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Items: 1 to 20 of 25

1.
Fibrillin-2 and Tenascin-C Bridge the Age Gap in Lung Epithelial Regeneration
Sarah E. Gilpin, Qiyao Li, Daniele Evangelista-Leite, Xi Ren, Dieter P. Reinhardt, Brian L. Frey, Harald C. Ott
Biomaterials. Author manuscript; available in PMC 2018 Sep 1.
Published in final edited form as: Biomaterials. 2017 Sep; 140: 212–219. Published online 2017 Jun 22. doi: 10.1016/j.biomaterials.2017.06.027
PMCID:
PMC5553709
AbstractArticlePDF–1.6M
2.
Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils
J Cell Biol. 1995 May 2; 129(4): 1165–1176. doi: 10.1083/jcb.129.4.1165
PMCID:
PMC2120487
SummaryPDF–6.4M
3.
Structure and expression of fibrillin-2, a novel microfibrillar component preferentially located in elastic matrices
J Cell Biol. 1994 Mar 1; 124(5): 855–863. doi: 10.1083/jcb.124.5.855
PMCID:
PMC2119952
SummaryPDF–7.5M
4.
A Novel Splicing Mutation in the FBN2 Gene in a Family With Congenital Contractural Arachnodactyly
Peiwen Xu, Ruirui Li, Sexin Huang, Menghan Sun, Jiaolong Liu, Yuping Niu, Yang Zou, Jie Li, Ming Gao, Xiaolei Li, Xuan Gao, Yuan Gao
Front Genet. 2020; 11: 143. Published online 2020 Feb 28. doi: 10.3389/fgene.2020.00143
PMCID:
PMC7058790
AbstractArticlePDF–1.1M
5.
CeRNA Expression Profiling Identifies KIT-Related circRNA-miRNA-mRNA Networks in Gastrointestinal Stromal Tumour
Ning Jia, Hanxing Tong, Yong Zhang, Hiroshi Katayama, Yuan Wang, Weiqi Lu, Sumei Zhang, Jin Wang
Front Genet. 2019; 10: 825. Published online 2019 Sep 10. doi: 10.3389/fgene.2019.00825
PMCID:
PMC6746987
AbstractArticlePDF–2.1M
6.
Characterization of Two Novel Intronic Variants Affecting Splicing in FBN1-Related Disorders
Carmela Fusco, Silvia Morlino, Lucia Micale, Alessandro Ferraris, Paola Grammatico, Marco Castori
Genes (Basel) 2019 Jun; 10(6): 442. Published online 2019 Jun 10. doi: 10.3390/genes10060442
PMCID:
PMC6627396
AbstractArticlePDF–1.7M
7.
The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance
Davut Pehlivan, Yavuz Bayram, Nilay Gunes, Zeynep Coban Akdemir, Anju Shukla, Tatjana Bierhals, Burcu Tabakci, Yavuz Sahin, Alper Gezdirici, Jawid M. Fatih, Elif Yilmaz Gulec, Gozde Yesil, Jaya Punetha, Zeynep Ocak, Christopher M. Grochowski, Ender Karaca, Hatice Mutlu Albayrak, Periyasamy Radhakrishnan, Haktan Bagis Erdem, Ibrahim Sahin, Timur Yildirim, Ilhan A. Bayhan, Aysegul Bursali, Muhsin Elmas, Zafer Yuksel, Ozturk Ozdemir, Fatma Silan, Onur Yildiz, Osman Yesilbas, Sedat Isikay, Burhan Balta, Shen Gu, Shalini N. Jhangiani, Harsha Doddapaneni, Jianhong Hu, Donna M. Muzny, Baylor-Hopkins Center for Mendelian Genomics, Eric Boerwinkle, Richard A. Gibbs, Konstantinos Tsiakas, Maja Hempel, Katta Mohan Girisha, Davut Gul, Jennifer E. Posey, Nursel H. Elcioglu, Beyhan Tuysuz, James R. Lupski
Am J Hum Genet. 2019 Jul 3; 105(1): 132–150. Published online 2019 Jun 20. doi: 10.1016/j.ajhg.2019.05.015
PMCID:
PMC6612529
AbstractArticlePDF–1.9M
8.
