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Clinical Chemistry
|
December 1, 1983
Coproporphyrin in urine of newborns with meconium aspiration syndrome
J Francoual, A Lindenbaum, M Dehan, et al.
European Journal of Biochemistry
|
November 3, 1998
Immunological, enzymatic and biochemical studies of uroporphyrinogen III-synthase deficiency in 20 patients with congenital erythropoietic porphyria
A G Freesemann, U Gross, M Bensidhoum, et al.
Biochemical Pharmacology
|
March 15, 1983
Study of anaesthetic agents for their ability to elicit porphyrin biosynthesis in chick embryo liver
H de Verneuil, J C Deybach, N Phung, et al.
The Journal of Biological Chemistry
|
June 5, 1991
Characterization of hypersensitive sites, protein-binding motifs, and regulatory elements in both promoters of the mouse porphobilinogen deaminase gene
C Porcher, G Pitiot, M Plumb, et al.
The Journal of Clinical Investigation
|
September 1, 1983
Harderoporphyria: a variant hereditary coproporphyria
Y Nordmann, B Grandchamp, H de Verneuil, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
March 10, 2009
Congenital erythropoietic porphyria: mutation update and correlations between genotype and phenotype
C Ged, F Moreau-Gaudry, E Richard, et al.
Blood
|
July 9, 1999
Correction of uroporphyrinogen decarboxylase deficiency (hepatoerythropoietic porphyria) in Epstein-Barr virus-transformed B-cell lines by retrovirus-mediated gene transfer: fluorescence-based selection of transduced cells
A Fontanellas, F Mazurier, F Moreau-Gaudry, et al.
Folia Biologica
|
January 21, 2016
Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients
M S Farrag, I Mikula, E Richard, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research
|
July 11, 2000
Retroviral coexpression of IFN-alpha and IFN-gamma genes and inhibitory effects in chronic myeloid leukemia cells
S Salesse, V Lagarde, C Ged, et al.
Biochemical and Biophysical Research Communications
|
December 16, 1991
Human erythropoietic protoporphyria: two point mutations in the ferrochelatase gene
J Lamoril, S Boulechfar, H de Verneuil, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 89) with videos related to
Sort By:
Page
of 9
Clinical Chemistry
|
December 1, 1983
Coproporphyrin in urine of newborns with meconium aspiration syndrome
J Francoual, A Lindenbaum, M Dehan, et al.
European Journal of Biochemistry
|
November 3, 1998
Immunological, enzymatic and biochemical studies of uroporphyrinogen III-synthase deficiency in 20 patients with congenital erythropoietic porphyria
A G Freesemann, U Gross, M Bensidhoum, et al.
Biochemical Pharmacology
|
March 15, 1983
Study of anaesthetic agents for their ability to elicit porphyrin biosynthesis in chick embryo liver
H de Verneuil, J C Deybach, N Phung, et al.
The Journal of Biological Chemistry
|
June 5, 1991
Characterization of hypersensitive sites, protein-binding motifs, and regulatory elements in both promoters of the mouse porphobilinogen deaminase gene
C Porcher, G Pitiot, M Plumb, et al.
The Journal of Clinical Investigation
|
September 1, 1983
Harderoporphyria: a variant hereditary coproporphyria
Y Nordmann, B Grandchamp, H de Verneuil, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
March 10, 2009
Congenital erythropoietic porphyria: mutation update and correlations between genotype and phenotype
C Ged, F Moreau-Gaudry, E Richard, et al.
Blood
|
July 9, 1999
Correction of uroporphyrinogen decarboxylase deficiency (hepatoerythropoietic porphyria) in Epstein-Barr virus-transformed B-cell lines by retrovirus-mediated gene transfer: fluorescence-based selection of transduced cells
A Fontanellas, F Mazurier, F Moreau-Gaudry, et al.
Folia Biologica
|
January 21, 2016
Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients
M S Farrag, I Mikula, E Richard, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research
|
July 11, 2000
Retroviral coexpression of IFN-alpha and IFN-gamma genes and inhibitory effects in chronic myeloid leukemia cells
S Salesse, V Lagarde, C Ged, et al.
Biochemical and Biophysical Research Communications
|
December 16, 1991
Human erythropoietic protoporphyria: two point mutations in the ferrochelatase gene
J Lamoril, S Boulechfar, H de Verneuil, et al.
Page
of 9