-
1
-
-
80052233389
-
Endosome maturation
-
Huotari J., Helenius A. Endosome maturation. EMBO J. 2011, 30:3481-3500.
-
(2011)
EMBO J.
, vol.30
, pp. 3481-3500
-
-
Huotari, J.1
Helenius, A.2
-
2
-
-
33846286901
-
Shaping the actin cytoskeleton using microtubule tips
-
Basu R., Chang F. Shaping the actin cytoskeleton using microtubule tips. Curr. Opin. Cell Biol. 2007, 19:88-94.
-
(2007)
Curr. Opin. Cell Biol.
, vol.19
, pp. 88-94
-
-
Basu, R.1
Chang, F.2
-
3
-
-
68049105101
-
Rab GTPases as coordinators of vesicle traffic
-
Stenmark H. Rab GTPases as coordinators of vesicle traffic. Nat. Rev. Mol. Cell Biol. 2009, 10:513-525.
-
(2009)
Nat. Rev. Mol. Cell Biol.
, vol.10
, pp. 513-525
-
-
Stenmark, H.1
-
4
-
-
74749099537
-
The early endosome: a busy sorting station for proteins at the crossroads
-
Jovic M., et al. The early endosome: a busy sorting station for proteins at the crossroads. Histol. Histopathol. 2010, 25:99-112.
-
(2010)
Histol. Histopathol.
, vol.25
, pp. 99-112
-
-
Jovic, M.1
-
5
-
-
32644434386
-
Huntingtin-HAP40 complex is a novel Rab5 effector that regulates early endosome motility and is up-regulated in Huntington's disease
-
Pal A., et al. Huntingtin-HAP40 complex is a novel Rab5 effector that regulates early endosome motility and is up-regulated in Huntington's disease. J. Cell Biol. 2006, 172:605-618.
-
(2006)
J. Cell Biol.
, vol.172
, pp. 605-618
-
-
Pal, A.1
-
6
-
-
63449090757
-
Huntingtin as an essential integrator of intracellular vesicular trafficking
-
Caviston J.P., Holzbaur E.L. Huntingtin as an essential integrator of intracellular vesicular trafficking. Trends Cell Biol. 2009, 19:147-155.
-
(2009)
Trends Cell Biol.
, vol.19
, pp. 147-155
-
-
Caviston, J.P.1
Holzbaur, E.L.2
-
7
-
-
77955956961
-
Rab GTPases-dependent endocytic pathways regulate neuronal migration and maturation through N-cadherin trafficking
-
Kawauchi T., et al. Rab GTPases-dependent endocytic pathways regulate neuronal migration and maturation through N-cadherin trafficking. Neuron 2010, 67:588-602.
-
(2010)
Neuron
, vol.67
, pp. 588-602
-
-
Kawauchi, T.1
-
8
-
-
0037598589
-
Role of Drosophila Rab5 during endosomal trafficking at the synapse and evoked neurotransmitter release
-
Wucherpfennig T.M., et al. Role of Drosophila Rab5 during endosomal trafficking at the synapse and evoked neurotransmitter release. J. Cell Biol. 2003, 161:609-624.
-
(2003)
J. Cell Biol.
, vol.161
, pp. 609-624
-
-
Wucherpfennig, T.M.1
-
9
-
-
53349168419
-
Spatial control of branching within dendritic arbors by dynein-dependent transport of Rab5-endosomes
-
Satoh D., et al. Spatial control of branching within dendritic arbors by dynein-dependent transport of Rab5-endosomes. Nat. Cell Biol. 2010, 10:1164-1171.
-
(2010)
Nat. Cell Biol.
, vol.10
, pp. 1164-1171
-
-
Satoh, D.1
-
10
-
-
0034785509
-
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
-
Yang Y., et al. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nat. Genet. 2001, 29:160-165.
-
(2001)
Nat. Genet.
, vol.29
, pp. 160-165
-
-
Yang, Y.1
-
11
-
-
81155154300
-
Alsin and SOD1(G93A) proteins regulate endosomal reactive oxygen species production by glial cells and proinflammatory pathways responsible for neurotoxicity
-
Li Q., et al. Alsin and SOD1(G93A) proteins regulate endosomal reactive oxygen species production by glial cells and proinflammatory pathways responsible for neurotoxicity. J. Biol. Chem. 2011, 286:40151-40162.
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 40151-40162
-
-
Li, Q.1
-
12
-
-
84901273024
-
Signalling endosomes in axonal transport: Travel updates on the molecular highway
-
pii: S1084-9521(13)00109-2
-
Schmieg N., et al. Signalling endosomes in axonal transport: Travel updates on the molecular highway. Semin. Cell Dev. Biol. 2013, pii: S1084-9521(13)00109-2. 10.1016/j.semcdb.2013.10.004.
-
(2013)
Semin. Cell Dev. Biol.
-
-
Schmieg, N.1
-
13
-
-
84862728987
-
Sbf/MTMR13 coordinates PI(3)P and Rab21 regulation in endocytic control of cellular remodeling
-
Jean S., et al. Sbf/MTMR13 coordinates PI(3)P and Rab21 regulation in endocytic control of cellular remodeling. Mol. Biol. Cell 2012, 23:2723-2740.
-
(2012)
Mol. Biol. Cell
, vol.23
, pp. 2723-2740
-
-
Jean, S.1
-
14
-
-
42449113004
-
Loss of the inactive myotubularin-related phosphatase Mtmr13 leads to a Charcot-Marie-Tooth 4B2-like peripheral neuropathy in mice
-
Robinson F.L., et al. Loss of the inactive myotubularin-related phosphatase Mtmr13 leads to a Charcot-Marie-Tooth 4B2-like peripheral neuropathy in mice. Proc. Natl. Acad. Sci. U.S.A. 2008, 105:4916-4921.
-
(2008)
Proc. Natl. Acad. Sci. U.S.A.
