ; Tavakoli, Ahmad ; Jazayeri, Seyed Mohammad ; Ghaffari, Hadi ; Ataei-Pirkooh, Angila ; Monavari, Seyed Hamidreaz ; Bokharaei-Salim, Farah
Publisher:London: BioMed Central Ltd
Journal title:Infectious agents and cancer, 2020-06, Vol.15 (1), p.1-10, Article 37
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Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability
Author / Creator:Dashti Sepide ; Salehpour Shadab ; Mohammad-Reza, Ghasemi ; Sadeghi Hossein ; Rostami Masoumeh ; Hashemi-Gorji Farzad ; Mirfakhraie Reza ; Yassaee, Vahid Reza ; Miryounesi Mohammad
Publisher:Milano: Springer Nature B.V
Journal title:Neurological sciences, 2022-04, Vol.43 (4), p.2859-2863
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Alopecia areata-like pattern of baldness: the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 gene
Author / Creator:Moeinafshar, Aysan ; Tehrani Fateh, Sahand ; Sadeghi, Hossein ; Karimzadeh, Parvaneh ; Mirfakhraie, Reza ; Hashemi-Gorji, Farzad ; Larki, Pegah ; Miryounesi, Mohammad ; Ghasemi, Mohammad-Reza
Publisher:Milano: Springer Nature B.V
Journal title:Neurological sciences, 2023-11, Vol.44 (11), p.4041-4048
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Assessment of CTNNB1 gene mutations and β-catenin immunoexpression in salivary gland pleomorphic adenomas and adenoid cystic carcinomas
Author / Creator:Roberta Barroso Cavalcante ; Cassiano Francisco Weege Nonaka ; Hellen Bandeira de Pontes Santos ; Silvia Helena Barem Rabenhorst ; Leão Pereira Pinto ; Lélia Batista de Souza
Publisher:Heidelberg: Springer Nature B.V
Journal title:Virchows Archiv : an international journal of pathology, 2018-06, Vol.472 (6), p.999-1005
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In Silico Analysis of the Missense Variants of Uncertain Significance of CTNNB1 Gene Reported in GnomAD Database
Author / Creator:Caballero-Avendaño, Arturo ; Gutiérrez-Angulo, Melva ; Ayala-Madrigal, María de la Luz ; Moreno-Ortiz, José Miguel ; González-Mercado, Anahí ; Peregrina-Sandoval, Jorge
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2024-07, Vol.15 (8), p.972
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Wnt/ β-catenin and CTNNB1 gene mutation in hepatocellular carcinoma, a case study in Egyptian patients
Author / Creator:Abdelsalam, Ramy A. ; El-Shawaf, Ibrahim M. ; Abdel-Aziz, Azza ; Bismar, Tarek A. ; Yussif, Shaimaa M.
Publisher:BMC
Journal title:Surgical and experimental pathology, 2025-01, Vol.8 (1), p.1-13, Article 1
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Identification of a novel splice mutation in CTNNB1 gene in a Chinese family with both severe intellectual disability and serious visual defects
Author / Creator:Wang, Hui ; Zhao, Yiqi ; Yang, Liwei ; Han, Shuai ; Qi, Ming
Publisher:Milano: Springer Nature B.V
Journal title:Neurological sciences, 2019-08, Vol.40 (8), p.1701-1704
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Screening and computational analysis of colorectal associated non-synonymous polymorphism in CTNNB1 gene in Pakistani population
Author / Creator:Razak, Suhail ; Bibi, Nousheen ; Dar, Javid Ahmad ; Afsar, Tayyaba ; Almajwal, Ali ; Parveen, Zahida ; Jahan, Sarwat
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2019-11, Vol.20 (1), p.171-12, Article 171
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Bioinformatics Analysis Identifies Precision Treatment with Paclitaxel for Hepatocellular Carcinoma Patients Harboring Mutant TP53 or Wild-Type CTNNB1 Gene
Author / Creator:Lin, Jiunn-Chang ; Liu, Tsang-Pai ; Andriani, Vivin ; Athoillah, Muhammad ; Wang, Chih-Yang ; Yang, Pei-Ming
Publisher:Basel: MDPI AG
Journal title:Journal of personalized medicine, 2021-11, Vol.11 (11), p.1199
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Thymus neuroendocrine tumors with CTNNB1 gene mutations, disarrayed ß-catenin expression, and dual intra-tumor Ki-67 labeling index compartmentalization challenge the concept of secondary high-grade n...
Author / Creator:Fabbri, Alessandra ; Cossa, Mara ; Sonzogni, Angelica ; Bidoli, Paolo ; Canova, Stefania ; Cortinovis, Diego ; Abbate, Maria Ida ; Calabrese, Fiorella ; Nannini, Nazarena ; Lunardi, Francesca ; Rossi, Giulio ; La Rosa, Stefano ; Capella, Carlo ; Tamborini, Elena ; Perrone, Federica ; Busico, Adele ; Capone, Iolanda ; Valeri, Barbara ; Pastorino, Ugo ; Albini, Adriana ; Pelosi, Giuseppe
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Virchows Archiv : an international journal of pathology, 2017-07, Vol.471 (1), p.31-47
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Correction to: Screening and computational analysis of colorectal associated non-synonymous polymorphism in CTNNB1 gene in Pakistani population
Author / Creator:Razak, S. ; Bibi, N. ; Dar, J. A. ; Afsar, T. ; Almajwal, A. ; Parveen, Z. ; Jahan, S.
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2020-02, Vol.21 (1), p.39-1, Article 39
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Whole Exome Sequencing Identified two Novel Truncation Mutations in the CTNNB1 Gene Associated with Neurodevelopmental Disorder, Language Dysfunction, and Microcephaly in Chinese Children
Author / Creator:Ji, Yongchun ; Xia, Qin ; Zhang, Hewei ; Huo, Hongliang ; Cao, Xujun ; Wang, Weiwei ; Gu, Qin
Publisher:Los Angeles, CA: SAGE Publications
Journal title:Child neurology open, 2023-01, Vol.10, p.2329048X231184184
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β-Catenin accumulation and S33F mutation of CTNNB1 gene in colorectal cancer in Saudi Arabia
Author / Creator:Alomar, Suliman Y. ; Mansour, Lamjed ; Abuderman, Abdulwahab ; Alkhuriji, Afrah ; Arafah, Maha ; Alwasel, Saleh ; Harrath, Abdel Halim ; Almutairi, Mikhlid ; Trayhyrn, Paul ; Dar, Javid Ahmad
Publisher:Poland: Termedia Publishing House
Journal title:Polish journal of pathology, 2016-01, Vol.2 (2), p.156-162
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Activating mutations in CTNNB1 in aldosterone producing adenomas
Author / Creator:Åkerström, Tobias ; Maharjan, Rajani ; Sven Willenberg, Holger ; Cupisti, Kenko ; Ip, Julian ; Moser, Ana ; Stålberg, Peter ; Robinson, Bruce ; Alexander Iwen, K. ; Dralle, Henning ; Walz, Martin K. ; Lehnert, Hendrik ; Sidhu, Stan ; Gomez-Sanchez, Celso ; Hellman, Per ; Björklund, Peyman
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2016-01, Vol.6 (1), p.19546-19546, Article 19546
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A Mosaic Variant in CTNNB1/β-catenin as a Novel Cause for Osteopathia Striata With Cranial Sclerosis
Author / Creator:Huybrechts, Yentl ; Appelman-Dijkstra, Natasha M ; Steenackers, Ellen ; Van Beylen, Wouter ; Mortier, Geert ; Hendrickx, Gretl ; Van Hul, Wim
Publisher:US: Oxford University Press
Journal title:The journal of clinical endocrinology and metabolism, 2024-07, Vol.109 (7), p.1891-1898
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Novel truncating variants in CTNNB1 cause familial exudative vitreoretinopathy
Author / Creator:He, Yunqi ; Yang, Mu ; Zhao, Rulian ; Peng, Li ; Dai, Erkuan ; Huang, Lulin ; Zhao, Peiquan ; Li, Shujin ; Yang, Zhenglin
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2023-02, Vol.60 (2), p.174-182
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Gain-of-function mutant p53 together with ERG proto-oncogene drive prostate cancer by beta-catenin activation and pyrimidine synthesis
Author / Creator:Ding, Donglin ; Blee, Alexandra M. ; Zhang, Jianong ; Pan, Yunqian ; Becker, Nicole A. ; Maher, L. James ; Jimenez, Rafael ; Wang, Liguo ; Huang, Haojie
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2023-08, Vol.14 (1), p.4671-19, Article 4671
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Showing 1 to 20 of 260 results

