Search

Search results

60 results found

Multi-dimensional Transcriptional Remodeling by Physiological Insulin In Vivo.

Publication: Journal Article

TM, Batista, Garcia-Martin R, Cai W, Konishi M, O’Neill BT, Sakaguchi M, Kim JH, Jung DY, Kim JK, and Kahn CR. 2019. “Multi-Dimensional Transcriptional Remodeling by Physiological Insulin In Vivo.”. Cell Reports 26 (12): 3429-43.

Regulation of UCP1 and Mitochondrial Metabolism in Brown Adipose Tissue by Reversible Succinylation.

Publication: Journal Article

G, Wang, Meyer JG, Cai W, Softic S, Li ME, Verdin E, Newgard C, Schilling B, and Kahn CR. 2019. “Regulation of UCP1 and Mitochondrial Metabolism in Brown Adipose Tissue by Reversible Succinylation.”. Molecular Cell S1097-2765 (19): 30225-4.

The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome

Publication: Journal Article

Berner, Daniel, Ursula Hoja, Matthias Zenkel, James Julian Ross, Steffen Uebe, Daniela Paoli, Paolo Frezzotti, et al. 2019. “The Protective Variant Rs7173049 at LOXL1 Locus Impacts on Retinoic Acid Signaling Pathway in Pseudoexfoliation Syndrome”. Hum Mol Genet.

Stem cell-derived tissue-associated regulatory T cells suppress the activity of pathogenic cells in autoimmune diabetes

Publication: Journal Article

Haque, Mohammad, Fengyang Lei, Xiaofang Xiong, Jugal Kishore Das, Xingcong Ren, Deyu Fang, Shahram Salek-Ardakani, Jin-Ming Yang, and Jianxun Song. 2019. “Stem Cell-Derived Tissue-Associated Regulatory T Cells Suppress the Activity of Pathogenic Cells in Autoimmune Diabetes”. JCI Insight 4 (7).

Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B

Publication: Journal Article

Khateb, Samer, Marco Nassisi, Kinga Bujakowska, Cécile Méjécase, Christel Condroyer, Aline Antonio, Marine Foussard, et al. 2019. “Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B”. JAMA Ophthalmol.

ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder

Publication: Journal Article

Williams, Lloyd, Asif Javed, Amin Sabri, Denise Morgan, Chad Huff, John Grigg, Xiu Ting Heng, et al. 2019. “ALPK1 Missense Pathogenic Variant in Five Families Leads to ROSAH Syndrome, an Ocular Multisystem Autosomal Dominant Disorder”. Genet Med 21 (9): 2103-15.

Monocanalicular Stents in Eyelid Lacerations: A Report by the American Academy of Ophthalmology

Publication: Journal Article

Wladis, Edward, Vinay Aakalu, Jeremiah Tao, Rachel Sobel, Suzanne Freitag, Jill Foster, and Louise Mawn. 2019. “Monocanalicular Stents in Eyelid Lacerations: A Report by the American Academy of Ophthalmology”. Ophthalmology 126 (9): 1324-29.

Genes with High Network Connectivity Are Enriched for Disease Heritability

Publication: Journal Article

Kim, Samuel, Chengzhen Dai, Farhad Hormozdiari, Bryce Geijn, Steven Gazal, Yongjin Park, Luke O’Connor, et al. 2019. “Genes With High Network Connectivity Are Enriched for Disease Heritability”. Am J Hum Genet 104 (5): 896-913.

Highlights from the 2019 ARVO Annual Meeting

News: May 07, 2019

The Department of Ophthalmology was well represented at this year’s Association for Research and Vision in Ophthalmology (ARVO) Annual Meeting, held April 22 through May 2 in Vancouver, British Columbia. More than 160 faculty and trainees participated as course instructors, panelists, lecturers and...

Recent Collaborative Publications

Page

Alterations in Chromatin at Antigen Receptor Loci Define Lineage Progression During B Lymphopoiesis. Lion M, Muhire B, Namiki Y, Tolstorukov MY, Oettinger MA. PNAS March 10, 2020 117 (10) 5453-5462. Link to paper The histone deacetylase SIRT6 restrains transcription elongation via promoter-proximal...