檢索結果 - Anand, Deepti

Systems Biology of Lens Development: a Paradigm for Disease Gene Discovery in the Eye 由 Anand, Deepti, Lachke, Salil A.

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Mutation Update of Transcription Factor Genes FOXE3, HSF4, MAF and PITX3 Causing Cataracts and Other Developmental Ocular Defects 由 Anand, Deepti, Agrawal, Smriti A., Slavotinek, Anne, Lachke, Salil A.

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RNA-sequencing-based transcriptomic profiles of embryonic lens development for cataract gene discovery 由 Anand, Deepti, Kakrana, Atul, Siddam, Archana D., Huang, Hongzhan, Saadi, Irfan, Lachke, Salil A.

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Molecular characterization of the human lens epithelium-derived cell line SRA01/04 由 Weatherbee, Bailey A. T., Barton, Joshua R., Siddam, Archana D., Anand, Deepti, Lachke, Salil A.

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An integrative approach to analyze microarray datasets for prioritization of genes relevant to lens biology and disease 由 Anand, Deepti, Agrawal, Smriti A., Siddam, Archana D., Motohashi, Hozumi, Yamamoto, Masayuki, Lachke, Salil A.

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β1-Integrin Deletion From the Lens Activates Cellular Stress Responses Leading to Apoptosis and Fibrosis 由 Wang, Yichen, Terrell, Anne M., Riggio, Brittany A., Anand, Deepti, Lachke, Salil A., Duncan, Melinda K.

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Genome-Wide Analysis of Differentially Expressed miRNAs and Their Associated Regulatory Networks in Lenses Deficient for the Congenital Cataract-Linked Tudor Domain Containing Prot... 由 Anand, Deepti, Al Saai, Salma, Shrestha, Sanjaya K., Barnum, Carrie E., Chuma, Shinichiro, Lachke, Salil A.

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iSyTE 2.0: a database for expression-based gene discovery in the eye 由 Kakrana, Atul, Yang, Andrian, Anand, Deepti, Djordjevic, Djordje, Ramachandruni, Deepti, Singh, Abhyudai, Huang, Hongzhan, Ho, Joshua W K, Lachke, Salil A

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High-throughput transcriptome analysis reveals that the loss of Pten activates a novel NKX6-1/RASGRP1 regulatory module to rescue microphthalmia caused by Fgfr2-deficient lenses 由 Padula, Stephanie L., Anand, Deepti, Hoang, Thanh V., Chaffee, Blake R., Liu, Lin, Liang, Chun, Lachke, Salil A., Robinson, Michael L.

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Molecular Characterization of Mouse Lens Epithelial Cell Lines and their Suitability to Study RNA Granules and Cataract Associated Genes 由 Terrell, Anne M., Anand, Deepti, Smith, Sylvie F., Dang, Christine A., Waters, Stephanie M., Pathania, Mallika, Beebe, David C., Lachke, Salil A.

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MS/MS in silico subtraction-based proteomic profiling as an approach to facilitate disease gene discovery: application to lens development and cataract 由 Aryal, Sandeep, Anand, Deepti, Hernandez, Francisco G., Weatherbee, Bailey A. T., Huang, Hongzhan, Reddy, Ashok P., Wilmarth, Phillip A., David, Larry L., Lachke, Salil A.

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A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects 由 Choquet, Hélène, Melles, Ronald B., Anand, Deepti, Yin, Jie, Cuellar-Partida, Gabriel, Wang, Wei, Hoffmann, Thomas J., Nair, K. Saidas, Hysi, Pirro G., Lachke, Salil A., Jorgenson, Eric

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The RNA-binding protein Celf1 post-transcriptionally regulates p27(Kip1) and Dnase2b to control fiber cell nuclear degradation in lens development 由 Siddam, Archana D., Gautier-Courteille, Carole, Perez-Campos, Linette, Anand, Deepti, Kakrana, Atul, Dang, Christine A., Legagneux, Vincent, Méreau, Agnès, Viet, Justine, Gross, Jeffrey M., Paillard, Luc, Lachke, Salil A.

