主页文献库搜索
Purification of PASII/PMP22--an extremely hydrophobic glycoprotein of PNS mye...

Sedzik(J),Kotake(Y),Uyemura(K) Neuroreport 1998-08-24

...PMP22, suitable for crystallization trials. We usually obtained 10-20 mg PASII/PMP22 from 10 g bovine spinal roots. It i...

Mutation analysis of the nerve specific promoter of the peripheral myelin pro...

Nelis(E),De Jonghe(P),De Vriendt(E),Patel(... J Med Genet 1998-10-01

We analysed the nerve specific promoter of the peripheral myelin protein 22 gene (PMP22) in a set of 15 unrelated patien...

Many facets of the peripheral myelin protein PMP22 in myelination and disease...

Naef(R),Suter(U) Microsc Res Tech 1998-09-17

...PMP22 as a structural component of myelin, PMP22 has also been proposed as a regulator of Schwann cell proliferation and...

Efficient neurophysiologic selection of X-linked Charcot-Marie-Tooth families...

Nicholson(G A),Yeung(L),Corbett(A) Neurology 1998-12-03

...PMP22, Po, or connexin 32) should be screened for mutations.,The yield of connexin 32 mutations was compared in possible...

A novel PMP22 point mutation causing HNPP phenotype: studies on nerve xenogra...

Sahenk(Z),Chen(L),Freimer(M) Neurology 1998-10-20

...PMP22) gene. Point mutations that lie deep within transmembrane (TM) domains causing major structural changes in PMP22 a...

Progressive central and peripheral demyelinating disease of adult onset in a ...

Hagen(K),Boman(H),Mellgren(S I),Lindal(S),... Arch Neurol 1998-12-01

...PMP22 (17q), APP (21q), CMTX1 (Xq), or PLP (Xq).,Progressive central and peripheral demyelinating disease seems to be a ...

Induction of experimental autoimmune neuritis with peripheral myelin protein-22.

Gabriel(C M),Hughes(R A),Moore(S E),Smith(... Brain 1998-11-20

...PMP22), the gene for which is duplicated in hereditary motor sensory neuropathy type la, can also induce EAN. PMP22 cDNA...

Major histocompatibility complex class II expression and macrophage responses...

Stoll(G),Gabreëls-Festen(A A),Jander(S),Mü... Muscle Nerve 1998-10-27

...PMP22 gene, MHC class II expression was consistently up-regulated and not closely related to the extent of macrophage in...

Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease an...

Silander(K),Meretoja(P),Juvonen(V),Ignatiu... Hum Mutat 1998-08-06

...PMP22) by direct sequencing. All patients chosen for mutation screening were negative for the 1.5 Mb duplication/deletio...

Absence of mutations in peripheral myelin protein-22, myelin protein zero, an...

Stögbauer(F),Young(P),Wiebusch(H),Timmerma... Neurosci Lett 1998-04-01

...PMP22) or myelin protein zero (MPZ). Heterozygous mutations in either of these two genes are also responsible for other ...

上一页 63 64 65 66 67 68 69 70 71 下一页 67 / 共 82

联系地址

山东省济南市章丘区文博路2号

齐鲁师范学院 genelibs生信实验室

山东省济南市高新区舜华路750号

大学科技园北区F座4单元2楼

电话: 0531-88819269

微信公众号

关注微信订阅号,实时查看信息,关注医学生物学动态。


商务邮箱

E-mail: [email protected]