نتایج جستجو برای: paucity
تعداد نتایج: 12516 فیلتر نتایج به سال:
Journal:
:Clinical Orthopaedics & Related Research
2010
Journal:
:Alternatives: Global, Local, Political
2020
Journal:
:PLoS ONE
2008
Julie Lozier
Brent McCright
Thomas Gridley
BACKGROUND Alagille syndrome is a developmental disorder caused predominantly by mutations in the Jagged1 (JAG1) gene, which encodes a ligand for Notch family receptors. A characteristic feature of Alagille syndrome is intrahepatic bile duct paucity. We described previously that mice doubly heterozygous for Jag1 and Notch2 mutations are an excellent model for Alagille syndrome. However, our pre...
Journal:
:NeuroReport
2012
Journal:
:Meteoritics & Planetary Science
1998
Journal:
:Monthly Notices of the Royal Astronomical Society: Letters
2016
Journal:
:The Astronomical Journal
2014
Journal:
:The Astrophysical Journal
2006
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