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Similar articles for PubMed (Select 11668633)

2.

Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.

Borun P, De Rosa M, Nedoszytko B, Walkowiak J, Plawski A.

Fam Cancer. 2015 Apr 5. [Epub ahead of print]

PMID:
25841653
3.

Gene mutations in chronic kidney disease patients with secondary hyperparathyroidism and Sagliker syndrome.

Demirhan O, Arslan A, Sagliker Y, Akbal E, Ergun S, Bayraktar R, Sagliker HS, Dogan E, Gunesacar R, Ozkaynak PS.

J Ren Nutr. 2015 Mar;25(2):176-86. doi: 10.1053/j.jrn.2014.12.008. Review.

PMID:
25701941
4.

Somatic STK11 and concomitant STK11/KRAS mutational frequency in stage IV lung adenocarcinoma adrenal metastases.

Gleeson FC, Kipp BR, Levy MJ, Voss JS, Campion MB, Minot DM, Tu ZJ, Klee EW, Lazaridis KN, Kerr SE.

J Thorac Oncol. 2015 Mar;10(3):531-4. doi: 10.1097/JTO.0000000000000391.

PMID:
25695224
5.

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 Feb 18;7(1). pii: 1759091415568914. doi: 10.1177/1759091415568914. Print 2015 Jan-Feb.

6.

Identification and expression analysis of a novel intragenic EFNB1 mutation causing craniofrontonasal syndrome.

Chacon-Camacho OF, Arce-Gonzalez R, Villegas-Ruiz V, Pelcastre-Luna E, Uría-Gómez CE, Granillo-Alvarez M, Zenteno JC.

Meta Gene. 2013 Nov 28;2:25-31. doi: 10.1016/j.mgene.2013.11.001. eCollection 2014 Dec.

7.

Microdeletion of 19p13.3 in a girl with Peutz-Jeghers syndrome, intellectual disability, hypotonia, and distinctive features.

Kuroda Y, Saito T, Nagai J, Ida K, Naruto T, Masuno M, Kurosawa K.

Am J Med Genet A. 2015 Feb;167A(2):389-93. doi: 10.1002/ajmg.a.36813. Epub 2014 Dec 8.

PMID:
25487640
8.

Short intronic repeat sequences facilitate circular RNA production.

Liang D, Wilusz JE.

Genes Dev. 2014 Oct 15;28(20):2233-47. doi: 10.1101/gad.251926.114. Epub 2014 Oct 3.

9.

Impact of G-quadruplex structures and intronic polymorphisms rs17878362 and rs1642785 on basal and ionizing radiation-induced expression of alternative p53 transcripts.

Perriaud L, Marcel V, Sagne C, Favaudon V, Guédin A, De Rache A, Guetta C, Hamon F, Teulade-Fichou MP, Hainaut P, Mergny JL, Hall J.

Carcinogenesis. 2014 Dec;35(12):2706-15. doi: 10.1093/carcin/bgu206. Epub 2014 Sep 30.

PMID:
25269805
10.

Loss of LKB1 in high-grade endometrial carcinoma: LKB1 is a novel transcriptional target of p53.

Co NN, Iglesias D, Celestino J, Kwan SY, Mok SC, Schmandt R, Lu KH.

Cancer. 2014 Nov 15;120(22):3457-68. doi: 10.1002/cncr.28854. Epub 2014 Jul 16.

PMID:
25042259
11.

Peutz-Jeghers syndrome with germline mutation of STK11.

Chae HD, Jeon CH.

Ann Surg Treat Res. 2014 Jun;86(6):325-30. doi: 10.4174/astr.2014.86.6.325. Epub 2014 May 23.

12.

[Mutation analysis of STK11 gene in a Chinese family with Peutz-Jeghers syndrome].

Zhao X, Huang Y, Yang B, Zhao Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):294-7. doi: 10.3760/cma.j.issn.1003-9406.2014.03.008. Chinese.

PMID:
24928005
13.

Identification of novel mutations in the VPS33B gene involved in arthrogryposis, renal dysfunction, and cholestasis syndrome.

Seo SH, Hwang SM, Ko JM, Ko JS, Hyun YJ, Cho SI, Park H, Kim SY, Seong MW, Park SS.

Clin Genet. 2015 Jul;88(1):80-4. doi: 10.1111/cge.12442. Epub 2014 Aug 7.

PMID:
24917129
14.

Umbilical pigmentation in Peutz-Jeghers syndrome.

Morrison PT, Donnelly DE, Morrison PJ.

Clin Dysmorphol. 2014 Jul;23(3):114-5. doi: 10.1097/MCD.0000000000000044. No abstract available.

PMID:
24878829
15.

Three uncommon KEL alleles in one family with unusual Kell phenotypes explain a 35-year old conundrum.

Karamatic Crew V, Poole J, Burton N, Daniels G.

Vox Sang. 2014 Apr;106(3):242-7.

PMID:
24795954
16.

Intronic splicing mutations in PTCH1 cause Gorlin syndrome.

Bholah Z, Smith MJ, Byers HJ, Miles EK, Evans DG, Newman WG.

Fam Cancer. 2014 Sep;13(3):477-80. doi: 10.1007/s10689-014-9712-9.

PMID:
24659465
17.

STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.

Wang Z, Wu B, Mosig RA, Chen Y, Ye F, Zhang Y, Gong W, Gong L, Huang F, Wang X, Nie B, Zheng H, Cui M, Wang Y, Wang J, Chen C, Polydorides AD, Zhang DY, Martignetti JA, Jiang B.

Hum Mutat. 2014 Jul;35(7):851-8. doi: 10.1002/humu.22549. Epub 2014 Jun 3.

PMID:
24652667
18.

Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene.

Caridi G, Dagnino M, Erdeve O, Di Duca M, Yildiz D, Alan S, Atasay B, Arsan S, Campagnoli M, Galliano M, Minchiotti L.

Biochem Med (Zagreb). 2014 Feb 15;24(1):151-8. doi: 10.11613/BM.2014.017. eCollection 2014.

19.

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. doi: 10.1007/s10620-014-3077-7. Epub 2014 Mar 7.

PMID:
24604241
20.

A tumor of the uterine cervix with a complex histology in a Peutz-Jeghers syndrome patient with genomic deletion of the STK11 exon 1 region.

Kobayashi Y, Masuda K, Kimura T, Nomura H, Hirasawa A, Banno K, Susumu N, Sugano K, Aoki D.

Future Oncol. 2014 Feb;10(2):171-7. doi: 10.2217/fon.13.180.

PMID:
24490603
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