Search Results - "Cojocaru, Radu I"

Conditional ablation of the Notch2 receptor in the ocular lens by Saravanamuthu, Senthil S., Le, Tien T., Gao, Chun Y., Cojocaru, Radu I., Pandiyan, Pushpa, Liu, Chunqiao, Zhang, Jun, Zelenka, Peggy S., Brown, Nadean L.

“…Notch signaling is essential for proper lens development, however the specific requirements of individual Notch receptors have not been investigated. Here we…”
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Ciliary neurotrophic factor induces genes associated with inflammation and gliosis in the retina: a gene profiling study of flow-sorted, Müller cells by Xue, Wei, Cojocaru, Radu I, Dudley, V Joseph, Brooks, Matthew, Swaroop, Anand, Sarthy, Vijay P

“…Ciliary neurotrophic factor (CNTF), a member of the interleukin-6 cytokine family, has been implicated in the development, differentiation and survival of…”
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Distinct signature of altered homeostasis in aging rod photoreceptors: implications for retinal diseases by Parapuram, Sunil K, Cojocaru, Radu I, Chang, Jessica R, Khanna, Ritu, Brooks, Matthew, Othman, Mohammad, Zareparsi, Sepideh, Khan, Naheed W, Gotoh, Norimoto, Cogliati, Tiziana, Swaroop, Anand

“…Advanced age contributes to clinical manifestations of many retinopathies and represents a major risk factor for age-related macular degeneration, a leading…”
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Protective gene expression changes elicited by an inherited defect in photoreceptor structure by Sharma, Yagya V, Cojocaru, Radu I, Ritter, Linda M, Khattree, Nidhi, Brooks, Matthew, Scott, Alison, Swaroop, Anand, Goldberg, Andrew F X

“…Inherited defects in retinal photoreceptor structure impair visual transduction, disrupt relationship with the retinal pigment epithelium (RPE), and compromise…”
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Preservation of cone photoreceptors after a rapid yet transient degeneration and remodeling in cone-only Nrl-/- mouse retina by Roger, Jerome E, Ranganath, Keerthi, Zhao, Lian, Cojocaru, Radu I, Brooks, Matthew, Gotoh, Norimoto, Veleri, Shobi, Hiriyanna, Avinash, Rachel, Rivka A, Campos, Maria Mercedes, Fariss, Robert N, Wong, Wai T, Swaroop, Anand

“…Cone photoreceptors are the primary initiator of visual transduction in the human retina. Dysfunction or death of rod photoreceptors precedes cone loss in many…”
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Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa by 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

“…Retinitis pigmentosa (RP) refers to a genetically heterogeneous group of progressive neurodegenerative diseases that result in dysfunction and/or death of rod…”
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