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/vufind/Search/Results?lookfor=%22Kannabiran+Chitra%22&type=Person&sort=year
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PubPharm (121)
1
Generation of two induced pluripotent stem cell lines (LVPEIi004-A and LVPEIi005-A) from probands with Leber Congenital Amaurosis 2 (LCA2) and harboring mutations in RPE65
enthalten in:
Stem cell research
| 2024
von
Maddileti, S.
|
Mahato, S.
|
Agrawal, T.
| +7
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2
Generation of two induced pluripotent stem cell lines (LVPEIi007-B, LVPEIi008-B) from patients harboring homozygous mutation in ABCA4 (c.6088C>T) using non-integrative Sendai virus-based approach
enthalten in:
Stem cell research
| 2024
von
Pidishetty, D.
|
Maddileti, S.
|
Mahato, S.
| +6
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3
Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3
enthalten in:
Stem cell research
| 2024
von
Mahato, S.
|
Maddileti, S.
|
Naik, M.
| +3
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4
RPE65 mutations in Leber congenital amaurosis, early-onset severe retinal dystrophy, and retinitis pigmentosa from a tertiary eye care center in India
enthalten in:
Ophthalmic genetics
| 2024
von
Parameswarappa, D.
|
Bagga, D.
|
Upadhyaya, A.
| +5
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5
Updates on congenital hereditary endothelial dystrophy
enthalten in:
Taiwan journal of ophthalmology
| 2023
von
Mehta, N.
|
Verma, A.
|
Achanta, D.
| +6
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6
Correction to : identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Salman, M.
|
Verma, A.
|
Chaurasia, S.
| +4
ErratumFor: Orphanet J Rare Dis. 2022 Sep 17;17(1):361. - PMID 36115991
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7
Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Salman, M.
|
Verma, A.
|
Chaurasia, S.
| +4
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8
Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Salman, M.
|
Verma, A.
|
Chaurasia, S.
| +4
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9
Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy
enthalten in:
Orphanet journal of rare diseases
| 2022
von
Salman, M.
|
Verma, A.
|
Chaurasia, S.
| +4
ErratumIn: Orphanet J Rare Dis. 2023 Jun 29;18(1):170. - PMID 37386499
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10
Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy
enthalten in:
Orphanet journal of rare diseases
| 2022
von
Salman, M.
|
Verma, A.
|
Chaurasia, S.
| +4
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118
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Journal of genetics
7
Indian journal of ophthalmology
7
Molecular vision
6
Documenta ophthalmologica
6
Investigative ophthalmology & visual science
6
Orphanet journal of rare diseases
5
Human mutation
4
Journal of biosciences
4
Journal of medical genetics
4
Ophthalmic genetics
3
Cornea
3
Journal of Genetics
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Stem cell research
3
Survey of ophthalmology
2
American journal of human genetics
2
American journal of ophthalmology
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American journal of ophthalmology <New York, NY>
2
Archives of pathology & laboratory medicine
2
Archives of pathology and laboratory medicine
2
Documenta ophthalmologica. Advances in ophthalm...
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Thema
55
Journal Article
32
Research Support, Non-U.S. Gov't
12
genetics
11
Review
8
mutations
6
Research Support, N.I.H., Extramural
6
retinitis pigmentosa
6
retinoblastoma
5
Anion Transport Proteins
5
Antiporters
5
Case Reports
5
Eye Proteins
5
SLC4A11 protein, human
4
CHED
4
DNA
4
RB1
4
corneal endothelium
4
gene mapping
3
148710-76-3
3
9007-49-2
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Erscheinungszeitraum
19
2020-
39
2010-2019
54
2000-2009
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