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1  primary deficiencies of LAMP-2, a principal lysosomal membrane protein.
2 ene product, cystinosin, is a novel integral lysosomal membrane protein.
3 rane protein, cystinosin, with features of a lysosomal membrane protein.
4 complex-related intracellular trafficking of lysosomal membrane proteins.
5 vitro and in vivo and impairs the sorting of lysosomal membrane proteins.
6  human chromosome 13 is LAMP1, which encodes lysosomal membrane protein 1.
7                                              Lysosomal membrane protein 2 (LAMP-2) is a target of ant
8 no acids of the N-terminal domain of NPC1, a lysosomal membrane protein, abolish its cholesterol bind
9 ulate in lysosomes, alter the trafficking of lysosomal membrane proteins, and inhibit the degradation
10 e that AP-3 defines a novel pathway by which lysosomal membrane proteins are transported from tubular
11  Mutations in the CLN3 gene, which encodes a lysosomal membrane protein, are responsible for the neur
12                                 Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familia
13 plex has been implicated in the transport of lysosomal membrane proteins, but its precise site of act
14 perforin expression and up-regulation of the lysosomal membrane protein CD107a after SIV Gag stimulat
15 sults in increased surface expression of the lysosomal membrane proteins CD63, lamp-1, and lamp-2, bu
16 d normal distribution and trafficking of the lysosomal membrane proteins, CD63 and Lamp-1.
17 nts where both selected synaptic vesicle and lysosomal membrane proteins coexist with the adaptor pro
18  is caused by mutation of a novel, endosomal/lysosomal membrane protein encoded by CLN3.
19 -linked oligosaccharides protect a subset of lysosomal membrane proteins from proteolytic digestion i
20 und to the cytosolic tail of a 96-kilodalton lysosomal membrane protein in two different binding assa
21 ove the Asn-linked glycans from fully folded lysosomal membrane proteins in living cells.
22  colocalization of C. neoformans and the MDM lysosomal membrane protein LAMP-1 was demonstrated, esta
23  cells by processing the sialic acids on the lysosomal membrane protein LAMP-1.
24 ay that measures transient surface levels of lysosomal membrane proteins LAMP-1 (CD107a) and LAMP-2 (
25 e, required for substrate uptake, and of the lysosomal membrane protein (lamp) type 2a, previously id
26 y normal distribution and trafficking of the lysosomal membrane protein, Lamp-2, in contrast to fibro
27 of the CD-MPR to the cytoplasmic tail of the lysosomal membrane protein Lamp1 was sufficient to parti
28                             Knockdown of the lysosomal membrane proteins LAMP1 and LAMP2 resulted in
29 coproteins and mannose-6-phosphate or to the lysosomal membrane protein, lgp120, distributed to endos
30 ignaling pathways, little is known about how lysosomal membrane protein lifetimes are regulated.
31              Mutations in the late endosomal/lysosomal membrane protein Niemann-Pick C1 (NPC1) are kn
32 surface glycoprotein (VSG221) as well as the lysosomal membrane protein p67 was observed in Deltatbns
33                     This screen revealed the lysosomal membrane protein SLC46A3, the genetic attenuat
34                   Acid beta-glucosidase is a lysosomal membrane protein that cleaves the O-beta-D-glu
35                  Niemann-Pick C1 (NPC1) is a lysosomal membrane protein that exports cholesterol deri
36 the nuclear envelope and as a chimera with a lysosomal membrane protein to demonstrate rapid interlys
37 ginine requires SLC38A9, a poorly understood lysosomal membrane protein with homology to amino acid t

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