BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 38412859)

  • 1. CRB1-associated retinal degeneration is dependent on bacterial translocation from the gut.
    Peng S; Li JJ; Song W; Li Y; Zeng L; Liang Q; Wen X; Shang H; Liu K; Peng P; Xue W; Zou B; Yang L; Liang J; Zhang Z; Guo S; Chen T; Li W; Jin M; Xing XB; Wan P; Liu C; Lin H; Wei H; Lee RWJ; Zhang F; Wei L
    Cell; 2024 Mar; 187(6):1387-1401.e13. PubMed ID: 38412859
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.
    Quinn PM; Mulder AA; Henrique Alves C; Desrosiers M; de Vries SI; Klooster J; Dalkara D; Koster AJ; Jost CR; Wijnholds J
    Hum Mol Genet; 2019 Jan; 28(1):105-123. PubMed ID: 30239717
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Crb1 is a determinant of retinal apical Müller glia cell features.
    van de Pavert SA; Sanz AS; Aartsen WM; Vos RM; Versteeg I; Beck SC; Klooster J; Seeliger MW; Wijnholds J
    Glia; 2007 Nov; 55(14):1486-97. PubMed ID: 17705196
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mthfr as a modifier of the retinal phenotype of Crb1(rd8/rd8) mice.
    Markand S; Saul A; Tawfik A; Cui X; Rozen R; Smith SB
    Exp Eye Res; 2016 Apr; 145():164-172. PubMed ID: 26646559
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A single amino acid substitution (Cys249Trp) in Crb1 causes retinal degeneration and deregulates expression of pituitary tumor transforming gene Pttg1.
    van de Pavert SA; Meuleman J; Malysheva A; Aartsen WM; Versteeg I; Tonagel F; Kamphuis W; McCabe CJ; Seeliger MW; Wijnholds J
    J Neurosci; 2007 Jan; 27(3):564-73. PubMed ID: 17234588
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human CRB1 and CRB2 form homo- and heteromeric protein complexes in the retina.
    Stehle IF; Imventarza JA; Woerz F; Hoffmann F; Boldt K; Beyer T; Quinn PM; Ueffing M
    Life Sci Alliance; 2024 Jun; 7(6):. PubMed ID: 38570189
    [No Abstract]   [Full Text] [Related]  

  • 7. Targeted deletion of Crb1/Crb2 in the optic vesicle models key features of leber congenital amaurosis 8.
    Cho SH; Nahar A; Kim JH; Lee M; Kozmik Z; Kim S
    Dev Biol; 2019 Sep; 453(2):141-154. PubMed ID: 31145883
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Current perspectives in Leber congenital amaurosis type 8 mouse modeling.
    Nahar A; Cho SH
    Dev Dyn; 2022 Jul; 251(7):1094-1106. PubMed ID: 35150033
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CRB2 Loss in Rod Photoreceptors Is Associated with Progressive Loss of Retinal Contrast Sensitivity.
    Alves CH; Boon N; Mulder AA; Koster AJ; Jost CR; Wijnholds J
    Int J Mol Sci; 2019 Aug; 20(17):. PubMed ID: 31438467
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 mice.
    Kwon YS; Tham A; Lopez AJ; Edwards S; Woods S; Chen J; Wong-Fortunato J; Quiroz Alonso A; Javier S; Au I; Clarke M; Humpal D; Lloyd KCK; Thomasy S; Murphy C; Glaser TM; Moshiri A
    Dev Biol; 2020 Feb; 458(2):141-152. PubMed ID: 31634437
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations.
    Beryozkin A; Zelinger L; Bandah-Rozenfeld D; Harel A; Strom TA; Merin S; Chowers I; Banin E; Sharon D
    Invest Ophthalmol Vis Sci; 2013 Mar; 54(3):2068-75. PubMed ID: 23449718
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Coat's like vasculopathy in leber congenital amaurosis secondary to homozygous mutations in CRB1: a case report and discussion of the management options.
    Hasan SM; Azmeh A; Mostafa O; Megarbane A
    BMC Res Notes; 2016 Feb; 9():91. PubMed ID: 26872607
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CRB1: one gene, many phenotypes.
    Ehrenberg M; Pierce EA; Cox GF; Fulton AB
    Semin Ophthalmol; 2013; 28(5-6):397-405. PubMed ID: 24138049
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CRB1 is required for recycling by RAB11A+ vesicles in human retinal organoids.
    Buck TM; Quinn PMJ; Pellissier LP; Mulder AA; Jongejan A; Lu X; Boon N; Koot D; Almushattat H; Arendzen CH; Vos RM; Bradley EJ; Freund C; Mikkers HMM; Boon CJF; Moerland PD; Baas F; Koster AJ; Neefjes J; Berlin I; Jost CR; Wijnholds J
    Stem Cell Reports; 2023 Sep; 18(9):1793-1810. PubMed ID: 37541258
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of CRB1 Pathogenic Variants Correctable with CRISPR Base and Prime Editing.
    da Costa BL; Jenny LA; Maumenee IH; Tsang SH; Quinn PMJ
    Adv Exp Med Biol; 2023; 1415():103-107. PubMed ID: 37440021
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Foveal Hypoplasia in
    Rodriguez-Martinez AC; Higgins BE; Tailor-Hamblin V; Malka S; Cheloni R; Collins AM; Bladen J; Henderson R; Moosajee M
    Int J Mol Sci; 2023 Sep; 24(18):. PubMed ID: 37762234
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Crumbs homologue 1 is required for maintenance of photoreceptor cell polarization and adhesion during light exposure.
    van de Pavert SA; Kantardzhieva A; Malysheva A; Meuleman J; Versteeg I; Levelt C; Klooster J; Geiger S; Seeliger MW; Rashbass P; Le Bivic A; Wijnholds J
    J Cell Sci; 2004 Aug; 117(Pt 18):4169-77. PubMed ID: 15316081
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model.
    Aleman TS; Cideciyan AV; Aguirre GK; Huang WC; Mullins CL; Roman AJ; Sumaroka A; Olivares MB; Tsai FF; Schwartz SB; Vandenberghe LH; Limberis MP; Stone EM; Bell P; Wilson JM; Jacobson SG
    Invest Ophthalmol Vis Sci; 2011 Aug; 52(9):6898-910. PubMed ID: 21757580
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Microglial Cell Dysfunction in CRB1-Associated Retinopathies.
    Alves CH; Wijnholds J
    Adv Exp Med Biol; 2019; 1185():159-163. PubMed ID: 31884605
    [TBL] [Abstract][Full Text] [Related]  

  • 20. In Silico Analysis of Pathogenic
    Bellingrath JS; McClements ME; Kaukonen M; Fischer MD; MacLaren RE
    Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946856
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.