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Journal of Inherited Metabolic Disease
|
August 13, 1998
Aberrant phenylalanine metabolism in phenylketonuria heterozygotes
P Guldberg, K F Henriksen, H C Lou, et al.
Human Mutation
|
January 1, 1996
DGGE analysis as supplement to SSCP analysis of the phenylalanine hydroxylase gene: detection of eight (one de novo, seven inherited) of nine remaining Norwegian PKU mutations
H G Eiken, P M Knappskog, P Guldberg, et al.
The Journal of Biological Chemistry
|
August 18, 2001
Methylation-dependent silencing of the reduced folate carrier gene in inherently methotrexate-resistant human breast cancer cells
J Worm, A F Kirkin, K N Dzhandzhugazyan, et al.
European Journal of Human Genetics : EJHG
|
February 5, 1998
A molecular survey of phenylketonuria in Iceland: identification of a founding mutation and evidence of predominant Norse settlement
P Guldberg, J Zschocke, A Dagbjartsson, et al.
Genomics
|
May 15, 1994
Molecular heterogeneity of nonphenylketonuria hyperphenylalaninemia in 25 Danish patients
P Guldberg, K F Henriksen, B Thöny, et al.
Acta Oncologica (Stockholm, Sweden)
|
September 15, 2000
TP53 mutation is an independent prognostic marker for poor outcome in both node-negative and node-positive breast cancer
J Overgaard, M Yilmaz, P Guldberg, et al.
Blood
|
May 30, 1998
Alterations of the MMAC1/PTEN gene in lymphoid malignancies
K Grønbaek, J Zeuthen, P Guldberg, et al.
The Journal of Investigative Dermatology
|
January 29, 2000
Mutation and allelic loss of the PTEN/MMAC1 gene in primary and metastatic melanoma biopsies
A Birck, V Ahrenkiel, J Zeuthen, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 29, 2000
Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients
J Alsner, M Yilmaz, P Guldberg, et al.
Molecular Genetics and Metabolism
|
June 5, 1999
Long-term beneficial effects of the phenylalanine-restricted diet in late-diagnosed individuals with phenylketonuria
R Koch, K Moseley, J Ning, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 101) with videos related to
Sort By:
Page
of 11
Journal of Inherited Metabolic Disease
|
August 13, 1998
Aberrant phenylalanine metabolism in phenylketonuria heterozygotes
P Guldberg, K F Henriksen, H C Lou, et al.
Human Mutation
|
January 1, 1996
DGGE analysis as supplement to SSCP analysis of the phenylalanine hydroxylase gene: detection of eight (one de novo, seven inherited) of nine remaining Norwegian PKU mutations
H G Eiken, P M Knappskog, P Guldberg, et al.
The Journal of Biological Chemistry
|
August 18, 2001
Methylation-dependent silencing of the reduced folate carrier gene in inherently methotrexate-resistant human breast cancer cells
J Worm, A F Kirkin, K N Dzhandzhugazyan, et al.
European Journal of Human Genetics : EJHG
|
February 5, 1998
A molecular survey of phenylketonuria in Iceland: identification of a founding mutation and evidence of predominant Norse settlement
P Guldberg, J Zschocke, A Dagbjartsson, et al.
Genomics
|
May 15, 1994
Molecular heterogeneity of nonphenylketonuria hyperphenylalaninemia in 25 Danish patients
P Guldberg, K F Henriksen, B Thöny, et al.
Acta Oncologica (Stockholm, Sweden)
|
September 15, 2000
TP53 mutation is an independent prognostic marker for poor outcome in both node-negative and node-positive breast cancer
J Overgaard, M Yilmaz, P Guldberg, et al.
Blood
|
May 30, 1998
Alterations of the MMAC1/PTEN gene in lymphoid malignancies
K Grønbaek, J Zeuthen, P Guldberg, et al.
The Journal of Investigative Dermatology
|
January 29, 2000
Mutation and allelic loss of the PTEN/MMAC1 gene in primary and metastatic melanoma biopsies
A Birck, V Ahrenkiel, J Zeuthen, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 29, 2000
Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients
J Alsner, M Yilmaz, P Guldberg, et al.
Molecular Genetics and Metabolism
|
June 5, 1999
Long-term beneficial effects of the phenylalanine-restricted diet in late-diagnosed individuals with phenylketonuria
R Koch, K Moseley, J Ning, et al.
Page
of 11