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Characterization of Ras effector mutant interactions with the NF1-GAP related d…

Marshall(M S),Hettich(L A) Oncogene 1993-02-26

...NF1-GAP related domain (NF1-GRD) were investigated. The NF1-GRD was unable to stimulate the GTPase of Ras[Asn33], Ras[Se...

A search for evidence of somatic mutations in the NF1 gene.

John(A M),Ruggieri(M),Ferner(R),Upadhyaya(M) J Med Genet 2000-02-18

...NF1 germline and two somatic mutations. In a plexiform neurofibroma from an NF1 patient, mutations in both NF1 alleles h...

Leukemia-associated NF1 inactivation in patients with pediatric T-ALL and AML l…

Balgobind(Brian V),Van Vlierberghe(Pieter),v… Blood 2008-05-13

...NF1) is an autosomal dominant genetic disorder caused by mutations in the NF1 gene. Patients with NF1 have a higher risk...

Neurofibromin-deficient Schwann cells have increased lysophosphatidic acid depe…

Nebesio(Todd D),Ming(Wenyu),Chen(Shi),Clegg(… Glia 2007-03-20

...NF1 gene (Nf1-/-). LPA promoted F-actin polymerization and increased migration and survival of Nf1-/- SCs as compared to...

Somatic deletion of the NF1 gene in a neurofibromatosis type 1-associated malig…

Rübben(Albert),Bausch(Birke),Nikkels(Arjen) Mol Cancer 2006-10-10

...NF1. The classical double-hit inactivation of the NF1 gene suggests that the NF1 genetic background promoted melanoma ge...

Genetic and cellular evidence of vascular inflammation in neurofibromin-deficie…

Lasater(Elisabeth A),Li(Fang),Bessler(Waylan… J Clin Invest 2010-03-31

...NF1) results from mutations in the NF1 tumor suppressor gene, which encodes the protein neurofibromin. NF1 patients disp...

NF1 molecular characterization and neurofibromatosis type I genotype-phenotype …

Sabbagh(Audrey),Pasmant(Eric),Imbard(Apollin… Hum Mutat 2014-05-08

...NF1 patients have private loss-of-function mutations scattered along the NF1 gene. Here, we present an original NF1 inve...

Clustering of mutations in the 5' tertile of the NF1 gene in Slovakia patients …

Bolcekova(A),Nemethova(M),Zatkova(A),Hlinkov… Neoplasma 2013-11-14

...NF1; OMIM 162200). Genotype-phenotype correlations in patients with NF1 may help to determine the risk group for develop...

Cardiac characterization of 16 patients with large NF1 gene deletions.

Nguyen(R),Mir(T S),Kluwe(L),Jett(K),Kentsch(… Clin Genet 2014-04-08

...NF1) and large deletions of the NF1 gene region. The study participants were 16 patients with large NF1 deletions and 16...

Parent-of-origin in individuals with familial neurofibromatosis type 1 and opti…

Johnson(K J),Fisher(M J),Listernick(R L),Nor… Fam Cancer 2013-04-23

...NF1) is one of the most common autosomal dominant cancer syndromes worldwide. Individuals with NF1 have a wide variety o...

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