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Molecular Pathology : MP
|
February 12, 2002
An R201H activating mutation of the GNAS1 (Gsalpha) gene in a corticotroph pituitary adenoma
M Riminucci, M T Collins, R Lala, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1989
Immunocytochemical identification of osteogenic bone tumors by osteonectin antibodies
G Jundt, A Schulz, K H Berghäuser, et al.
Human Molecular Genetics
|
August 1, 1997
PHOG, a candidate gene for involvement in the short stature of Turner syndrome
J W Ellison, Z Wardak, M F Young, et al.
Nucleic Acids Research
|
December 22, 1986
Characterization of bone PG II cDNA and its relationship to PG II mRNA from other connective tissues
A A Day, C I Ramis, L W Fisher, et al.
Journal of Dental Research
|
November 25, 2003
Comparison of stem-cell-mediated osteogenesis and dentinogenesis
S Batouli, M Miura, J Brahim, et al.
Journal of Dental Research
|
July 31, 2002
Stem cell properties of human dental pulp stem cells
S Gronthos, J Brahim, W Li, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
January 8, 1998
Functional characterization of the human biglycan 5'-flanking DNA and binding of the transcription factor c-Krox
A M Heegaard, P Gehron Robey, W Vogel, et al.
Journal of Cellular Physiology
|
November 10, 1998
Receptor tyrosine kinase expression in human bone marrow stromal cells
K Satomura, A R Derubeis, N S Fedarko, et al.
Journal of Cellular Biochemistry
|
January 5, 2000
Differential display of human marrow stromal cells reveals unique mRNA expression patterns in response to dexamethasone
S C Dieudonné, J M Kerr, T Xu, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
July 10, 2002
Phenotypic effects of biglycan deficiency are linked to collagen fibril abnormalities, are synergized by decorin deficiency, and mimic Ehlers-Danlos-like changes in bone and other connective tissues
A Corsi, T Xu, X D Chen, et al.
Page
of 2
Search research articles
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Molecular Pathology : MP
|
February 12, 2002
An R201H activating mutation of the GNAS1 (Gsalpha) gene in a corticotroph pituitary adenoma
M Riminucci, M T Collins, R Lala, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1989
Immunocytochemical identification of osteogenic bone tumors by osteonectin antibodies
G Jundt, A Schulz, K H Berghäuser, et al.
Human Molecular Genetics
|
August 1, 1997
PHOG, a candidate gene for involvement in the short stature of Turner syndrome
J W Ellison, Z Wardak, M F Young, et al.
Nucleic Acids Research
|
December 22, 1986
Characterization of bone PG II cDNA and its relationship to PG II mRNA from other connective tissues
A A Day, C I Ramis, L W Fisher, et al.
Journal of Dental Research
|
November 25, 2003
Comparison of stem-cell-mediated osteogenesis and dentinogenesis
S Batouli, M Miura, J Brahim, et al.
Journal of Dental Research
|
July 31, 2002
Stem cell properties of human dental pulp stem cells
S Gronthos, J Brahim, W Li, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
January 8, 1998
Functional characterization of the human biglycan 5'-flanking DNA and binding of the transcription factor c-Krox
A M Heegaard, P Gehron Robey, W Vogel, et al.
Journal of Cellular Physiology
|
November 10, 1998
Receptor tyrosine kinase expression in human bone marrow stromal cells
K Satomura, A R Derubeis, N S Fedarko, et al.
Journal of Cellular Biochemistry
|
January 5, 2000
Differential display of human marrow stromal cells reveals unique mRNA expression patterns in response to dexamethasone
S C Dieudonné, J M Kerr, T Xu, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
July 10, 2002
Phenotypic effects of biglycan deficiency are linked to collagen fibril abnormalities, are synergized by decorin deficiency, and mimic Ehlers-Danlos-like changes in bone and other connective tissues
A Corsi, T Xu, X D Chen, et al.
Page
of 2