Prameela Kantheti

Mutation in AP-3 δ in the mocha Mouse Links Endosomal Transport to Storage Deficiency in Platelets, Melanosomes, and Synaptic Vesicles

Prameela Kantheti, Xiaoxi Qiao, María E. Díaz et al. · Neuron · 1998 · 397 citations · Full text

Signal Transduction, Genetics, Synaptic Vesicles +11

Genetic and phenotypic analysis of the mouse mutant mh 2J , an Ap3d allele caused by IAP element insertion

Prameela Kantheti, María Elena Díaz, Andrew A. Peden et al. · Mammalian Genome · 2003 · 35 citations

Knockout Mouse, Iap Element Insertion, Phenotypic Analysis +8

Comparative Maps of Human 19p13.3 and Mouse Chromosome 10 Allow Identification of Sequences at Evolutionary Breakpoints

Radhika Puttagunta, Laurie Gordon, Gary Meyer et al. · Genome Research · 2000 · 35 citations · Full text

Cytogenetics, Genetics, Molecular Genetics +18

Expression of Caytaxin Protein in Cayman Ataxia Mouse Models Correlates with Phenotype Severity

Kristine M. Sikora, LaGina Merie Nosavanh, Prameela Kantheti et al. · PLoS ONE · 2012 · 18 citations · Full text

Genetics, Human Cayman Ataxia, Social Sciences +17

Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: Identification of novel mutations that affect PAH RNA

Murali Dharan Bashyam, Ajay Kumar Chaudhary, E. Chandrakanth Reddy et al. · Molecular Genetics and Metabolism · 2010 · 12 citations

Genetic Disorder, Genetics, Inherited Metabolic Disease +6