Detalhe da pesquisa
1.
A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish patients.
Mol Vis
; 27: 588-600, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34703197
2.
Tuftelin's involvement in embryonic development.
J Exp Zool B Mol Dev Evol
; 332(5): 125-135, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31045321
3.
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects.
Ophthalmology
; 125(5): 725-734, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29276052
4.
Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular disease.
Graefes Arch Clin Exp Ophthalmol
; 256(11): 2157-2164, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30167917
5.
[FROM THE LAB BENCH TO THE PATIENT - CAN INJURED SKELETAL TISSUES REGENERATE?]
Harefuah
; 157(3): 183-187, 2018 Mar.
Artigo
em Hebraico
| MEDLINE | ID: mdl-29582951
6.
Skeletal ligament healing using the recombinant human amelogenin protein.
J Cell Mol Med
; 20(5): 815-24, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26917487
7.
Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene Therapy.
Ophthalmology
; 122(5): 997-1007, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25616768
8.
Visual acuity improvement in children with albinism beyond the first decade of life.
PLoS One
; 19(1): e0296744, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38232104
9.
Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli Population.
Invest Ophthalmol Vis Sci
; 65(2): 39, 2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38411968
10.
The prevalence of autism among children with albinism.
Eur J Ophthalmol
; : 11206721231206091, 2023 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37787167
11.
Regeneration of injured articular cartilage using the recombinant human amelogenin protein.
Bone Joint Res
; 12(10): 615-623, 2023 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37783468
12.
Childhood visual impairment and blindness: 5-year data from a tertiary low vision center in Israel.
Eye (Lond)
; 36(10): 2052-2056, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34426656
13.
The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences.
Invest Ophthalmol Vis Sci
; 63(1): 19, 2022 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35029636
14.
The induction of tuftelin expression in PC12 cell line during hypoxia and NGF-induced differentiation.
J Cell Physiol
; 226(1): 165-72, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20658530
15.
Biphasic influence of hypoxia on tuftelin expression in mouse mesenchymal C3H10T1/2 stem cells.
Eur J Oral Sci
; 119 Suppl 1: 55-61, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22243227
16.
Regeneration of grade 3 ankle sprain, using the recombinant human amelogenin protein (rHAM+ ) in a rat model.
J Orthop Res
; 39(7): 1540-1547, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32410235
17.
Regeneration of bone and periodontal ligament induced by recombinant amelogenin after periodontitis.
J Cell Mol Med
; 13(6): 1110-24, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19228267
18.
Amelogenin in cranio-facial development: the tooth as a model to study the role of amelogenin during embryogenesis.
J Exp Zool B Mol Dev Evol
; 312B(5): 445-57, 2009 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19097165
19.
Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli families.
Prenat Diagn
; 29(10): 939-46, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19626598
20.
Tuftelin Is Required for NGF-Induced Differentiation of PC12 Cells.
J Mol Neurosci
; 68(1): 135-143, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30903486