BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 38054352)

  • 1. The functional study of a novel MKRN3 missense mutation associated with familial central precocious puberty.
    Chen Z; You Q; Wang J; Dong Z; Wang W; Yang Y; Ma X; Li C; Lu W
    Am J Med Genet A; 2024 Apr; 194(4):e63460. PubMed ID: 38054352
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Key Roles of Makorin RING Finger Protein 3 (MKRN3) During the Development of Pubertal Initiation and Central Precocious Puberty (CPP).
    Liu J; Li T; Peng M; Luo M; Gui Z; Long S; Mo Z; He W
    Curr Mol Med; 2023 May; 23(7):668-677. PubMed ID: 35748557
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial central precocious puberty: two novel MKRN3 mutations.
    Varimo T; Iivonen AP; Känsäkoski J; Wehkalampi K; Hero M; Vaaralahti K; Miettinen PJ; Niedziela M; Raivio T
    Pediatr Res; 2021 Aug; 90(2):431-435. PubMed ID: 33214675
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 Mutations.
    Seraphim CE; Canton APM; Montenegro L; Piovesan MR; Macedo DB; Cunha M; Guimaraes A; Ramos CO; Benedetti AFF; de Castro Leal A; Gagliardi PC; Antonini SR; Gryngarten M; Arcari AJ; Abreu AP; Kaiser UB; Soriano-Guillén L; Escribano-Muñoz A; Corripio R; Labarta JI; Travieso-Suárez L; Ortiz-Cabrera NV; Argente J; Mendonca BB; Brito VN; Latronico AC
    J Clin Endocrinol Metab; 2021 Mar; 106(4):1041-1050. PubMed ID: 33383582
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Novel Loss-of-Function
    Yin X; Wang J; Han T; Tingting Z; Li Y; Dong Z; Wang W; Li C; Lu W
    Front Genet; 2021; 12():663746. PubMed ID: 34421985
    [No Abstract]   [Full Text] [Related]  

  • 6. Outcomes of Patients with Central Precocious Puberty Due to Loss-of-Function Mutations in the MKRN3 Gene after Treatment with Gonadotropin-Releasing Hormone Analog.
    Ramos CO; Macedo DB; Canton APM; Cunha-Silva M; Antonini SRR; Stecchini MF; Seraphim CE; Rodrigues T; Mendonca BB; Latronico AC; Brito VN
    Neuroendocrinology; 2020; 110(7-8):705-713. PubMed ID: 31671431
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel heterozygous MKRN3 nonsense mutation in a Chinese girl with idiopathic central precocious puberty: A case report.
    Liu M; Fan L; Gong CX
    Medicine (Baltimore); 2020 Sep; 99(38):e22295. PubMed ID: 32957387
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular analysis of
    Kırkgöz T; Kaygusuz SB; Alavanda C; Helvacıoğlu D; Abalı ZY; Tosun BG; Eltan M; Menevşe TS; Guran T; Arman A; Turan S; Bereket A
    J Pediatr Endocrinol Metab; 2023 Apr; 36(4):401-408. PubMed ID: 36883204
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty.
    Simon D; Ba I; Mekhail N; Ecosse E; Paulsen A; Zenaty D; Houang M; Jesuran Perelroizen M; de Filippo GP; Salerno M; Simonin G; Reynaud R; Carel JC; Léger J; de Roux N
    Eur J Endocrinol; 2016 Jan; 174(1):1-8. PubMed ID: 26431553
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel MKRN3 Missense Mutations Associated With Central Precocious Puberty Reveal Distinct Effects on Ubiquitination.
    Magnotto JC; Mancini A; Bird K; Montenegro L; Tütüncüler F; Pereira SA; Simas V; Garcia L; Roberts SA; Macedo D; Magnuson M; Gagliardi P; Mauras N; Witchel SF; Carroll RS; Latronico AC; Kaiser UB; Abreu AP
    J Clin Endocrinol Metab; 2023 Jun; 108(7):1646-1656. PubMed ID: 36916482
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comparison of Makorin Ring Finger Protein 3 Levels Between Obese and Normal Weight Patients with Central Precocious Puberty.
    Eren SE; Şimşek E
    J Clin Res Pediatr Endocrinol; 2023 May; 15(2):182-189. PubMed ID: 36728292
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MKRN3 and KISS1R mutations in precocious and early puberty.
    Pagani S; Calcaterra V; Acquafredda G; Montalbano C; Bozzola E; Ferrara P; Gasparri M; Villani A; Bozzola M
    Ital J Pediatr; 2020 Mar; 46(1):39. PubMed ID: 32228714
    [TBL] [Abstract][Full Text] [Related]  

  • 13. MKRN3 role in regulating pubertal onset: the state of art of functional studies.
    Palumbo S; Cirillo G; Aiello F; Papparella A; Miraglia Del Giudice E; Grandone A
    Front Endocrinol (Lausanne); 2022; 13():991322. PubMed ID: 36187104
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel MKRN3 missense mutation causing familial precocious puberty.
    de Vries L; Gat-Yablonski G; Dror N; Singer A; Phillip M
    Hum Reprod; 2014 Dec; 29(12):2838-43. PubMed ID: 25316453
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Central precocious puberty caused by mutations in the imprinted gene MKRN3.
    Abreu AP; Dauber A; Macedo DB; Noel SD; Brito VN; Gill JC; Cukier P; Thompson IR; Navarro VM; Gagliardi PC; Rodrigues T; Kochi C; Longui CA; Beckers D; de Zegher F; Montenegro LR; Mendonca BB; Carroll RS; Hirschhorn JN; Latronico AC; Kaiser UB
    N Engl J Med; 2013 Jun; 368(26):2467-75. PubMed ID: 23738509
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3.
    Macedo DB; Abreu AP; Reis AC; Montenegro LR; Dauber A; Beneduzzi D; Cukier P; Silveira LF; Teles MG; Carroll RS; Junior GG; Filho GG; Gucev Z; Arnhold IJ; de Castro M; Moreira AC; Martinelli CE; Hirschhorn JN; Mendonca BB; Brito VN; Antonini SR; Kaiser UB; Latronico AC
    J Clin Endocrinol Metab; 2014 Jun; 99(6):E1097-103. PubMed ID: 24628548
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Makorin ring finger 3 gene analysis in Koreans with familial precocious puberty.
    Jeong HR; Lee HS; Hwang JS
    J Pediatr Endocrinol Metab; 2017 Oct; 30(11):1197-1201. PubMed ID: 28988223
    [TBL] [Abstract][Full Text] [Related]  

  • 18. MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations.
    Aiello F; Palumbo S; Cirillo G; Tornese G; Fava D; Wasniewska M; Faienza MF; Bozzola M; Luongo C; Festa A; Miraglia Del Giudice E; Grandone A
    J Endocrinol Invest; 2024 Jun; 47(6):1477-1485. PubMed ID: 38112911
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical and molecular genetic features of 3 family cases of the central precocious puberty, due to
    Zubkova NA; Kolodkina AA; Makretskaya NA; Okorokov PL; Pogoda TV; Vasiliev EV; Petrov VM; Tiulpakov AN
    Probl Endokrinol (Mosk); 2021 May; 67(3):55-61. PubMed ID: 34297502
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A missense mutation in MKRN3 in a Danish girl with central precocious puberty and her brother with early puberty.
    Känsäkoski J; Raivio T; Juul A; Tommiska J
    Pediatr Res; 2015 Dec; 78(6):709-11. PubMed ID: 26331766
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.