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Literature DB >> 31152729

Bespoke Babies: Genome Editing in Cystic Fibrosis Embryos.

Kyle B Brothers¹, Mary Devereaux², Robert M Sade³.

Abstract

Entities: Chemical Disease Gene Species

Year: 2019 PMID： 31152729 PMCID： PMC6931252 DOI： 10.1016/j.athoracsur.2019.04.030

Source DB: PubMed Journal: Ann Thorac Surg ISSN： 0003-4975 Impact factor: 4.330

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11 in total

Review 1. Human Germline Genome Editing.

Authors: Kelly E Ormond; Douglas P Mortlock; Derek T Scholes; Yvonne Bombard; Lawrence C Brody; W Andrew Faucett; Nanibaa' A Garrison; Laura Hercher; Rosario Isasi; Anna Middleton; Kiran Musunuru; Daniel Shriner; Alice Virani; Caroline E Young
Journal: Am J Hum Genet Date: 2017-08-03 Impact factor: 11.025

2. A contemporary survival analysis of individuals with cystic fibrosis: a cohort study.

Authors: Anne L Stephenson; Melissa Tom; Yves Berthiaume; Lianne G Singer; Shawn D Aaron; G A Whitmore; Sanja Stanojevic
Journal: Eur Respir J Date: 2014-11-13 Impact factor: 16.671

Review 3. A systematic review of factors associated with health-related quality of life in adolescents and adults with cystic fibrosis.

Authors: Al-Rahim R Habib; Jamil Manji; Pearce G Wilcox; Amin R Javer; Jane A Buxton; Bradley S Quon
Journal: Ann Am Thorac Soc Date: 2015-03

Bespoke Babies: Genome Editing in Cystic Fibrosis Embryos.

Review 1. Human Germline Genome Editing.

2. A contemporary survival analysis of individuals with cystic fibrosis: a cohort study.

Review 3. A systematic review of factors associated with health-related quality of life in adolescents and adults with cystic fibrosis.

Review 4. Zinc finger nuclease technology heralds a new era in mammalian transgenesis.

5. U.S. attitudes on human genome editing.

6. Shock greets claim of CRISPR-edited babies.

7. Rethink public engagement for gene editing.

8. Diabetes-related mortality in adults with cystic fibrosis. Role of genotype and sex.

9. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.

10. Repair of double-strand breaks induced by CRISPR-Cas9 leads to large deletions and complex rearrangements.

1. Human genome editing and the identity politics of genetic disability.

Review 2. Clinical Trial Design for Disease-Modifying Therapies for Genetic Epilepsies.