Wen T. Qin

London, ON N6A3K7, Canada

Last Updated: 09/26/2026

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Found 11 publications

The Transcriptional Repressor BS69 is a Conserved Target of the E1A Proteins from Several Human Adenovirus Species.

The Transcriptional Repressor BS69 is a Conserved Target of the E1A Proteins from Several Human Adenovirus Species.

Journal: Viruses

Published: October 31, 2018

Surface Loops in a Single SH2 Domain Are Capable of Encoding the Spectrum of Specificity of the SH2 Family.

Surface Loops in a Single SH2 Domain Are Capable of Encoding the Spectrum of Specificity of the SH2 Family.

Journal: Molecular & cellular proteomics : MCP

Published: September 28, 2018

Infantile Myofibromatosis With Intracranial Extradural Involvement and PDGFRB Mutation: A Case Report and Review of the Literature.

Infantile Myofibromatosis With Intracranial Extradural Involvement and PDGFRB Mutation: A Case Report and Review of the Literature.

Journal: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society

Published: August 15, 2018

Integration of A Deep Learning Classifier with A Random Forest Approach for Predicting Malonylation Sites.

Integration of A Deep Learning Classifier with A Random Forest Approach for Predicting Malonylation Sites.

Journal: Genomics, proteomics & bioinformatics

Published: January 26, 2018

Novel 25 kb Deletion of MERTK Causes Retinitis Pigmentosa With Severe Progression.

Novel 25 kb Deletion of MERTK Causes Retinitis Pigmentosa With Severe Progression.

Journal: Investigative ophthalmology & visual science

Published: March 22, 2017

Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability.

Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability.

Journal: American journal of human genetics

Published: September 15, 2015

Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation.

Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation.

Journal: American journal of medical genetics. Part A

Published: September 10, 2015

Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8.

Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8.

Journal: American journal of human genetics

Published: July 08, 2015

Identification of a Recognizable Progressive Skeletal Dysplasia Caused by RSPRY1 Mutations.

Identification of a Recognizable Progressive Skeletal Dysplasia Caused by RSPRY1 Mutations.

Journal: American journal of human genetics

Published: June 17, 2015

Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability.

Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability.

Journal: Human molecular genetics

Published: May 23, 2015

A novel mutation in two Hmong families broadens the range of STRA6-related malformations to include contractures and camptodactyly.

A novel mutation in two Hmong families broadens the range of STRA6-related malformations to include contractures and camptodactyly.

Journal: American journal of medical genetics. Part A

Published: February 03, 2015

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Last Updated: 09/26/2026