By manipulating the genome, it is possible to correct hereditary diseases in humans. Ensuring the birth of healthy children by diagnosing and selecting, for in vitro fertilization, an embryo that does not contain a pathogenic mutation is a serious prospect in modern genomic research. However, the legislative approaches of states towards this issue remain very ambiguous due to the complexity of the ethical and legal sides of this problem. We believe that a single consensus international position should be adopted on the issues of intervention in the human genome, otherwise permission to conduct in one country may lead to negative reactions in other states and lay criminal risks in this area
The aim of this article is to address the current risk of the increasingly progressive development o...
This article aims to examine clinical problems of genetic modification in human embryo and current i...
In April 2015, scientists used a new genetic engineering tool known as CRISPR to edit the genes of a...
Gene editing of human embryos is an interdisciplinary topic regarding science, ethics, religion, soc...
Although the potential advantages of clinical germline genome editing (GGE) over currently available...
To use human embryos outside of the ordinary course of nature is exceptional. Although it raises pro...
Perhaps the two most significant pioneering biomedical discoveries with immediate clinical implicati...
The CRISPR/Cas9 genome engineering platform is the first method of gene editing that could potential...
Purposes of pre-implantation genetic diagnosis (PGD) include screening for single gene mutation...
In this article we examine processes of ethical deliberation, legislative developments, and social a...
This paper examines current controversies around the use of gene editing on human embryos. Gene edit...
The use of genome embryo editing tools in reproduction is often touted as a way to ensure the birth ...
Scientists now have the ability to manipulate the DNA of human embryos in ways that could allow them...
As the sophistication of technology advances, it introduces new issues that had previously not been ...
AbstractGenome editing based on site-directed nucleases facilitated efficient and versatile genetic ...
The aim of this article is to address the current risk of the increasingly progressive development o...
This article aims to examine clinical problems of genetic modification in human embryo and current i...
In April 2015, scientists used a new genetic engineering tool known as CRISPR to edit the genes of a...
Gene editing of human embryos is an interdisciplinary topic regarding science, ethics, religion, soc...
Although the potential advantages of clinical germline genome editing (GGE) over currently available...
To use human embryos outside of the ordinary course of nature is exceptional. Although it raises pro...
Perhaps the two most significant pioneering biomedical discoveries with immediate clinical implicati...
The CRISPR/Cas9 genome engineering platform is the first method of gene editing that could potential...
Purposes of pre-implantation genetic diagnosis (PGD) include screening for single gene mutation...
In this article we examine processes of ethical deliberation, legislative developments, and social a...
This paper examines current controversies around the use of gene editing on human embryos. Gene edit...
The use of genome embryo editing tools in reproduction is often touted as a way to ensure the birth ...
Scientists now have the ability to manipulate the DNA of human embryos in ways that could allow them...
As the sophistication of technology advances, it introduces new issues that had previously not been ...
AbstractGenome editing based on site-directed nucleases facilitated efficient and versatile genetic ...
The aim of this article is to address the current risk of the increasingly progressive development o...
This article aims to examine clinical problems of genetic modification in human embryo and current i...
In April 2015, scientists used a new genetic engineering tool known as CRISPR to edit the genes of a...