(Q33582790)

28 July 2017

title

Impact of human pathogenic micro-insertions and micro-deletions on post-transcriptional regulation (English)

1 reference

28 July 2017

1 reference

28 July 2017

Huiying Zhao

0 references

Yaoqi Zhou

0 references

Matthew Mort

1 reference

28 July 2017

Xinjun Zhang

1 reference

28 July 2017

Hai Lin

series ordinal

1 reference

28 July 2017

Yangyang Hao

series ordinal

1 reference

28 July 2017

Yunlong Liu

series ordinal

1 reference

28 July 2017

language of work or name

English

0 references

publication date

16 January 2014

1 reference

28 July 2017

published in

Human Molecular Genetics

1 reference

28 July 2017

1 reference

28 July 2017

1 reference

28 July 2017

page(s)

3024-3034

1 reference

The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine

28 July 2017

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

21 June 2018

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Colorectal cancer and genetic alterations in the Wnt pathway

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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A secondary structure that contains the 5' and 3' splice sites suppresses splicing of duck hepatitis B virus pregenomic RNA.

21 June 2018

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21 June 2018

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Conserved stem-loop structures in the HIV-1 RNA region containing the A3 3' splice site and its cis-regulatory element: possible involvement in RNA splicing

21 June 2018

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An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease.

21 June 2018

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21 June 2018

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Insertion/deletion polymorphism of the angiotensin-converting enzyme gene is strongly associated with coronary heart disease in non-insulin-dependent diabetes mellitus

21 June 2018

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A DNA insertion/deletion necessitates an aberrant RNA splice accounting for a mu heavy chain disease protein

21 June 2018

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21 June 2018

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21 June 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Linking C5 deficiency to an exonic splicing enhancer mutation

21 January 2018

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Differential GC Content between Exons and Introns Establishes Distinct Strategies of Splice-Site Recognition

21 January 2018

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21 January 2018

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Bayesian Network Classifiers

21 January 2018

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Multilayer feedforward networks are universal approximators

21 January 2018

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Identifying Important Risk Factors for Survival in Kidney Graft Failure Patients Using Random Survival Forests

21 January 2018

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Alternative splicing in disease and therapy

21 January 2018

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Predicting protein associations with long noncoding RNAs

21 January 2018

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Association between a complex insertion/deletion polymorphism in NOD1 (CARD4) and susceptibility to inflammatory bowel disease

21 January 2018

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A Heterozygous Frameshift Mutation in the V1 Domain of Keratin 5 in a Family with Dowling–Degos Disease

21 January 2018

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Angiotensin-converting enzyme insertion/deletion polymorphism and cerebrovascular disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24436305

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A six-nucleotide insertion-deletion polymorphism in the CASP8 promoter is associated with susceptibility to multiple cancers

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24436305

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association of polymorphisms across the tyrosine kinase gene, TYK2 in UK SLE families

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24436305

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDU019

1 reference

28 July 2017

1 reference

28 July 2017

1 reference