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Search Results - swaroop
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Gene Therapy for Treatment of CRX-Autosomal Dominant Retinopathies
Abstract: Mutations in the cone rod homeobox (CRX) transcription factor lead to distinct retinopathy phenotypes, including early-onset vision impairment in dominant Leber congenital amaurosis (LCA). Adeno-Associated virus (AAV) vector-mediated delivery of a CRX cDNA under the control of a CRX promoter region partially restored photoreceptor phenotype...
Published: 12/6/2024
|
Inventor(s):
Anand
Swaroop
,
Kamil Kruczek
,
Suja Hiriyanna
,
Zhijian Wu
Keywords(s):
AAV
,
Adeno-associated Virus
,
Cone-rod Dystrophy
,
CRD
,
GENE THERAPY
,
LCA
,
Leber Congenital Amaurosis
,
Lentivirus
,
NEI
,
rare disease
,
Retinitis Pigmentosa
,
Retinopathies
,
RP
,
Swaroop
Category(s):
Collaboration Sought > Licensing
,
Application > Therapeutics
,
Collaboration Sought > Collaboration
,
TherapeuticArea > Ear, Nose, & Throat
,
TherapeuticArea > Ophthalmology
Induced Pluripotent Stem Cells Derived from Patients with CEP290-associated Ciliopathies and Unaffected Family Members
Abstract: Approximately one-third of non-syndromic retinal dystrophies involve a defect in a ciliary protein. Non-syndromic retinal ciliopathies include retinitis pigmentosa, cone dystrophy, cone-rod dystrophy, macular dystrophy, and Leber-congenital amaurosis (LCA). Many CEP290-LCA patients also exhibit auditory and olfactory defects. Induced pluripotent...
Published: 12/6/2024
|
Inventor(s):
Anand
Swaroop
,
Hiroko Shimada-Ishii
,
Yu Holly Chen
,
Milton English
Keywords(s):
Anosmia
,
Cell therapy
,
Ciliopathies
,
Congenital Blindness
,
Drug Development
,
GENE THERAPY
,
hearing loss
,
iPS
,
National Eye Institute
,
NEI
,
Pluripotent Stem Cells
,
Primary Cilia
,
Retina
,
Retinal degeneration
,
Swaroop
,
VISION
Category(s):
Application > Research Materials
,
Collaboration Sought > Licensing
,
Collaboration Sought > Collaboration
,
TherapeuticArea > Ear, Nose, & Throat
,
TherapeuticArea > Ophthalmology