Pages that link to "Q32425901"

The following pages link to Leonardo Almeida-Souza (Q32425901):

Displaying 20 items.

• Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type I (Q24301846) (← links)
• Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritance (Q24339600) (← links)
• Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy (Q24632623) (← links)
• HSPB1 facilitates the formation of non-centrosomal microtubules (Q27314539) (← links)
• Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy (Q28115297) (← links)
• Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency (Q28254422) (← links)
• Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach (Q30009313) (← links)
• Endophilin marks and controls a clathrin-independent endocytic pathway. (Q38927789) (← links)
• MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets (Q38989183) (← links)
• Mutant HSPB8 causes motor neuron-specific neurite degeneration. (Q39694541) (← links)
• Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease (Q41199733) (← links)
• PhD survival guide. Some brief advice for PhD students. (Q41773050) (← links)
• Acute injury in the peripheral nervous system triggers an alternative macrophage response. (Q42276078) (← links)
• HSPB1 facilitates ERK-mediated phosphorylation and degradation of BIM to attenuate endoplasmic reticulum stress-induced apoptosis. (Q42358226) (← links)
• Characterization of New Transgenic Mouse Models for Two Charcot-Marie-Tooth-Causing HspB1 Mutations using the Rosa26 Locus. (Q48427387) (← links)
• Small heat-shock protein HSPB1 mutants stabilize microtubules in Charcot-Marie-Tooth neuropathy. (Q50509111) (← links)
• Sensory-Neuropathy-Causing Mutations in ATL3 Cause Aberrant ER Membrane Tethering. (Q55396745) (← links)
• Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia (Q55671551) (← links)
• A Flat BAR Protein Promotes Actin Polymerization at the Base of Clathrin-Coated Pits (Q57752490) (← links)
• Multidimensional Dynamics of the Proteome in the Neurodegenerative and Aging Mammalian Brain (Q112302798) (← links)