FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Carlo Rivolta

Research Profile

Disorders

Physiology

Procedures

Chemicals & Drugs

Concepts & Ideas

Pedigree

Genes & Molecular Sequences

Living Beings

Heterozygote

Anatomy

Cell Line

Co-author Network

Publications

TOP 3
Carlo Rivolta; Terri L McGee; Thomas Rio Frio; Roderick V Jensen; Eliot L Berson; Thaddeus P Dryja
Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.
Carlo Rivolta; Eliot L Berson; Thaddeus P Dryja
Mutation screening of the peropsin gene, a retinal pigment epithelium specific rhodopsin homolog, in patients with retinitis pigmentosa and allied diseases.
Babak Jian Seyedahmadi; Carlo Rivolta; Julia A Keene; Eliot L Berson; Thaddeus P Dryja
Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Carlo Rivolta (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2006: Carlo Rivolta; Terri L McGee; Thomas Rio Frio; Roderick V Jensen; Eliot L Berson; Thaddeus P Dryja
Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.
Human mutation 2006;27(7):644-53.
2006: Carlo Rivolta; Eliot L Berson; Thaddeus P Dryja
Mutation screening of the peropsin gene, a retinal pigment epithelium specific rhodopsin homolog, in patients with retinitis pigmentosa and allied diseases.
Molecular vision 2006;12():1511-5.
2004: Babak Jian Seyedahmadi; Carlo Rivolta; Julia A Keene; Eliot L Berson; Thaddeus P Dryja
Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.
Experimental eye research 2004;79(2):167-73.
2003: Carlo Rivolta; Radha Ayyagari; Paul Sieving; Eliot L Berson; Thaddeus P Dryja
Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis.
Molecular vision 2003;9():49-51.
2002: Xuejiao Wang; Siqun Xu; Carlo Rivolta; Lili Y Li; Guang-Hua Peng; Prabodh K Swain; Ching-Hwa Sung; Anand Swaroop; Eliot L Berson; Thaddeus P Dryja; Shiming Chen
Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function.
The Journal of biological chemistry 2002;277(45):43288-300.
2002: Carlo Rivolta; Eliot L Berson; Thaddeus P Dryja
Paternal uniparental heterodisomy with partial isodisomy of chromosome 1 in a patient with retinitis pigmentosa without hearing loss and a missense mutation in the Usher syndrome type II gene USH2A.
Archives of ophthalmology 2002;120(11):1566-71.
2002: Carlo Rivolta; Dror Sharon; Margaret DeAngelis; Thaddeus P Dryja
Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns.
Human molecular genetics 2002;11(10):1219-27.
2001: Carlo Rivolta; N E Peck; A B Fulton; Gerald A Fishman; Eliot L Berson; Thaddeus P Dryja
Novel frameshift mutations in CRX associated with Leber congenital amaurosis.
Human mutation 2001;18(6):550-1.
2001: Carlo Rivolta; Eliot L Berson; Thaddeus P Dryja
Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX.
Human mutation 2001;18(6):488-98.
2000: Carlo Rivolta; E A Sweklo; Eliot L Berson; Thaddeus P Dryja
Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss.
American journal of human genetics 2000;66(6):1975-8.