Congenital disorders of glycosylation: narration of a story through its patents.
Congenital disorders of glycosylation: narration of a story through its patents.
复制标题
DOI:
10.1186/s13023-023-02852-w
复制
发表时间:
2023-08-29
影响因子:
3.7
通讯作者:
中科院分区:
文献类型:
--
作者:
Congenital disorders of glycosylation are a group of more than 160 rare genetic defects in protein and lipid glycosylation. Since the first clinical report in 1980 of PMM2-CDG, the most common CDG worldwide, research made great strides, but nearly all of them are still missing a cure. CDG diagnosis has been at a rapid pace since the introduction of whole-exome/whole-genome sequencing as a diagnostic tool. Here, we retrace the history of CDG by analyzing all the patents associated with the topic. To this end, we explored the Espacenet database, extracted a list of patents, and then divided them into three major groups: (1) Drugs/therapeutic approaches for CDG, (2) Drug delivery tools for CDG, (3) Diagnostic tools for CDG. Despite the enormous scientific progress experienced in the last 30 years, diagnostic tools, drugs, and biomarkers are still urgently needed. The online version contains supplementary material available at 10.1186/s13023-023-02852-w.
登录
查看更多内容
影响因子:
3.5
作者:
Gicquel, Evelyne;Maizonnier, Natacha;Richard, Isabelle
通讯作者:
Richard, Isabelle
影响因子:
2
作者:
Andreotti, Giuseppina;Pedone, Emilia;Giordano, Assunta;Cubellis, Maria Vittoria
通讯作者:
Cubellis, Maria Vittoria
DOI:
10.1006/bmme.1997.2574
发表时间:
1997-04-01
期刊:
BIOCHEMICAL AND MOLECULAR MEDICINE
影响因子:
--
作者:
Alton, G;Kjaergaard, S;Freeze, HH
通讯作者:
Freeze, HH
影响因子:
4.2
作者:
Čechová A;Altassan R;Borgel D;Bruneel A;Correia J;Girard M;Harroche A;Kiec-Wilk B;Mohnike K;Pascreau T;Pawliński Ł;Radenkovic S;Vuillaumier-Barrot S;Aldamiz-Echevarria L;Couce ML;Martins EG;Quelhas D;Morava E;de Lonlay P;Witters P;Honzík T
通讯作者:
Honzík T
影响因子:
5.9
作者:
Witters P;Cassiman D;Morava E
通讯作者:
Morava E