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 *

129 related articles for article (PubMed ID: 26030385)

  • 21. The potential importance of autophagy genes expression profile dysregulation and ATG polymorphisms in COVID-19 pathogenesis.
    Yousefi P; Tabibzadeh A; Keyvani H; Esghaei M; Karampoor S; Razizadeh MH; Mousavizadeh L
    APMIS; 2023 Apr; 131(4):161-169. PubMed ID: 36478304
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Analysis of rs1864182 and rs1864183 variants in ATG10 gene and antineutrophil cytoplasmic autoantibody-associated vasculitis in Chinese Guangxi population.
    Huang S; Rao J; Wei J; Huang Q; Zhu Y; Li W; Xue C
    J Clin Lab Anal; 2022 Feb; 36(2):e24193. PubMed ID: 34961976
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Seeking the elusive etiology of Paget disease: a progress report.
    Siris ES
    J Bone Miner Res; 1996 Nov; 11(11):1599-601. PubMed ID: 8915766
    [No Abstract]   [Full Text] [Related]  

  • 24. Lack of association of the autophagy-related gene polymorphism ATG16L1 rs2241880 in RA predisposition.
    Chatzikyriakidou A; Voulgari PV; Drosos AA
    Rheumatol Int; 2014 Apr; 34(4):477-9. PubMed ID: 23535819
    [No Abstract]   [Full Text] [Related]  

  • 25. Paget's disease of bone is not associated with common polymorphisms in interleukin-6, interleukin-8 and tumor necrosis factor alpha genes.
    Corral-Gudino L; del Pino-Montes J; García-Aparicio J; Alonso-Garrido M; González-Sarmiento R
    Cytokine; 2010 Dec; 52(3):146-50. PubMed ID: 20709566
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Allele, genotype, and composite genotype effects of IL-1A +4845 and IL-1B +3954 polymorphisms for chronic periodontitis in an Indian population.
    Gayathri R; Saadi AV; Bhat KM; Bhat SG; Satyamoorthy K
    Indian J Dent Res; 2011; 22(4):612. PubMed ID: 22124068
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic polymorphisms of 17 β-hydroxysteroid dehydrogenase 3 and the risk of hypospadias.
    Sata F; Kurahashi N; Ban S; Moriya K; Tanaka KD; Ishizuka M; Nakao H; Yahata Y; Imai H; Kakizaki H; Nonomura K; Kishi R
    J Sex Med; 2010 Aug; 7(8):2729-38. PubMed ID: 20059664
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Carrier-state of D allele in ACE gene insertion/deletion polymorphism is associated with coronary artery disease, in contrast to the C677-->T transition in the MTHFR gene.
    Zak I; Niemiec P; Sarecka B; Balcerzyk A; Ciemniewski Z; Rudowska E; Dylag S
    Acta Biochim Pol; 2003; 50(2):527-34. PubMed ID: 12833177
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Analysis of single nucleotide polymorphisms in the 5'-flanking region of tumor necrosis factor-alpha gene in Japanese patients with early-onset periodontitis.
    Endo M; Tai H; Tabeta K; Kobayashi T; Yamazaki K; Yoshie H
    J Periodontol; 2001 Nov; 72(11):1554-9. PubMed ID: 11759867
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Contribution of genetic factors to the pathogenesis of Paget's disease of bone and related disorders.
    Lucas GJ; Daroszewska A; Ralston SH
    J Bone Miner Res; 2006 Dec; 21 Suppl 2():P31-7. PubMed ID: 17229006
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Vitamin D receptor, oestrogen receptor-alpha and calcium-sensing receptor genotypes, bone mineral density and biochemical markers in Paget's disease of bone.
    Donáth J; Speer G; Poór G; Gergely P; Tabák A; Lakatos P
    Rheumatology (Oxford); 2004 Jun; 43(6):692-5. PubMed ID: 14997007
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Lack of association of three GRIN2B polymorphisms with bipolar disorder.
    Szczepankiewicz A; Skibinska M; Rybakowski J; Leszczynska-Rodziewicz A; Tomaszewska M; Twarowska-Hauser J
    World J Biol Psychiatry; 2009; 10(4 Pt 2):469-73. PubMed ID: 19005876
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Alleles and haplotypes of the interleukin 10 gene polymorphisms are associated with risk of developing acute coronary syndrome in Mexican patients.
    Fragoso JM; Vallejo M; Alvarez-León E; Delgadillo H; Peña-Duque MA; Cardoso-Saldaña G; Posadas-Romero C; Martínez-Ríos MA; Vargas-Alarcón G
    Cytokine; 2011 Jul; 55(1):29-33. PubMed ID: 21481602
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular prediction of disease risk and severity in a large Dutch Crohn's disease cohort.
    Weersma RK; Stokkers PC; van Bodegraven AA; van Hogezand RA; Verspaget HW; de Jong DJ; van der Woude CJ; Oldenburg B; Linskens RK; Festen EA; van der Steege G; Hommes DW; Crusius JB; Wijmenga C; Nolte IM; Dijkstra G;
    Gut; 2009 Mar; 58(3):388-95. PubMed ID: 18824555
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Osteoporotic fractures are associated with an 86-base pair repeat polymorphism in the interleukin-1--receptor antagonist gene but not with polymorphisms in the interleukin-1beta gene.
    Langdahl BL; Løkke E; Carstens M; Stenkjaer LL; Eriksen EF
    J Bone Miner Res; 2000 Mar; 15(3):402-14. PubMed ID: 10750554
    [TBL] [Abstract][Full Text] [Related]  

  • 36. HLA DRB1, DQB1 and insulin promoter VNTR polymorphisms: interactions and the association with adult-onset diabetes mellitus in Czech patients.
    Cejkova P; Novota P; Cerna M; Kolostova K; Novakova D; Kucera P; Novak J; Andel M; Weber P; Zdarsky E
    Int J Immunogenet; 2008 Apr; 35(2):133-40. PubMed ID: 18279373
    [TBL] [Abstract][Full Text] [Related]  

  • 37. ZNF687 Mutations in Severe Paget Disease of Bone Associated with Giant Cell Tumor.
    Divisato G; Formicola D; Esposito T; Merlotti D; Pazzaglia L; Del Fattore A; Siris E; Orcel P; Brown JP; Nuti R; Strazzullo P; Benassi MS; Cancela ML; Michou L; Rendina D; Gennari L; Gianfrancesco F
    Am J Hum Genet; 2016 Feb; 98(2):275-86. PubMed ID: 26849110
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Association of single nucleotide autophagy-related protein 5 gene polymorphism rs2245214 with susceptibility to non-small cell lung cancer.
    Nikseresht M; Shahverdi M; Dehghani M; Abidi H; Mahmoudi R; Ghalamfarsa G; Manzouri L; Ghavami S
    J Cell Biochem; 2019 Feb; 120(2):1924-1931. PubMed ID: 30242869
    [TBL] [Abstract][Full Text] [Related]  

  • 39. ARG5 rs2245214 C/G Polymorphism Frequency in a Romanian Population.
    Burada F; Florescu DN; Cucu MG; Cimpoeru AL; Gheonea DI
    Curr Health Sci J; 2015; 41(2):121-125. PubMed ID: 30364870
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Heterogeneity in Paget disease of the bone.
    Nance MA; Nuttall FQ; Econs MJ; Lyles KW; Viles KD; Vance JM; Pericak-Vance MA; Speer MC
    Am J Med Genet; 2000 Jun; 92(5):303-7. PubMed ID: 10861657
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.