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Items: 1 to 20 of 31

1.
Characterization of βB2‐crystallin tryptophan mutants reveals two different folding states in solution
Jiayue Sun, Ken Morishima, Rintaro Inoue, Masaaki Sugiyama, Takumi Takata
Protein Sci. 2024 Jul; 33(7): e5092. Published online 2024 Jun 26. doi: 10.1002/pro.5092
PMCID:
PMC11201810
AbstractArticlePDF–6.6M
2.
An ATCUN-like copper site in βB2-crystallin plays a protective role in cataract-associated aggregation
Martin E. Tovar-Ramírez, Nils Schuth, Oscar Rodríguez, Thomas Kroll, Gloria Saab-Rincon, Miguel Costas, Kirsten Lampi, Liliana Quintanar
Inorg Chem. Author manuscript; available in PMC 2024 Jul 10.
Published in final edited form as: Inorg Chem. 2023 Jul 10; 62(27): 10592–10604. Published online 2023 Jun 28. doi: 10.1021/acs.inorgchem.3c00794
PMCID:
PMC11156493
AbstractArticlePDF–2.1M
3.
Insight into Pathogenic Mechanism Underlying the Hereditary Cataract Caused by βB2-G149V Mutation
Jing Wu, Silong Chen, Jingjie Xu, Wanyue Xu, Sifan Zheng, Qing Tian, Chenqi Luo, Xiangjun Chen, Xingchao Shentu
Biomolecules. 2023 May; 13(5): 864. Published online 2023 May 19. doi: 10.3390/biom13050864
PMCID:
PMC10216223
AbstractArticlePDF–4.2M
4.
Polymorphisms in CRYBB2 encoding βB2-crystallin are associated with antisaccade performance and memory function
Ina Giegling, Annette M. Hartmann, Just Genius, Bettina Konte, Stephan Maul, Andreas Straube, Thomas Eggert, Christoph Mulert, Gregor Leicht, Susanne Karch, Ulrich Hegerl, Oliver Pogarell, Sabine M. Hölter, Hans-Jürgen Möller, Jochen Graw, Dan Rujescu
Transl Psychiatry. 2020; 10: 113. Published online 2020 Apr 21. doi: 10.1038/s41398-020-0791-0
PMCID:
PMC7174396
AbstractArticlePDF–1.0M
5.
Human βB2-crystallin forms a face-en-face dimer in solution - an integrated NMR and SAXS study
Zhaoyong Xi, Matthew J. Whitley, Angela M. Gronenborn
Structure. Author manuscript; available in PMC 2018 Mar 7.
Published in final edited form as: Structure. 2017 Mar 7; 25(3): 496–505. Published online 2017 Feb 23. doi: 10.1016/j.str.2017.02.001
PMCID:
PMC5381515
AbstractArticlePDF–1.0M
6.
Analyzing the Association of Polymorphisms in the CRYBB2 Gene with Prostate Cancer Risk in African Americans
MEZBAH U. FARUQUE, RABINDRA PAUL, LUISEL RICKS-SANTI, EMMANUEL Y. JINGWI, CHILEDUM A. AHAGHOTU, GEORGIA M. DUNSTON
Anticancer Res. Author manuscript; available in PMC 2016 May 1.
Published in final edited form as: Anticancer Res. 2015 May; 35(5): 2565–2570.
PMCID:
PMC4743665
AbstractArticlePDF–348K
7.
Congenital cataracts: de novo gene conversion event in CRYBB2
Sarah J. Garnai, Jeroen R. Huyghe, David M. Reed, Kathleen M. Scott, Jeffrey M. Liebmann, Michael Boehnke, Julia E. Richards, Robert Ritch, Hemant Pawar
Mol Vis. 2014; 20: 1579–1593. Published online 2014 Nov 6.
PMCID:
PMC4225141
AbstractArticlePDF–4.1M
8.
A Missense Mutation in CRYBB2 Leads to Progressive Congenital Membranous Cataract by Impacting the Solubility and Function of βB2-Crystallin
Weirong Chen, Xiaoyun Chen, Zhengmao Hu, Haotian Lin, Fengqi Zhou, Lixia Luo, Xinyu Zhang, Xiaojian Zhong, Ye Yang, Changrui Wu, Zhuoling Lin, Shaobi Ye, Yizhi Liu, for the study group of CCPMOH
PLoS One. 2013; 8(11): e81290. Published online 2013 Nov 28. doi: 10.1371/journal.pone.0081290
PMCID:
PMC3842955
AbstractArticlePDF–6.0M
9.
The Congenital Cataract-Linked A2V Mutation Impairs Tetramer Formation and Promotes Aggregation of βB2-Crystallin
Jia Xu, Sha Wang, Wei-Jie Zhao, Yi-Bo Xi, Yong-Bin Yan, Ke Yao
PLoS One. 2012; 7(12): e51200. Published online 2012 Dec 6. doi: 10.1371/journal.pone.0051200
PMCID:
PMC3516508
AbstractArticlePDF–865K
10.
