Next-generation sequencing facilitates quantitative analysis of wild-type and Nrl(−/−) retinal transcriptomes

Por Brooks, Matthew J., Rajasimha, Harsha K., Roger, Jerome E., Swaroop, Anand
Publicado em 2011

Transcriptome Profiling of NIH3T3 Cell Lines Expressing Opsin and the P23H Opsin Mutant Identifies Candidate Drugs for the Treatment of Retinitis Pigmentosa

Por Chen, Yuanyuan, Brooks, Matthew J, Gieser, Linn, Swaroop, Anand, Palczewski, Krzysztof
Publicado no Pharmacol Res (2016)

An unusual cause of transient ischemic attack

Por Brooks, Matthew J, Hannan, Liam M, Ng, AiVee, Irving, Louis, Aggarwal, Anu
Publicado em 2013

Amiodarone-Induced Destructive Thyroiditis Associated with Coronary Artery Vasospasm and Recurrent Ventricular Fibrillation

Por Brooks, Matthew J., Pattison, David A., Teo, Eliza P., Price, Sarah, Gurvitch, Ronen
Publicado em 2013

Next Generation Sequencing Technology and Genomewide Data Analysis: Perspectives for Retinal Research

Por Chaitankar, Vijender, Karakülah, Gökhan, Ratnapriya, Rinki, Giuste, Felipe O., Brooks, Matthew J., Swaroop, Anand
Publicado no Prog Retin Eye Res (2016)

Regulation of Noncoding Transcriptome in Developing Photoreceptors by Rod Differentiation Factor NRL

Por Zelinger, Lina, Karakülah, Gökhan, Chaitankar, Vijender, Kim, Jung-Woong, Yang, Hyun-Jin, Brooks, Matthew J., Swaroop, Anand
Publicado no Invest Ophthalmol Vis Sci (2017)

Transcriptome analysis using next generation sequencing reveals molecular signatures of diabetic retinopathy and efficacy of candidate drugs

Por Kandpal, Raj P., Rajasimha, Harsha K., Brooks, Matthew J., Nellissery, Jacob, Wan, Jun, Qian, Jiang, Kern, Timothy S., Swaroop, Anand
Publicado em 2012

Global expression profiling of peripheral Qa-1-restricted CD8αα+TCRαβ+ regulatory T Cells reveals innate-like features: implications for immune regulatory repertoire

Por Fanchiang, Shaohsuan S., Cojocaru, Radu, Othman, Mohammad, Khanna, Ritu, Brooks, Matthew J., Smith, Trevor, Tang, Xiaolei, Maricic, Igor, Swaroop, Anand, Kumar, Vipin
Publicado em 2011

The cellular and compartmental profile of mouse retinal glycolysis, tricarboxylic acid cycle, oxidative phosphorylation, and ~P transferring kinases

Por Rueda, Elda M., Johnson, Jerry E., Giddabasappa, Anand, Swaroop, Anand, Brooks, Matthew J., Sigel, Irena, Chaney, Shawnta Y., Fox, Donald A.
Publicado no Mol Vis (2016)

Synergistically acting agonists and antagonists of G protein–coupled receptors prevent photoreceptor cell degeneration

Por Chen, Yu, Palczewska, Grazyna, Masuho, Ikuo, Gao, Songqi, Jin, Hui, Dong, Zhiqian, Gieser, Linn, Brooks, Matthew J., Kiser, Philip D., Kern, Timothy S., Martemyanov, Kirill A., Swaroop, Anand, Palczewski, Krzysztof
Publicado no Sci Signal (2016)

A role for prenylated rab acceptor 1 in vertebrate photoreceptor development

Por Dickison Virginia M, Richmond Angela M, Abu Irqeba Ameair, Martak Joshua G, Hoge Sean CE, Brooks Matthew J, Othman Mohammed I, Khanna Ritu, Mears Alan J, Chowdhury Adnan Y, Swaroop Anand, Ogilvie Judith Mosinger
Publicado em 2012-12-01

A role for prenylated rab acceptor 1 in vertebrate photoreceptor development

Por Dickison, Virginia M, Richmond, Angela M, Abu Irqeba, Ameair, Martak, Joshua G, Hoge, Sean CE, Brooks, Matthew J, Othman, Mohammed I, Khanna, Ritu, Mears, Alan J, Chowdhury, Adnan Y, Swaroop, Anand, Ogilvie, Judith Mosinger
Publicado em 2012

REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survival

Por Veleri, Shobi, Nellissery, Jacob, Mishra, Bibhudatta, Manjunath, Souparnika H., Brooks, Matthew J., Dong, Lijin, Nagashima, Kunio, Qian, Haohua, Gao, Chun, Sergeev, Yuri V., Huang, Xiu-Feng, Qu, Jia, Lu, Fan, Cideciyan, Artur V., Li, Tiansen, Jin, Zi-Bing, Fariss, Robert N., Ratnapriya, Rinki, Jacobson, Samuel G., Swaroop, Anand
Publicado no Hum Mol Genet (2017)

Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 mice

Por Friedman, James S., Chang, Bo, Krauth, Daniel S., Lopez, Irma, Waseem, Naushin H., Hurd, Ron E., Feathers, Kecia L., Branham, Kari E., Shaw, Manessa, Thomas, George E., Brooks, Matthew J., Liu, Chunqiao, Bakeri, Hirva A., Campos, Maria M., Maubaret, Cecilia, Webster, Andrew R., Rodriguez, Ignacio R., Thompson, Debra A., Bhattacharya, Shomi S., Koenekoop, Robert K., Heckenlively, John R., Swaroop, Anand
Publicado em 2010

Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa

Por Friedman, James S., Ray, Joseph W., Waseem, Naushin, Johnson, Kory, Brooks, Matthew J., Hugosson, Therése, Breuer, Debra, Branham, Kari E., Krauth, Daniel S., Bowne, Sara J., Sullivan, Lori S., Ponjavic, Vesna, Gränse, Lotta, Khanna, Ritu, Trager, Edward H., Gieser, Linn M., Hughbanks-Wheaton, Dianna, Cojocaru, Radu I., Ghiasvand, Noor M., Chakarova, Christina F., Abrahamson, Magnus, Göring, Harald H.H., Webster, Andrew R., Birch, David G., Abecasis, Goncalo R., Fann, Yang, Bhattacharya, Shomi S., Daiger, Stephen P., Heckenlively, John R., Andréasson, Sten, Swaroop, Anand
Publicado em 2009