, vol.105
, pp. 4916-4921
-
-
Robinson, F.L.1
-
15
-
-
77954630191
-
A novel function for the Rab5 effector Rabenosyn-5 in planar cell polarity
-
Mottola G., et al. A novel function for the Rab5 effector Rabenosyn-5 in planar cell polarity. Development 2010, 137:2353-2364.
-
(2010)
Development
, vol.137
, pp. 2353-2364
-
-
Mottola, G.1
-
16
-
-
28544438939
-
Endocytic control of epithelial polarity and proliferation in Drosophila
-
Lu H., Bilder D. Endocytic control of epithelial polarity and proliferation in Drosophila. Nat. Cell Biol. 2005, 7:1232-1239.
-
(2005)
Nat. Cell Biol.
, vol.7
, pp. 1232-1239
-
-
Lu, H.1
Bilder, D.2
-
17
-
-
84883284087
-
NDRG1 functions in LDL receptor trafficking by regulating endosomal recycling and degradation
-
Pietiainen V., et al. NDRG1 functions in LDL receptor trafficking by regulating endosomal recycling and degradation. J. Cell Sci. 2013, 126:3961-3971.
-
(2013)
J. Cell Sci.
, vol.126
, pp. 3961-3971
-
-
Pietiainen, V.1
-
18
-
-
0033869715
-
Endocytic pathway abnormalities precede amyloid beta deposition in sporadic Alzheimer's disease and Down syndrome: differential effects of APOE genotype and presenilin mutations
-
Cataldo A.M., et al. Endocytic pathway abnormalities precede amyloid beta deposition in sporadic Alzheimer's disease and Down syndrome: differential effects of APOE genotype and presenilin mutations. Am. J. Pathol. 2000, 157:277-286.
-
(2000)
Am. J. Pathol.
, vol.157
, pp. 277-286
-
-
Cataldo, A.M.1
-
19
-
-
84856956771
-
Probing sporadic and familial Alzheimer's disease using induced pluripotent stem cells
-
Israel M.A., et al. Probing sporadic and familial Alzheimer's disease using induced pluripotent stem cells. Nature 2012, 482:216-220.
-
(2012)
Nature
, vol.482
, pp. 216-220
-
-
Israel, M.A.1
-
20
-
-
33749620373
-
Rab5 and Rab7 control endocytic sorting along the axonal retrograde transport pathway
-
Deinhardt K., et al. Rab5 and Rab7 control endocytic sorting along the axonal retrograde transport pathway. Neuron 2006, 52:293-305.
-
(2006)
Neuron
, vol.52
, pp. 293-305
-
-
Deinhardt, K.1
-
21
-
-
33847003020
-
Activation of endosomal dynein motors by stepwise assembly of Rab7-RILP-p150Glued, ORP1L, and the receptor betalll spectrin
-
Johansson M., et al. Activation of endosomal dynein motors by stepwise assembly of Rab7-RILP-p150Glued, ORP1L, and the receptor betalll spectrin. J. Cell Biol. 2007, 176:459-471.
-
(2007)
J. Cell Biol.
, vol.176
, pp. 459-471
-
-
Johansson, M.1
-
22
-
-
0035865135
-
Rab-interacting lysosomal protein (RILP): the Rab7 effector required for transport to lysosomes
-
Cantalupo G., et al. Rab-interacting lysosomal protein (RILP): the Rab7 effector required for transport to lysosomes. EMBO J. 2001, 20:683-693.
-
(2001)
EMBO J.
, vol.20
, pp. 683-693
-
-
Cantalupo, G.1
-
23
-
-
0035975946
-
The Rab7 effector protein RILP controls lysosomal transport by inducing the recruitment of dynein-dynactin motors
-
Jordens I., et al. The Rab7 effector protein RILP controls lysosomal transport by inducing the recruitment of dynein-dynactin motors. Curr. Biol. 2001, 11:1680-1685.
-
(2001)
Curr. Biol.
, vol.11
, pp. 1680-1685
-
-
Jordens, I.1
-
24
-
-
84883382591
-
Late endosomal transport and tethering are coupled processes controlled by RILP and the cholesterol sensor ORP1L
-
van der Kant R., et al. Late endosomal transport and tethering are coupled processes controlled by RILP and the cholesterol sensor ORP1L. J. Cell Sci. 2013, 126:3462-3474.
-
(2013)
J. Cell Sci.
, vol.126
, pp. 3462-3474
-
-
van der Kant, R.1
-
25
-
-
67649600680
-
Cholesterol sensor ORP1L contacts the ER protein VAP to control Rab7-RILP-p150 Glued and late endosome positioning
-
Rocha N., et al. Cholesterol sensor ORP1L contacts the ER protein VAP to control Rab7-RILP-p150 Glued and late endosome positioning. J. Cell Biol. 2009, 185:1209-1225.
-
(2009)
J. Cell Biol.
, vol.185
, pp. 1209-1225
-
-
Rocha, N.1
-
26
-
-
83455229793
-
Arl8 and SKIP act together to link lysosomes to kinesin-1
-
Rosa-Ferreira C., Munro S. Arl8 and SKIP act together to link lysosomes to kinesin-1. Dev. Cell 2011, 21:1171-1178.
-
(2011)
Dev. Cell
, vol.21
, pp. 1171-1178
-
-
Rosa-Ferreira, C.1
Munro, S.2
-
27
-
-
80051876839
-
Lysosomal trafficking, antigen presentation, and microbial killing are controlled by the Arf-like GTPase Arl8b
-
Garg S., et al. Lysosomal trafficking, antigen presentation, and microbial killing are controlled by the Arf-like GTPase Arl8b. Immunity 2011, 35:182-193.
-
(2011)
Immunity
, vol.35
, pp. 182-193
-
-
Garg, S.1
-
28
-
-
0035818998
-
Kinesin-mediated axonal transport of a membrane compartment containing beta-secretase and presenilin-1 requires APP
-
Kamal A., et al. Kinesin-mediated axonal transport of a membrane compartment containing beta-secretase and presenilin-1 requires APP. Nature 2001, 414:643-648.
