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Humoral and cellular immune responses to myelin protein peptides in chronic i...

Sanvito(L),Makowska(A),Mahdi-Rogers(M),Had... J Neurol Neurosurg Psychiat... 2009-03-05

...PMP22.,Antibodies to P0, P2 or PMP22 peptides were detected in only a minority of CIDP, both not treated (nT-CIDP) and t...

Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: m...

Leal(Alejandro),Huehne(Kathrin),Bauer(Finn... Neurogenetics 2009-12-07

...Pmp22 gene dosage and expression in transgenic mice and rats. These results suggest a potential role of this protein in ...

[Hereditary peripheral neuropathies].

Vallat(Jean-Michel),Tazir(Mériem),Calvo(Ju... Presse Med 2009-09-29

...PMP22gene. In its axonal forms (CMT2), 10-20% of the cases may be associated with a mutation of the MFN2gene. For North ...

Intermittent fasting alleviates the neuropathic phenotype in a mouse model of...

Madorsky(Irina),Opalach(Katherine),Waber(A... Neurobiol Dis 2009-05-05

Charcot-Marie-Tooth type 1A (CMT1A) neuropathies linked to the misexpression of peripheral myelin protein 22 (PMP22) are...

Analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Uk...

Hryshchenko(N V),Livshits(L A) Tsitol Genet 2009-12-18

...PMP22 gene dosage measuring by means of quantitative Real- Time PCR. It has been carried out detection and analysis of 1...

Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Ch...

Keckarevic-Markovic(Milica),Milic-Rasic(Ve... J Peripher Nerv Syst 2009-10-27

...PMP22, EGR2, and LITAF/SIMPLE in 57 Charcot-Marie-Tooth (CMT) patients of Serbian origin without the PMP22 duplication. ...

Myelin sheaths are formed with proteins that originated in vertebrate lineage...

Gould(Robert M),Oakley(Todd),Goldstone(Jar... Neuron Glia Biol 2009-10-30

...PMP22) and (6) stathmin-1 (STMN1). Although widely distributed in gnathostome/vertebrate genomes, neither MBP nor MPZ ar...

[Charcot-Marie-Tooth disease].

Birouk(Nazha) Presse Med 2009-03-11

...PMP22 gene, and CMTX, due to mutations in the connexin 32 gene. Autosomal recessive forms are more frequent in North Afr...

[Diagnosis of the peripheral hereditary neuropathies and its molecular geneti...

Hernández-Zamora(Edgar),Arenas-Sordo(María... Acta Ortop Mex 2009-01-07

...PMP22. So far, there five different types of CMT (1,2,3,4,X) with approximately 32 subtypes, associated with more than 3...

Overexpression and purification of rat peroxisomal membrane protein 22, PMP22...

Egawa(Kyoko),Shibata(Hiroyuki),Yamashita(S... Protein Expr Purif 2009-02-12

...PMP22 (rPMP22) with the use of a methylotrophic yeast, Pichia pastoris, as a host. rPMP22 was localized not to peroxisom...

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