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 *

174 related articles for article (PubMed ID: 33631011)

  • 21. The Dual Oxidase Duox2 stabilized with DuoxA2 in an enzymatic complex at the surface of the cell produces extracellular H
    Poncelet L; Dumont JE; Miot F; De Deken X
    Exp Cell Res; 2019 Nov; 384(1):111620. PubMed ID: 31513783
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases].
    Enacán RE; Masnata ME; Belforte F; Papendieck P; Olcese MC; Siffo S; Gruñeiro-Papendieck L; Targovnik H; Rivolta CM; Chiesa AE
    Arch Argent Pediatr; 2017 Jun; 115(3):e162-e165. PubMed ID: 28504502
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Genetic mutation profiles for children with congenital hypothyroidism in Fujian province].
    Cheng F; Su YQ; Wang XR; Wu FY; Sun F; Fang Y; Zhang RJ; Zhao SX; Song HD
    Zhonghua Yi Xue Za Zhi; 2023 Feb; 103(5):336-343. PubMed ID: 36740391
    [No Abstract]   [Full Text] [Related]  

  • 24. Compound heterozygosity for a novel hemizygous missense mutation and a partial deletion affecting the catalytic core of the H2O2-generating enzyme DUOX2 associated with transient congenital hypothyroidism.
    Hoste C; Rigutto S; Van Vliet G; Miot F; De Deken X
    Hum Mutat; 2010 Apr; 31(4):E1304-19. PubMed ID: 20187165
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Patients with Thyroid Dyshormonogenesis and
    Baz-Redón N; Antolín M; Clemente M; Campos A; Mogas E; Fernández-Cancio M; Zafon E; García-Arumí E; Soler L; González-Llorens N; Aguilar-Riera C; Camats-Tarruella N; Yeste D
    Int J Mol Sci; 2024 Aug; 25(15):. PubMed ID: 39126042
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Correlation of DUOX2 residual enzymatic activity with phenotype in congenital hypothyroidism caused by biallelic DUOX2 defects.
    Sun F; Zhang RJ; Cheng F; Fang Y; Yang RM; Ye XP; Han B; Zhao SX; Dong M; Song HD
    Clin Genet; 2021 Dec; 100(6):713-721. PubMed ID: 34564849
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic and Phenotypic Characteristics of Congenital Hypothyroidism in a Chinese Cohort.
    Long W; Guo F; Yao R; Wang Y; Wang H; Yu B; Xue P
    Front Endocrinol (Lausanne); 2021; 12():705773. PubMed ID: 34539567
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism.
    Kollati Y; Akella RRD; Naushad SM; Borkar D; Thalla M; Nagalingam S; Lingappa L; Patel RK; Reddy GB; Dirisala VR
    Mol Biol Rep; 2020 Oct; 47(10):7467-7475. PubMed ID: 32930933
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7.
    Acar S; Gürsoy S; Arslan G; Nalbantoğlu Ö; Hazan F; Köprülü Ö; Özkaya B; Özkan B
    J Endocrinol Invest; 2022 Apr; 45(4):773-786. PubMed ID: 34780050
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical and genetic investigation in patients with permanent congenital hypothyroidism.
    Zhou L; Liu S; Long W; Wang LL; Yu B
    Clin Chim Acta; 2023 Jan; 539():1-6. PubMed ID: 36423704
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Functional Characterization of DUOX Enzymes in Reconstituted Cell Models.
    Korzeniowska A; Donkó ÁP; Morand S; Leto TL
    Methods Mol Biol; 2019; 1982():173-190. PubMed ID: 31172473
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Disorders of H
    Muzza M; Fugazzola L
    Best Pract Res Clin Endocrinol Metab; 2017 Mar; 31(2):225-240. PubMed ID: 28648510
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism.
    Aycan Z; Cangul H; Muzza M; Bas VN; Fugazzola L; Chatterjee VK; Persani L; Schoenmakers N
    J Clin Endocrinol Metab; 2017 Sep; 102(9):3085-3090. PubMed ID: 28633507
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
    Bruellman RJ; Watanabe Y; Ebrhim RS; Creech MK; Abdullah MA; Dumitrescu AM; Refetoff S; Weiss RE
    J Clin Endocrinol Metab; 2020 May; 105(5):1564-72. PubMed ID: 31867598
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism.
    Zamproni I; Grasberger H; Cortinovis F; Vigone MC; Chiumello G; Mora S; Onigata K; Fugazzola L; Refetoff S; Persani L; Weber G
    J Clin Endocrinol Metab; 2008 Feb; 93(2):605-10. PubMed ID: 18042646
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Inhibition of the thyroid hormonogenic H
    Giusti N; Gillotay P; Trubiroha A; Opitz R; Dumont JE; Costagliola S; De Deken X
    Mol Cell Endocrinol; 2020 Jan; 500():110635. PubMed ID: 31678421
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Characteristics of DUOXA2 gene mutation in children with congenital hypothyroidism].
    Tan MY; Huang YL; Li B; Jiang X; Chen QY; Jia XF; Tang CF; Liu L
    Zhongguo Dang Dai Er Ke Za Zhi; 2017 Jan; 19(1):59-63. PubMed ID: 28100324
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identification of the maturation factor for dual oxidase. Evolution of an eukaryotic operon equivalent.
    Grasberger H; Refetoff S
    J Biol Chem; 2006 Jul; 281(27):18269-72. PubMed ID: 16651268
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients.
    Fu C; Wang J; Luo S; Yang Q; Li Q; Zheng H; Hu X; Su J; Zhang S; Chen R; Luo J; Zhang Y; Shen Y; Wei H; Meng D; Gui B; Zeng Z; Fan X; Chen S
    Clin Chim Acta; 2016 Nov; 462():127-132. PubMed ID: 27637299
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The Prevalence, Clinical, and Molecular Characteristics of Congenital Hypothyroidism Caused by DUOX2 Mutations: A Population-Based Cohort Study in Guangzhou.
    Tan M; Huang Y; Jiang X; Li P; Tang C; Jia X; Chen Q; Chen W; Sheng H; Feng Y; Wu D; Liu L
    Horm Metab Res; 2016 Sep; 48(9):581-8. PubMed ID: 27557340
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.