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Screening for mutations in a genetically heterogeneous disorder: DHPLC versus...

Takashima(H),Boerkoel(C F),Lupski(J R) Genet Med 2002-01-31

...PMP22, MPZ, GJB1 and EGR2. (2) Comparison of DHPLC with DNA sequencing for mutation detection in 168 patient DNA samples...

Two different targeting signals direct human peroxisomal membrane protein 22 ...

Brosius(Ute),Dehmel(Thomas),Gärtner(Jutta) J Biol Chem 2002-01-24

...PMP22 and most other peroxisomal membrane proteins, we showed that human as well as rat PMP22 contains two distinct and ...

Competitive binding of triplex-forming oligonucleotides in the two alternate ...

Hai(M),Bidichandani(S I),Hogan(M E),Patel(... Antisense Nucleic Acid Drug... 2002-03-05

...PMP22) causes the inherited peripheral neuropathy, Charcot-Marie-Tooth disease type 1A (CMT1A). In an attempt to alter P...

Peripheral myelin protein 22 is a constituent of intercellular junctions in e...

Notterpek(L),Roux(K J),Amici(S A),Yazdanpo... Proc Natl Acad Sci U S A 2002-01-10

...PMP22 expression is highest in myelinating Schwann cells of peripheral nerves; however, significant levels of PMP22 mRNA...

Human Connexin 32, a gap junction protein altered in the X-linked form of Cha...

Bondurand(N),Girard(M),Pingault(V),Lemort(... Hum Mol Genet 2002-03-13

...PMP22 and Connexin 32, three major proteins of the peripheral myelin. Our study shows that this factor, in synergy with ...

Progesterone synthesis and myelin formation in peripheral nerves.

Schumacher(M),Guennoun(R),Mercier(G),Désar... Brain Res Brain Res Rev 2002-02-11

...PMP22). Recently, it has been proposed that progesterone may indirectly regulate myelin formation by influencing gene ex...

Neuroactive steroids and peripheral myelin proteins.

Magnaghi(V),Cavarretta(I),Galbiati(M),Mart... Brain Res Brain Res Rev 2002-02-11

...PMP22)) in the peripheral nervous system. Utilizing different in vivo (aged and adult male rats) and in vitro (Schwann c...

Disease mechanisms and potential therapeutic strategies in Charcot-Marie-Toot...

Young(P),Suter(U) Brain Res Brain Res Rev 2002-02-08

...pmp22) gene in the Trembler mouse in 1992, the groundwork was laid down for a novel chapter in the elucidation of the mo...

Hereditary neuropathy with liability to pressure palsies associated with cent...

Dacković(J),Rakocević-Stojanović(V),Pavlov... Eur J Neurol 2002-03-01

...PMP22) gene. Mutations resulting in functional loss of one PMP22 gene copy are less frequent. We present a 51-year-old p...

Congenital hypomyelination neuropathy in a newborn infant: unusual cause of d...

Hahn(J S),Henry(M),Hudgins(L),Madan(A) Pediatrics 2001-12-14

...PMP22, and EGR2 was negative. Several attempts at extubation failed and the infant became increasingly ventilator-depend...

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