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Myelin basic protein gene dosage effects in the PNS.

Smith-Slatas(C),Barbarese(E) Mol Cell Neurosci 2000-08-02

...PMP22), two structural components of compact myelin, remain constant. The levels of P0, PMP22, Cx32, and MAG mRNA do not...

Density dependent regulation of human Schwann cell proliferation.

Casella(G T),Wieser(R),Bunge(R P),Margitic... Glia 2000-04-27

...PMP22) in regulating growth was studied. Thymidine-labeling of HSCs on collagen-coated dishes was inhibited at cell dens...

Anti-PMP22 antibodies in patients with inflammatory neuropathy.

Gabriel(C M),Gregson(N A),Hughes(R A) J Neuroimmunol 2000-04-14

...PMP22). We have investigated whether PMP22 may be important in inducing human inflammatory neuropathy. We examined sera ...

Characterisation of autoantibodies to peripheral myelin protein 22 in patient...

Ritz(M F),Lechner-Scott(J),Scott(R J),Fuhr... J Neuroimmunol 2000-04-14

...PMP22-expressing COS cells revealed that these sera did not recognise endogenous PMP22. Our results indicate that anti-P...

Role of the peripheral myelin protein 22 N-linked glycan in oligomer stabilit...

Ryan(M C),Notterpek(L),Tobler(A R),Liu(N),... J Neurochem 2000-10-05

...PMP22 facilitates, in part, the stability of the PMP22 oligomer; however, the implications of PMP22 oligomerization rema...

Exposure at the cell surface is required for gas3/PMP22 To regulate both cell...

Brancolini(C),Edomi(P),Marzinotto(S),Schne... Mol Biol Cell 2000-12-07

...PMP22 is a tetraspan membrane protein highly expressed in myelinating Schwann cells. Point mutations in the gas3/PMP22 g...

Mosaicism for Charcot-Marie-Tooth disease type 1A: onset in childhood suggest...

Rautenstrauss(B),Liehr(T),Fuchs(C),Bevot(A... Int J Mol Med 1999-03-22

...PMP22 specific probe c132G8 revealed in peripheral blood lymphocytes 60% of interphase nuclei with CMT1A duplication ind...

Autosomal dominant Charcot-Marie-Tooth disease type 1A and hereditary neuropa...

Leonardis(L),Zidar(J),Ekici(A),Peterlin(B)... Int J Mol Med 1999-03-22

...PMP22 amino acid substitution. Dominantly inherited CMT1A duplications and HNPP deletions on chromosome 17p11.2 are thus...

Temporal expression pattern of peripheral myelin protein 22 during in vivo an...

Notterpek(L),Snipes(G J),Shooter(E M) Glia 1999-06-29

...PMP22) was initially described as a minor component of peripheral myelin. Mutations affecting the PMP22 gene cause demye...

Charcot-Marie-Tooth polyneuropathy: duplication, gene dosage, and genetic het...

Lupski(J R) Pediatr Res 1999-04-16

...PMP22, located within the duplication is responsible for the demyelinating neuropathy by virtue of a gene dosage effect....

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