about
Discovery of the elusive leptin in birds: identification of several 'missing links' in the evolution of leptin and its receptorThe C-terminal domain of SRA1p has a fold more similar to PRP18 than to an RRM and does not directly bind to the SRA1 RNA STR7 regionDifferential mechanisms of activation of the Ang peptide receptors AT1, AT2, and MAS: using in silico techniques to differentiate the three receptorsMethylation specific targeting of a chromatin remodeling complex from sponges to humansOn the Molecular Evolution of Leptin, Leptin Receptor, and EndospaninRefined mapping of a hypertension susceptibility locus on rat chromosome 12.MAS promoter regulation: a role for Sry and tyrosine nitration of the KRAB domain of ZNF274 as a feedback mechanism.Analysis of Sry duplications on the Rattus norvegicus Y-chromosomeLeptin in teleost fishes: an argument for comparative study.Structural libraries of protein models for multiple species to understand evolution of the renin-angiotensin system.An evolutionarily conserved DNA architecture determines target specificity of the TWIST family bHLH transcription factors.Mutation of SH2B3 (LNK), a genome-wide association study candidate for hypertension, attenuates Dahl salt-sensitive hypertension via inflammatory modulation.Similarities and differences of X and Y chromosome homologous genes, SRY and SOX3, in regulating the renin-angiotensin system promoters.From rat to human: regulation of Renin-Angiotensin system genes by sry.Chromosome Y genetic variants: impact in animal models and on human diseaseThe phenotypic impact of the male-specific region of chromosome-Y in inbred mating: the role of genetic variants and gene duplications in multiple inbred rat strains.The Tumor-suppressive Small GTPase DiRas1 Binds the Noncanonical Guanine Nucleotide Exchange Factor SmgGDS and Antagonizes SmgGDS Interactions with Oncogenic Small GTPasesSry, more than testis determination?Molecular evolution of GPCRs: Melanocortin/melanocortin receptors.Differences in the Phosphorylation-Dependent Regulation of Prenylation of Rap1A and Rap1B.Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy.Beyond thermoregulation: metabolic function of cetacean blubber in migrating bowhead and beluga whales.The tumor-suppressive small GTPase DiRas1 binds the noncanonical guanine nucleotide exchange factor SmgGDS and antagonizes SmgGDS interactions with oncogenic small GTPases.Familial and Somatic BAP1 Mutations Inactivate ASXL1/2-Mediated Allosteric Regulation of BAP1 Deubiquitinase by Targeting Multiple Independent Domains.Genetic Fine-Mapping and Identification of Candidate Genes and Variants for Adiposity Traits in Outbred Rats.Molecular modeling in the age of clinical genomics, the enterprise of the next generation.Functional domain analysis of SOX18 transcription factor using a single-chain variable fragment-based approach.Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD.Genome Sequencing in the Clinic: The Past, Present, and Future of Genomic Medicine.De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder.Lethal NARS2-Related Disorder Associated With Rapidly Progressive Intractable Epilepsy and Global Brain AtrophyDe novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delayRNF213 variants in a child with PHACE syndrome and moyamoya vasculopathyEvolution of the phenotype of craniosynostosis with dental anomalies syndrome and report of IL11RA variant population frequencies in a Crouzon-like autosomal recessive syndromeGenome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
Jeremy W Prokop
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Jeremy W Prokop
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Jeremy W Prokop
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Jeremy W Prokop
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Jeremy W Prokop
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Jeremy W Prokop
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Jeremy W Prokop
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Jeremy W Prokop
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prefLabel
Jeremy W Prokop
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Jeremy W Prokop
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Jeremy W Prokop
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Jeremy W Prokop
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P106
P1153
54279363500
P31
P496
0000-0002-1818-9695