Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mary Alice Crawford"'
Autor:
Ruth Ashery-Padan, Jonathan P. Katz, Joram Piatigorsky, Mary Alice Crawford, Klaus H. Kaestner, Shivalingappa K. Swamynathan
Publikováno v:
Molecular and Cellular Biology. 27:182-194
The Krüppel-like transcription factor KLF4 is among the most highly expressed transcription factors in the mouse cornea (B. Norman, J. Davis, and J. Piatigorsky, Investig. Ophthalmol. Vis. Sci. 45:429-440, 2004). Here, we deleted the Klf4 gene selec
Autor:
M.R. Meltzer, N. Smaoui, Mary Alice Crawford, Benjamin I. Rubin, Ekaterini Tsilou, Chi-Chao Chan, Rafael C. Caruso, O’Neil M. Biscette
Publikováno v:
RETINAL Cases & Brief Reports. 1:232-235
PURPOSE To report variations in the inheritance pattern and clinical presentation of crystalline retinopathies. METHODS Two different families with crystalline retinopathy were studied with a complete family history and ophthalmologic examination inc
Autor:
Mary Alice Crawford, Joram Piatigorsky, Shivalingappa K. Swamynathan, W. Gerald Robison, Jyotshnabala Kanungo
Publikováno v:
The FASEB Journal. 17:1996-2005
The water meniscus bisects the eyes of the “four-eyed” fish Anableps anableps, resulting in simultaneous vision in air and water. We compare the structure and macromolecular compositions of the Anableps dorsal (air) and ventral (water) corneas wi
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 6:319-327
Purpose: To search for the presence of, and qualitatively characterize the microscopic anatomy of, nerve terminals in the tendino-scleral (enthesial) area of the extraocular muscle tendon. Methods: Extraocular rectus muscle tendino-scleralspecimens f
Autor:
Rafael C. Caruso, Muriel I. Kaiser-Kupfer, Thomas C. Markello, Chi-Chao Chan, Mary Alice Crawford, Karl G. Csaky, Juanru Guo, William A. Gahl
Publikováno v:
American Journal of Ophthalmology. 118:569-582
We examined three affected members of a Chinese-American family with Bietti's crystalline retinopathy. The clinical characteristics of a 24-year-old proband are contrasted to the clinical findings of her grandmother, for whom we have 26 years of foll
Publikováno v:
Cornea. 12:451-460
Anterior corneal dystrophies involving Bowman's membrane and anterior stroma include several subtypes of uncertain etiology: the Reis-Bückler, Thiel-Behnke, Grayson-Wilbrandt, and "honeycomb" dystrophies. The clinical and pathologic features of thes
Publikováno v:
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus. 12(2)
Background Papillorenal syndrome is an autosomal-dominant disease caused by mutations in the PAX2 transcription factor gene. Patients often exhibit congenital excavation of the optic nerve and a spectrum of congenital kidney abnormalities. Using a no
Autor:
Dody Avichezer, Chi-Chao Chan, John M. Nickerson, Rachel R. Caspi, Giavonni M. Lewis, Mary Alice Crawford, Gregory I. Liou, Larry A. Donoso, Barbara Wiggert
Publikováno v:
Journal of autoimmunity. 21(3)
Experimental autoimmune uveitis (EAU) and pinealitis (EAP) can be induced in susceptible mice by immunization with immunologically privileged retinal antigens. In the present study, we analyzed the immunologic and immunopathologic responses of mice d
Autor:
Gerald J. Chader, Susan Gentleman, Rhea A Lloyd-Muhammad, Anita Pikus, Muriel I. Kaiser-Kupfer, W. Gerald Robison, Richard J. Sherins, Rafael C. Caruso, Mary Alice Crawford
Publikováno v:
Human pathology. 27(1)
This study examined the ultrastructural morphology and posttranslationally modified alpha-tubulin isoforms in the sperm flagella of a patient presenting with infertility and retinal degeneration. Clinical evaluation showed impaired motility and gross
Autor:
Simon W. M. John, J. Fielding Hejtmancik, Richard A. Hess, Denise M. Larson, Mary Alice Crawford, Brian P. Brooks, Xiaodong Jiao, Richard S. Smith, Marjan Huizing, Arvydas Maminishkis, Ronald A. Bush, Chi-Chao Chan, Sten Kjellstrom, Lynn Lamoreux, William J. Pavan
Publikováno v:
Investigative Opthalmology & Visual Science. 48:3905
PURPOSE: To characterize the ocular phenotype resulting from mutation of Rab38, a candidate gene for Hermansky-Pudlak syndrome.METHODS: Chocolate mice (cht, Rab38(cht/cht)) and control heterozygous (Rab38(cht/)(+)) and wild-type mice were examined cl