-
(2001)
Nature
, vol.414
, pp. 643-648
-
-
Kamal, A.1
-
29
-
-
84866411994
-
The balance between receptor recycling and trafficking toward lysosomes determines synaptic strength during long-term depression
-
Fernandez-Monreal M., et al. The balance between receptor recycling and trafficking toward lysosomes determines synaptic strength during long-term depression. J. Neurosci. 2012, 32:13200-13205.
-
(2012)
J. Neurosci.
, vol.32
, pp. 13200-13205
-
-
Fernandez-Monreal, M.1
-
30
-
-
0037371509
-
Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy
-
Verhoeven K., et al. Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy. Am. J. Hum. Genet. 2003, 72:722-727.
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 722-727
-
-
Verhoeven, K.1
-
31
-
-
39549098329
-
Functional characterization of Rab7 mutant proteins associated with Charcot-Marie-Tooth type 2B disease
-
Spinosa M.R., et al. Functional characterization of Rab7 mutant proteins associated with Charcot-Marie-Tooth type 2B disease. J. Neurosci. 2008, 28:1640-1648.
-
(2008)
J. Neurosci.
, vol.28
, pp. 1640-1648
-
-
Spinosa, M.R.1
-
32
-
-
77950686629
-
Disease mutations in Rab7 result in unregulated nucleotide exchange and inappropriate activation
-
McCray B.A., et al. Disease mutations in Rab7 result in unregulated nucleotide exchange and inappropriate activation. Hum. Mol. Genet. 2010, 19:1033-1047.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 1033-1047
-
-
McCray, B.A.1
-
33
-
-
77956184372
-
CMT2B-associated Rab7 mutants inhibit neurite outgrowth
-
Cogli L., et al. CMT2B-associated Rab7 mutants inhibit neurite outgrowth. Acta Neuropathol. 2010, 120:491-501.
-
(2010)
Acta Neuropathol.
, vol.120
, pp. 491-501
-
-
Cogli, L.1
-
34
-
-
84876555190
-
Defective axonal transport of Rab7 GTPase results in dysregulated trophic signaling
-
Zhang K., et al. Defective axonal transport of Rab7 GTPase results in dysregulated trophic signaling. J. Neurosci. 2013, 33:7451-7462.
-
(2013)
J. Neurosci.
, vol.33
, pp. 7451-7462
-
-
Zhang, K.1
-
35
-
-
0037382240
-
Mutant dynactin in motor neuron disease
-
Puls I., et al. Mutant dynactin in motor neuron disease. Nat. Genet. 2003, 33:455-456.
-
(2003)
Nat. Genet.
, vol.33
, pp. 455-456
-
-
Puls, I.1
-
36
-
-
84878717611
-
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
-
Poirier K., et al. Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. Nat. Genet. 2013, 45:639-647.
-
(2013)
Nat. Genet.
, vol.45
, pp. 639-647
-
-
Poirier, K.1
-
37
-
-
84861542834
-
Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy
-
Harms M.B., et al. Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy. Neurology 2012, 78:1714-1720.
-
(2012)
Neurology
, vol.78
, pp. 1714-1720
-
-
Harms, M.B.1
-
38
-
-
84871351575
-
Charcot-Marie-Tooth neuropathy type 2
-
University of Washington, R.A. Pagon (Ed.)
-
Bird T.D., et al. Charcot-Marie-Tooth neuropathy type 2. GeneReviews 1993, University of Washington. R.A. Pagon (Ed.).
-
(1993)
GeneReviews
-
-
Bird, T.D.1
-
39
-
-
84878883752
-
Mutations in BICD2, which encodes a golgin and important motor adaptor, cause congenital autosomal-dominant spinal muscular atrophy
-
Neveling K., et al. Mutations in BICD2, which encodes a golgin and important motor adaptor, cause congenital autosomal-dominant spinal muscular atrophy. Am. J. Hum. Genet. 2013, 92:946-954.
-
(2013)
Am. J. Hum. Genet.
, vol.92
, pp. 946-954
-
-
Neveling, K.1
-
40
-
-
84878835790
-
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia
-
Oates E.C., et al. Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia. Am. J. Hum. Genet. 2013, 92:965-973.
-
(2013)
Am. J. Hum. Genet.
, vol.92
, pp. 965-973
-
-
Oates, E.C.1
-
41
-
-
84878892093
-
Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritance
-
Peeters K., et al. Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritance. Am. J. Hum. Genet. 2013, 92:955-964.
-
(2013)
Am. J. Hum. Genet.
, vol.92
, pp. 955-964
-
-
Peeters, K.1
-
42
-
-
84886953670
-
Cytoplasmic dynein heavy chain: the servant of many masters
-
Schiavo G., et al. Cytoplasmic dynein heavy chain: the servant of many masters. Trends Neurosci. 2013, 36:641-651.
-
(2013)
Trends Neurosci.
, vol.36
, pp. 641-651
-
-
Schiavo, G.1
-
43
-
-
59149097039
-
DCTN1 mutations in Perry syndrome
-
Farrer M.J., et al. DCTN1 mutations in Perry syndrome. Nat. Genet. 2009, 41:163-165.
-
(2009)
Nat. Genet.
, vol.41
, pp. 163-165
-
-
Farrer, M.J.1
-
44
-
-
84870489243
-
De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia
-
Xu B., et al. De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia. Nat. Genet. 2012, 44:1365-1369.
-
(2012)
Nat. Genet.
, vol.44
, pp. 1365-1369
-
-
Xu, B.1
-
45
-
-
12144290067
-
Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome
-
Gissen P., et al. Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome. Nat. Genet. 2004, 36:400-404.
-
(2004)
Nat. Genet.
