Contributors |
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ix | |
Preface |
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xi | |
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1 Pathogen and host genetics underpinning cryptococcal disease |
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1 | (66) |
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2 | (1) |
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2 Cryptococcus spp. genetics and genomics |
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3 | (27) |
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30 | (16) |
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46 | (1) |
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46 | (21) |
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2 Role of RNA-interacting proteins in modulating plant-microbe interactions |
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67 | (28) |
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68 | (8) |
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2 Crossing barriers: HIGS into action |
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76 | (1) |
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3 RNA-interacting proteins at the verge of plant-pathogen interaction |
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77 | (1) |
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4 RNA chaperone-sRNA interplay in host-microbe interaction |
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78 | (7) |
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5 Pathogenic sRNAs to impede host defense |
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85 | (1) |
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6 sRNAs on the move: Mechanistic insights into cross-kingdom sRNA movement |
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86 | (1) |
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87 | (1) |
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88 | (1) |
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88 | (7) |
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3 FMRP ribonucleoprotein complexes and RNA homeostasis |
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95 | (42) |
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Gabriela Aparecida Marcondes Suardi |
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96 | (3) |
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2 FMR1-associated clinical conditions |
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99 | (5) |
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3 FMRP is a synaptic regulator |
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104 | (2) |
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4 FMRP in ribonucleoprotein (RNP) complexes |
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106 | (14) |
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120 | (1) |
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121 | (1) |
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121 | (16) |
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4 "Electrifying dysmorphology": Potassium channelopathies causing dysmorphic syndromes |
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137 | (38) |
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138 | (1) |
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2 Potassium channel structure and function |
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139 | (2) |
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3 Andersen-Tawil syndrome |
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141 | (4) |
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4 Bauer-Tartaglia (FHEIG) syndrome |
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145 | (3) |
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5 Birk-Barel syndrome (BBS) |
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148 | (2) |
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150 | (4) |
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7 Keppen-Lubinsky syndrome (KLS) |
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154 | (4) |
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8 Temple-Baraitser syndrome (TBS) |
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158 | (4) |
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9 Zimmermann-Laband syndrome (ZLS) |
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162 | (4) |
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166 | (1) |
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167 | (1) |
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167 | (8) |
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5 Recent advances in oomycete genomics |
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175 | (54) |
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176 | (4) |
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180 | (10) |
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190 | (4) |
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4 Oomycete mitochondrial genomes |
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194 | (2) |
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5 The impact of horizontal gene transfer on oomycete evolution |
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196 | (3) |
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6 Genome mining for oomycete effectors |
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199 | (7) |
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206 | (6) |
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8 Tools for oomycete genomics |
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212 | (2) |
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9 Oomycetes in the post-genomic era |
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214 | (3) |
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10 Conclusions and future outlook |
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217 | (1) |
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218 | (1) |
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218 | (11) |
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6 Antibiotic drug discovery: Challenges and perspectives in the light of emerging antibiotic resistance |
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229 | (64) |
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231 | (1) |
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2 History of novel antibiotic discovery |
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232 | (2) |
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3 Metabolite biosynthesizing microbes |
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234 | (1) |
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4 Antibiotics classification and their mode of actions |
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235 | (1) |
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5 Antibiotic resistance and evolution of superbugs |
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235 | (2) |
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6 Problem of antimicrobial resistance |
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237 | (1) |
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7 Foundation of antibiotic era |
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238 | (1) |
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8 Qualities to qualify as an antibiotic |
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238 | (1) |
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9 Antibiotics developmental pipeline and causes of discovery void |
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239 | (1) |
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10 Maintenance of antibiotics pipeline |
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240 | (1) |
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241 | (3) |
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244 | (1) |
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13 Characteristics of versatile surrogate chassis hosts |
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245 | (1) |
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14 Silent/cryptic gene clusters, their roles and significance |
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246 | (1) |
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15 Secondary metabolic cluster (presence of biosynthetic, resistance and transporters) |
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247 | (1) |
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16 Complex cascade regulation of antibiotic biosynthesis in actinomycetes (Nikkomycin biosynthetic cluster as an example) |
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247 | (3) |
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17 Classical approaches for detection of novel antibiotics |
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250 | (8) |
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18 Bioactivity analysis of novel antimicrobial compounds |
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258 | (1) |
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19 Strategies for prediction, analysis and activation of BGC |
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259 | (11) |
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20 Alternative approaches to conventional antibiotics |
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270 | (4) |
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21 Perspectives, challenges and conclusions |
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274 | (1) |
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275 | (18) |
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7 Application of yeast to studying amyloid and prion diseases |
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293 | |
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Pavithra Chandramowlishwaran |
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296 | (4) |
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2 Overview of yeast prions |
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300 | (8) |
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3 Yeast models for polyglutamine aggregation |
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308 | (9) |
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4 Yeast models for aggregation of α-synuclein, associated with Parkinson's disease (PD) |
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317 | (3) |
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5 Yeast models for amyloid proteins associated with Alzheimer's disease (AD) and tauopathies |
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320 | (9) |
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6 Yeast models for aggregation of mammalian prion protein (PrP) |
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329 | (6) |
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7 Yeast models for proteins associated with amyotrophic lateral sclerosis (ALS) |
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335 | (11) |
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8 Aggregation of transthyretin in yeast |
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346 | (1) |
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9 Yeast assay for amyloid nucleation by mammalian proteins |
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347 | (5) |
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10 Conclusions and future directions |
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352 | (2) |
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354 | (1) |
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354 | |