Search research articles
Contact Us
Filters
Showing results (11-20 of 14) with videos related to
Page
of 2
Sort By:
You have reached the last page of results.
This site can display upto 14 results.
Developmental Biology
|
January 22, 2000
Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF
J Pispa, H S Jung, J Jernvall, et al.
American Journal of Human Genetics
|
January 1, 1996
Fine mapping of the EDA gene: a translocation breakpoint is associated with a CpG island that is transcribed
A K Srivastava, O Montonen, U Saarialho-Kere, et al.
Developmental Biology
|
February 24, 2001
TNF signaling via the ligand-receptor pair ectodysplasin and edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis
J Laurikkala, M Mikkola, T Mustonen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 16, 1997
The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains
A K Srivastava, J Pispa, A J Hartung, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 14) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 14 results.
Developmental Biology
|
January 22, 2000
Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF
J Pispa, H S Jung, J Jernvall, et al.
American Journal of Human Genetics
|
January 1, 1996
Fine mapping of the EDA gene: a translocation breakpoint is associated with a CpG island that is transcribed
A K Srivastava, O Montonen, U Saarialho-Kere, et al.
Developmental Biology
|
February 24, 2001
TNF signaling via the ligand-receptor pair ectodysplasin and edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis
J Laurikkala, M Mikkola, T Mustonen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 16, 1997
The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains
A K Srivastava, J Pispa, A J Hartung, et al.
Page
of 2