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Screening for candidate genes involved in the production of mouse subventricu...

Tabata(Hidenori),Hachiya(Tsuyoshi),Nagata(... Front Neuroanat 2013-08-05

...Pmp22 were stronger. Candidate molecules responsible for primate cortical expansion through an increase in bRGs may be i...

Biopsy in a patient with PMP22 exon 2 mutation recapitulates pathology of Tre...

Madrid(Ricardo E),Lofgren(Ann),Baets(Jonat... Neuromuscul Disord 2013-09-03

...PMP22 gene. The patient never walked independently and was wheelchair bound by age 18 years. Her parents and son were un...

Sequence motifs of myelin membrane proteins: towards the molecular basis of d...

Sedzik(Jan),Jastrzebski(Jan Pawel),Ikenaka... J Neurosci Res 2013-08-05

...PMP22 had the fewest myristoylation motifs, which was only one; rat PMP22 contained no such motifs. Cholesterol recognit...

Hereditary neuropathy with liability to pressure palsy: a recurrent and bilat...

Flor-de-Lima(Filipa),Macedo(Liliana),Taipa... Case Rep Pediatr 2013-11-19

...PMP22 deletion of chromosome 17p11.2. He started motor rehabilitation and avoidance of stressing factors with progressiv...

Differential regulation of Wnt/beta-catenin signaling by Liver X Receptors in...

Shackleford(Ghjuvan'Ghjacumu),Makoukji(Joe... Biochem Pharmacol 2013-09-19

...PMP22) expression: 25-OH inhibits MPZ and PMP22 in Schwann cell line but not in oligodendrocyte cell line. Importantly, ...

Parental mosaicism of a novel PMP22 mutation with a minimal neuropathic pheno...

Taioli(Federica),Bertolasi(Laura),Ajena(Do... J Peripher Nerv Syst 2013-06-11

...PMP22) associated with an early-onset demyelinating CMT type 1 E (CMT1E) in two siblings born from asymptomatic non-cons...

Pemphigus vulgaris autoantibody profiling by proteomic technique.

Kalantari-Dehaghi(Mina),Anhalt(Grant J),Ca... PLoS One 2013-09-06

...PMP22 and HLA-E genes as well as mitochondrial proteins encoded by the NDUFS1, CYB5B, SOD2, PDHA1 and FH genes. The high...

[Therapeutic strategies for Charcot-Marie-Tooth disease].

Nakagawa(Masanori) Rinsho Shinkeigaku 2012-09-18

...PMP22 expression, and read-through of stop codon methods are expected in the near features. In addition, development of ...

Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth disease.

Maeda(Meiko Hashimoto),Mitsui(Jun),Soong(B... Ann Neurol 2012-03-09

...PMP22, MPZ, or GJB1 and gene dosage study of PMP22 did not reveal causative mutations. Hence, we applied a custom-design...

Aging of myelinating glial cells predominantly affects lipid metabolism and i...

Verdier(Valérie),Csárdi(Gábor),de Preux-Ch... Glia 2012-11-19

...Pmp22, SCAP, or Lpin1, we found that the majority of age-related transcripts were also affected in myelin mutants (54.4%...

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