377 results on '"Chrast, Roman"'
Search Results
52. Complement factors in adult peripheral nerve: a potential role in energy metabolism
53. Gene replacement therapy in a model of Charcot-Marie-Tooth 4C neuropathy
54. Schwann cell demyelination is triggered by a transient mitochondrial calcium release through Voltage Dependent Anion Channel 1
55. Characterization of molecular mechanisms underlying the axonal Charcot–Marie–Tooth neuropathy caused by MORC2 mutations
56. Differential gene expression studies to explore the molecular pathophysiology of Down syndrome
57. Disrupted function of lactate transporter MCT1, but not MCT4, in Schwann cells affects the maintenance of motor end‐plate innervation.
58. Oligodendroglial myelination requires astrocyte-derived lipids
59. Lipin1 is required for skeletal muscle development by regulating MEF2c and MyoD expression
60. Neuromuscular Junction Changes in a Mouse Model of Charcot-Marie-Tooth Disease Type 4C
61. Lipin1 deficiency causes sarcoplasmic reticulum stress and chaperone‐responsive myopathy
62. CMT disease 2A and demyelination decouple ATP and ROS production by axonal mitochondria
63. Loss of lipin 1‐mediated phosphatidic acid phosphohydrolase activity in muscle leads to skeletal myopathy in mice
64. Macrophage-associated lipin-1 enzymatic activity contributes to modified low-density lipoprotein-induced pro-inflammatory signaling and atherosclerosis.
65. PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease
66. Oligodendroglial myelination requires astrocyte-derived lipids
67. Oligodendroglial myelination requires astrocyte-derived lipids
68. Reply: Is SIGMAR1 a confirmed FTD/MND gene?
69. Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome
70. PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease
71. SH3TC2, a protein mutant in Charcot-Marie-Tooth neuropathy, links peripheral nerve myelination to endosomal recycling
72. Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathies
73. Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor
74. Phosphatidic acid mediates demyelination in Lpin1 mutant mice
75. Charcot–Marie–Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challenges
76. The Role of Peripheral Myelin Protein 2 in Remyelination
77. Diagnostic Challenges due to Atypical presentations of CMT in Charcot Marie Tooth Disease type 4C associated with SH3TC2 mutations (P5.124)
78. Local regulation of fat metabolism in peripheral nerves
79. Altered interplay between endoplasmic reticulum and mitochondria in Charcot-Marie-Tooth type 2A neuropathy.
80. Lipin1 is required for skeletal muscle development by regulating MEF2c and MyoD expression.
81. Loss of lipin 1-mediated phosphatidic acid phosphohydrolase activity in muscle leads to skeletal myopathy in mice.
82. Myeloid Cell-Specific Lipin-1 Deficiency Stimulates Endocrine Adiponectin-FGF15 Axis and Ameliorates Ethanol-Induced Liver Injury in Mice
83. Charcot-Marie-Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challenges.
84. Erratum: Corrigendum: Transcriptional regulator PRDM12 is essential for human pain perception
85. Missense mutations inTENM4, a regulator of axon guidance and central myelination, cause essential tremor
86. Reply: IsSIGMAR1a confirmed FTD/MND gene?
87. Loss of function mutations inHARScause a spectrum of inherited peripheral neuropathies
88. Transcriptional regulator PRDM12 is essential for human pain perception
89. Lack of GDAP1 Induces Neuronal Calcium and Mitochondrial Defects in a Knockout Mouse Model of Charcot-Marie-Tooth Neuropathy
90. Distribution of Monocarboxylate Transporters in the Peripheral Nervous System Suggests Putative Roles in Lactate Shuttling and Myelination
91. A role of peripheral myelin protein 2 in lipid homeostasis of myelinating Schwann cells.
92. A Missense Mutation in Myelin Oligodendrocyte Glycoprotein as a Cause of Familial Narcolepsy with Cataplexy
93. Global Transcript Expression Profiling by Serial Analysis of Gene Expression (SAGE)
94. Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) gene
95. Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations
96. New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations
97. Neuronal activity in the hub of extrasynaptic Schwann cell-axon interactions
98. Akt Regulates Axon Wrapping and Myelin Sheath Thickness in the PNS.
99. Mice with an adipocyte-specific lipin 1 separation-of-function allele reveal unexpected roles for phosphatidic acid in metabolic regulation
100. Cell Autonomous Lipin 1 Function Is Essential for Development and Maintenance of White and Brown Adipose Tissue
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.