Lista de obras - Chitra Kannabiran - Dominio Público Uruguay

A Fluorescent Quantitative Multiplex PCR Method to Detect Copy Number Changes in the RB1 Gene

artículo científico publicado en 2018

A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma.

artículo científico publicado en 2009

A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration.

artículo científico publicado en 2016

Allelic heterogeneity of the carbohydrate sulfotransferase-6 gene in patients with macular corneal dystrophy

artículo científico publicado en 2005

Association of Human Leukocyte Antigen Class 1 genes with Stevens Johnson Syndrome with severe ocular complications in an Indian population.

artículo científico publicado en 2017

Bilateral granular dystrophy: A clinicopathogenetic correlation after alcohol assisted debridement with phototherapeutic keratectomy.

artículo científico publicado en 2012

Coexistence of Congenital Hereditary Endothelial Dystrophy and Fuchs Endothelial Corneal Dystrophy Associated With SLC4A11 Mutations in Affected Families

artículo científico publicado en 2020

Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening

scientific article published on April 2009

Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophy.

artículo científico publicado en 2005

Homozygous Null Mutations in the ABCA4 Gene in Two Families With Autosomal Recessive Retinal Dystrophy

artículo científico publicado en 2006

Identification of Key Genes and Pathways in Persistent Hyperplastic Primary Vitreous of the Eye Using Bioinformatic Analysis

artículo científico publicado en 2021

Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23

artículo científico publicado en 2011

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract

artículo científico publicado en 2007

Mutational screening of the RB1 gene in Indian patients with retinoblastoma reveals eight novel and several recurrent mutations

artículo científico publicado en 2003

NMNAT1 mutations cause Leber congenital amaurosis

artículo científico publicado en 2012

Phenotypic characterization of retinoblastoma for the presence of putative cancer stem-like cell markers by flow cytometry.

artículo científico publicado en 2008

Posterior microphthalmos pigmentary retinopathy syndrome

artículo científico publicado en 2011

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration

artículo científico publicado en 2006

RB1 gene mutations in retinoblastoma and its clinical correlation

artículo científico publicado en 2010

Reliability of nested polymerase chain reaction in the diagnosis of bacterial endophthalmitis.

artículo científico publicado en 2002

Screening for homozygosity by descent in families with autosomal recessive retinitis pigmentosa

artículo científico publicado en 2002

Share, learn and get together: knowledge and information interactions at the XLV International Symposium of ISCEV - Hyderabad, India, 25-29 August 2007.

artículo científico publicado en 2007

Splicing aberrations caused by constitutional RB1 gene mutations in retinoblastoma.

artículo científico publicado en 2011

Stevens-Johnson syndrome: The role of an ophthalmologist.

artículo científico publicado en 2016

TGFBI gene mutations in corneal dystrophies.

artículo científico publicado en 2006

Therapeutic avenues for hereditary forms of retinal blindness

artículo científico publicado en 2018

Trans-ethnic study confirmed independent associations of HLA-A02:06 and HLA-B44:03 with cold medicine-related Stevens-Johnson syndrome with severe ocular surface complications.

artículo científico publicado en 2014

Lista de obras de Chitra Kannabiran

A Fluorescent Quantitative Multiplex PCR Method to Detect Copy Number Changes in the RB1 Gene

A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma.

A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration.

Allelic heterogeneity of the carbohydrate sulfotransferase-6 gene in patients with macular corneal dystrophy

Association of Human Leukocyte Antigen Class 1 genes with Stevens Johnson Syndrome with severe ocular complications in an Indian population.

Bilateral granular dystrophy: A clinicopathogenetic correlation after alcohol assisted debridement with phototherapeutic keratectomy.

Coexistence of Congenital Hereditary Endothelial Dystrophy and Fuchs Endothelial Corneal Dystrophy Associated With SLC4A11 Mutations in Affected Families

Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening

Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophy.

Homozygous Null Mutations in the ABCA4 Gene in Two Families With Autosomal Recessive Retinal Dystrophy

Identification of Key Genes and Pathways in Persistent Hyperplastic Primary Vitreous of the Eye Using Bioinformatic Analysis

Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract

Mutational screening of the RB1 gene in Indian patients with retinoblastoma reveals eight novel and several recurrent mutations

NMNAT1 mutations cause Leber congenital amaurosis

Phenotypic characterization of retinoblastoma for the presence of putative cancer stem-like cell markers by flow cytometry.

Posterior microphthalmos pigmentary retinopathy syndrome

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration

RB1 gene mutations in retinoblastoma and its clinical correlation

Reliability of nested polymerase chain reaction in the diagnosis of bacterial endophthalmitis.

Screening for homozygosity by descent in families with autosomal recessive retinitis pigmentosa

Share, learn and get together: knowledge and information interactions at the XLV International Symposium of ISCEV - Hyderabad, India, 25-29 August 2007.

Splicing aberrations caused by constitutional RB1 gene mutations in retinoblastoma.

Stevens-Johnson syndrome: The role of an ophthalmologist.

TGFBI gene mutations in corneal dystrophies.

Therapeutic avenues for hereditary forms of retinal blindness

Trans-ethnic study confirmed independent associations of HLA-A*02:06 and HLA-B*44:03 with cold medicine-related Stevens-Johnson syndrome with severe ocular surface complications.

Trans-ethnic study confirmed independent associations of HLA-A02:06 and HLA-B44:03 with cold medicine-related Stevens-Johnson syndrome with severe ocular surface complications.