BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 36833358)

  • 1. Homozygous Missense Variant in the Solute Carrier Organic Anion Transporter 2A1 (
    Umair M; Bilal M; Shah K; Said G; Ahmad F
    Genes (Basel); 2023 Feb; 14(2):. PubMed ID: 36833358
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Three novel mutations in the SLCO2A1 gene in two Chinese families with primary hypertrophic osteoarthropathy.
    Cheng R; Li M; Guo Y; Yao Y; Gao C; Yao Z
    Eur J Dermatol; 2013; 23(5):636-9. PubMed ID: 24153155
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pachydermoperiostosis of the complete type: A novel missense mutation c.101T > C in the SLCO2A1 gene.
    Ma W; Guo S; Li Y; Li Z
    Eur J Med Genet; 2017 Aug; 60(8):433-436. PubMed ID: 28602931
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype-genotype correlation in Japanese patients with pachydermoperiostosis.
    Sasaki T; Niizeki H; Shimizu A; Shiohama A; Hirakiyama A; Okuyama T; Seki A; Kabashima K; Otsuka A; Ishiko A; Tanese K; Miyakawa S; Sakabe J; Kuwahara M; Amagai M; Okano H; Suematsu M; Kudoh J
    J Dermatol Sci; 2012 Oct; 68(1):36-44. PubMed ID: 22906430
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inactivating mutation in the prostaglandin transporter gene, SLCO2A1, associated with familial digital clubbing, colon neoplasia, and NSAID resistance.
    Guda K; Fink SP; Milne GL; Molyneaux N; Ravi L; Lewis SM; Dannenberg AJ; Montgomery CG; Zhang S; Willis J; Wiesner GL; Markowitz SD
    Cancer Prev Res (Phila); 2014 Aug; 7(8):805-12. PubMed ID: 24838973
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC).
    Tariq M; Azeem Z; Ali G; Chishti MS; Ahmad W
    J Med Genet; 2009 Jan; 46(1):14-20. PubMed ID: 18805827
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy.
    Zhang Z; Xia W; He J; Zhang Z; Ke Y; Yue H; Wang C; Zhang H; Gu J; Hu W; Fu W; Hu Y; Li M; Liu Y
    Am J Hum Genet; 2012 Jan; 90(1):125-32. PubMed ID: 22197487
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two novel mutations in the SLCO2A1 gene in a Chinese patient with primary hypertrophic osteoarthropathy.
    Zhang Z; He JW; Fu WZ; Zhang CQ; Zhang ZL
    Gene; 2014 Jan; 534(2):421-3. PubMed ID: 24185079
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of mutations in the prostaglandin transporter gene SLCO2A1 and phenotypic comparison between two subtypes of primary hypertrophic osteoarthropathy (PHO): A single-center study.
    Hou Y; Lin Y; Qi X; Yuan L; Liao R; Pang Q; Cui L; Jiang Y; Wang O; Li M; Dong J; Xia W
    Bone; 2018 Jan; 106():96-102. PubMed ID: 28963081
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Touraine-Solente-Gole syndrome: pathogenic variant in SLCO2A1 presented with polyarthralgia and digital clubbing.
    Nicolau R; Beirão T; Guimarães F; Aguiar F; Ganhão S; Rodrigues M; Grangeia A; Brito I
    Pediatr Rheumatol Online J; 2023 May; 21(1):48. PubMed ID: 37226222
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbing.
    Busch J; Frank V; Bachmann N; Otsuka A; Oji V; Metze D; Shah K; Danda S; Watzer B; Traupe H; Bolz HJ; Kabashima K; Bergmann C
    J Invest Dermatol; 2012 Oct; 132(10):2473-2476. PubMed ID: 22696055
    [No Abstract]   [Full Text] [Related]  

  • 12. Mutations in the prostaglandin transporter encoding gene SLCO2A1 cause primary hypertrophic osteoarthropathy and isolated digital clubbing.
    Seifert W; Kühnisch J; Tüysüz B; Specker C; Brouwers A; Horn D
    Hum Mutat; 2012 Apr; 33(4):660-4. PubMed ID: 22331663
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of the Mutations in the Prostaglandin Transporter Gene, SLCO2A1 and Clinical Characterization in Korean Patients with Pachydermoperiostosis.
    Lee S; Park SY; Kwon HJ; Lee CH; Kim OH; Rhee Y
    J Korean Med Sci; 2016 May; 31(5):735-42. PubMed ID: 27134495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Primary hypertrophic osteoarthropathy due to a novel
    Mangupli R; Daly AF; Cuauro E; Camperos P; Krivoy J; Beckers A
    Endocrinol Diabetes Metab Case Rep; 2017; 2017():. PubMed ID: 28469926
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Monoallelic mutations in SLCO2A1 cause autosomal dominant primary hypertrophic osteoarthropathy.
    Xu Y; Zhang Z; Yue H; Li S; Zhang Z
    J Bone Miner Res; 2021 Aug; 36(8):1459-1468. PubMed ID: 33852188
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel mutation in the SLCO2A1 gene in a Chinese family with primary hypertrophic osteoarthropathy.
    Zhang Z; He JW; Fu WZ; Zhang CQ; Zhang ZL
    Gene; 2013 May; 521(1):191-4. PubMed ID: 23531451
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Homozygous SLCO2A1 translation initiation codon mutation in a Pakistani family with recessive isolated congenital nail clubbing.
    Shah K; Ferrara TM; Jan A; Umair M; Irfanullah ; Khan S; Ahmad W; Spritz RA
    Br J Dermatol; 2017 Aug; 177(2):546-548. PubMed ID: 27681482
    [No Abstract]   [Full Text] [Related]  

  • 18. A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family.
    Khan AK; Muhammad N; Khan SA; Ullah W; Nasir A; Afzal S; Ramzan K; Basit S; Khan S
    Ann Hum Genet; 2018 May; 82(3):171-176. PubMed ID: 29282707
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Primary Hypertrophic Osteoarthropathy Mimicking Juvenile Idiopathic Arthritis: A Novel SLCO2A1 Mutation and Imaging Findings.
    Torgutalp M; Durmaz CD; Karabulut HG; Seifert W; Horn D; Akkaya Z; Turgay M
    Cytogenet Genome Res; 2019; 158(3):126-132. PubMed ID: 31203270
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy.
    Guo T; Yang K; Liu L; Tan ZP; Luo H
    Mol Med Rep; 2017 May; 15(5):2977-2982. PubMed ID: 28339061
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.