Involvement of tazarotene‐induced gene 1 in proliferation and differentiation of human adipose tissue‐derived mesenchymal stem cells
S. Ohnishi, K. Okabe, H. Obata, K. Otani, S. Ishikane, H. Ogino, S. Kitamura, N. Nagaya
Cell Prolif. 2009 Jun; 42(3): 309–316. Published online 2009 Feb 24. doi: 10.1111/j.1365-2184.2008.00592.x
PMCID:
PMC6496132
AbstractArticlePDF–433K
9.
A novel FBN2 mutation cosegregates with congenital contractural arachnodactyly in a five‐generation Chinese family
Shiyuan Zhou, Fengyu Wang, Yongheng Dou, Jiping Zhou, Gefang Hao, Chengqi Xu, Qing K. Wang, Haili Wang, Pengyun Wang
Clin Case Rep. 2018 Aug; 6(8): 1612–1617. Published online 2018 Jul 3. doi: 10.1002/ccr3.1693
PMCID:
PMC6099051
AbstractArticlePDF–398K
10.
Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly
Guoling You, Bailing Zu, Bo Wang, Zhigang Wang, Yunlan Xu, Qihua Fu
Int J Mol Sci. 2017 Apr; 18(4): 626. Published online 2017 Apr 5. doi: 10.3390/ijms18040626
PMCID:
PMC5412266
AbstractArticlePDF–8.4M
11.
Comparison of Stemness and Gene Expression between Gingiva and Dental Follicles in Children
Chung-Min Kang, Seong-Oh Kim, Mijeong Jeon, Hyung-Jun Choi, Han-Sung Jung, Jae-Ho Lee
Stem Cells Int. 2016; 2016: 8596520. Published online 2016 Aug 30. doi: 10.1155/2016/8596520
PMCID:
PMC5021492
AbstractArticlePDF–3.4M
12.
Dose- and Time-Dependent Transcriptional Response of Ishikawa Cells Exposed to Genistein
Jorge M. Naciff, Zubin S. Khambatta, Gregory J. Carr, Jay P. Tiesman, David W. Singleton, Sohaib A. Khan, George P. Daston
Toxicol Sci. 2016 May; 151(1): 71–87. Published online 2016 Feb 10. doi: 10.1093/toxsci/kfw024
PMCID:
PMC4914796
AbstractArticlePDF–285K
13.
Effects of a Closed Space Environment on Gene Expression in Hair Follicles of Astronauts in the International Space Station
Masahiro Terada, Masaya Seki, Rika Takahashi, Shin Yamada, Akira Higashibata, Hideyuki J. Majima, Masamichi Sudoh, Chiaki Mukai, Noriaki Ishioka
PLoS One. 2016; 11(3): e0150801. Published online 2016 Mar 30. doi: 10.1371/journal.pone.0150801
Correction in:
PLoS One. 2016; 11(5): e0156190.
PMCID:
PMC4814050
AbstractArticlePDF–1.7M
14.
Acceleration of Age-Associated Methylation Patterns in HIV-1-Infected Adults
Tammy M. Rickabaugh, Ruth M. Baxter, Mary Sehl, Janet S. Sinsheimer, Patricia M. Hultin, Lance E. Hultin, Austin Quach, Otoniel Martínez-Maza, Steve Horvath, Eric Vilain, Beth D. Jamieson
PLoS One. 2015; 10(3): e0119201. Published online 2015 Mar 25. doi: 10.1371/journal.pone.0119201
PMCID:
PMC4373843
AbstractArticlePDF–901K
15.
A novel FBN2 mutation in a Chinese family with congenital contractural arachnodactyly
Wei Liu, Ning Zhao, Xue-fu Li, Hong Wang, Yu Sui, Yong-ping Lu, Wen-hua Feng, Chao Ma, Wei-tian Han, Miao Jiang
FEBS Open Bio. 2015; 5: 163–166. Published online 2015 Mar 5. doi: 10.1016/j.fob.2015.02.005
PMCID:
PMC4359973
AbstractArticlePDF–1.2M
16.
