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 *

133 related articles for article (PubMed ID: 28390009)

  • 1. Mutations in proteasome-related genes are associated with thyroid hemiagenesis.
    Budny B; Szczepanek-Parulska E; Zemojtel T; Szaflarski W; Rydzanicz M; Wesoly J; Handschuh L; Wolinski K; Piatek K; Niedziela M; Ziemnicka K; Figlerowicz M; Zabel M; Ruchala M
    Endocrine; 2017 May; 56(2):279-285. PubMed ID: 28390009
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Thyroid Hemiagenesis: Incidence, Clinical Significance, and Genetic Background.
    Szczepanek-Parulska E; Zybek-Kocik A; Wartofsky L; Ruchala M
    J Clin Endocrinol Metab; 2017 Sep; 102(9):3124-3137. PubMed ID: 28666345
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The absence of mutations in homeobox candidate genes HOXA3, HOXB3, HOXD3 and PITX2 in familial and sporadic thyroid hemiagenesis.
    Kizys MM; Nesi-França S; Cardoso MG; Harada MY; Melo MC; Chiamolera MI; Dias-da-Silva MR; Maciel RM
    J Pediatr Endocrinol Metab; 2014 Mar; 27(3-4):317-22. PubMed ID: 24127533
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Compound heterozygous GLI3 variants in siblings with thyroid hemiagenesis.
    Szczepanek-Parulska E; Budny B; Borowczyk M; Zawadzka K; Sztromwasser P; Ruchała M
    Endocrine; 2021 Feb; 71(2):514-519. PubMed ID: 32696176
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.
    Kühnen P; Turan S; Fröhler S; Güran T; Abali S; Biebermann H; Bereket A; Grüters A; Chen W; Krude H
    J Clin Endocrinol Metab; 2014 Jan; 99(1):E169-76. PubMed ID: 24248179
    [TBL] [Abstract][Full Text] [Related]  

  • 6. NKX2-5 Variant in Two Siblings with Thyroid Hemiagenesis.
    Szczepanek-Parulska E; Budny B; Borowczyk M; Zhukov I; Szutkowski K; Zawadzka K; Tahir R; Minczykowski A; Niedziela M; Ruchała M
    Int J Mol Sci; 2022 Mar; 23(6):. PubMed ID: 35328834
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Thyroid hemiagenesis is a rare variant of thyroid dysgenesis with a familial component but without Pax8 mutations in a cohort of 22 cases.
    Castanet M; Leenhardt L; Léger J; Simon-Carré A; Lyonnet S; Pelet A; Czernichow P; Polak M
    Pediatr Res; 2005 Jun; 57(6):908-13. PubMed ID: 15845640
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Possible non-Mendelian mechanisms of thyroid dysgenesis.
    Deladoëy J; Vassart G; Van Vliet G
    Endocr Dev; 2007; 10():29-42. PubMed ID: 17684388
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prevalence of thyroid hemiagenesis in an asymptomatic schoolchildren population.
    Korpal-Szczyrska M; Kosiak W; Swieton D
    Thyroid; 2008 Jun; 18(6):637-9. PubMed ID: 18578613
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FOXE1 polyalanine tract length polymorphism in patients with thyroid hemiagenesis and subjects with normal thyroid.
    Szczepanek E; Ruchala M; Szaflarski W; Budny B; Kilinska L; Jaroniec M; Niedziela M; Zabel M; Sowinski J
    Horm Res Paediatr; 2011; 75(5):329-34. PubMed ID: 21311165
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Slc:Wistar/ST rats develop unilateral thyroid dysgenesis: A novel animal model of thyroid hemiagenesis.
    Nakamura T; Ichii O; Sunden Y; Elewa YHA; Yoshiyasu T; Hattori H; Tatsumi O; Kon Y; Nagasaki KI
    PLoS One; 2019; 14(8):e0221939. PubMed ID: 31465501
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.
    Al Taji E; Biebermann H; Límanová Z; Hníková O; Zikmund J; Dame C; Grüters A; Lebl J; Krude H
    Eur J Endocrinol; 2007 May; 156(5):521-9. PubMed ID: 17468187
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Screening chromosomal aberrations by array comparative genomic hybridization in 80 patients with congenital hypothyroidism and thyroid dysgenesis.
    Thorwarth A; Mueller I; Biebermann H; Ropers HH; Grueters A; Krude H; Ullmann R
    J Clin Endocrinol Metab; 2010 Jul; 95(7):3446-52. PubMed ID: 20427504
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 22q11.2 Microduplication with thyroid hemiagenesis.
    Kim HJ; Jo HS; Yoo EG; Chung IH; Kim SW; Lee KH; Chang YH
    Horm Res Paediatr; 2013; 79(4):243-9. PubMed ID: 23364243
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Thyroid hemiagenesis associated with medullary or papillary carcinoma: report of cases.
    Wang J; Gao L; Song C
    Head Neck; 2014 Nov; 36(11):E106-11. PubMed ID: 24115043
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
    Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
    Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification and characterization of four PAX8 rare sequence variants (p.T225M, p.L233L, p.G336S and p.A439A) in patients with congenital hypothyroidism and dysgenetic thyroid glands.
    Esperante SA; Rivolta CM; Miravalle L; Herzovich V; Iorcansky S; Baralle M; Targovnik HM
    Clin Endocrinol (Oxf); 2008 May; 68(5):828-35. PubMed ID: 17980011
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic analysis of the paired box transcription factor (PAX8) gene in a cohort of Polish patients with primary congenital hypothyroidism and dysgenetic thyroid glands.
    Kumorowicz-Czoch M; Madetko-Talowska A; Dudek A; Tylek-Lemanska D
    J Pediatr Endocrinol Metab; 2015 Jul; 28(7-8):735-43. PubMed ID: 25720050
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in BOREALIN cause thyroid dysgenesis.
    Carré A; Stoupa A; Kariyawasam D; Gueriouz M; Ramond C; Monus T; Léger J; Gaujoux S; Sebag F; Glaser N; Zenaty D; Nitschke P; Bole-Feysot C; Hubert L; Lyonnet S; Scharfmann R; Munnich A; Besmond C; Taylor W; Polak M
    Hum Mol Genet; 2017 Feb; 26(3):599-610. PubMed ID: 28025328
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations.
    Ramos HE; Carré A; Chevrier L; Szinnai G; Tron E; Cerqueira TL; Léger J; Cabrol S; Puel O; Queinnec C; De Roux N; Guillot L; Castanet M; Polak M
    Eur J Endocrinol; 2014 Oct; 171(4):499-507. PubMed ID: 25214233
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.