BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 33413516)

  • 1. Molecular screening of PROKR2 gene in girls with idiopathic central precocious puberty.
    Aiello F; Cirillo G; Cassio A; Di Mase R; Tornese G; Umano GR; Miraglia Del Giudice E; Grandone A
    Ital J Pediatr; 2021 Jan; 47(1):5. PubMed ID: 33413516
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early puberty.
    Fukami M; Suzuki E; Izumi Y; Torii T; Narumi S; Igarashi M; Miyado M; Katsumi M; Fujisawa Y; Nakabayashi K; Hata K; Umezawa A; Matsubara Y; Yamauchi J; Ogata T
    J Cell Mol Med; 2017 Oct; 21(10):2623-2626. PubMed ID: 28338294
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Mutations of the KISS1 gene in disorders of puberty.
    Silveira LG; Noel SD; Silveira-Neto AP; Abreu AP; Brito VN; Santos MG; Bianco SD; Kuohung W; Xu S; Gryngarten M; Escobar ME; Arnhold IJ; Mendonca BB; Kaiser UB; Latronico AC
    J Clin Endocrinol Metab; 2010 May; 95(5):2276-80. PubMed ID: 20237166
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 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. 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]  

  • 10. The response to gonadotropin releasing hormone (GnRH) stimulation test does not predict the progression to true precocious puberty in girls with onset of premature thelarche in the first three years of life.
    Bizzarri C; Spadoni GL; Bottaro G; Montanari G; Giannone G; Cappa M; Cianfarani S
    J Clin Endocrinol Metab; 2014 Feb; 99(2):433-9. PubMed ID: 24297793
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Central precocious puberty in a girl and early puberty in her brother caused by a novel mutation in the MKRN3 gene.
    Settas N; Dacou-Voutetakis C; Karantza M; Kanaka-Gantenbein C; Chrousos GP; Voutetakis A
    J Clin Endocrinol Metab; 2014 Apr; 99(4):E647-51. PubMed ID: 24438377
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.
    Abreu AP; Trarbach EB; de Castro M; Frade Costa EM; Versiani B; Matias Baptista MT; Garmes HM; Mendonca BB; Latronico AC
    J Clin Endocrinol Metab; 2008 Oct; 93(10):4113-8. PubMed ID: 18682503
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways.
    Libri DV; Kleinau G; Vezzoli V; Busnelli M; Guizzardi F; Sinisi AA; Pincelli AI; Mancini A; Russo G; Beck-Peccoz P; Loche S; Crivellaro C; Maghnie M; Krausz C; Persani L; Bonomi M;
    J Clin Endocrinol Metab; 2014 Mar; 99(3):E458-63. PubMed ID: 24276467
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Absence of GPR54 and TACR3 mutations in sporadic cases of idiopathic central precocious puberty.
    Leka-Emiri S; Louizou E; Kambouris M; Chrousos G; De Roux N; Kanaka-Gantenbein C
    Horm Res Paediatr; 2014; 81(3):177-81. PubMed ID: 24434351
    [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. 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]  

  • 18. Genetic Variations of the KISS1R Gene in Korean Girls with Central Precocious Puberty.
    Oh YJ; Rhie YJ; Nam HK; Kim HR; Lee KH
    J Korean Med Sci; 2017 Jan; 32(1):108-114. PubMed ID: 27914139
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes: pathophysiology and genotype-phenotype correlations.
    Sarfati J; Dodé C; Young J
    Front Horm Res; 2010; 39():121-132. PubMed ID: 20389090
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GPR54 polymorphisms in Chinese girls with central precocious puberty.
    Luan X; Yu H; Wei X; Zhou Y; Wang W; Li P; Gan X; Wei D; Xiao J
    Neuroendocrinology; 2007; 86(2):77-83. PubMed ID: 17700012
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.