Results 81 to 90 of about 737 (163)
Characterization of IKAP localization in PNS WT and FD hESC-derived cultured neurons.
Immunofluorescence confocal microscopy analysis was performed as shown in Fig 3. IKAP together with peripherin and Rab3a expression are shown within hESC derived neurons in WT (A-F) and FD (G-L) genetic backgrounds. Images B and H show the expression and
Miguel Weil (222465) +14 more
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Confocal micrographs of hESC derived PNS neurons double-stained with Rabbit anti-hIKAP antibodies combined with either antibodies against synaptic vesicular markers, synaptic vesicle 2 (SV2) (A-G) or with Rab3a (H-J).
Miguel Weil (222465) +14 more
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Familial Dysautonomia: Mechanisms and Models
Hereditary Sensory and Autonomic Neuropathies (HSANs) compose a heterogeneous group of genetic disorders characterized by sensory and autonomic dysfunctions.
Paula Dietrich, Ioannis Dragatsis
doaj +3 more sources
Desa Cibogo merupakan salah satu desa yang ada dalam wilayah Kecamatan Cisauk, Kabupaten Tangerang. Desa Cibogo terletak di lokasi yang sangat strategis karena berdampingan dengan kawasan modern Bumi Serpong Damai dan stasiun kereta rel listrik Cisauk ...
Ambang Aries Yudanto +2 more
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IKAP expression in WT and FD early and mature neurons.
(A) RT-PCR analysis of the expression of IKBKAP showing WT (upper lane) and FD (mis-spliced, lower lane) mRNA isoforms at the stage of early neuronal precursors, early and mature neurons.
Miguel Weil (222465) +14 more
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Penelitian ini bertujuan untuk mengetahui gambaran sikap terhadap pelaksanaan tata tertib sekolah siswa yang diasuh dengan pola asuh demokratis, otoriter, dan permisif serta untuk mengetahui perbedaan pengaruh pola asuh demokratis, otoriter, dan permisif
Fatwiasih Al Humaira +2 more
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FD cells were treated for 5 days either with (A) 50 μg/ml PS or 10 μM kinetin (Kin) or the combination of both drugs, and (B) 50 μg/ml PS or 100 ng/ml TSA or the combination of both drugs. Upper panels: Western blotting of FD cell lysates after indicated
Maya Donyo (234098) +3 more
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Familial dysautonomia (FD) patients have reduced levels of the modified wobble nucleoside mcm5s2U in tRNA [PDF]
Familial dysautonomia (FD) is a recessive neurodegenerative genetic disease. FD is caused by a mutation in the IKBKAP gene resulting in a splicing defect and reduced levels of full length IKAP protein.
Karlsborn, Tony, +6 more
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(A-D) FD cells were treated with 0, 10, 100, 500, 1000, and 10,000 nM of pridopidine. Control treatment was done with vehicle only. (A) Western blotting of FD cell lysates with and without pridopidine treatment for 10 days.
Maya Donyo (234098) +3 more
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Caractérisation des rôles biologiques de la protéine IKAP et du complexe Elongator
As the first step in the complex process of gene expression, the transcription of genes from DNA to RNA by RNA polymerase II is subject to a multiplicity of controls and is thereby the endpoint of multiple cell regulatory pathways. We focused here on the
Close, Pierre
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