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Article title matches
- Category:Neurofibromatosis (48 bytes)
1: List of pages with the keyword Neurofibromatosis - Category:Type i neurofibromatosis (55 bytes)
1: List of pages with the keyword Type i neurofibromatosis - Category:Neurofibromatosis type 1 (55 bytes)
1: List of pages with the keyword Neurofibromatosis type 1 - Category:Neurofibromatosis type i (55 bytes)
1: List of pages with the keyword Neurofibromatosis type i
Page text matches
- 7lwh (5,189 bytes)
11: ...t/MERL_HUMAN MERL_HUMAN] Neurofibromatosis type 3;Neurofibromatosis type 2. The disease is caused by mutations affect...
16: The Neurofibromatosis type 2 gene encodes the Nf2/merlin tumor suppress... - 1h4r (5,314 bytes)
2: ...ystal Structure of the FERM domain of Merlin, the Neurofibromatosis 2 Tumor Suppressor Protein.==
11: ...t/MERL_HUMAN MERL_HUMAN] Neurofibromatosis type 3;Neurofibromatosis type 2. The disease is caused by mutations affect...
26: Neurofibromatosis type 2 is an autosomal dominant disorder characte...
28: The structure of the FERM domain of merlin, the neurofibromatosis type 2 gene product.,Kang BS, Cooper DR, Devedjie... - 1n99 (4,337 bytes)
24: ...d with merlin, the product of the causal gene for neurofibromatosis type II. We report a crystal structure of the fun... - 1nf1 (7,228 bytes)
10: ...ID:11704931</ref> Defects in NF1 are a cause of neurofibromatosis-Noonan syndrome (NFNS) [MIM:[https://omim.org/ent...
25: ...alteration is responsible for the pathogenesis of neurofibromatosis type 1 (NF1), one of the most frequent genetic di... - 2d4q (5,342 bytes)
2: ...ystal structure of the Sec-PH domain of the human neurofibromatosis type 1 protein==
11: ...ID:11704931</ref> Defects in NF1 are a cause of neurofibromatosis-Noonan syndrome (NFNS) [MIM:[https://omim.org/ent... - 2e2x (7,626 bytes)
11: ...ID:11704931</ref> Defects in NF1 are a cause of neurofibromatosis-Noonan syndrome (NFNS) [MIM:[https://omim.org/ent...
26: ...sible for the pathogenesis of the common disorder Neurofibromatosis type I (NF1). The only well-characterized functio... - Sandbox Reserved 720 (8,377 bytes)
12: ... an inheritable autosomal dominant disorder : the Neurofibromatosis type 2. This desease is characterized by tumor pr... - 1isn (4,412 bytes)
23: Neurofibromatosis type 2 (NF2) is a dominantly inherited disease as...
25: Structural basis for neurofibromatosis type 2. Crystal structure of the merlin FERM doma... - Xavière Lornage/Sandbox1 (7,830 bytes)
10: ... an inheritable autosomal dominant disorder : the Neurofibromatosis type 2. This desease is characterized by tumor pr... - Category:Neurofibromatosis (48 bytes)
1: List of pages with the keyword Neurofibromatosis - Sandbox Reserved 705 (8,208 bytes)
11: ... is encoded by the Neurofibromatosis-2(Nf2) gene. Neurofibromatosis type 2 is an inheritable autosomal dominant disor... - Category:Type i neurofibromatosis (55 bytes)
1: List of pages with the keyword Type i neurofibromatosis - 3p7z (6,404 bytes)
11: ...ID:11704931</ref> Defects in NF1 are a cause of neurofibromatosis-Noonan syndrome (NFNS) [MIM:[https://omim.org/ent...
16: Neurofibromatosis type 1 (NF1) is a common genetic disorder caused ... - 3peg (6,445 bytes)
11: ...ID:11704931</ref> Defects in NF1 are a cause of neurofibromatosis-Noonan syndrome (NFNS) [MIM:[https://omim.org/ent...
16: Neurofibromatosis type 1 (NF1) is a common genetic disorder caused ... - 3pg7 (6,286 bytes)
11: ...ID:11704931</ref> Defects in NF1 are a cause of neurofibromatosis-Noonan syndrome (NFNS) [MIM:[https://omim.org/ent...
16: Neurofibromatosis type 1 (NF1) is a common genetic disorder caused ... - 3u8z (2,596 bytes)
10: ...t/MERL_HUMAN MERL_HUMAN] Neurofibromatosis type 3;Neurofibromatosis type 2. The disease is caused by mutations affect... - 4eqc (6,155 bytes)
14: ...a requirement for the PAKs in the pathogenesis of Neurofibromatosis type 2 (NF2), a dominantly inherited cancer disor...
16: ... p21-activated Kinases, Inhibits Tumorigenesis of Neurofibromatosis Type 2 (NF2)-associated Schwannomas.,Licciulli S,... - 3wa0 (4,461 bytes)
13: Merlin, a tumor suppressor encoded by the neurofibromatosis type 2 gene, has been shown to suppress tumorigen... - 4tu7 (4,367 bytes)
14: ...the major class of 3' splice sites. We found that neurofibromatosis- or retinitis pigmentosa-causing mutations in the... - 4tu8 (4,337 bytes)
14: ...the major class of 3' splice sites. We found that neurofibromatosis- or retinitis pigmentosa-causing mutations in the...
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