Angelika A. Noegel

Joseph Stelzmann Str. 52
Koeln, NW, Germany

Last Updated: 09/26/2026

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Found 73 publications

Evolution of microRNAs in Amoebozoa and implications for the origin of multicellularity.

Evolution of microRNAs in Amoebozoa and implications for the origin of multicellularity.

Journal: Nucleic acids research

Published: November 14, 2023

Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling.

Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 29, 2021

De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway.

De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway.

Journal: HGG advances

Published: November 29, 2021

Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism.

Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism.

Journal: Genes

Published: June 30, 2021

A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome.

A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome.

Journal: Clinical genetics

Published: May 24, 2021

Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies.

Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: March 19, 2021

Abundantly expressed class of noncoding RNAs conserved through the multicellular evolution of dictyostelid social amoebas.

Abundantly expressed class of noncoding RNAs conserved through the multicellular evolution of dictyostelid social amoebas.

Journal: Genome research

Published: October 08, 2020

An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan.

An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan.

Journal: Molecular genetics & genomic medicine

Published: January 30, 2020

Lack of a Retinal Phenotype in a Syne-2/Nesprin-2 Knockout Mouse Model.

Lack of a Retinal Phenotype in a Syne-2/Nesprin-2 Knockout Mouse Model.

Journal: Cells

Published: September 17, 2019

CRN2 binds to TIMP4 and MMP14 and promotes perivascular invasion of glioblastoma cells.

CRN2 binds to TIMP4 and MMP14 and promotes perivascular invasion of glioblastoma cells.

Journal: European journal of cell biology

Published: June 04, 2019

Nesprin-1 impact on tumorigenic cell phenotypes.

Nesprin-1 impact on tumorigenic cell phenotypes.

Journal: Molecular biology reports

Published: March 17, 2019

Depletion of Nesprin-2 is associated with an embryonic lethal phenotype in mice.

Depletion of Nesprin-2 is associated with an embryonic lethal phenotype in mice.

Journal: Nucleus (Austin, Tex.)

Published: September 18, 2018

Showing 1-12 of 73

Last Updated: 09/26/2026