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A novel RAB7 mutation associated with ulcero‐mutilating neuropathy
Annals of Neurology, 2004AbstractThere are two known autosomal dominant genes for the hereditary ulcero‐mutilating neuropathies: SPTLC1 (hereditary sensory neuropathy type 1) and RAB7 (Charcot–Marie–Tooth disease type 2B). We report a family with autosomal dominant ulcero‐mutilating neuropathy, developing in the teens and characterized by ulcers, amputations, sensory ...
Henry, Houlden +6 more
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Rab‐interacting lysosomal protein (RILP): the Rab7 effector required for transport to lysosomes
EMBO Journal, 2001Cecilia Bucci +2 more
exaly
Reciprocal effects of rab7 deletion in activated and neglected T cells
Autophagy, 2013Lomon So, Aimee L Edinger
exaly
USE OF RAB7 GTPASE (RAB7) INHIBITORS IN ENHANCING PERMEABILITY OF THE BLOOD BRAIN BARRIER (BBB)
2020MOSES MARSHA A, MORAD GOLNAZ
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Dissection of Rab7 localization on phagosome
Biochemical and Biophysical Research Communications, 2009Sohkichi Matsumoto +2 more
exaly

