Associated Papers
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Elife, 2024
38277211 (PubMed )
Supplement: elife-89762-supp1.xlsx › Variants
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Biorxiv : the Preprint Server for Biology, 2023
37292598 (PubMed )
Supplement: media-1.xlsx › Variants
Sensitization of Patient-Derived Colorectal Cancer Organoids to Photon and Proton Radiation by Targeting DNA Damage Response Mechanisms.
Pape K et al.
Cancers, 2022
36291768 (PubMed )
Supplement: cancers-14-04984-s001.zip › Table_S2.xlsx › DD204
Analysis of genomic pathogenesis according to the revised Bethesda guidelines and additional criteria.
Kim JC et al.
Journal of Cancer Research and Clinical Oncology, 2021
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
Calender A et al.
Bmc Medical Genomics, 2018
29510755 (PubMed )
Supplement: 12920_2018_338_MOESM6_ESM.xlsx › Feuil3
Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon-Lefevre syndrome in a Saudi family.
Alkhiary YM et al.
Saudi Journal of Biological Sciences, 2016
27579005 (PubMed )
Supplement: mmc1.xlsx › Sheet1
MMP3 and TIMP1 variants contribute to chronic periodontitis and may be implicated in disease progression.
Letra A et al.
Journal of Clinical Periodontology, 2012
Association of MMP3 and TIMP2 promoter polymorphisms with nonsyndromic oral clefts.
Letra A et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2012
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