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 *

186 related articles for article (PubMed ID: 30334930)

  • 1. Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation.
    Zhao HM; Yang YJ; Duan JQ; Ouyang HJ; Liu L; Yi LC; Xiao ZH; Zheng Y; Peng L; Attard TM; Li DY; You JY
    J Pediatr Gastroenterol Nutr; 2019 Feb; 68(2):199-206. PubMed ID: 30334930
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Clinical and Molecular Genetic Study in 11 Chinese Children With Peutz-Jeghers Syndrome.
    Zheng B; Wang C; Jia Z; Liu Z; Li M; Jin Y; Pan J
    J Pediatr Gastroenterol Nutr; 2017 Apr; 64(4):559-564. PubMed ID: 27467201
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Germline mutation analysis of STK11 gene using direct sequencing and multiplex ligation-dependent probe amplification assay in Korean children with Peutz-Jeghers syndrome.
    Yang HR; Ko JS; Seo JK
    Dig Dis Sci; 2010 Dec; 55(12):3458-65. PubMed ID: 20393878
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome.
    Tan H; Mei L; Huang Y; Yang P; Li H; Peng Y; Chen C; Wei X; Pan Q; Liang D; Wu L
    BMC Med Genet; 2016 Nov; 17(1):77. PubMed ID: 27821076
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome.
    Huang Z; Miao S; Wang L; Zhang P; Wu B; Wu J; Huang Y
    BMC Gastroenterol; 2015 Nov; 15():166. PubMed ID: 26607058
    [TBL] [Abstract][Full Text] [Related]  

  • 6. First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.
    McKay V; Cairns D; Gokhale D; Mountford R; Greenhalgh L
    Fam Cancer; 2016 Jan; 15(1):57-61. PubMed ID: 26386697
    [TBL] [Abstract][Full Text] [Related]  

  • 7. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
    Aretz S; Stienen D; Uhlhaas S; Loff S; Back W; Pagenstecher C; McLeod DR; Graham GE; Mangold E; Santer R; Propping P; Friedl W
    Hum Mutat; 2005 Dec; 26(6):513-9. PubMed ID: 16287113
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients.
    Papp J; Kovacs ME; Solyom S; Kasler M; Børresen-Dale AL; Olah E
    BMC Med Genet; 2010 Nov; 11():169. PubMed ID: 21118512
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Large deletions and splicing-site mutations in the STK11 gene in Peutz-Jeghers Chilean families.
    Orellana P; López-Köstner F; Heine C; Suazo C; Pinto E; Church J; Carvallo P; Alvarez K
    Clin Genet; 2013 Apr; 83(4):365-9. PubMed ID: 22775437
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome.
    Yoo JH; Yoo JH; Choi YJ; Kang JG; Sun YK; Ki CS; Lee KA; Choi JR
    BMC Med Genet; 2008 May; 9():44. PubMed ID: 18495044
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype-phenotype correlations in Peutz-Jeghers syndrome.
    Amos CI; Keitheri-Cheteri MB; Sabripour M; Wei C; McGarrity TJ; Seldin MF; Nations L; Lynch PM; Fidder HH; Friedman E; Frazier ML
    J Med Genet; 2004 May; 41(5):327-33. PubMed ID: 15121768
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two novel STK11 mutations in three Chinese families with Peutz-Jeghers syndrome.
    Zuo YG; Xu KJ; Su B; Ho MG; Liu YH
    Chin Med J (Engl); 2007 Jul; 120(13):1183-6. PubMed ID: 17637250
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus.
    Chow E; Meldrum CJ; Crooks R; Macrae F; Spigelman AD; Scott RJ
    Clin Genet; 2006 Nov; 70(5):409-14. PubMed ID: 17026623
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients.
    Thakur N; Reddy DN; Rao GV; Mohankrishna P; Singh L; Chandak GR
    BMC Med Genet; 2006 Sep; 7():73. PubMed ID: 17010210
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.
    Zhao ZY; Jiang YL; Li BR; Yang F; Li J; Jin XW; Ning SB; Sun SH
    BMC Med Genet; 2017 Nov; 18(1):130. PubMed ID: 29141581
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.
    Hearle NC; Rudd MF; Lim W; Murday V; Lim AG; Phillips RK; Lee PW; O'donohue J; Morrison PJ; Norman A; Hodgson SV; Lucassen A; Houlston RS
    J Med Genet; 2006 Apr; 43(4):e15. PubMed ID: 16582077
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mutations of the STK11 and FHIT genes among patients with Peutz-Jeghers syndrome].
    Mao X; Zhang Y; Wang H; Mao G; Ning S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):186-90. PubMed ID: 27060312
    [TBL] [Abstract][Full Text] [Related]  

  • 18. STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients.
    Jiang YL; Zhao ZY; Li BR; Wang H; Yu ED; Ning SB
    Cancer Genet; 2019 Jan; 230():47-57. PubMed ID: 30528796
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome.
    Mehenni H; Resta N; Guanti G; Mota-Vieira L; Lerner A; Peyman M; Chong KA; Aissa L; Ince A; Cosme A; Costanza MC; Rossier C; Radhakrishna U; Burt RW; Picard D
    Dig Dis Sci; 2007 Aug; 52(8):1924-33. PubMed ID: 17404884
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation analysis of related genes in hamartoma polyp tissue of Peutz-Jeghers syndrome.
    Zhang Z; Duan FX; Gu GL; Yu PF
    World J Gastroenterol; 2020 Apr; 26(16):1926-1937. PubMed ID: 32390703
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.