Lista de obras - Jeremy W Prokop - Dominio Público Uruguay

An evolutionarily conserved DNA architecture determines target specificity of the TWIST family bHLH transcription factors.

artículo científico publicado en 2015

Analysis of Sry duplications on the Rattus norvegicus Y-chromosome

artículo científico publicado en 2013

Balancing precision versus cohort transcriptomic analysis of acute and recovery phase of viral bronchiolitis

artículo científico publicado en 2021

Beyond thermoregulation: metabolic function of cetacean blubber in migrating bowhead and beluga whales

artículo científico publicado en 2016

Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD.

artículo científico publicado en 2018

Chromosome Y genetic variants: impact in animal models and on human disease

artículo científico publicado en 2015

De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder.

artículo científico publicado en 2018

De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay

artículo científico publicado en 2018

Differences in the Phosphorylation-Dependent Regulation of Prenylation of Rap1A and Rap1B.

artículo científico publicado en 2016

Differential mechanisms of activation of the Ang peptide receptors AT1, AT2, and MAS: using in silico techniques to differentiate the three receptors

artículo científico publicado en 2013

Discovery of the elusive leptin in birds: identification of several 'missing links' in the evolution of leptin and its receptor

artículo científico publicado en 2014

Evolution of the phenotype of craniosynostosis with dental anomalies syndrome and report of IL11RA variant population frequencies in a Crouzon-like autosomal recessive syndrome

artículo científico publicado en 2019

Familial and Somatic BAP1 Mutations Inactivate ASXL1/2-Mediated Allosteric Regulation of BAP1 Deubiquitinase by Targeting Multiple Independent Domains.

artículo científico publicado en 2017

From rat to human: regulation of Renin-Angiotensin system genes by sry.

artículo científico publicado en 2012

Functional domain analysis of SOX18 transcription factor using a single-chain variable fragment-based approach.

artículo científico publicado en 2018

Genetic Fine-Mapping and Identification of Candidate Genes and Variants for Adiposity Traits in Outbred Rats.

artículo científico publicado en 2017

Genome Sequencing in the Clinic: The Past, Present, and Future of Genomic Medicine.

artículo científico publicado en 2018

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

scientific article published on 13 December 2019

Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy

artículo científico publicado en 2016

Leptin in teleost fishes: an argument for comparative study.

artículo científico publicado en 2011

Lethal NARS2-Related Disorder Associated With Rapidly Progressive Intractable Epilepsy and Global Brain Atrophy

artículo científico publicado en 2018

MAS promoter regulation: a role for Sry and tyrosine nitration of the KRAB domain of ZNF274 as a feedback mechanism.

artículo científico publicado en 2014

Methylation specific targeting of a chromatin remodeling complex from sponges to humans

artículo científico publicado en 2017

Molecular evolution of GPCRs: Melanocortin/melanocortin receptors

artículo científico publicado en 2014

Molecular modeling in the age of clinical genomics, the enterprise of the next generation.

artículo científico publicado en 2017

Mutation of SH2B3 (LNK), a genome-wide association study candidate for hypertension, attenuates Dahl salt-sensitive hypertension via inflammatory modulation

artículo científico publicado en 2015

On the Molecular Evolution of Leptin, Leptin Receptor, and Endospanin

artículo científico publicado en 2017

RNF213 variants in a child with PHACE syndrome and moyamoya vasculopathy

artículo científico publicado en 2017

Refined mapping of a hypertension susceptibility locus on rat chromosome 12.

artículo científico publicado en 2014

SARS-CoV-2 (COVID-19) structural and evolutionary dynamicome: Insights into functional evolution and human genomics

artículo científico publicado en 2020

Similarities and differences of X and Y chromosome homologous genes, SRY and SOX3, in regulating the renin-angiotensin system promoters.

artículo científico publicado en 2015

Sry, more than testis determination?

artículo científico publicado en 2011

Structural libraries of protein models for multiple species to understand evolution of the renin-angiotensin system

artículo científico publicado en 2014

The 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 region

artículo científico publicado en 2014

The Tumor-suppressive Small GTPase DiRas1 Binds the Noncanonical Guanine Nucleotide Exchange Factor SmgGDS and Antagonizes SmgGDS Interactions with Oncogenic Small GTPases

artículo científico publicado en 2016

The 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.

artículo científico publicado en 2016

The tumor-suppressive small GTPase DiRas1 binds the noncanonical guanine nucleotide exchange factor SmgGDS and antagonizes SmgGDS interactions with oncogenic small GTPases

artículo científico publicado en 2016

Lista de obras de Jeremy W Prokop

An evolutionarily conserved DNA architecture determines target specificity of the TWIST family bHLH transcription factors.

Analysis of Sry duplications on the Rattus norvegicus Y-chromosome

Balancing precision versus cohort transcriptomic analysis of acute and recovery phase of viral bronchiolitis

Beyond thermoregulation: metabolic function of cetacean blubber in migrating bowhead and beluga whales

Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD.

Chromosome Y genetic variants: impact in animal models and on human disease

De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder.

De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay

Differences in the Phosphorylation-Dependent Regulation of Prenylation of Rap1A and Rap1B.

Differential mechanisms of activation of the Ang peptide receptors AT1, AT2, and MAS: using in silico techniques to differentiate the three receptors

Discovery of the elusive leptin in birds: identification of several 'missing links' in the evolution of leptin and its receptor

Evolution of the phenotype of craniosynostosis with dental anomalies syndrome and report of IL11RA variant population frequencies in a Crouzon-like autosomal recessive syndrome

Familial and Somatic BAP1 Mutations Inactivate ASXL1/2-Mediated Allosteric Regulation of BAP1 Deubiquitinase by Targeting Multiple Independent Domains.

From rat to human: regulation of Renin-Angiotensin system genes by sry.

Functional domain analysis of SOX18 transcription factor using a single-chain variable fragment-based approach.

Genetic Fine-Mapping and Identification of Candidate Genes and Variants for Adiposity Traits in Outbred Rats.

Genome Sequencing in the Clinic: The Past, Present, and Future of Genomic Medicine.

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy

Leptin in teleost fishes: an argument for comparative study.

Lethal NARS2-Related Disorder Associated With Rapidly Progressive Intractable Epilepsy and Global Brain Atrophy

MAS promoter regulation: a role for Sry and tyrosine nitration of the KRAB domain of ZNF274 as a feedback mechanism.

Methylation specific targeting of a chromatin remodeling complex from sponges to humans

Molecular evolution of GPCRs: Melanocortin/melanocortin receptors

Molecular modeling in the age of clinical genomics, the enterprise of the next generation.

Mutation of SH2B3 (LNK), a genome-wide association study candidate for hypertension, attenuates Dahl salt-sensitive hypertension via inflammatory modulation

On the Molecular Evolution of Leptin, Leptin Receptor, and Endospanin

RNF213 variants in a child with PHACE syndrome and moyamoya vasculopathy

Refined mapping of a hypertension susceptibility locus on rat chromosome 12.

SARS-CoV-2 (COVID-19) structural and evolutionary dynamicome: Insights into functional evolution and human genomics

Similarities and differences of X and Y chromosome homologous genes, SRY and SOX3, in regulating the renin-angiotensin system promoters.

Sry, more than testis determination?

Structural libraries of protein models for multiple species to understand evolution of the renin-angiotensin system

The 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 region

The Tumor-suppressive Small GTPase DiRas1 Binds the Noncanonical Guanine Nucleotide Exchange Factor SmgGDS and Antagonizes SmgGDS Interactions with Oncogenic Small GTPases

The 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 GTPases