%E0%A6%AE%E0%A6%BF%E0%A6%A4%E0%A6%BE%E0%A6%B2%E0%A6%BF_%E0%A6%AE%E0%A7%81%E0%A6%96%E0%A6%BE%E0%A6%B0%E0%A7%8D%E0%A6%9C%E0%A7%80Mitali_Mukerji%E0%A4%AE%E0%A4%BF%E0%A4%A4%E0%A4%BE%E0%A4%B2%E0%A5%80_%E0%A4%AE%E0%A5%81%E0%A4%96%E0%A4%B0%E0%A5%8D%E0%A4%9C%E0%A5%80%E0%B0%AE%E0%B0%BF%E0%B0%A5%E0%B0%BE%E0%B0%B2%E0%B1%80_%E0%B0%AE%E0%B1%81%E0%B0%96%E0%B0%B0%E0%B1%8D%E0%B0%9C%E0%B1%80Q15972945
about
Genome-wide prediction of G4 DNA as regulatory motifs: role in Escherichia coli global regulationEvolution and distribution of RNA polymerase II regulatory sites from RNA polymerase III dependant mobile Alu elementsMapping human genetic diversity in AsiaRecent Admixture in an Indian Population of African AncestrySNPs in stress-responsive rice genes: validation, genotyping, functional relevance and population structureInfantile onset spinocerebellar ataxia 2 (SCA2): a clinical report with review of previous cases.MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease.EGLN1 involvement in high-altitude adaptation revealed through genetic analysis of extreme constitution types defined in Ayurveda.Complex patterns of genomic admixture within southern AfricaSpinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic populationCombined genetic effects of EGLN1 and VWF modulate thrombotic outcome in hypoxia revealed by Ayurgenomics approachHeat shock factor binding in Alu repeats expands its involvement in stress through an antisense mechanism.Transcriptome-wide expansion of non-coding regulatory switches: evidence from co-occurrence of Alu exonization, antisense and editing.From 'JUNK' to just unexplored noncoding knowledge: the case of transcribed Alus.SMARCA2 and THAP11: potential candidates for polyglutamine disorders as evidenced from polymorphism and protein-folding simulation studies.Genomic insights into ayurvedic and western approaches to personalized medicine.Ayurgenomics for stratified medicine: TRISUTRA consortium initiative across ethnically and geographically diverse Indian populations.Extensive copy number variations in admixed Indian population of African ancestry: potential involvement in adaptation.Comparative Genomics of Host-Symbiont and Free-Living Oceanobacillus Species.Recapitulation of Ayurveda constitution types by machine learning of phenotypic traits.IGVBrowser--a genomic variation resource from diverse Indian populations.SCA-LSVD: a repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.Finding Alu in primate genomes with AF-1.From diversity to delivery: the case of the Indian Genome Variation initiative.Origin and instability of GAA repeats: insights from Alu elements.Utilizing linkage disequilibrium information from Indian Genome Variation Database for mapping mutations: SCA12 case study.A genome-wide search for non-UGT1A1 markers associated with unconjugated bilirubin level reveals significant association with a polymorphic marker near a gene of the nucleoporin family.North and South Indian populations share a common ancestral origin of Friedreich's ataxia but vary in age of GAA repeat expansion.Spectrum of large copy number variations in 26 diverse Indian populations: potential involvement in phenotypic diversity.Deletion of the APOBEC3B gene strongly impacts susceptibility to falciparum malaria.Ayurgenomics: a new way of threading molecular variability for stratified medicine.Targeted exome sequencing in anti-factor H antibody negative HUS reveals multiple variations.Human satellite-III non-coding RNAs modulate heat-shock-induced transcriptional repression.A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7-CAG Expansion Loci in the Indian and Mexican Population.Alu repeat analysis in the complete human genome: trends and variations with respect to genomic composition.Ancestral Variations of the PCDHG Gene Cluster Predispose to Dyslexia in a Multiplex Family.Western Indian Rural Gut Microbial Diversity in Extreme Prakriti Endo-Phenotypes Reveals Signature Microbes.SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.Complex phenotypes in an Indian family with homozygous SCA2 mutations.Population diversity and adaptive evolution in keratinization genes: impact of environment in shaping skin phenotypes.
P50
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P50
description
Indian scientist
@en
Indian scientist
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Indian scientist
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biologa indiana
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biologiste indienne
@fr
biologo indiarra
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biòloga índia
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bióloga india
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bióloga india
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bióloga indiana
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name
Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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मिताली मुखर्जी
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
@fr
Mitali Mukerji
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Mitali Mukerji
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मिताली मुखर्जी
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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Mitali Mukerji
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मिताली मुखर्जी
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P101
P106
P108
P21
P27
P31
P551
P569
1967-01-01T00:00:00Z