, vol.36
, pp. 400-404
-
-
Gissen, P.1
-
46
-
-
77950300024
-
Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization
-
Cullinane A.R., et al. Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization. Nat. Genet. 2010, 42:303-312.
-
(2010)
Nat. Genet.
, vol.42
, pp. 303-312
-
-
Cullinane, A.R.1
-
47
-
-
25844507433
-
Arthrogryposis, renal tubular acidosis and cholestasis (ARC) syndrome: two new cases and review
-
Abu-Sa'da O., et al. Arthrogryposis, renal tubular acidosis and cholestasis (ARC) syndrome: two new cases and review. Clin. Dysmorphol. 2005, 14:191-196.
-
(2005)
Clin. Dysmorphol.
, vol.14
, pp. 191-196
-
-
Abu-Sa'da, O.1
-
48
-
-
39849109338
-
Autophagy fights disease through cellular self-digestion
-
Mizushima N., et al. Autophagy fights disease through cellular self-digestion. Nature 2008, 451:1069-1075.
-
(2008)
Nature
, vol.451
, pp. 1069-1075
-
-
Mizushima, N.1
-
49
-
-
84865202328
-
The Rab interacting lysosomal protein (RILP) homology domain functions as a novel effector domain for small GTPase Rab36: Rab36 regulates retrograde melanosome transport in melanocytes
-
Matsui T.N., et al. The Rab interacting lysosomal protein (RILP) homology domain functions as a novel effector domain for small GTPase Rab36: Rab36 regulates retrograde melanosome transport in melanocytes. J. Biol. Chem. 2012, 287:28619-28631.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 28619-28631
-
-
Matsui, T.N.1
-
50
-
-
72049084499
-
Rab36 regulates the spatial distribution of late endosomes and lysosomes through a similar mechanism to Rab34
-
Chen L., et al. Rab36 regulates the spatial distribution of late endosomes and lysosomes through a similar mechanism to Rab34. Mol. Membr. Biol. 2010, 27:24-31.
-
(2010)
Mol. Membr. Biol.
, vol.27
, pp. 24-31
-
-
Chen, L.1
-
51
-
-
81955164789
-
The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplication
-
Piccione M., et al. The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplication. Am. J. Med. Genet. A 2011, 155A:3054-3059.
-
(2011)
Am. J. Med. Genet. A
, vol.155 A
, pp. 3054-3059
-
-
Piccione, M.1
-
52
-
-
0035369084
-
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta
-
Zhao C., et al. Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta. Cell 2001, 105:587-597.
-
(2001)
Cell
, vol.105
, pp. 587-597
-
-
Zhao, C.1
-
53
-
-
1642327748
-
A novel kinesin-like protein, KIF1Bbeta3 is involved in the movement of lysosomes to the cell periphery in non-neuronal cells
-
Matsushita M., et al. A novel kinesin-like protein, KIF1Bbeta3 is involved in the movement of lysosomes to the cell periphery in non-neuronal cells. Traffic 2004, 5:140-1451.
-
(2004)
Traffic
, vol.5
, pp. 140-1451
-
-
Matsushita, M.1
-
54
-
-
0030744142
-
Kinesin hydrolyses one ATP per 8nm step
-
Schnitzer M.J., Block S.M. Kinesin hydrolyses one ATP per 8nm step. Nature 1997, 388:386-390.
-
(1997)
Nature
, vol.388
, pp. 386-390
-
-
Schnitzer, M.J.1
Block, S.M.2
-
55
-
-
0030844286
-
Coupling of kinesin steps to ATP hydrolysis
-
Hua W., et al. Coupling of kinesin steps to ATP hydrolysis. Nature 1997, 388:390-393.
-
(1997)
Nature
, vol.388
, pp. 390-393
-
-
Hua, W.1
-
56
-
-
84861429431
-
Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity
-
Funfschilling U., et al. Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity. Nature 2012, 485:517-521.
-
(2012)
Nature
, vol.485
, pp. 517-521
-
-
Funfschilling, U.1
-
57
-
-
84873323723
-
Vesicular glycolysis provides on-board energy for fast axonal transport
-
Zala D., et al. Vesicular glycolysis provides on-board energy for fast axonal transport. Cell 2013, 152:479-491.
-
(2013)
Cell
, vol.152
, pp. 479-491
-
-
Zala, D.1
-
58
-
-
34547193908
-
Huntingtin facilitates dynein/dynactin-mediated vesicle transport
-
Caviston J.P., et al. Huntingtin facilitates dynein/dynactin-mediated vesicle transport. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:10045-10050.
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 10045-10050
-
-
Caviston, J.P.1
-
59
-
-
0032519646
-
Interaction of huntingtin-associated protein with dynactin P150Glued
-
Li S.H., et al. Interaction of huntingtin-associated protein with dynactin P150Glued. J. Neurosci. 1998, 18:1261-1269.
-
(1998)
J. Neurosci.
, vol.18
, pp. 1261-1269
-
-
Li, S.H.1
-
60
-
-
0030726894
-
Huntingtin-associated protein 1 (HAP1) interacts with the p150Glued subunit of dynactin
-
Engelender S., et al. Huntingtin-associated protein 1 (HAP1) interacts with the p150Glued subunit of dynactin. Hum. Mol. Genet. 1997, 6:2205-22012.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2205-22012
-
-
Engelender, S.1
-
61
-
-
33745233087
-
Regulation of intracellular trafficking of huntingtin-associated protein-1 is critical for TrkA protein levels and neurite outgrowth
-
Rong J., et al. Regulation of intracellular trafficking of huntingtin-associated protein-1 is critical for TrkA protein levels and neurite outgrowth. J. Neurosci. 2006, 26:6019-6030.
-
(2006)
J. Neurosci.
, vol.26
, pp. 6019-6030
-
-
Rong, J.1
-
62
-
-
79960225411
-
The ESCRT pathway
-
Henne W.M., et al. The ESCRT pathway. Dev. Cell 2011, 21:77-91.
