These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 36837600)

  • 1.
    Sobolewska M; Świerczyńska M; Dorecka M; Wyględowska-Promieńska D; Krawczyński MR; Mrukwa-Kominek E
    Medicina (Kaunas); 2023 Feb; 59(2):. PubMed ID: 36837600
    [No Abstract]   [Full Text] [Related]  

  • 2. A rare case of
    Mermeklieva E; Kamenarova K; Mihova K; Shakola F; Kaneva R
    Ophthalmic Genet; 2021 Dec; 42(6):747-752. PubMed ID: 34229535
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotypic and Genetic Alterations in Adult-Onset Cone and Cone-Rod Dystrophy.
    Kim DJ; Woo SJ; Joo K
    Ophthalmic Res; 2024; 67(1):9-22. PubMed ID: 38091967
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical Phenotypes of
    Malechka VV; Cukras CA; Chew EY; Sergeev YV; Blain D; Jeffrey BG; Ullah E; Hufnagel RB; Brooks BP; Huryn LA; Zein WM
    Genes (Basel); 2022 May; 13(5):. PubMed ID: 35627310
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hypomorphic
    Farag S; Yusuf IH; Kaukonen M; Taylor LJ; Charbel Issa P; MacLaren RE
    Ophthalmic Genet; 2024 Apr; 45(2):201-206. PubMed ID: 37728066
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical characteristics, imaging findings, and genetic results of a patient with
    Vilaplana F; Ros A; Garcia B; Blanco I; Castellanos E; Edwards NJ; Valldeperas X; Ruiz-Bilbao S; Sabala A
    Ophthalmic Genet; 2021 Aug; 42(4):474-479. PubMed ID: 33886416
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Specific Macula-Predominant Retinal Phenotype Is Associated With the CDHR1 Variant c.783G>A, a Silent Mutation Leading to In-Frame Exon Skipping.
    Charbel Issa P; Gliem M; Yusuf IH; Birtel J; Müller PL; Mangold E; Downes SM; MacLaren RE; Betz C; Bolz HJ
    Invest Ophthalmol Vis Sci; 2019 Aug; 60(10):3388-3397. PubMed ID: 31387115
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deep phenotyping of the Cdhr1
    Yusuf IH; McClements ME; MacLaren RE; Charbel Issa P
    Exp Eye Res; 2021 Jul; 208():108603. PubMed ID: 33964272
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical characteristics of recessive retinal degeneration due to mutations in the CDHR1 gene and a review of the literature.
    Bessette AP; DeBenedictis MJ; Traboulsi EI
    Ophthalmic Genet; 2018; 39(1):51-55. PubMed ID: 28885867
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of the cone-rod dystrophy retinal phenotype caused by novel homozygous DRAM2 mutations.
    Abad-Morales V; Burés-Jelstrup A; Navarro R; Ruiz-Nogales S; Méndez-Vendrell P; Corcóstegui B; Pomares E
    Exp Eye Res; 2019 Oct; 187():107752. PubMed ID: 31394102
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Case Report: Multimodal Imaging Features of an ABCA4 Cone Dystrophy.
    Monferrer-Adsuara C; Montero-Hernández J; Castro-Navarro V; Remolí-Sargues L; Cervera-Taulet E
    Optom Vis Sci; 2022 Feb; 99(2):195-201. PubMed ID: 34897229
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characteristic Ocular Features in Cases of Autosomal Recessive PROM1 Cone-Rod Dystrophy.
    Collison FT; Fishman GA; Nagasaki T; Zernant J; McAnany JJ; Park JC; Allikmets R
    Invest Ophthalmol Vis Sci; 2019 May; 60(6):2347-2356. PubMed ID: 31136651
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel splice site mutation of CDHR1 in a consanguineous Israeli Christian Arab family segregating autosomal recessive cone-rod dystrophy.
    Cohen B; Chervinsky E; Jabaly-Habib H; Shalev SA; Briscoe D; Ben-Yosef T
    Mol Vis; 2012; 18():2915-21. PubMed ID: 23233793
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1.
    Arno G; Hull S; Carss K; Dev-Borman A; Chakarova C; Bujakowska K; van den Born LI; Robson AG; Holder GE; Michaelides M; Cremers FP; Pierce E; Raymond FL; Moore AT; Webster AR
    Invest Ophthalmol Vis Sci; 2016 Sep; 57(11):4806-13. PubMed ID: 27623334
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Quantitative Fundus Autofluorescence and Genetic Associations in Macular, Cone, and Cone-Rod Dystrophies.
    Gliem M; Müller PL; Birtel J; Herrmann P; McGuinness MB; Holz FG; Charbel Issa P
    Ophthalmol Retina; 2020 Jul; 4(7):737-749. PubMed ID: 32646556
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rescue of cone and rod photoreceptor function in a CDHR1-model of age-related retinal degeneration.
    Yusuf IH; Burgoyne T; Salman A; McClements ME; MacLaren RE; Charbel Issa P
    Mol Ther; 2024 May; 32(5):1445-1460. PubMed ID: 38504520
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutation in
    Ahn J; Chiang J; Gorin MB
    Ophthalmic Genet; 2020 Aug; 41(4):386-389. PubMed ID: 32594822
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction.
    Roosing S; van den Born LI; Hoyng CB; Thiadens AA; de Baere E; Collin RW; Koenekoop RK; Leroy BP; van Moll-Ramirez N; Venselaar H; Riemslag FC; Cremers FP; Klaver CC; den Hollander AI
    Ophthalmology; 2013 Jun; 120(6):1239-46. PubMed ID: 23499059
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Retinal dystrophy associated with a single-base deletion mutation in mitochondrial DNA 3271 in patient with MELAS syndrome.
    Ozawa K; Mochizuki K; Manabe Y; Yoshikura N; Shimohata T; Nishino I; Goto YI
    Doc Ophthalmol; 2019 Apr; 138(2):147-152. PubMed ID: 30701423
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical characteristics of early retinal disease due to CDHR1 mutation.
    Ba-Abbad R; Sergouniotis PI; Plagnol V; Robson AG; Michaelides M; Holder GE; Webster AR
    Mol Vis; 2013; 19():2250-9. PubMed ID: 24265541
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.