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Journal of Ophthalmic & Vision Research
|
November 28, 2018
Targeted Screening for Predominant CYP1B1 Mutations in Primary Congenital Glaucoma
Mansoor Sarfarazi
Journal of Ophthalmic & Vision Research
|
October 2, 2015
Common Molecular Challenges in Glaucoma
Mansoor Sarfarazi
Ophthalmology Clinics of North America
|
January 27, 2004
Optineurin in primary open angle glaucoma
Mansoor Sarfarazi, Tayebeh Rezaie
Genomics
|
December 21, 2004
Molecular cloning, genomic structure, and protein characterization of mouse optineurin
Tayebeh Rezaie, Mansoor Sarfarazi
American Journal of Ophthalmology
|
February 20, 2008
The use of microarray technology in deciphering the cause of genetic eye diseases: LOXL1 and exfoliation syndrome
Elias I Traboulsi, Mansoor Sarfarazi
Molecular Vision
|
September 26, 2007
Embryonic expression of the optineurin (glaucoma) gene in different stages of mouse development
Tayebeh Rezaie, Ivaylo Stoilov, Mansoor Sarfarazi
Ophthalmology Clinics of North America
|
January 27, 2004
Genetics and biochemistry of primary congenital glaucoma
Mansoor Sarfarazi, Ivaylo Stoilov, John B Schenkman
Ophthalmic Genetics
|
July 16, 2005
Analysis of rare variants and common haplotypes in the optineurin gene in Swedish glaucoma cases
Mattias Jansson, Claes Wadelius, Tayebeh Rezaie, et al.
Pharmacogenetics and Genomics
|
July 16, 2008
Characterization of the biochemical and structural phenotypes of four CYP1B1 mutations observed in individuals with primary congenital glaucoma
Dharamainder Choudhary, Ingela Jansson, Mansoor Sarfarazi, et al.
Drug Metabolism Reviews
|
November 24, 2004
Xenobiotic-metabolizing cytochromes P450 in ontogeny: evolving perspective
Dharamainder Choudhary, Ingela Jansson, Mansoor Sarfarazi, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 33) with videos related to
Sort By:
Page
of 4
Journal of Ophthalmic & Vision Research
|
November 28, 2018
Targeted Screening for Predominant CYP1B1 Mutations in Primary Congenital Glaucoma
Mansoor Sarfarazi
Journal of Ophthalmic & Vision Research
|
October 2, 2015
Common Molecular Challenges in Glaucoma
Mansoor Sarfarazi
Ophthalmology Clinics of North America
|
January 27, 2004
Optineurin in primary open angle glaucoma
Mansoor Sarfarazi, Tayebeh Rezaie
Genomics
|
December 21, 2004
Molecular cloning, genomic structure, and protein characterization of mouse optineurin
Tayebeh Rezaie, Mansoor Sarfarazi
American Journal of Ophthalmology
|
February 20, 2008
The use of microarray technology in deciphering the cause of genetic eye diseases: LOXL1 and exfoliation syndrome
Elias I Traboulsi, Mansoor Sarfarazi
Molecular Vision
|
September 26, 2007
Embryonic expression of the optineurin (glaucoma) gene in different stages of mouse development
Tayebeh Rezaie, Ivaylo Stoilov, Mansoor Sarfarazi
Ophthalmology Clinics of North America
|
January 27, 2004
Genetics and biochemistry of primary congenital glaucoma
Mansoor Sarfarazi, Ivaylo Stoilov, John B Schenkman
Ophthalmic Genetics
|
July 16, 2005
Analysis of rare variants and common haplotypes in the optineurin gene in Swedish glaucoma cases
Mattias Jansson, Claes Wadelius, Tayebeh Rezaie, et al.
Pharmacogenetics and Genomics
|
July 16, 2008
Characterization of the biochemical and structural phenotypes of four CYP1B1 mutations observed in individuals with primary congenital glaucoma
Dharamainder Choudhary, Ingela Jansson, Mansoor Sarfarazi, et al.
Drug Metabolism Reviews
|
November 24, 2004
Xenobiotic-metabolizing cytochromes P450 in ontogeny: evolving perspective
Dharamainder Choudhary, Ingela Jansson, Mansoor Sarfarazi, et al.
Page
of 4