hyaluronoglucosaminidase has been researched along with Cor Triatriatum in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chowdhury, B; Dolinsky, VW; Muggenthaler, M; Triggs-Raine, B; Xiang, B | 1 |
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, K | 1 |
2 other study(ies) available for hyaluronoglucosaminidase and Cor Triatriatum
Article | Year |
---|---|
Hyaluronidase 2 deficiency is a molecular cause of cor triatriatum sinister in mice.
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.
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 |