检索结果 - Eileen Boye
- Showing 1 - 5 results of 5
-
1
-
2
-
3
-
4
Determination of the Genomic Structure of the COL4A4 Gene and of Novel Mutations Causing Autosomal Recessive Alport Syndrome 由 Eileen Boye, Géraldine Mollet, Lionel Forestier, L Cohen-Solal, Laurence Heidet, Pierre Cochat, Jean‐Pierre Grünfeld, Jean‐Bernard Palcoux, Marie‐Claire Gubler, Corinne Antignac
出版 1998Artigo -
5
Knobloch syndrome: Novel mutations in<i>COL18A1</i>, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin 由 Olivier Menzel, Reidunn C.J. Bekkeheien, Alexandre Reymond, Naomi Fukai, Eileen Boye, György Kosztolányi, Salim Aftimos, Samuel Deutsch, Hamish S. Scott, Bjørn R. Olsen, Stylianos E. Antonarakis, Michel Guipponi
出版 2003Artigo
相关主题
Biology
Angiogenesis
Gene
Genetics
Medicine
Cancer research
Endostatin
Hemangioma
Mutation
Pathology
Alport syndrome
Cell
Cell biology
Chemistry
Computational biology
Exon
Frameshift mutation
Glomerular basement membrane
Glomerulonephritis
Integrin
Kidney
Kinase insert domain receptor
Laminin
Lesion
Locus (genetics)
Missense mutation
Molecular biology
NFAT
Receptor
Resection