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Compound mouse mutants of bZIP transcription factors Mafg and Mafk reveal a regulatory network of non-crystallin genes associated with cataract 由 Agrawal, Smriti A., Anand, Deepti, Siddam, Archana D., Kakrana, Atul, Dash, Soma, Scheiblin, David A., Dang, Christine A., Terrell, Anne M., Waters, Stephanie M., Singh, Abhyudai, Motohashi, Hozumi, Yamamoto, Masayuki, Lachke, Salil A.

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N-myc regulates growth and fiber cell differentiation in lens development 由 Cavalheiro, Gabriel R., Matos-Rodrigues, Gabriel E., Zhao, Yilin, Gomes, Anielle L., Anand, Deepti, Predes, Danilo, de Lima, Silmara, Abreu, Jose G., Zheng, Deyou, Lachke, Salil A., Cvekl, Ales, Martins, Rodrigo A. P.

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Six2 regulates Pax9 expression, palatogenesis and craniofacial bone formation 由 Sweat, Yan Yan, Sweat, Mason, Mansaray, Maurisa, Cao, Huojun, Eliason, Steven, Adeyemo, Waisu L., Gowans, Lord J.J., Eshete, Mekonen A, Anand, Deepti, Chalkley, Camille, Saadi, Irfan, Lachke, Salil A., Butali, Azeez, Amendt, Brad A.

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Exome Sequencing Provides Additional Evidence for the Involvement of ARHGAP29 in Mendelian Orofacial Clefting and Extends the Phenotypic Spectrum to Isolated Cleft Palate 由 Liu, Huan, Busch, Tamara, Eliason, Steven, Anand, Deepti, Bullard, Steven, Gowans, Lord J.J, Nidey, Nichole, Petrin, Aline, Augustine-Akpan, Eno-Abasi, Saadi, Irfan, Dunnwald, Martine, Lachke, Salil A., Zhu, Ying, Adeyemo, Adebowale, Amendt, Brad, Roscioli, Tony, Cornell, Robert, Murray, Jeffrey, Butali, Azeez

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The Tudor-domain protein TDRD7, mutated in congenital cataract, controls the heat shock protein HSPB1 (HSP27) and lens fiber cell morphology 由 Barnum, Carrie E, Al Saai, Salma, Patel, Shaili D, Cheng, Catherine, Anand, Deepti, Xu, Xiaolu, Dash, Soma, Siddam, Archana D, Glazewski, Lisa, Paglione, Emily, Polson, Shawn W, Chuma, Shinichiro, Mason, Robert W, Wei, Shuo, Batish, Mona, Fowler, Velia M, Lachke, Salil A

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Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract 由 Patel, Nisha, Anand, Deepti, Monies, Dorota, Maddirevula, Sateesh, Khan, Arif O., Algoufi, Talal, Alowain, Mohammed, Faqeih, Eissa, Alshammari, Muneera, Qudair, Ahmed, Alsharif, Hadeel, Aljubran, Fatimah, Alsaif, Hessa S., Ibrahim, Niema, Abdulwahab, Firdous M., Hashem, Mais, Alsedairy, Haifa, Aldahmesh, Mohammed A., Lachke, Salil A., Alkuraya, Fowzan S.

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A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals 由 Carlson, Jenna C., Anand, Deepti, Butali, Azeez, Buxo, Carmen J., Christensen, Kaare, Deleyiannis, Frederic, Hecht, Jacqueline T., Moreno, Lina M., Orioli, Ieda M., Padilla, Carmencita, Shaffer, John R., Vieira, Alexandre R., Wehby, George L., Weinberg, Seth M., Murray, Jeffrey C., Beaty, Terri H., Saadi, Irfan, Lachke, Salil A., Marazita, Mary L., Feingold, Eleanor, Leslie, Elizabeth J.

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