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 *

60 related articles for article (PubMed ID: 24604241)

  • 1. Novel and recurrent mutations of STK11 gene in six Chinese cases with Peutz-Jeghers syndrome.
    Dai L; Fu L; Liu D; Zhang K; Wu Y; Meng H; Zhang B; Guan X; Guo H; Bai Y
    Dig Dis Sci; 2014 Aug; 59(8):1856-61. PubMed ID: 24604241
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Two missense
    Liu J; Zeng SC; Wang A; Cheng HY; Zhang QJ; Lu GX
    World J Gastrointest Oncol; 2024 Apr; 16(4):1532-1546. PubMed ID: 38660671
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multidisciplinary management for Peutz-Jeghers syndrome and prevention of vertical transmission to offspring using preimplantation genetic testing.
    Xu X; Song R; Hu K; Li Y; Jin H; Chen B; Song W; Zhang Y; Xu J; Sun Y
    Orphanet J Rare Dis; 2022 Feb; 17(1):64. PubMed ID: 35189935
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The molecular basis and clinical aspects of Peutz-Jeghers syndrome.
    Hemminki A
    Cell Mol Life Sci; 1999 May; 55(5):735-50. PubMed ID: 10379360
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Distinctive Adnexal (Usually Paratubal) Neoplasm Often Associated With Peutz-Jeghers Syndrome and Characterized by STK11 Alterations (STK11 Adnexal Tumor): A Report of 22 Cases.
    Bennett JA; Young RH; Howitt BE; Croce S; Wanjari P; Zhen C; Da Cruz Paula A; Meserve E; Schoolmeester JK; Westbom-Fremer S; Benzi E; Patil NM; Kooreman L; El-Bahrawy M; Zannoni GF; Krausz T; McCluggage WG; Weigelt B; Ritterhouse LL; Oliva E
    Am J Surg Pathol; 2021 Aug; 45(8):1061-1074. PubMed ID: 33534223
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lobular endocervical glandular hyperplasia and peritoneal pigmentation associated with Peutz-Jeghers syndrome due to a germline mutation of STK11.
    Hirasawa A; Akahane T; Tsuruta T; Kobayashi Y; Masuda K; Banno K; Fujii T; Susumu N; Itsubo T; Kameyama K; Sugano K; Aoki D
    Ann Oncol; 2012 Nov; 23(11):2990-2992. PubMed ID: 23038761
    [No Abstract]   [Full Text] [Related]  

  • 9. Changes of gut microbiota and short chain fatty acids in patients with Peutz-Jeghers syndrome.
    Zhou A; Tang B; Xie Y; Li S; Xiao X; Wu L; Tu D; Wang S; Feng Y; Feng X; Lai Y; Ning S; Yang S
    BMC Microbiol; 2023 Nov; 23(1):373. PubMed ID: 38036954
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prediction of Deleterious Non-synonymous SNPs of Human STK11 Gene by Combining Algorithms, Molecular Docking, and Molecular Dynamics Simulation.
    Islam MJ; Khan AM; Parves MR; Hossain MN; Halim MA
    Sci Rep; 2019 Nov; 9(1):16426. PubMed ID: 31712642
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Generation of an iPSC line (TSHSUi001-A) from a patient with Peutz-Jeghers syndrome due to STK11 mutation.
    Wang T; Zhu K; Yu W; Peng L; Wang H; Wu Q
    Stem Cell Res; 2023 Sep; 71():103152. PubMed ID: 37392704
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel stop codon mutation in STK11 gene is associated with Peutz-Jeghers Syndrome and elevated cancer risk: a case study.
    Khanabadi B; Najafgholizadeh Seyfi D; Rejali L; Taleghani MY; Tavallaei M; Shahrokh S; Daskar Abkenar E; Naderi Noukabadi F; Asadzadeh Aghdaei H; Nazemalhosseini Mojarad E
    Gastroenterol Hepatol Bed Bench; 2023; 16(3):341-346. PubMed ID: 37767326
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical characteristics and genetic analysis of gene mutations in a Chinese pedigree with Peutz-Jeghers syndrome.
    Qiu Y; Xuan T; Yin M; Gao Z; Guo P; Chen X; Ye Y; Shen Z
    Clin Case Rep; 2019 Apr; 7(4):735-739. PubMed ID: 30997075
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expression of
    Alkaf A; Al-Jafari A; Wani TA; Alqattan S; Zargar S
    3 Biotech; 2017 Dec; 7(6):362. PubMed ID: 29043114
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A single-nucleotide polymorphism in serine-threonine kinase 11, the gene encoding liver kinase B1, is a risk factor for multiple sclerosis.
    Boullerne AI; Skias D; Hartman EM; Testai FD; Kalinin S; Polak PE; Feinstein DL
    ASN Neuro; 2015; 7(1):. PubMed ID: 25694554
    [TBL] [Abstract][Full Text] [Related]  

  • 16. STK11 Adnexal Tumor in an Adolescent Female: Diagnostic Pitfalls of a Recently Described Entity.
    Sharma AE; Slack JC; Parra-Herran CE; Quade BJ; Shusterman S; Church AJ; Kolin DL; Carreon CK
    Pediatr Dev Pathol; 2023; 26(5):486-493. PubMed ID: 37334562
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exploring the histogenesis of STK11 adnexal tumour using electron microscopy.
    Mascaro N; Aboelnasr LS; Masood M; Yague E; Moran L; El-Bahrawy M
    Virchows Arch; 2024 Feb; ():. PubMed ID: 38376618
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel
    Forte G; Cariola F; De Marco K; Manghisi A; Guglielmi FA; Armentano R; Lippolis G; Giorgio P; Simone C; Disciglio V
    Genes Dis; 2022 Mar; 9(2):288-291. PubMed ID: 35224145
    [No Abstract]   [Full Text] [Related]  

  • 19. Corrigendum to 'A novel
    Forte G; Cariola F; De Marco K; Manghisi A; Guglielmi FA; Armentano R; Lippolis G; Giorgio P; Simone C; Disciglio V
    Genes Dis; 2024 Mar; 11(2):1082-1083. PubMed ID: 37692472
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing.
    Bodian DL; McCutcheon JN; Kothiyal P; Huddleston KC; Iyer RK; Vockley JG; Niederhuber JE
    PLoS One; 2014; 9(4):e94554. PubMed ID: 24728327
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.