-
(2011)
Dev. Cell
, vol.21
, pp. 77-91
-
-
Henne, W.M.1
-
63
-
-
23044471011
-
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
-
Skibinski G., et al. Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nat. Genet. 2005, 37:806-808.
-
(2005)
Nat. Genet.
, vol.37
, pp. 806-808
-
-
Skibinski, G.1
-
64
-
-
33745139797
-
SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutations
-
Latour P., et al. SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutations. J. Peripher. Nerv. Syst. 2006, 11:148-155.
-
(2006)
J. Peripher. Nerv. Syst.
, vol.11
, pp. 148-155
-
-
Latour, P.1
-
65
-
-
20244367606
-
SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation
-
Saifi G.M., et al. SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation. Hum. Mutat. 2005, 25:372-383.
-
(2005)
Hum. Mutat.
, vol.25
, pp. 372-383
-
-
Saifi, G.M.1
-
66
-
-
11144356764
-
SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve
-
Bennett C.L., et al. SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve. Ann. Neurol. 2004, 55:713-720.
-
(2004)
Ann. Neurol.
, vol.55
, pp. 713-720
-
-
Bennett, C.L.1
-
67
-
-
80054037232
-
Mutations associated with Charcot-Marie-Tooth disease cause SIMPLE protein mislocalization and degradation by the proteasome and aggresome-autophagy pathways
-
Lee S.M., et al. Mutations associated with Charcot-Marie-Tooth disease cause SIMPLE protein mislocalization and degradation by the proteasome and aggresome-autophagy pathways. J. Cell Sci. 2011, 124:3319-3331.
-
(2011)
J. Cell Sci.
, vol.124
, pp. 3319-3331
-
-
Lee, S.M.1
-
68
-
-
84871997901
-
Charcot-Marie-Tooth disease-linked protein SIMPLE functions with the ESCRT machinery in endosomal trafficking
-
Lee S.M., et al. Charcot-Marie-Tooth disease-linked protein SIMPLE functions with the ESCRT machinery in endosomal trafficking. J. Cell Biol. 2012, 199:799-816.
-
(2012)
J. Cell Biol.
, vol.199
, pp. 799-816
-
-
Lee, S.M.1
-
69
-
-
34447133038
-
Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J
-
Chow C.Y., et al. Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J. Nature 2007, 448:68-72.
-
(2007)
Nature
, vol.448
, pp. 68-72
-
-
Chow, C.Y.1
-
70
-
-
0034062698
-
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
-
Bolino A., et al. Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2. Nat. Genet. 2000, 25:17-19.
-
(2000)
Nat. Genet.
, vol.25
, pp. 17-19
-
-
Bolino, A.1
-
71
-
-
79955538881
-
Endosomal targeting of the phosphoinositide 3-phosphatase MTMR2 is regulated by an N-terminal phosphorylation site
-
Franklin N.E., et al. Endosomal targeting of the phosphoinositide 3-phosphatase MTMR2 is regulated by an N-terminal phosphorylation site. J. Biol. Chem. 2011, 286:15841-15853.
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 15841-15853
-
-
Franklin, N.E.1
-
72
-
-
84872183810
-
The retromer complex - endosomal protein recycling and beyond
-
Seaman M.N. The retromer complex - endosomal protein recycling and beyond. J. Cell Sci. 2012, 125:4693-4702.
-
(2012)
J. Cell Sci.
, vol.125
, pp. 4693-4702
-
-
Seaman, M.N.1
-
73
-
-
79952103459
-
Transport according to GARP: receiving retrograde cargo at the trans-Golgi network
-
Bonifacino J.S., Hierro A. Transport according to GARP: receiving retrograde cargo at the trans-Golgi network. Trends Cell Biol. 2011, 21:159-167.
-
(2011)
Trends Cell Biol.
, vol.21
, pp. 159-167
-
-
Bonifacino, J.S.1
Hierro, A.2
-
74
-
-
80051488602
-
VPS35 mutations in Parkinson disease
-
Vilarino-Guell C., et al. VPS35 mutations in Parkinson disease. Am. J. Hum. Genet. 2011, 89:162-167.
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 162-167
-
-
Vilarino-Guell, C.1
-
75
-
-
80051534540
-
A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease
-
Zimprich A., et al. A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease. Am. J. Hum. Genet. 2011, 89:168-175.
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 168-175
-
-
Zimprich, A.1
-
76
-
-
84873730294
-
Wnt5a cooperates with canonical Wnts to generate midbrain dopaminergic neurons in vivo and in stem cells
-
Andersson E.R., et al. Wnt5a cooperates with canonical Wnts to generate midbrain dopaminergic neurons in vivo and in stem cells. Proc. Natl. Acad. Sci. U.S.A. 2013, 110:E602-E610.
-
(2013)
Proc. Natl. Acad. Sci. U.S.A.
, vol.110
-
-
Andersson, E.R.1
-
77
-
-
84863012293
-
RAB-6.2 and the retromer regulate glutamate receptor recycling through a retrograde pathway
-
Zhang D., et al. RAB-6.2 and the retromer regulate glutamate receptor recycling through a retrograde pathway. J. Cell Biol. 2012, 196:85-101.
-
(2012)
J. Cell Biol.
, vol.196
, pp. 85-101
-
-
Zhang, D.1
-
78
-
-
84877111389
-
Novel role of sorting nexin 5 in renal D(1) dopamine receptor trafficking and function: implications for hypertension
-
Villar V.A., et al. Novel role of sorting nexin 5 in renal D(1) dopamine receptor trafficking and function: implications for hypertension. FASEB J. 2013, 27:1808-1819.
-
(2013)
FASEB J.
, vol.27
, pp. 1808-1819
-
-
Villar, V.A.1
-
79
-
-
77953898430
-
Disease-associated mutations in the p150(Glued) subunit destabilize the CAP-gly domain
-
Ahmed S., et al. Disease-associated mutations in the p150(Glued) subunit destabilize the CAP-gly domain. Biochemistry 2010, 49:5083-5085.
