List of works - Jonathan K Alder

Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis.

scientific article

Another building in the IPF Manhattan plot skyline

scientific article published on 20 October 2017

CRISPR-Cas9 directed knock-out of a constitutively expressed gene using lance array nanoinjection

scientific article

Cellular Senescence: The Trojan Horse in Chronic Lung Diseases

scientific article published on 01 July 2019

Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript

scientific article

Comparative Analysis of Lipid-Mediated CRISPR-Cas9 Genome Editing Techniques

scientific article published on 19 February 2018

GDF15 is an epithelial-derived biomarker of idiopathic pulmonary fibrosis

scientific article published on 21 August 2019

Phenotypic Diversity Caused by Differential Expression of SFTPC-Cre Transgenic Alleles

scientific article published on 24 March 2020

Rapid direct sequence analysis of the dystrophin gene

scientific article

Short telomere syndromes cause a primary T cell immunodeficiency

scientific article published on 22 October 2018

Short telomeres are a risk factor for idiopathic pulmonary fibrosis

scholarly article

Short telomeres are sufficient to cause the degenerative defects associated with aging

scientific article published on December 2009

Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase ⬇️

scientific article published on March 24, 2011

Telomerase mutations in smokers with severe emphysema.

scientific article

Telomere Phenotypes in Females with Heterozygous Mutations in the Dyskeratosis Congenita 1 (DKC1) Gene ⬇️

scientific article published on September 11, 2013

Telomere length is a determinant of emphysema susceptibility.

scientific article published on 14 July 2011

List of works by Jonathan K Alder

Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis.

Another building in the IPF Manhattan plot skyline

CRISPR-Cas9 directed knock-out of a constitutively expressed gene using lance array nanoinjection

Cellular Senescence: The Trojan Horse in Chronic Lung Diseases

Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript

Comparative Analysis of Lipid-Mediated CRISPR-Cas9 Genome Editing Techniques

GDF15 is an epithelial-derived biomarker of idiopathic pulmonary fibrosis

Phenotypic Diversity Caused by Differential Expression of SFTPC-Cre Transgenic Alleles

Rapid direct sequence analysis of the dystrophin gene

Short telomere syndromes cause a primary T cell immunodeficiency

Short telomeres are a risk factor for idiopathic pulmonary fibrosis

Short telomeres are sufficient to cause the degenerative defects associated with aging

Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase ⬇️

Telomerase mutations in smokers with severe emphysema.

Telomere Phenotypes in Females with Heterozygous Mutations in the Dyskeratosis Congenita 1 (DKC1) Gene ⬇️

Telomere length is a determinant of emphysema susceptibility.