17999388 24218100 18300207 16906226 11735023 10543400 10929333 25161109 12403553 11068991 23522726 27130733 9788554 11258625 34646065 17335073 9584942 9328481 10712197 11258624 10862084 16033085 27617404 17876295 12687660 9793647 22108604 27013922 25 - Search Results

Year	Number of Results
1997	1
1998	4
1999	3
2000	6
2001	2
2002	2
2003	1
2005	1
2006	1
2007	2
2008	2
2011	1
2012	1
2013	2
2014	2
2016	3
2021	1
2022	0

1

p53 regulates FAK expression in human tumor cells.

Golubovskaya VM, Finch R, Kweh F, Massoll NA, Campbell-Thompson M, Wallace MR, Cance WG. Golubovskaya VM, et al. Mol Carcinog. 2008 May;47(5):373-82. doi: 10.1002/mc.20395. Mol Carcinog. 2008. PMID: 17999388 Free PMC article.

2

Cerebral vasculopathy in a Chinese family with neurofibromatosis type I mutation.

Liang JT, Huo LR, Bao YH, Wang ZY, Ling F. Liang JT, et al. Neurosci Bull. 2013 Dec;29(6):708-14. doi: 10.1007/s12264-013-1388-x. Epub 2013 Nov 11. Neurosci Bull. 2013. PMID: 24218100 Free PMC article.

3

Development of a simple and highly sensitive mutation screening system by enzyme mismatch cleavage with optimized conditions for standard laboratories.

Tsuji T, Niida Y. Tsuji T, et al. Electrophoresis. 2008 Apr;29(7):1473-83. doi: 10.1002/elps.200700729. Electrophoresis. 2008. PMID: 18300207 Free article.

4

The neurofibromin GAP-related domain rescues endothelial but not neural crest development in Nf1 mice.

Ismat FA, Xu J, Lu MM, Epstein JA. Ismat FA, et al. J Clin Invest. 2006 Sep;116(9):2378-84. doi: 10.1172/JCI28341. Epub 2006 Aug 10. J Clin Invest. 2006. PMID: 16906226 Free PMC article.

5

Evaluation of denaturing high performance liquid chromatography (DHPLC) for the mutational analysis of the neurofibromatosis type 1 ( NF1) gene.

Han SS, Cooper DN, Upadhyaya MN. Han SS, et al. Hum Genet. 2001 Nov;109(5):487-97. doi: 10.1007/s004390100594. Epub 2001 Oct 11. Hum Genet. 2001. PMID: 11735023

6

Evaluation of the protein truncation test and mutation detection in the NF1 gene: mutational analysis of 15 known and 40 unknown mutations.

Osborn MJ, Upadhyaya M. Osborn MJ, et al. Hum Genet. 1999 Oct;105(4):327-32. doi: 10.1007/s004399900135. Hum Genet. 1999. PMID: 10543400

7

[Treatment of scoliosis and scoliokyphosis in Recklinghausen neurofibromatosis].

Metz-Stavenhagen P, Krebs S, Seidel T, Krämer F, Völpel HJ. Metz-Stavenhagen P, et al. Orthopade. 2000 Jun;29(6):524-34. doi: 10.1007/s001320050491. Orthopade. 2000. PMID: 10929333 German.

8

Cognitive and behavioral problems in children with neurofibromatosis type 1: challenges and future directions.

Schwetye KE, Gutmann DH. Schwetye KE, et al. Expert Rev Neurother. 2014 Oct;14(10):1139-52. doi: 10.1586/14737175.2014.953931. Epub 2014 Aug 27. Expert Rev Neurother. 2014. PMID: 25161109 Review.

9

NF1 mutations and molecular testing.

Thomson SA, Fishbein L, Wallace MR. Thomson SA, et al. J Child Neurol. 2002 Aug;17(8):555-61; discussion 571-2, 646-51. doi: 10.1177/088307380201700803. J Child Neurol. 2002. PMID: 12403553 Review.

10

Identification of two novel frame shift mutations of the NF1 gene in Korean patients with neurofibromatosis type 1.

Park KC, Choi HO, Han WS, Hwang JH, Park KH, Kim KH, Chung JH, Eun HC. Park KC, et al. J Korean Med Sci. 2000 Oct;15(5):542-4. doi: 10.3346/jkms.2000.15.5.542. J Korean Med Sci. 2000. PMID: 11068991 Free PMC article.

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