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Trisomy 21 Is a Cause of Permanent Neonatal Diabetes That Is Autoimmune but Not HLA Associated.
Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease.
A Genomic Link From Heart Failure to Atrial Fibrillation Risk: FOG2 Modulates a TBX5/GATA4-Dependent Atrial Gene Regulatory Network.
Identification of different ALK mutations in a pair of neuroblastoma cell lines established at diagnosis and relapse.
Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms.
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Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms.
Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms. Hum Mol Genet. 2016 07 15; 25(14):3011-3028.
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PubMed
subject areas
Animals
Axonemal Dyneins
Body Patterning
Cilia
Disease Models, Animal
Ethylnitrosourea
Exome
Gene Expression Regulation
Heart
Heart Septal Defects
Hedgehog Proteins
Humans
Mice
Mutation
Proteins
Signal Transduction
authors with profiles
Ozanna Burnicka-Turek
Ivan Moskowitz
Xinan Yang
Junghun Kweon