BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 37755482)

  • 1. CYP26B1-related disorder: expanding the ends of the spectrum through clinical and molecular evidence.
    Silveira KC; Fonseca IC; Oborn C; Wengryn P; Ghafoor S; Beke A; Dreseris ES; Wong C; Iacovone A; Soltys CL; Babul-Hirji R; Artigalas O; Antolini-Tavares A; Gingras AC; Campos E; Cavalcanti DP; Kannu P
    Hum Genet; 2023 Nov; 142(11):1571-1586. PubMed ID: 37755482
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nonlethal presentations of CYP26B1-related skeletal anomalies and multiple synostoses syndrome.
    Grand K; Skraban CM; Cohen JL; Dowsett L; Mazzola S; Tarpinian J; Bedoukian E; Nesbitt A; Denenberg B; Lulis L; Santani A; Zackai EH; Deardorff MA
    Am J Med Genet A; 2021 Sep; 185(9):2766-2775. PubMed ID: 34160123
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial monoallelic CYP26B1 truncating variant causes a syndromic craniosynostosis due to haploinsufficiency ?
    Sarma AS; Peter Mathew R; Dalal A; Bhat V; Patil SJ
    Eur J Med Genet; 2023 Jul; 66(7):104772. PubMed ID: 37100236
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes.
    Morton JE; Frentz S; Morgan T; Sutherland-Smith AJ; Robertson SP
    Am J Med Genet A; 2016 Oct; 170(10):2706-10. PubMed ID: 27410456
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mucopolysaccharidosis IIIB and mild skeletal anomalies: coexistence of NAGLU and CYP26B1 missense variations in the same patient in a Chinese family.
    Li J; Xie H; Jiang Y
    BMC Med Genet; 2018 Apr; 19(1):51. PubMed ID: 29606097
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A variant in CYP26B1 associated with esophageal squamous cell carcinoma risk by affecting retinoic acid metabolism.
    Niu S; Shi K; Yue X; Pan M; Song L; Gu L; Tan Y; Miao X; Tian J; Chang J
    Mol Carcinog; 2023 Jul; 62(7):991-1000. PubMed ID: 37042568
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid.
    Laue K; Pogoda HM; Daniel PB; van Haeringen A; Alanay Y; von Ameln S; Rachwalski M; Morgan T; Gray MJ; Breuning MH; Sawyer GM; Sutherland-Smith AJ; Nikkels PG; Kubisch C; Bloch W; Wollnik B; Hammerschmidt M; Robertson SP
    Am J Hum Genet; 2011 Nov; 89(5):595-606. PubMed ID: 22019272
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Loss of Angelman Syndrome Protein E6AP Disrupts a Novel Antagonistic Estrogen-Retinoic Acid Transcriptional Crosstalk in Neurons.
    El Hokayem J; Weeber E; Nawaz Z
    Mol Neurobiol; 2018 Sep; 55(9):7187-7200. PubMed ID: 29388081
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cloning and functional studies of a splice variant of CYP26B1 expressed in vascular cells.
    Elmabsout AA; Kumawat A; Saenz-Méndez P; Krivospitskaya O; Sävenstrand H; Olofsson PS; Eriksson LA; Strid A; Valen G; Törmä H; Sirsjö A
    PLoS One; 2012; 7(5):e36839. PubMed ID: 22666329
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Direct protein-protein interactions and substrate channeling between cellular retinoic acid binding proteins and CYP26B1.
    Nelson CH; Peng CC; Lutz JD; Yeung CK; Zelter A; Isoherranen N
    FEBS Lett; 2016 Aug; 590(16):2527-35. PubMed ID: 27416800
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Accelerated Skeletal Maturation in Disorders of Retinoic Acid Metabolism: A Case Report and Focused Review of the Literature.
