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 *

102 related articles for article (PubMed ID: 10207042)

  • 21. Opposite Profiles of Complement in Antiphospholipid Syndrome (APS) and Systemic Lupus Erythematosus (SLE) Among Patients With Antiphospholipid Antibodies (aPL).
    Savelli SL; Roubey RAS; Kitzmiller KJ; Zhou D; Nagaraja HN; Mulvihill E; Barbar-Smiley F; Ardoin SP; Wu YL; Yu CY
    Front Immunol; 2019; 10():885. PubMed ID: 31134052
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Increased Risk of Autoimmune Disorders in 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study.
    Falhammar H; Frisén L; Hirschberg AL; Nordenskjöld A; Almqvist C; Nordenström A
    J Endocr Soc; 2019 May; 3(5):1039-1052. PubMed ID: 31065621
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline.
    Speiser PW; Arlt W; Auchus RJ; Baskin LS; Conway GS; Merke DP; Meyer-Bahlburg HFL; Miller WL; Murad MH; Oberfield SE; White PC
    J Clin Endocrinol Metab; 2018 Nov; 103(11):4043-4088. PubMed ID: 30272171
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Congenital Adrenal Hyperplasia (CAH) due to 21-Hydroxylase Deficiency: A Comprehensive Focus on 233 Pathogenic Variants of CYP21A2 Gene.
    Concolino P; Costella A
    Mol Diagn Ther; 2018 Jun; 22(3):261-280. PubMed ID: 29450859
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A
    Silva-Grecco RLD; de Paula Michelatto D; Lincoln-de-Carvalho CR; Henrique PP; da Cunha HM; Palandi-de-Mello M
    Mol Genet Metab Rep; 2015 Dec; 5():98-102. PubMed ID: 28649552
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India.
    Dubey S; Tardy V; Chowdhury MR; Gupta N; Jain V; Deka D; Sharma P; Morel Y; Kabra M
    Indian J Med Res; 2017 Feb; 145(2):194-202. PubMed ID: 28639595
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis.
    Li N; Zhang J; Liao D; Yang L; Wang Y; Hou S
    Sci Rep; 2017 Feb; 7():42628. PubMed ID: 28205620
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Choi JH; Kim GH; Yoo HW
    Ann Pediatr Endocrinol Metab; 2016 Mar; 21(1):1-6. PubMed ID: 27104172
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune Diseases.
    Lintner KE; Wu YL; Yang Y; Spencer CH; Hauptmann G; Hebert LA; Atkinson JP; Yu CY
    Front Immunol; 2016; 7():36. PubMed ID: 26913032
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations.
    Chen JY; Wu YL; Mok MY; Wu YJ; Lintner KE; Wang CM; Chung EK; Yang Y; Zhou B; Wang H; Yu D; Alhomosh A; Jones K; Spencer CH; Nagaraja HN; Lau YL; Lau CS; Yu CY
    Arthritis Rheumatol; 2016 Jun; 68(6):1442-1453. PubMed ID: 26814708
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis.
    Lintner KE; Patwardhan A; Rider LG; Abdul-Aziz R; Wu YL; Lundström E; Padyukov L; Zhou B; Alhomosh A; Newsom D; White P; Jones KB; O'Hanlon TP; Miller FW; Spencer CH; Yu CY
    Ann Rheum Dis; 2016 Sep; 75(9):1599-606. PubMed ID: 26493816
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations.
    Milacic I; Barac M; Milenkovic T; Ugrin M; Klaassen K; Skakic A; Jesic M; Joksic I; Mitrovic K; Todorovic S; Vujovic S; Pavlovic S; Stojiljkovic M
    J Endocrinol Invest; 2015 Nov; 38(11):1199-210. PubMed ID: 26233337
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels.
    Doleschall M; Szabó JA; Pázmándi J; Szilágyi Á; Koncz K; Farkas H; Tóth M; Igaz P; Gláz E; Prohászka Z; Korbonits M; Rácz K; Füst G; Patócs A
    PLoS One; 2014; 9(9):e107244. PubMed ID: 25210767
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Investigation of complement component C4 copy number variation in human longevity.
    Flachsbart F; Caliebe A; Heinsen FA; Hemming-Karlsen T; Schreiber S; Franke A; Nebel A
    PLoS One; 2014; 9(1):e86188. PubMed ID: 24465950
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Comprehensive mutation analysis of the CYP21A2 gene: an efficient multistep approach to the molecular diagnosis of congenital adrenal hyperplasia.
    Xu Z; Chen W; Merke DP; McDonnell NB
    J Mol Diagn; 2013 Nov; 15(6):745-53. PubMed ID: 24071710
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Sequencing and comparative analysis of the gorilla MHC genomic sequence.
    Wilming LG; Hart EA; Coggill PC; Horton R; Gilbert JG; Clee C; Jones M; Lloyd C; Palmer S; Sims S; Whitehead S; Wiley D; Beck S; Harrow JL
    Database (Oxford); 2013; 2013():bat011. PubMed ID: 23589541
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Tenascin-X haploinsufficiency associated with Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia.
    Merke DP; Chen W; Morissette R; Xu Z; Van Ryzin C; Sachdev V; Hannoush H; Shanbhag SM; Acevedo AT; Nishitani M; Arai AE; McDonnell NB
    J Clin Endocrinol Metab; 2013 Feb; 98(2):E379-87. PubMed ID: 23284009
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Intraspecific evolution of human RCCX copy number variation traced by haplotypes of the CYP21A2 gene.
    Bánlaki Z; Szabó JA; Szilágyi Á; Patócs A; Prohászka Z; Füst G; Doleschall M
    Genome Biol Evol; 2013; 5(1):98-112. PubMed ID: 23241443
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.
    Rabbani B; Mahdieh N; Haghi Ashtiani MT; Akbari MT; Rabbani A
    Iran J Pediatr; 2011 Jun; 21(2):139-50. PubMed ID: 23056780
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mutational characterization of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Malaysia.
    Balraj P; Lim PG; Sidek H; Wu LL; Khoo AS
    J Endocrinol Invest; 2013 Jun; 36(6):366-74. PubMed ID: 23027774
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.