Page last updated: 2024-08-22

hyaluronoglucosaminidase and Cor Triatriatum

hyaluronoglucosaminidase has been researched along with Cor Triatriatum in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chowdhury, B; Dolinsky, VW; Muggenthaler, M; Triggs-Raine, B; Xiang, B1
Alkuraya, FS; Baple, EL; Behr, ER; Blakley, B; Chioza, BA; Chowdhury, B; Crosby, AH; Cross, HE; Cross, L; Dolinsky, V; Faqeih, E; Harlalka, GV; Hasan, SN; Ishida, M; Jackson, M; Lees, M; Mark, B; Muggenthaler, MM; Patton, MA; Salter, C; Sharma, S; Stanier, P; Triggs-Raine, B; Zahka, K1

Other Studies

2 other study(ies) available for hyaluronoglucosaminidase and Cor Triatriatum

ArticleYear
Hyaluronidase 2 deficiency is a molecular cause of cor triatriatum sinister in mice.
    International journal of cardiology, 2016, Apr-15, Volume: 209

    Topics: Animals; Cor Triatriatum; GPI-Linked Proteins; Hyaluronic Acid; Hyaluronoglucosaminidase; Mice; Mice, Knockout; Mucopolysaccharidoses

2016
Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice.
    PLoS genetics, 2017, Volume: 13, Issue:1

    Topics: Adolescent; Animals; Cell Adhesion Molecules; Child; Child, Preschool; Cleft Lip; Cleft Palate; Cor Triatriatum; Female; GPI-Linked Proteins; Humans; Hyaluronoglucosaminidase; Male; Mice; Mice, Inbred C57BL; Mutation; Pedigree; Penetrance; Syndrome

2017