Genes & Diseases

ISSN 2352-4820 e-ISSN 2352-3042 CN 50-1221/R
Editors-in-Chief: Ailong Huang, Tong-Chuan He
Open Access
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Keyword: mutation
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Open Access Review Article
Unraveling the molecular genetics of head and neck cancer through genome-wide approaches
https://doi.org/10.1016/j.gendis.2014.07.002
Published: 23 July 2014
2014, 1 (1): 75-86
Downloads: 2 | Views: 121 | PDF (1.3 MB)
Open Access Review Article
CRISPR/Cas9 system and its applications in nervous system diseases
https://doi.org/10.1016/j.gendis.2023.03.017
Published: 13 April 2023
2024, 11 (2): 675-686
Downloads: 2 | Views: 87 | PDF (759.6 KB)
Open Access Review Article
How genetic errors in GPCRs affect their function: Possible therapeutic strategies
https://doi.org/10.1016/j.gendis.2015.02.005
Published: 25 February 2015
2015, 2 (2): 108-132
Downloads: 2 | Views: 141 | PDF (2.2 MB)
Open Access View on News
Human endogenous retroviruses – An ongoing evolutionary tango
https://doi.org/10.1016/j.gendis.2015.05.002
Published: 29 May 2015
2015, 2 (3): 224
Downloads: 1 | Views: 80 | PDF (216.2 KB)
Open Access Review Article
ESR1 mutations: Pièce de résistance
https://doi.org/10.1016/j.gendis.2016.03.005
Published: 19 April 2016
2016, 3 (2): 124-129
Downloads: 3 | Views: 129 | PDF (550.2 KB)
Open Access Short Communication
An EGLN1 mutation may regulate hypoxic response in cyanotic congenital heart disease through the PHD2/HIF-1A pathway
https://doi.org/10.1016/j.gendis.2018.03.003
Published: 13 March 2018
2019, 6 (1): 35-42
Downloads: 2 | Views: 134 | PDF (967.8 KB)
Open Access Full Length Article
Clinical phenotype of a Chinese patient with RIPK1 deficiency due to novel mutation
https://doi.org/10.1016/j.gendis.2019.10.008
Published: 21 October 2019
2020, 7 (1): 122-127
Downloads: 2 | Views: 197 | PDF (904.8 KB)
Open Access Research Article
A novel ABCD1 G1202A mutation in a Chinese patient with pure adrenomyeloneuropathy and literature review
https://doi.org/10.1016/j.gendis.2020.01.009
Published: 28 January 2020
2021, 8 (5): 709-714
Downloads: 1 | Views: 133 | PDF (604 KB)
Open Access Short Communication
The R168G heterozygous mutation of tropomyosin 3 (TPM3) was identified in three family members and has manifestations ranging from asymptotic to serve scoliosis and respiratory complications
https://doi.org/10.1016/j.gendis.2020.01.010
Published: 25 January 2020
2021, 8 (5): 715-720
Downloads: 3 | Views: 140 | PDF (1.3 MB)
Open Access Review Article
Mutational landscape of gastric adenocarcinoma in Latin America: A genetic approach for precision medicine
https://doi.org/10.1016/j.gendis.2021.04.002
Published: 24 April 2021
2022, 9 (4): 928-940
Downloads: 2 | Views: 180 | PDF (1.5 MB)
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