Similar articles for PMID: 15987703

Year	Number of Results
1997	1
1998	9
1999	16
2000	11
2001	12
2002	12
2003	15
2004	18
2005	15
2006	18
2007	13
2008	11
2009	9
2010	6
2011	10
2012	6
2013	7
2014	5
2015	3
2016	4
2017	4
2018	6
2019	6
2020	6
2021	3
2022	2
2023	1
2024	0

1

LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes.

Mehenni H, Lin-Marq N, Buchet-Poyau K, Reymond A, Collart MA, Picard D, Antonarakis SE. Mehenni H, et al. Hum Mol Genet. 2005 Aug 1;14(15):2209-19. doi: 10.1093/hmg/ddi225. Epub 2005 Jun 29. Hum Mol Genet. 2005. PMID: 15987703

2

Loss of cytoplasmic retention ability of mutant LKB1 found in Peutz-Jeghers syndrome patients.

Nezu J, Oku A, Shimane M. Nezu J, et al. Biochem Biophys Res Commun. 1999 Aug 11;261(3):750-5. doi: 10.1006/bbrc.1999.1047. Biochem Biophys Res Commun. 1999. PMID: 10441497

3

Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients.

Boudeau J, Kieloch A, Alessi DR, Stella A, Guanti G, Resta N. Boudeau J, et al. Hum Mutat. 2003 Feb;21(2):172. doi: 10.1002/humu.9112. Hum Mutat. 2003. PMID: 12552571

4

LKB1, a novel serine/threonine protein kinase and potential tumour suppressor, is phosphorylated by cAMP-dependent protein kinase (PKA) and prenylated in vivo.

Collins SP, Reoma JL, Gamm DM, Uhler MD. Collins SP, et al. Biochem J. 2000 Feb 1;345 Pt 3(Pt 3):673-80. Biochem J. 2000. PMID: 10642527 Free PMC article.

5

De novo germline mutation in the serine-threonine kinase STK11/LKB1 gene associated with Peutz-Jeghers syndrome.

Hernan I, Roig I, Martin B, Gamundi MJ, Martinez-Gimeno M, Carballo M. Hernan I, et al. Clin Genet. 2004 Jul;66(1):58-62. doi: 10.1111/j.0009-9163.2004.00266.x. Clin Genet. 2004. PMID: 15200509

6

Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families.

Westerman AM, Entius MM, Boor PP, Koole R, de Baar E, Offerhaus GJ, Lubinski J, Lindhout D, Halley DJ, de Rooij FW, Wilson JH. Westerman AM, et al. Hum Mutat. 1999;13(6):476-81. doi: 10.1002/(SICI)1098-1004(1999)13:6<476::AID-HUMU7>3.0.CO;2-2. Hum Mutat. 1999. PMID: 10408777

7

Stability of the Peutz-Jeghers syndrome kinase LKB1 requires its binding to the molecular chaperones Hsp90/Cdc37.

Nony P, Gaude H, Rossel M, Fournier L, Rouault JP, Billaud M. Nony P, et al. Oncogene. 2003 Dec 11;22(57):9165-75. doi: 10.1038/sj.onc.1207179. Oncogene. 2003. PMID: 14668798

8

Mutations in the human LKB1/STK11 gene.

Launonen V. Launonen V. Hum Mutat. 2005 Oct;26(4):291-7. doi: 10.1002/humu.20222. Hum Mutat. 2005. PMID: 16110486 Review.

9

Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients.

Resta N, Stella A, Susca FC, Di Giacomo M, Forleo G, Miccolis I, Rossini FP, Genuardi M, Piepoli A, Grammatico P, Guanti G. Resta N, et al. Hum Mutat. 2002 Jul;20(1):78-9. doi: 10.1002/humu.9046. Hum Mutat. 2002. PMID: 12112668

10

A novel germline mutation of the LKB1 gene in a patient with Peutz-Jeghers syndrome with early-onset gastric cancer.

Takahashi M, Sakayori M, Takahashi S, Kato T, Kaji M, Kawahara M, Suzuki T, Kato S, Kato S, Shibata H, Murakawa Y, Yoshioka T, Ishioka C. Takahashi M, et al. J Gastroenterol. 2004 Dec;39(12):1210-4. doi: 10.1007/s00535-004-1474-y. J Gastroenterol. 2004. PMID: 15622488

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