Identification of a novel CRYBB2 missense mutation causing congenital autosomal dominant cataract
Nicole Weisschuh, Sabine Aisenbrey, Bernd Wissinger, Angelika Riess
Mol Vis. 2012; 18: 174–180. Published online 2012 Jan 21.
PMCID:
PMC3272051
AbstractArticlePDF–662K
11.
Characterization of a novel mutation in the CRYBB2 gene associated with autosomal dominant congenital posterior subcapsular cataract in a Chinese family
Ke Yao, Jinyu Li, Chongfei Jin, Wei Wang, Yanan Zhu, Xingchao Shentu, Qiwei Wang
Mol Vis. 2011; 17: 144–152. Published online 2011 Jan 13.
PMCID:
PMC3021577
AbstractArticlePDF–741K
12.
Mutation analysis in a German family identified a new cataract-causing allele in the CRYBB2 gene
Silke Pauli, Torben Söker, Norman Klopp, Thomas Illig, Wolfgang Engel, Jochen Graw
Mol Vis. 2007; 13: 962–967. Published online 2007 Jun 19.
PMCID:
PMC2774456
AbstractArticlePDF–464K
13.
Mutation analysis of congenital cataract in a Basotho family identified a new missense allele in CRYBB2
Maneo Emily Mothobi, Shuren Guo, Yuanyuan Liu, Qiang Chen, Ali Said Yussuf, Xinli Zhu, Zheng Fang
Mol Vis. 2009; 15: 1470–1475. Published online 2009 Jul 30.
PMCID:
PMC2718852
AbstractArticlePDF–1.4M
14.
Deamidation in Human Lens βB2-Crystallin Destabilizes the Dimer
Kirsten J. Lampi, Kencee K. Amyx, Petra Ahmann, Eric A. Steel
Biochemistry. Author manuscript; available in PMC 2008 Sep 9.
Published in final edited form as: Biochemistry. 2006 Mar 14; 45(10): 3146–3153. doi: 10.1021/bi052051k
PMCID:
PMC2533042
AbstractArticlePDF–722K
15.
Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts
Fei-feng Li, Si-quan Zhu, Shu-zhen Wang, Chang Gao, Shang-zhi Huang, Meng Zhang, Xu Ma
Mol Vis. 2008; 14: 750–755. Published online 2008 Apr 24.
PMCID:
PMC2335123
AbstractArticlePDF–3.3M
16.
Amino acid sequence of human lens beta B2-crystallin.
L. R. Miesbauer, J. B. Smith, D. L. Smith
Protein Sci. 1993 Feb; 2(2): 290–291. doi: 10.1002/pro.5560020217
PMCID:
PMC2142348
SummaryPDF–214K
17.
CRYβB2 enhances tumorigenesis through upregulation of nucleolin in triple negative breast cancer
Yu Yan, Athira Narayan, Soonweng Cho, Zhiqiang Cheng, Jun O. Liu, Heng Zhu, Guannan Wang, Bryan Wharram, Ala Lisok, Mary Brummet, Harumi Saeki, Tao Huang, Kathleen Gabrielson, Edward Gabrielson, Leslie Cope, Yasmine M. Kanaan, Ali Afsari, Tammey Naab, Harris G. Yfantis, Stefan Ambs, Martin G. Pomper, Saraswati Sukumar, Vanessa F. Merino
Oncogene. Author manuscript; available in PMC 2023 Mar 31.
Published in final edited form as: Oncogene. 2021 Sep; 40(38): 5752–5763. Published online 2021 Aug 2. doi: 10.1038/s41388-021-01975-3
PMCID:
PMC10064491
AbstractArticlePDF–2.5M
18.
Cataract-Associated New Mutants S175G/H181Q of βΒ2-Crystallin and P24S/S31G of γD-Crystallin Are Involved in Protein Aggregation by Structural Changes
In-Kang Song, Seungjin Na, Eunok Paek, Kong-Joo Lee
Int J Mol Sci. 2020 Sep; 21(18): 6504. Published online 2020 Sep 5. doi: 10.3390/ijms21186504
PMCID:
PMC7555777
AbstractArticlePDF–2.4M
19.
A functional role for the cancer disparity-linked genes, CRYβB2 and CRYβB2P1, in the promotion of breast cancer
Maya A. Barrow, Megan E. Martin, Alisha Coffey, Portia L. Andrews, Gieira S. Jones, Denise K. Reaves, Joel S. Parker, Melissa A. Troester, Jodie M. Fleming
Breast Cancer Res. 2019; 21: 105. Published online 2019 Sep 11. doi: 10.1186/s13058-019-1191-3
PMCID:
PMC6739962
AbstractArticlePDF–2.7M
20.
Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms
Sathiyavedu T. Santhiya, Ganesan Senthil Kumar, Pridhvi Sudhakar, Navnit Gupta, Norman Klopp, Thomas Illig, Torben Söker, Marco Groth, Matthias Platzer, Puthiya M. Gopinath, Jochen Graw
Mol Vis. 2010; 16: 1837–1847. Published online 2010 Sep 10.
PMCID:
PMC2956670
AbstractArticlePDF–953K

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