Associated Papers
Early-onset hereditary isolated non-neurogenic orthostatic hypotension in a Swedish family.
Fagius J et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society, 2023
37460866 (PubMed )
Supplement: 10286_2023_963_MOESM2_ESM.xlsx › Variants
Somatic Mutation of PRKAR1A in Four Cases of Sporadic Cardiac Myxoma.
Sun Y et al.
Archives of Iranian Medicine, 2023
38310436 (PubMed )
Supplement: aim-26-346-s001.pdf
Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type.
Wu J et al.
Frontiers in Genetics, 2022
35368703 (PubMed )
Supplement: DataSheet1.zip › 823861_SupMaterial › Data_Sheet_1.ZIP › raw_datas › patient_2__NGS_raw_data.xlsx › Sheet1
Effects of microRNAs polymorphism in cancer progression.
SiamiGorji S et al.
Medical Journal of the Islamic Republic of Iran, 2020
Comprehensive analysis of damage associated SNPs of MMP9 gene: A computational approach.
Bhatnager R et al.
Computational Biology and Chemistry, 2018
Role of N-glycosylation in activation of proMMP-9. A molecular dynamics simulations study.
Kumar S et al.
Plos One, 2018
Functional Roles of N-Linked Glycosylation of Human Matrix Metalloproteinase 9.
Duellman T et al.
Traffic (copenhagen, Denmark), 2015
Single nucleotide polymorphism-specific regulation of matrix metalloproteinase-9 by multiple miRNAs targeting the coding exon.
Duellman T et al.
Nucleic Acids Research, 2014
Polymorphisms in metalloproteinase-9 are associated with the risk for asthma in Mexican pediatric patients.
Jiménez-Morales S et al.
Human Immunology, 2013
Matrix metalloproteinase-9 genotype as a potential genetic marker for abdominal aortic aneurysm.
Duellman T et al.
Circulation. Cardiovascular Genetics, 2012
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009
19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeI_
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