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Nuclear β-catenin localization and mutation of the CTNNB1 gene: a context-dependent association

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Prognostic Value of CTNNB1 Gene Mutation in Primary Sporadic Aggressive Fibromatosis

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Familial exudative vitreoretinopathy caused by CTNNB1 gene de novo mutation in a Chinese family: a case report

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Investigation of CTNNB1 gene mutations and expression in hepatocellular carcinoma and cirrhosis in association with hepatitis B virus infection

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Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability

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Alopecia areata-like pattern of baldness: the most recent update and the expansion of novel phenotype and genotype in the CTNNB1 gene

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Assessment of CTNNB1 gene mutations and β-catenin immunoexpression in salivary gland pleomorphic adenomas and adenoid cystic carcinomas

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In Silico Analysis of the Missense Variants of Uncertain Significance of CTNNB1 Gene Reported in GnomAD Database

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Wnt/ β-catenin and CTNNB1 gene mutation in hepatocellular carcinoma, a case study in Egyptian patients

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Identification of a novel splice mutation in CTNNB1 gene in a Chinese family with both severe intellectual disability and serious visual defects

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Screening and computational analysis of colorectal associated non-synonymous polymorphism in CTNNB1 gene in Pakistani population

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Bioinformatics Analysis Identifies Precision Treatment with Paclitaxel for Hepatocellular Carcinoma Patients Harboring Mutant TP53 or Wild-Type CTNNB1 Gene

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Thymus neuroendocrine tumors with CTNNB1 gene mutations, disarrayed ß-catenin expression, and dual intra-tumor Ki-67 labeling index compartmentalization challenge the concept of secondary high-grade n...

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Correction to: Screening and computational analysis of colorectal associated non-synonymous polymorphism in CTNNB1 gene in Pakistani population

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Whole Exome Sequencing Identified two Novel Truncation Mutations in the CTNNB1 Gene Associated with Neurodevelopmental Disorder, Language Dysfunction, and Microcephaly in Chinese Children

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β-Catenin accumulation and S33F mutation of CTNNB1 gene in colorectal cancer in Saudi Arabia

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Activating mutations in CTNNB1 in aldosterone producing adenomas

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A Mosaic Variant in CTNNB1/β-catenin as a Novel Cause for Osteopathia Striata With Cranial Sclerosis

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Novel truncating variants in CTNNB1 cause familial exudative vitreoretinopathy

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Gain-of-function mutant p53 together with ERG proto-oncogene drive prostate cancer by beta-catenin activation and pyrimidine synthesis

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