-
(2010)
Biochemistry
, vol.49
, pp. 5083-5085
-
-
Ahmed, S.1
-
80
-
-
84873281274
-
RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk
-
MacLeod D.A., et al. RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk. Neuron 2013, 77:425-439.
-
(2013)
Neuron
, vol.77
, pp. 425-439
-
-
MacLeod, D.A.1
-
81
-
-
33845991876
-
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia
-
Valdmanis P.N., et al. Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. Am. J. Hum. Genet. 2007, 80:152-161.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 152-161
-
-
Valdmanis, P.N.1
-
82
-
-
79958707744
-
Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability: the WASH complex member SWIP
-
Ropers F., et al. Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability: the WASH complex member SWIP. Hum. Mol. Genet. 2011, 20:2585-2590.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 2585-2590
-
-
Ropers, F.1
-
83
-
-
77955594318
-
Structural basis for the wobbler mouse neurodegenerative disorder caused by mutation in the Vps54 subunit of the GARP complex
-
Perez-Victoria F.J., et al. Structural basis for the wobbler mouse neurodegenerative disorder caused by mutation in the Vps54 subunit of the GARP complex. Proc. Natl. Acad. Sci. U.S.A. 2010, 107:12860-21285.
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 12860-21285
-
-
Perez-Victoria, F.J.1
-
84
-
-
55749083068
-
NPC2 facilitates bidirectional transfer of cholesterol between NPC1 and lipid bilayers, a step in cholesterol egress from lysosomes
-
Infante R.E., et al. NPC2 facilitates bidirectional transfer of cholesterol between NPC1 and lipid bilayers, a step in cholesterol egress from lysosomes. Proc. Natl. Acad. Sci. U.S.A. 2008, 105:15287-15292.
-
(2008)
Proc. Natl. Acad. Sci. U.S.A.
, vol.105
, pp. 15287-15292
-
-
Infante, R.E.1
-
85
-
-
78651328466
-
A role for oxysterol-binding protein-related protein 5 in endosomal cholesterol trafficking
-
Du X., et al. A role for oxysterol-binding protein-related protein 5 in endosomal cholesterol trafficking. J. Cell Biol. 2011, 192:121-135.
-
(2011)
J. Cell Biol.
, vol.192
, pp. 121-135
-
-
Du, X.1
-
87
-
-
2442444286
-
The ABCA1 transporter modulates late endocytic trafficking: insights from the correction of the genetic defect in Tangier disease
-
Neufeld E.B., et al. The ABCA1 transporter modulates late endocytic trafficking: insights from the correction of the genetic defect in Tangier disease. J. Biol. Chem. 2004, 279:15571-15578.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 15571-15578
-
-
Neufeld, E.B.1
-
88
-
-
18844471093
-
The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum
-
Lonka L., et al. The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum. Hum. Mol. Genet. 2000, 9:1691-1697.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1691-1697
-
-
Lonka, L.1
-
89
-
-
84871911332
-
Identifying protein partners of CLN8, an ER-resident protein involved in neuronal ceroid lipofuscinosis
-
Passantino R., et al. Identifying protein partners of CLN8, an ER-resident protein involved in neuronal ceroid lipofuscinosis. Biochim. Biophys. Acta 2013, 1833:529-540.
-
(2013)
Biochim. Biophys. Acta
, vol.1833
, pp. 529-540
-
-
Passantino, R.1
-
90
-
-
34848904785
-
Motor neuron disease-associated mutant vesicle-associated membrane protein-associated protein (VAP) B recruits wild-type VAPs into endoplasmic reticulum-derived tubular aggregates
-
Teuling E., et al. Motor neuron disease-associated mutant vesicle-associated membrane protein-associated protein (VAP) B recruits wild-type VAPs into endoplasmic reticulum-derived tubular aggregates. J. Neurosci. 2007, 27:9801-9815.
-
(2007)
J. Neurosci.
, vol.27
, pp. 9801-9815
-
-
Teuling, E.1
-
91
-
-
70350319531
-
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
-
Sidransky E., et al. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N. Engl. J. Med. 2009, 361:1651-1661.
-
(2009)
N. Engl. J. Med.
, vol.361
, pp. 1651-1661
-
-
Sidransky, E.1
-
92
-
-
84862838085
-
Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments
-
Uusi-Rauva K., et al. Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments. Cell. Mol. Life Sci. 2012, 69:2075-2089.
-
(2012)
Cell. Mol. Life Sci.
, vol.69
, pp. 2075-2089
-
-
Uusi-Rauva, K.1
-
93
-
-
0032905252
-
Action of BTN1, the yeast orthologue of the gene mutated in Batten disease
-
Pearce D.A., et al. Action of BTN1, the yeast orthologue of the gene mutated in Batten disease. Nat. Genet. 1999, 22:55-58.
-
(1999)
Nat. Genet.
, vol.22
, pp. 55-58
-
-
Pearce, D.A.1
-
94
-
-
79951552729
-
Interactions of the proteins of neuronal ceroid lipofuscinosis: clues to function
-
Getty A.L., Pearce D.A. Interactions of the proteins of neuronal ceroid lipofuscinosis: clues to function. Cell. Mol. Life Sci. 2011, 68:453-474.
-
(2011)
Cell. Mol. Life Sci.
, vol.68
, pp. 453-474
-
-
Getty, A.L.1
Pearce, D.A.2
-
95
-
-
84861379836
-
The role of ceroid lipofuscinosis neuronal protein 5 (CLN5) in endosomal sorting
-
Mamo A., et al. The role of ceroid lipofuscinosis neuronal protein 5 (CLN5) in endosomal sorting. Mol. Cell. Biol. 2012, 32:1855-1866.
