1 rocutaneous diseases neurofibromatosis 1 and
neurofibromatosis 2.
2 molecular bases for neurofibromatosis 1 and
neurofibromatosis 2.
3 ion as a mediator of pathologies relevant to
Neurofibromatosis 2.
4 of individuals with neurofibromatosis 1 and
neurofibromatosis 2.
5 the familial schwannomas and meningiomas of
neurofibromatosis 2 and their sporadic counterparts.
6 ncoded by the gene for the tumour suppressor
neurofibromatosis-2 and is a member of the Ezrin-Radixin
7 The genes for neurofibromatosis 1,
neurofibromatosis 2,
and one of two forms of tuberous sc
8 Neurofibromatosis 1,
neurofibromatosis 2,
and tuberous sclerosis are a set of
9 Neurofibromatosis 1 and
neurofibromatosis 2 are autosomal dominant genetic disor
10 Neurofibromatosis 2-
associated vestibular schwannomas ha
11 NF2 (
neurofibromatosis 2,
encoding the merlin protein) gene m
12 the tumor suppressor Merlin, encoded by the
neurofibromatosis 2 gene.
13 of Merlin, we are investigating a Drosophila
Neurofibromatosis-2 homologue, Merlin.
14 Neurofibromatosis-2 is an inherited disorder characteriz
15 er), a homolog of the human tumor suppressor
neurofibromatosis 2,
is required to coordinate prolifera
16 The
neurofibromatosis 2 (
NF2 ) gene product, merlin, is a t
17 the inherited cancer predisposition syndrome
neurofibromatosis 2 (
NF2) develop several central nervou
18 Neurofibromatosis 2 (
NF2) features bilateral vestibular
19 Biallelic mutations in the
neurofibromatosis 2 (
NF2) gene are linked to schwannoma
20 Mutations in the
neurofibromatosis 2 (
NF2) gene are the predominant cause
21 s bearing a loss-of-function mutation in the
neurofibromatosis 2 (
NF2) gene require MLK3.
22 Mutations in the
neurofibromatosis 2 (
NF2) gene with the resultant loss o
23 Merlin, encoded by the
Neurofibromatosis 2 (
NF2) gene, is a multifunctional tum
24 Inactivating mutations of the
neurofibromatosis 2 (
NF2) gene, NF2, result predominantl
25 ation of Stat-3 by a mechanism involving the
neurofibromatosis 2 (
NF2) gene.
26 Individuals with the
neurofibromatosis 2 (
NF2) inherited tumor predisposition
27 Neurofibromatosis 2 (
NF2) is a dominantly inherited diso
28 Neurofibromatosis 2 (
NF2) is a tumor predisposition synd
29 Neurofibromatosis 2 (
NF2) is a tumor suppressor, althoug
30 Neurofibromatosis 2 (
NF2) is an autosomal dominant disea
31 Neurofibromatosis 2 (
NF2) is an inherited cancer syndrom
32 Neurofibromatosis 2 (
NF2) is an inherited cancer syndrom
33 ted recently by the discovery that the human
neurofibromatosis 2 (
NF2) tumor suppressor gene encodes
34 Mutations of the
neurofibromatosis 2 (
NF2) tumor suppressor gene have fre
35 Mutation of the
Neurofibromatosis 2 (
NF2) tumor suppressor gene leads to
36 his finding led to the identification of the
neurofibromatosis 2 (
NF2) tumor suppressor gene on 22q12
37 The
neurofibromatosis 2 (
NF2) tumor suppressor gene product,
38 s motif that binds to MERLIN, the product of
Neurofibromatosis 2 (
NF2) tumor suppressor gene.
39 We further show that the
Neurofibromatosis 2 (
Nf2) tumor suppressor inhibits Yap
40 xamine the mechanism by which the Drosophila
Neurofibromatosis 2 (
NF2) tumor suppressor ortholog Merl
41 The
neurofibromatosis 2 (
NF2) tumor suppressor protein, merl
42 The
neurofibromatosis 2 (
NF2) tumor suppressor protein, schw
43 cer syndromes, neurofibromatosis 1 (NF1) and
neurofibromatosis 2 (
NF2), develop both benign and malig
44 homologue of the human tumor suppressor gene
Neurofibromatosis 2 (
NF2), is required for the regulatio
45 ry genes have been identified, including the
Neurofibromatosis 2 (
NF2), Tumor Suppressor in Lung Canc
46 is 1 (NF1) has been inextricably linked with
neurofibromatosis 2 (
NF2).
47 Here we show that the tumor suppressor
neurofibromatosis 2 (
Nf2; merlin) limits the expansion o
48 The
Neurofibromatosis-2 (
NF2) tumor suppressor merlin negati
49 we isolated earlier as an interactor of the
neurofibromatosis 2 protein merlin, was independently id
50 gnostic criteria for neurofibromatosis 1 and
neurofibromatosis 2,
recommendations for the care of pat
51 ologues of two well-studied genes, the human
Neurofibromatosis 2 tumor suppressor and the yeast CDC42
52 The
neurofibromatosis 2 tumor suppressor gene product merlin
53 eins, whose members include Protein 4.1, the
Neurofibromatosis 2 tumor suppressor Merlin, Expanded, t
54 The
neurofibromatosis 2 tumor suppressor protein schwannomin
55 Merlin, the
neurofibromatosis 2 tumor suppressor protein, has two ma
56 Merlin, the
neurofibromatosis 2 tumor suppressor protein, is related
57 The
neurofibromatosis 2 tumor suppressor protein, merlin or
58 HE-RF) as a novel interactor for merlin, the
neurofibromatosis 2 tumor suppressor protein.
59 The
Neurofibromatosis-2 tumor suppressor gene encodes Merlin