BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

295 related articles for article (PubMed ID: 32480405)

  • 1. Heterozygous Deletions in MKRN3 Cause Central Precocious Puberty Without Prader-Willi Syndrome.
    Meader BN; Albano A; Sekizkardes H; Delaney A
    J Clin Endocrinol Metab; 2020 Aug; 105(8):2732-9. PubMed ID: 32480405
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pathogenic and Low-Frequency Variants in Children With Central Precocious Puberty.
    Neocleous V; Fanis P; Toumba M; Gorka B; Kousiappa I; Tanteles GA; Iasonides M; Nicolaides NC; Christou YP; Michailidou K; Nicolaou S; Papacostas SS; Christoforidis A; Kyriakou A; Vlachakis D; Skordis N; Phylactou LA
    Front Endocrinol (Lausanne); 2021; 12():745048. PubMed ID: 34630334
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel Genetic and Biochemical Findings of DLK1 in Children with Central Precocious Puberty: A Brazilian-Spanish Study.
    Montenegro L; Labarta JI; Piovesan M; Canton APM; Corripio R; Soriano-Guillén L; Travieso-Suárez L; Martín-Rivada Á; Barrios V; Seraphim CE; Brito VN; Latronico AC; Argente J
    J Clin Endocrinol Metab; 2020 Oct; 105(10):. PubMed ID: 32676665
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Molecular Screening of MKRN3, DLK1, and KCNK9 Genes in Girls with Idiopathic Central Precocious Puberty.
    Grandone A; Capristo C; Cirillo G; Sasso M; Umano GR; Mariani M; Miraglia Del Giudice E; Perrone L
    Horm Res Paediatr; 2017; 88(3-4):194-200. PubMed ID: 28672280
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene.
    Grandone A; Cantelmi G; Cirillo G; Marzuillo P; Luongo C; Miraglia del Giudice E; Perrone L
    BMC Endocr Disord; 2015 Oct; 15():60. PubMed ID: 26499472
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies.
    Canton APM; Krepischi ACV; Montenegro LR; Costa S; Rosenberg C; Steunou V; Sobrier ML; Santana L; Honjo RS; Kim CA; de Zegher F; Idkowiak J; Gilligan LC; Arlt W; Funari MFA; Jorge AAL; Mendonca BB; Netchine I; Brito VN; Latronico AC
    Hum Reprod; 2021 Jan; 36(2):506-518. PubMed ID: 33313884
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome.
    Kanber D; Giltay J; Wieczorek D; Zogel C; Hochstenbach R; Caliebe A; Kuechler A; Horsthemke B; Buiting K
    Eur J Hum Genet; 2009 May; 17(5):582-90. PubMed ID: 19066619
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty.
    Dauber A; Cunha-Silva M; Macedo DB; Brito VN; Abreu AP; Roberts SA; Montenegro LR; Andrew M; Kirby A; Weirauch MT; Labilloy G; Bessa DS; Carroll RS; Jacobs DC; Chappell PE; Mendonca BB; Haig D; Kaiser UB; Latronico AC
    J Clin Endocrinol Metab; 2017 May; 102(5):1557-1567. PubMed ID: 28324015
    [TBL] [Abstract][Full Text] [Related]  

  • 13. High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic.
    Bessa DS; Macedo DB; Brito VN; França MM; Montenegro LR; Cunha-Silva M; Silveira LG; Hummel T; Bergadá I; Braslavsky D; Abreu AP; Dauber A; Mendonca BB; Kaiser UB; Latronico AC
    Neuroendocrinology; 2017; 105(1):17-25. PubMed ID: 27225315
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Central Precocious Puberty Caused by a Heterozygous Deletion in the MKRN3 Promoter Region.
    Macedo DB; França MM; Montenegro LR; Cunha-Silva M; Best DS; Abreu AP; Kaiser UB; Mendonca BB; Jorge AAL; Brito VN; Latronico AC
    Neuroendocrinology; 2018; 107(2):127-132. PubMed ID: 29763903
    [TBL] [Abstract][Full Text] [Related]  

  • 15. MKRN3 circulating levels in Prader-Willi syndrome: a pilot study.
    Mariani M; Fintini D; Cirillo G; Palumbo S; Del Giudice EM; Bocchini S; Manco M; Cappa M; Grandone A
    J Endocrinol Invest; 2022 Nov; 45(11):2165-2170. PubMed ID: 35854182
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A new pathway in the control of the initiation of puberty: the MKRN3 gene.
    Abreu AP; Macedo DB; Brito VN; Kaiser UB; Latronico AC
    J Mol Endocrinol; 2015 Jun; 54(3):R131-9. PubMed ID: 25957321
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.