-
(2012)
Mol. Cell. Biol.
, vol.32
, pp. 1855-1866
-
-
Mamo, A.1
-
96
-
-
0032706624
-
A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases
-
Verheijen F.W., et al. A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases. Nat. Genet. 1999, 23:462-465.
-
(1999)
Nat. Genet.
, vol.23
, pp. 462-465
-
-
Verheijen, F.W.1
-
97
-
-
0031945551
-
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis
-
Town M., et al. A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. Nat. Genet. 1998, 18:319-324.
-
(1998)
Nat. Genet.
, vol.18
, pp. 319-324
-
-
Town, M.1
-
98
-
-
18744363612
-
Identification and characterization of the single channel function of human mucolipin-1 implicated in mucolipidosis type IV, a disorder affecting the lysosomal pathway
-
LaPlante J.M., et al. Identification and characterization of the single channel function of human mucolipin-1 implicated in mucolipidosis type IV, a disorder affecting the lysosomal pathway. FEBS Lett. 2002, 532:183-187.
-
(2002)
FEBS Lett.
, vol.532
, pp. 183-187
-
-
LaPlante, J.M.1
-
99
-
-
77649136250
-
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
-
Van Deerlin V.M., et al. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nat. Genet. 2010, 42:234-239.
-
(2010)
Nat. Genet.
, vol.42
, pp. 234-239
-
-
Van Deerlin, V.M.1
-
100
-
-
0032775827
-
A new locus for variant late infantile neuronal ceroid lipofuscinosis-CLN7
-
Wheeler R.B., et al. A new locus for variant late infantile neuronal ceroid lipofuscinosis-CLN7. Mol. Genet. Metab. 1999, 66:337-338.
-
(1999)
Mol. Genet. Metab.
, vol.66
, pp. 337-338
-
-
Wheeler, R.B.1
-
101
-
-
80755139512
-
Mechanisms of polarized membrane trafficking in neurons - focusing in on endosomes
-
Lasiecka Z.M., Winckler B. Mechanisms of polarized membrane trafficking in neurons - focusing in on endosomes. Mol. Cell. Neurosci. 2011, 48:278-287.
-
(2011)
Mol. Cell. Neurosci.
, vol.48
, pp. 278-287
-
-
Lasiecka, Z.M.1
Winckler, B.2
-
102
-
-
84860668936
-
Harnessing the power of the endosome to regulate neural development
-
Yap C.C., Winckler B. Harnessing the power of the endosome to regulate neural development. Neuron 2012, 74:440-451.
-
(2012)
Neuron
, vol.74
, pp. 440-451
-
-
Yap, C.C.1
Winckler, B.2
-
103
-
-
84863222963
-
SnapShot: axonal transport
-
Twelvetrees A., et al. SnapShot: axonal transport. Cell 2012, 149:950.
-
(2012)
Cell
, vol.149
, pp. 950
-
-
Twelvetrees, A.1
-
104
-
-
0029813779
-
Dynamic organization of endocytic pathways in axons of cultured sympathetic neurons
-
Overly C.C., Hollenbeck P.J. Dynamic organization of endocytic pathways in axons of cultured sympathetic neurons. J. Neurosci. 1996, 16:6056-6064.
-
(1996)
J. Neurosci.
, vol.16
, pp. 6056-6064
-
-
Overly, C.C.1
Hollenbeck, P.J.2
-
105
-
-
78651377060
-
The role of endosomal-recycling in long-term potentiation
-
Kelly E.E., et al. The role of endosomal-recycling in long-term potentiation. Cell. Mol. Life Sci. 2011, 68:185-194.
-
(2011)
Cell. Mol. Life Sci.
, vol.68
, pp. 185-194
-
-
Kelly, E.E.1
-
106
-
-
36049044386
-
Message in a bottle: long-range retrograde signaling in the nervous system
-
Ibanez C.F. Message in a bottle: long-range retrograde signaling in the nervous system. Trends Cell Biol. 2007, 17:519-528.
-
(2007)
Trends Cell Biol.
, vol.17
, pp. 519-528
-
-
Ibanez, C.F.1
-
107
-
-
0037899137
-
NGF signaling in sensory neurons: evidence that early endosomes carry NGF retrograde signals
-
Delcroix J.D., et al. NGF signaling in sensory neurons: evidence that early endosomes carry NGF retrograde signals. Neuron 2003, 39:69-84.
-
(2003)
Neuron
, vol.39
, pp. 69-84
-
-
Delcroix, J.D.1
-
108
-
-
79955556527
-
Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis
-
Erlich Y., et al. Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis. Genome Res. 2011, 21:658-664.
-
(2011)
Genome Res.
, vol.21
, pp. 658-664
-
-
Erlich, Y.1
-
109
-
-
70349579493
-
The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling
-
Tsang H.T., et al. The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling. Hum. Mol. Genet. 2009, 18:3805-3821.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3805-3821
-
-
Tsang, H.T.1
-
110
-
-
48249095748
-
Down syndrome fibroblast model of Alzheimer-related endosome pathology: accelerated endocytosis promotes late endocytic defects
-
Cataldo A.M., et al. Down syndrome fibroblast model of Alzheimer-related endosome pathology: accelerated endocytosis promotes late endocytic defects. Am. J. Pathol. 2008, 173:370-384.
-
(2008)
Am. J. Pathol.
, vol.173
, pp. 370-384
-
-
Cataldo, A.M.1
-
111
-
-
78650803250
-
Regional selectivity of rab5 and rab7 protein upregulation in mild cognitive impairment and Alzheimer's disease
-
Ginsberg S.D., et al. Regional selectivity of rab5 and rab7 protein upregulation in mild cognitive impairment and Alzheimer's disease. J. Alzheimers Dis. 2010, 22:631-639.