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration
Rinki Ratnapriya, Xiaowei Zhan, Robert N. Fariss, Kari E. Branham, David Zipprer, Christina F. Chakarova, Yuri V. Sergeev, Maria M. Campos, Mohammad Othman, James S. Friedman, Arvydas Maminishkis, Naushin H. Waseem, Matthew Brooks, Harsha K. Rajasimha, Albert O. Edwards, Andrew Lotery, Barbara E. Klein, Barbara J. Truitt, Bingshan Li, Debra A. Schaumberg, Denise J. Morgan, Margaux A. Morrison, Eric Souied, Evangelia E. Tsironi, Felix Grassmann, Gerald A. Fishman, Giuliana Silvestri, Hendrik P.N. Scholl, Ivana K. Kim, Jacqueline Ramke, Jingsheng Tuo, Joanna E. Merriam, John C. Merriam, Kyu Hyung Park, Lana M. Olson, Lindsay A. Farrer, Matthew P. Johnson, Neal S. Peachey, Mark Lathrop, Robert V. Baron, Robert P. Igo, Jr, Ronald Klein, Stephanie A. Hagstrom, Yoichiro Kamatani, Tammy M. Martin, Yingda Jiang, Yvette Conley, Jose-Alan Sahel, Donald J. Zack, Chi-Chao Chan, Margaret A. Pericak-Vance, Samuel G. Jacobson, Michael B. Gorin, Michael L. Klein, Rando Allikmets, Sudha K. Iyengar, Bernhard H. Weber, Jonathan L. Haines, Thierry Léveillard, Margaret M. Deangelis, Dwight Stambolian, Daniel E. Weeks, Shomi S. Bhattacharya, Emily Y. Chew, John R. Heckenlively, Gonçalo R. Abecasis, Anand Swaroop
Hum Mol Genet. 2014 Nov 1; 23(21): 5827–5837. Published online 2014 Jun 4. doi: 10.1093/hmg/ddu276
PMCID:
PMC4189898
AbstractArticlePDF–14M
17.
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis
Jillian G. Buchan, David M. Alvarado, Gabe E. Haller, Carlos Cruchaga, Matthew B. Harms, Tianxiao Zhang, Marcia C. Willing, Dorothy K. Grange, Alan C. Braverman, Nancy H. Miller, Jose A. Morcuende, Nelson Leung-Sang Tang, Tsz-Ping Lam, Bobby Kin-Wah Ng, Jack Chun-Yiu Cheng, Matthew B. Dobbs, Christina A. Gurnett
Hum Mol Genet. 2014 Oct 1; 23(19): 5271–5282. Published online 2014 May 15. doi: 10.1093/hmg/ddu224
PMCID:
PMC4159151
AbstractArticlePDF–318K
18.
Transcriptomes of the major human pancreatic cell types
C. Dorrell, J. Schug, C. F. Lin, P. S. Canaday, A. J. Fox, O. Smirnova, R. Bonnah, P. R. Streeter, C. J. Stoeckert, Jr, K. H. Kaestner, M. Grompe
Diabetologia. Author manuscript; available in PMC 2014 Jan 3.
Published in final edited form as: Diabetologia. 2011 Nov; 54(11): 10.1007/s00125-011-2283-5. Published online 2011 Sep 1. doi: 10.1007/s00125-011-2283-5
Correction in:
volume 56 on page 1192
PMCID:
PMC3880150
AbstractArticlePDF–791K
19.
Unique Sex-Based Approach Identifies Transcriptomic Biomarkers Associated with Non-Syndromic Craniosynostosis
Brendan D. Stamper, Sarah S. Park, Richard P. Beyer, Theo K. Bammler, Michael L. Cunningham
Gene Regul Syst Bio. 2012; 6: 81–92. Published online 2012 May 16. doi: 10.4137/GRSB.S9693
PMCID:
PMC3362332
AbstractArticlePDF–759K
20.
Suppression of Death Receptor-mediated Apoptosis by 1,25-Dihydroxyvitamin D3 Revealed by Microarray Analysis
Xiaohui Zhang, Pengfei Li, Junying Bao, Santo V. Nicosia, Honggang Wang, Steven A. Enkemann, Wenlong Bai
J Biol Chem. Author manuscript; available in PMC 2012 Jan 3.
Published in final edited form as: J Biol Chem. 2005 Oct 21; 280(42): 35458–35468. Published online 2005 Aug 10. doi: 10.1074/jbc.M506648200
PMCID:
PMC3249976
AbstractArticlePDF–1.5M

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