HomeLiterature Search
Popular searches
The interferon consensus sequence-binding protein activates transcription of th…

Zhu(C),Saberwal(G),Lu(Y),Platanias(LC),Eklun… J Biol Chem 2004-12-03

...Nf1) as an ICSBP target gene, by chromatin immunoprecipitation. Additionally, we find decreased Nf1 expression in bone m...

NF1 regulates a Ras-dependent vascular smooth muscle proliferative injury respo…

Xu(J),Ismat(FA),Wang(T),Yang(J),Epstein(JA) Circulation 2007-11-06

...NF1 in vascular smooth muscle, we generated mice with homozygous loss of the murine homolog Nf1 in smooth muscle (Nf1smK...

Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosit…

Stewart(DR),Pemov(A),Van Loo(P),Beert(E),Bre… Genes Chromosomes Cancer 2012-05-00

...NF1) is a common, autosomal dominant, tumor-predisposition syndrome that arises secondary to mutations in NF1. Glomus tu...

JNK inhibitors increase osteogenesis in Nf1-deficient cells.

Sullivan(K),El-Hoss(J),Little(DG),Schindeler… Bone 2011-12-00

...Nf1-deficient and Nf1-null primary osteoblasts. C2C12 cells, which are highly responsive to rhBMP-2, were examined with ...

Neurofibromin 1 (NF1) defects are common in human ovarian serous carcinomas and…

Sangha(N),Wu(R),Kuick(R),Powers(S),Mu(D),Fia… Neoplasia 2008-12-00

...NF1 transcripts were detected in 5 of the 6 cell lines with loss of NF1 expression. Similarly, NF1 alterations including...

A controlled register-based study of 460 neurofibromatosis 1 patients: increase…

Heervä(E),Koffert(A),Jokinen(E),Kuorilehto(T… J Bone Miner Res 2012-11-00

...NF1 patients. Medical records of NF1 and control cohorts were screened for fractures according to the International Stat...

The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular orig…

Skuse(GR),Kosciolek(BA),Rowley(PT) Am J Hum Genet 1991-09-00

...NF1) is the most common hereditary syndrome predisposing to neoplasia. NF1 is an autosomal dominant disease caused by a ...

Neurofibromatosis type 1 gene haploinsufficiency reduces AP-1 gene expression w…

Yu(X),Milas(J),Watanabe(N),Rao(N),Murthy(S),… Calcif Tissue Int 2006-03-00

...Nf1 heterozygote (Nf1(+/-)) and wild type (Nf1(+/+)) mice were treated with recombinant human PTH(1-34) or vehicle once ...

NF1 deletions in S-100 protein-positive and negative cells of sporadic and neur…

Perry(A),Roth(KA),Banerjee(R),Fuller(CE),Gut… Am J Pathol 2001-07-00

...NF1). NF1 loss was detected in four of seven PNs and one atypical PN, with deletions entirely restricted to S-100 protei...

Histopathology and clinical outcome of NF1-associated vs. sporadic malignant pe…

Hagel(C),Zils(U),Peiper(M),Kluwe(L),Gotthard… J Neurooncol 2007-04-00

...NF1 patients and 14 sporadic patients. NF1 patients were significantly younger at diagnosis (p<0.001) and had a signific...

Previous 82 83 84 85 86 87 88 89 90 Next Vol. 86 / of 901 页

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com