-
(2010)
J. Alzheimers Dis.
, vol.22
, pp. 631-639
-
-
Ginsberg, S.D.1
-
112
-
-
77953913051
-
Lysosomal proteolysis and autophagy require presenilin 1 and are disrupted by Alzheimer-related PS1 mutations
-
Lee J.H., et al. Lysosomal proteolysis and autophagy require presenilin 1 and are disrupted by Alzheimer-related PS1 mutations. Cell 2010, 141:1146-1158.
-
(2010)
Cell
, vol.141
, pp. 1146-1158
-
-
Lee, J.H.1
-
113
-
-
84862883617
-
A role for presenilins in autophagy revisited: normal acidification of lysosomes in cells lacking PSEN1 and PSEN2
-
Zhang X., et al. A role for presenilins in autophagy revisited: normal acidification of lysosomes in cells lacking PSEN1 and PSEN2. J. Neurosci. 2012, 32:8633-8648.
-
(2012)
J. Neurosci.
, vol.32
, pp. 8633-8648
-
-
Zhang, X.1
-
114
-
-
84865086929
-
Lysosomal calcium homeostasis defects, not proton pump defects, cause endo-lysosomal dysfunction in PSEN-deficient cells
-
Coen K., et al. Lysosomal calcium homeostasis defects, not proton pump defects, cause endo-lysosomal dysfunction in PSEN-deficient cells. J. Cell Biol. 2012, 198:23-35.
-
(2012)
J. Cell Biol.
, vol.198
, pp. 23-35
-
-
Coen, K.1
-
115
-
-
84860919373
-
Membrane trafficking pathways in Alzheimer's disease
-
Rajendran L., Annaert W. Membrane trafficking pathways in Alzheimer's disease. Traffic 2012, 13:759-770.
-
(2012)
Traffic
, vol.13
, pp. 759-770
-
-
Rajendran, L.1
Annaert, W.2
-
116
-
-
79955670132
-
The many faces of tau
-
Morris M., et al. The many faces of tau. Neuron 2011, 70:410-4126.
-
(2011)
Neuron
, vol.70
, pp. 410-4126
-
-
Morris, M.1
-
117
-
-
41549153666
-
Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome
-
Hanein S., et al. Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. Am. J. Hum. Genet. 2008, 82:992-1002.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 992-1002
-
-
Hanein, S.1
-
118
-
-
77950510375
-
PtdIns(3)P controls cytokinesis through KIF13A-mediated recruitment of FYVE-CENT to the midbody
-
Sagona A.P., et al. PtdIns(3)P controls cytokinesis through KIF13A-mediated recruitment of FYVE-CENT to the midbody. Nat. Cell Biol. 2010, 12:362-371.
-
(2010)
Nat. Cell Biol.
, vol.12
, pp. 362-371
-
-
Sagona, A.P.1
-
119
-
-
84878830120
-
Lysosomal storage and advanced senescence in the brain of LAMP-2-deficient Danon disease
-
Furuta A., et al. Lysosomal storage and advanced senescence in the brain of LAMP-2-deficient Danon disease. Acta Neuropathol. 2013, 125:459-461.
-
(2013)
Acta Neuropathol.
, vol.125
, pp. 459-461
-
-
Furuta, A.1
-
120
-
-
84872038046
-
Adaptor protein complexes AP-4 and AP-5: new players in endosomal trafficking and progressive spastic paraplegia
-
Hirst J., et al. Adaptor protein complexes AP-4 and AP-5: new players in endosomal trafficking and progressive spastic paraplegia. Traffic 2013, 14:153-164.
-
(2013)
Traffic
, vol.14
, pp. 153-164
-
-
Hirst, J.1
-
121
-
-
0025897376
-
Saposin proteins: structure, function, and role in human lysosomal storage disorders
-
O'Brien J.S., Kishimoto Y. Saposin proteins: structure, function, and role in human lysosomal storage disorders. FASEB J. 1991, 5:301-308.
-
(1991)
FASEB J.
, vol.5
, pp. 301-308
-
-
O'Brien, J.S.1
Kishimoto, Y.2
-
122
-
-
84879143450
-
Gangliosides and gangliosidoses: principles of molecular and metabolic pathogenesis
-
Sandhoff K., Harzer K. Gangliosides and gangliosidoses: principles of molecular and metabolic pathogenesis. J. Neurosci. 2013, 33:10195-10208.
-
(2013)
J. Neurosci.
, vol.33
, pp. 10195-10208
-
-
Sandhoff, K.1
Harzer, K.2
-
123
-
-
84884776465
-
Christianson syndrome protein NHE6 modulates TrkB endosomal signaling required for neuronal circuit development
-
Ouyang Q., et al. Christianson syndrome protein NHE6 modulates TrkB endosomal signaling required for neuronal circuit development. Neuron 2013, 80:97-112.
-
(2013)
Neuron
, vol.80
, pp. 97-112
-
-
Ouyang, Q.1
-
124
-
-
84862189804
-
Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration
-
Dehay B., et al. Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration. Proc. Natl. Acad. Sci. U.S.A. 2012, 109:9611-9616.
-
(2012)
Proc. Natl. Acad. Sci. U.S.A.
, vol.109
, pp. 9611-9616
-
-
Dehay, B.1
-
125
-
-
84871351575
-
Charcot-Marie-Tooth neuropathy type 1
-
University of Washington, R.A. Pagon (Ed.)
-
Bird T.D., et al. Charcot-Marie-Tooth neuropathy type 1. GeneReviews 1993, University of Washington. R.A. Pagon (Ed.).
-
(1993)
GeneReviews
-
-
Bird, T.D.1
-
126
-
-
84866992578
-
Delivery of endosomes to lysosomes via microautophagy in the visceral endoderm of mouse embryos
-
Kawamura N., et al. Delivery of endosomes to lysosomes via microautophagy in the visceral endoderm of mouse embryos. Nat. Commun. 2012, 3:1071.
-
(2012)
Nat. Commun.
, vol.3
, pp. 1071
-
-
Kawamura, N.1
|