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The Journal of Investigative Dermatology
|
November 5, 1997
Erythropoietic protoporphyria: four novel frameshift mutations in the ferrochelatase gene
X Wang, S Piomelli, M Peacocke, et al.
Journal of the American Academy of Dermatology
|
February 3, 1998
Patterns of X chromosome inactivation in sporadic basal cell carcinomas: evidence for clonality
D S Walsh, M Peacocke, A Harrington, et al.
The Journal of Investigative Dermatology
|
March 1, 1996
Clonality of basal cell carcinoma--molecular analysis of an interesting case
D S Walsh, H C Tsou, A Harrington, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1988
Induction of nerve growth factor receptors on cultured human melanocytes
M Peacocke, M Yaar, C P Mansur, et al.
Experimental Dermatology
|
December 19, 1998
Similarities of cutaneous and breast pathology in Cowden's Syndrome
C A Schrager, D Schneider, A C Gruener, et al.
Experimental Cell Research
|
September 1, 1994
A beta 2RARE-LacZ transgene identifies retinoic acid-mediated transcriptional activation in distinct cutaneous sites
H C Tsou, S P Si, X Lee, et al.
Experimental Cell Research
|
February 25, 1996
RAR beta 2-mediated growth inhibition in HeLa cells
S P Si, X Lee, H C Tsou, et al.
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research
|
February 1, 1994
Down-regulation of retinoic acid receptor beta in mammary carcinoma cell lines and its up-regulation in senescing normal mammary epithelial cells
K Swisshelm, K Ryan, X Lee, et al.
Human Pathology
|
January 28, 1998
Clinical and pathological features of breast disease in Cowden's syndrome: an underrecognized syndrome with an increased risk of breast cancer
C A Schrager, D Schneider, A C Gruener, et al.
The Journal of Investigative Dermatology
|
November 26, 1999
Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2
J T Celebi, E L Tanzi, Y J Yao, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 56) with videos related to
Sort By:
Page
of 6
The Journal of Investigative Dermatology
|
November 5, 1997
Erythropoietic protoporphyria: four novel frameshift mutations in the ferrochelatase gene
X Wang, S Piomelli, M Peacocke, et al.
Journal of the American Academy of Dermatology
|
February 3, 1998
Patterns of X chromosome inactivation in sporadic basal cell carcinomas: evidence for clonality
D S Walsh, M Peacocke, A Harrington, et al.
The Journal of Investigative Dermatology
|
March 1, 1996
Clonality of basal cell carcinoma--molecular analysis of an interesting case
D S Walsh, H C Tsou, A Harrington, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1988
Induction of nerve growth factor receptors on cultured human melanocytes
M Peacocke, M Yaar, C P Mansur, et al.
Experimental Dermatology
|
December 19, 1998
Similarities of cutaneous and breast pathology in Cowden's Syndrome
C A Schrager, D Schneider, A C Gruener, et al.
Experimental Cell Research
|
September 1, 1994
A beta 2RARE-LacZ transgene identifies retinoic acid-mediated transcriptional activation in distinct cutaneous sites
H C Tsou, S P Si, X Lee, et al.
Experimental Cell Research
|
February 25, 1996
RAR beta 2-mediated growth inhibition in HeLa cells
S P Si, X Lee, H C Tsou, et al.
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research
|
February 1, 1994
Down-regulation of retinoic acid receptor beta in mammary carcinoma cell lines and its up-regulation in senescing normal mammary epithelial cells
K Swisshelm, K Ryan, X Lee, et al.
Human Pathology
|
January 28, 1998
Clinical and pathological features of breast disease in Cowden's syndrome: an underrecognized syndrome with an increased risk of breast cancer
C A Schrager, D Schneider, A C Gruener, et al.
The Journal of Investigative Dermatology
|
November 26, 1999
Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2
J T Celebi, E L Tanzi, Y J Yao, et al.
Page
of 6