    Nilsson O; Isoherranen N; Guo MH; Lui JC; Jee YH; Guttmann-Bauman I; Acerini C; Lee W; Allikmets R; Yanovski JA; Dauber A; Baron J
    Horm Metab Res; 2016 Nov; 48(11):737-744. PubMed ID: 27589347
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CYP26B1 and its implications in lymphangiogenesis: Literature review and study of rare variants in two families.
    Ricci M; Serrani R; Amato B; Compagna R; Veselenyiova D; Kenanoglu S; Kurti D; Baglivo M; Krajcovic J; Miggiano GAD; Aquilanti B; Matera G; Velluti V; Gagliardi L; Dundar M; Basha SH; Bertelli M
    Lymphology; 2020; 53(1):20-28. PubMed ID: 32521127
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A CYP26B1 polymorphism enhances retinoic acid catabolism and may aggravate atherosclerosis.
    Krivospitskaya O; Elmabsout AA; Sundman E; Söderström LA; Ovchinnikova O; Gidlöf AC; Scherbak N; Norata GD; Samnegård A; Törmä H; Abdel-Halim SM; Jansson JH; Eriksson P; Sirsjö A; Olofsson PS
    Mol Med; 2012 May; 18(1):712-8. PubMed ID: 22415012
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome-1 in two new patients with the same homozygous TMCO1 variant and review of the literature.
    Abdelrazek IM; Holling T; Harms FL; Alawi M; Omar T; Abdalla E; Kutsche K
    Eur J Med Genet; 2023 Mar; 66(3):104715. PubMed ID: 36708876
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expression of STRA8 is conserved in therian mammals but expression of CYP26B1 differs between marsupials and mice.
    Hickford DE; Wong SFL; Frankenberg SR; Shaw G; Yu H; Chew KY; Renfree MB
    Biol Reprod; 2017 Aug; 97(2):217-229. PubMed ID: 29044428
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of Tazarotenic Acid as the First Xenobiotic Substrate of Human Retinoic Acid Hydroxylase CYP26A1 and CYP26B1.
    Foti RS; Isoherranen N; Zelter A; Dickmann LJ; Buttrick BR; Diaz P; Douguet D
    J Pharmacol Exp Ther; 2016 May; 357(2):281-92. PubMed ID: 26937021
    [TBL] [Abstract][Full Text] [Related]  

  • 17. SHH propagates distal limb bud development by enhancing CYP26B1-mediated retinoic acid clearance via AER-FGF signalling.
    Probst S; Kraemer C; Demougin P; Sheth R; Martin GR; Shiratori H; Hamada H; Iber D; Zeller R; Zuniga A
    Development; 2011 May; 138(10):1913-23. PubMed ID: 21471156
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exome-wide analyses identify low-frequency variant in CYP26B1 and additional coding variants associated with esophageal squamous cell carcinoma.
    Chang J; Zhong R; Tian J; Li J; Zhai K; Ke J; Lou J; Chen W; Zhu B; Shen N; Zhang Y; Zhu Y; Gong Y; Yang Y; Zou D; Peng X; Zhang Z; Zhang X; Huang K; Wu T; Wu C; Miao X; Lin D
    Nat Genet; 2018 Mar; 50(3):338-343. PubMed ID: 29379198
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Endothelial Cyp26b1 restrains murine heart valve growth during development.
    Ahuja N; Hiltabidle MS; Rajasekhar H; Voss S; Lu SZ; Barlow HR; Cowdin MA; Daniel E; Vaddaraju V; Anandakumar T; Black E; Cleaver O; Maynard C
    Dev Biol; 2022 Jun; 486():81-95. PubMed ID: 35364055
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Differential expression of the retinoic acid-metabolizing enzymes CYP26A1 and CYP26B1 during murine organogenesis.
    Abu-Abed S; MacLean G; Fraulob V; Chambon P; Petkovich M; Dollé P
    Mech Dev; 2002 Jan; 110(1-2):173-7. PubMed ID: 11744378
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.