Byrappa Venkatesh
educated at: National University of Singapore
occupation: researcher
Articles 168
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Publisher Correction: Reconstruction of proto-vertebrate, protocyclostome and proto-gnathostome genomes provides new insights into early vertebrate evolution
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Reconstruction of proto-vertebrate, proto-cyclostome and proto-gnathostome genomes provides new insights into early vertebrate evolution
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Genome sequences reveal global dispersal routes and suggest convergent genetic adaptations in seahorse evolution
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Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
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Chromosome-level assembly of the horseshoe crab genome provides insights into its genome evolution
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Chromosome-level genome assembly of the coastal horseshoe crab (Tachypleus gigas)
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Conservation as well as divergence in Mcidas function underlies the differentiation of multiciliated cells in vertebrates
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A loss-of-function NUAK2 mutation in humans causes anencephaly due to impaired Hippo-YAP signaling
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Author Correction: Elephant shark genome provides unique insights into gnathostome evolution
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Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis
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Specific macrophage populations promote both cardiac scar deposition and subsequent resolution in adult zebrafish
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Transcriptional activation of elephant shark mineralocorticoid receptor by corticosteroids, progesterone, and spironolactone
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Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features
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Sydney Brenner—a personal perspective
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The Divergent Genomes of Teleosts.
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The Ancient Origins of Neural Substrates for Land Walking.
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Expansions, diversification, and interindividual copy number variations of AID/APOBEC family cytidine deaminase genes in lampreys.
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Comprehensive phylogeny of ray-finned fishes (Actinopterygii) based on transcriptomic and genomic data
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Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome
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Bone matrix hypermineralization associated with low bone turnover in a case of Nasu-Hakola disease
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Retention of fatty acyl desaturase 1 (fads1) in Elopomorpha and Cyclostomata provides novel insights into the evolution of long-chain polyunsaturated fatty acid biosynthesis in vertebrates
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Characterization of Gonadotropin-Releasing Hormone (GnRH) Genes From Cartilaginous Fish: Evolutionary Perspectives
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Whole exome sequencing identifies recessive germline mutations in FAM160A1 in familial NK/T cell lymphoma
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Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita
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CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays.
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Voltage-gated sodium channel gene repertoire of lampreys: gene duplications, tissue-specific expression and discovery of a long-lost gene.
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Reversal of Phenotypic Abnormalities by CRISPR/Cas9-Mediated Gene Correction in Huntington Disease Patient-Derived Induced Pluripotent Stem Cells.
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LXRα and LXRβ Nuclear Receptors Evolved in the Common Ancestor of Gnathostomes
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Draft genome of the lined seahorse, Hippocampus erectus
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Lampreys, the jawless vertebrates, contain only two ParaHox gene clusters
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Priming of lineage-specifying genes by Bcl11b is required for lineage choice in post-selection thymocytes.
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Corrigendum: The spotted gar genome illuminates vertebrate evolution and facilitates human-teleost comparisons.
Human - wd:Q28914672