Bowen-Conradi Syndrome Latest Advances

EMG1 cooperates with GRHL3 in β-catenin-mediated surface ectoderm differentiation to regulate neural tube closure.

Journal: Development (Cambridge, England)

Published: February 03, 2025

Chemical Modifications of Ribosomal RNA.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: July 07, 2022

Naturally occurring modified ribonucleosides.

Journal: Wiley interdisciplinary reviews. RNA

Published: January 12, 2020

Quantum Language of MicroRNA: Application for New Cancer Therapeutic Targets.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: February 13, 2018

Effects of the Bowen-Conradi syndrome mutation in EMG1 on its nuclear import, stability and nucleolar recruitment.

Journal: Human molecular genetics

Published: August 29, 2016

Nucleolar Enrichment of Brain Proteins with Critical Roles in Human Neurodevelopment.

Journal: Molecular & cellular proteomics : MCP

Published: May 15, 2015

A Hutterite condition that mimics Bowen-Conradi syndrome.

Journal: South Dakota medicine : the journal of the South Dakota State Medical Association

Published: April 25, 2015

Bowen-Conradi Syndrome: a trisomy 18-like autosomal recessive disorder common in Hutterites.

Journal: South Dakota medicine : the journal of the South Dakota State Medical Association

Published: March 25, 2015

Growth arrest in the ribosomopathy, Bowen-Conradi syndrome, is due to dramatically reduced cell proliferation and a defect in mitotic progression.

Journal: Biochimica et biophysica acta

Published: November 24, 2014

Mutation of EMG1 causing Bowen-Conradi syndrome results in reduced cell proliferation rates concomitant with G2/M arrest and 18S rRNA processing delay.

Journal: BBA clinical

Published: March 25, 2014

Human diseases of the SSU processome.

Journal: Biochimica et biophysica acta

Published: August 16, 2013

Bowen-Conradi: a common Hutterite condition that mimics trisomy 18.

Journal: South Dakota medicine : the journal of the South Dakota State Medical Association

Published: August 04, 2012

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EMG1 cooperates with GRHL3 in β-catenin-mediated surface ectoderm differentiation to regulate neural tube closure.

EMG1 cooperates with GRHL3 in β-catenin-mediated surface ectoderm differentiation to regulate neural tube closure.

Chemical Modifications of Ribosomal RNA.

Chemical Modifications of Ribosomal RNA.

Naturally occurring modified ribonucleosides.

Naturally occurring modified ribonucleosides.

Quantum Language of MicroRNA: Application for New Cancer Therapeutic Targets.

Quantum Language of MicroRNA: Application for New Cancer Therapeutic Targets.

Effects of the Bowen-Conradi syndrome mutation in EMG1 on its nuclear import, stability and nucleolar recruitment.

Effects of the Bowen-Conradi syndrome mutation in EMG1 on its nuclear import, stability and nucleolar recruitment.

Nucleolar Enrichment of Brain Proteins with Critical Roles in Human Neurodevelopment.

Nucleolar Enrichment of Brain Proteins with Critical Roles in Human Neurodevelopment.

A Hutterite condition that mimics Bowen-Conradi syndrome.

A Hutterite condition that mimics Bowen-Conradi syndrome.

Bowen-Conradi Syndrome: a trisomy 18-like autosomal recessive disorder common in Hutterites.

Bowen-Conradi Syndrome: a trisomy 18-like autosomal recessive disorder common in Hutterites.

Growth arrest in the ribosomopathy, Bowen-Conradi syndrome, is due to dramatically reduced cell proliferation and a defect in mitotic progression.

Growth arrest in the ribosomopathy, Bowen-Conradi syndrome, is due to dramatically reduced cell proliferation and a defect in mitotic progression.

Mutation of EMG1 causing Bowen-Conradi syndrome results in reduced cell proliferation rates concomitant with G2/M arrest and 18S rRNA processing delay.

Mutation of EMG1 causing Bowen-Conradi syndrome results in reduced cell proliferation rates concomitant with G2/M arrest and 18S rRNA processing delay.

Human diseases of the SSU processome.

Human diseases of the SSU processome.

Bowen-Conradi: a common Hutterite condition that mimics trisomy 18.

Bowen-Conradi: a common Hutterite condition that mimics trisomy 18.