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 *

288 related articles for article (PubMed ID: 27134495)

  • 21. A Common Mutation and a Novel Mutation in the HPGD Gene in Nine Patients with Primary Hypertrophic Osteoarthropathy.
    Yuan L; Chen L; Liao RX; Lin YY; Jiang Y; Wang O; Li M; Xing XP; Pang QQ; Jiajue R; Xia WB
    Calcif Tissue Int; 2015 Oct; 97(4):336-42. PubMed ID: 26135126
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. 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]  

  • 26. 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]  

  • 27. Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six-Month Prospective Clinical Intervention.
    Li SS; He JW; Fu WZ; Liu YJ; Hu YQ; Zhang ZL
    J Bone Miner Res; 2017 Aug; 32(8):1659-1666. PubMed ID: 28425581
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Case of pachydermoperiostosis with solute carrier organic anion transporter family, member 2A1 (SLCO2A1) mutations.
    Minakawa S; Kaneko T; Niizeki H; Mizukami H; Saito Y; Nigawara T; Kurose R; Nakabayashi K; Kabashima K; Sawamura D
    J Dermatol; 2015 Sep; 42(9):908-10. PubMed ID: 26072672
    [No Abstract]   [Full Text] [Related]  

  • 29. Novel SLCO2A1compound heterozygous mutation causing primary hypertrophic osteoarthropathy with Bartter-like hypokalemia in a Chinese family.
    Jiang Y; Du J; Song YW; Wang WB; Pang QQ; Li M; Wang O; Lian XL; Xing XP; Xia WB
    J Endocrinol Invest; 2019 Oct; 42(10):1245-1252. PubMed ID: 31004291
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Involvement of prostaglandin E2 in the first Japanese case of pachydermoperiostosis with HPGD mutation and recalcitrant leg ulcer.
    Nakazawa S; Niizeki H; Matsuda M; Nakabayashi K; Seki A; Mori T; Tokura Y
    J Dermatol Sci; 2015 May; 78(2):153-5. PubMed ID: 25757862
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. Pachydermoperiostosis: an update.
    Castori M; Sinibaldi L; Mingarelli R; Lachman RS; Rimoin DL; Dallapiccola B
    Clin Genet; 2005 Dec; 68(6):477-86. PubMed ID: 16283874
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Primary hypertrophic osteoarthropathy with digital clubbing and palmoplantar hyperhidrosis caused by 15-PGHD/HPGD loss-of-function mutations.
    Bergmann C; Wobser M; Morbach H; Falkenbach A; Wittenhagen D; Lassay L; Ott H; Zerres K; Girschick HJ; Hamm H
    Exp Dermatol; 2011 Jun; 20(6):531-3. PubMed ID: 21426412
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.
    Diggle CP; Parry DA; Logan CV; Laissue P; Rivera C; Restrepo CM; Fonseca DJ; Morgan JE; Allanore Y; Fontenay M; Wipff J; Varret M; Gibault L; Dalantaeva N; Korbonits M; Zhou B; Yuan G; Harifi G; Cefle K; Palanduz S; Akoglu H; Zwijnenburg PJ; Lichtenbelt KD; Aubry-Rozier B; Superti-Furga A; Dallapiccola B; Accadia M; Brancati F; Sheridan EG; Taylor GR; Carr IM; Johnson CA; Markham AF; Bonthron DT
    Hum Mutat; 2012 Aug; 33(8):1175-81. PubMed ID: 22553128
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genotype and phenotype characterization of primary hypertrophic osteoarthropathy type 2 and chronic enteropathy associated with SLCO2A1: Report of two cases and literature review.
    Kimball TN; Rivero-García P; Barrera-Godínez A; Domínguez-Cherit J
    Am J Med Genet A; 2024 Mar; 194(3):e63446. PubMed ID: 37915296
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Novel SLCO2A1 mutations cause gender differentiated pachydermoperiostosis.
    Yuan L; Chen X; Liu Z; Wu D; Lu J; Bao G; Zhang S; Wang L; Wu Y
    Endocr Connect; 2018 Aug; 7(11):1116-28. PubMed ID: 30352415
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The novel SLCO2A1 heterozygous missense mutation p.E427K and nonsense mutation p.R603* in a female patient with pachydermoperiostosis with an atypical phenotype.
    Niizeki H; Shiohama A; Sasaki T; Seki A; Kabashima K; Otsuka A; Takeshita M; Hirakiyama A; Okuyama T; Tanese K; Ishiko A; Amagai M; Kudoh J
    Br J Dermatol; 2014 May; 170(5):1187-9. PubMed ID: 24329728
    [No Abstract]   [Full Text] [Related]  

  • 39. Complete form of pachydermoperiostosis with SLCO2A1 gene mutation in a Korean family.
    Kim HJ; Koo KY; Shin DY; Kim DY; Lee JS; Lee MG
    J Dermatol; 2015 Jun; 42(6):655-7. PubMed ID: 25810087
    [No Abstract]   [Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 15.