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European Journal of Dermatology : EJD
|
August 30, 2001
Persistent urticaria--urticarial reaction caused by late phase reaction?
A Kitao, S Nobuhara, S Kore-Eda, et al.
American Journal of Human Genetics
|
November 1, 1993
High prevalence of the point mutation in exon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients in Tunisia
C Nishigori, M Zghal, T Yagi, et al.
Archives of Dermatology
|
March 1, 1993
A case of Rothmund-Thomson syndrome with reduced DNA repair capacity
A Shinya, C Nishigori, S Moriwaki, et al.
Oncogene
|
April 1, 1993
Activation of c-mos oncogene by integration of an endogenous long terminal repeat element during transfection of genomic DNA from mouse skin tumor cells
S Wang, C Nishigori, J Miyakoshi, et al.
The British Journal of Dermatology
|
January 1, 1993
A case of xeroderma pigmentosum complementation group F with neurological abnormalities
S Moriwaki, C Nishigori, S Imamura, et al.
The Journal of Investigative Dermatology
|
September 1, 1995
High prevalence of mutations in the p53 gene in poorly differentiated squamous cell carcinomas in xeroderma pigmentosum patients
Y Matsumura, M Sato, C Nishigori, et al.
European Journal of Pediatrics
|
May 1, 1993
IgG4 deficiency with Rothmund-Thomson syndrome: a case report
M Kubota, M Yasunaga, H Hashimoto, et al.
The Journal of Investigative Dermatology
|
July 1, 1993
Absence of DNA repair deficiency in the confirmed heterozygotes of xeroderma pigmentosum group A
S Moriwaki, C Nishigori, T Teramoto, et al.
Carcinogenesis
|
February 24, 1998
Complete restoration of normal DNA repair characteristics in group F xeroderma pigmentosum cells by over-expression of transfected XPF cDNA
T Yagi, Y Matsumura, M Sato, et al.
The British Journal of Dermatology
|
February 13, 2001
Useful applications of DNA repair tests for differential diagnosis of atypical dyschromatosis symmetrica hereditaria from xeroderma pigmentosum
E Ohtoshi, Y Matsumura, C Nishigori, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 56) with videos related to
Sort By:
Page
of 6
European Journal of Dermatology : EJD
|
August 30, 2001
Persistent urticaria--urticarial reaction caused by late phase reaction?
A Kitao, S Nobuhara, S Kore-Eda, et al.
American Journal of Human Genetics
|
November 1, 1993
High prevalence of the point mutation in exon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients in Tunisia
C Nishigori, M Zghal, T Yagi, et al.
Archives of Dermatology
|
March 1, 1993
A case of Rothmund-Thomson syndrome with reduced DNA repair capacity
A Shinya, C Nishigori, S Moriwaki, et al.
Oncogene
|
April 1, 1993
Activation of c-mos oncogene by integration of an endogenous long terminal repeat element during transfection of genomic DNA from mouse skin tumor cells
S Wang, C Nishigori, J Miyakoshi, et al.
The British Journal of Dermatology
|
January 1, 1993
A case of xeroderma pigmentosum complementation group F with neurological abnormalities
S Moriwaki, C Nishigori, S Imamura, et al.
The Journal of Investigative Dermatology
|
September 1, 1995
High prevalence of mutations in the p53 gene in poorly differentiated squamous cell carcinomas in xeroderma pigmentosum patients
Y Matsumura, M Sato, C Nishigori, et al.
European Journal of Pediatrics
|
May 1, 1993
IgG4 deficiency with Rothmund-Thomson syndrome: a case report
M Kubota, M Yasunaga, H Hashimoto, et al.
The Journal of Investigative Dermatology
|
July 1, 1993
Absence of DNA repair deficiency in the confirmed heterozygotes of xeroderma pigmentosum group A
S Moriwaki, C Nishigori, T Teramoto, et al.
Carcinogenesis
|
February 24, 1998
Complete restoration of normal DNA repair characteristics in group F xeroderma pigmentosum cells by over-expression of transfected XPF cDNA
T Yagi, Y Matsumura, M Sato, et al.
The British Journal of Dermatology
|
February 13, 2001
Useful applications of DNA repair tests for differential diagnosis of atypical dyschromatosis symmetrica hereditaria from xeroderma pigmentosum
E Ohtoshi, Y Matsumura, C Nishigori, et al.
Page
of 6