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I Hombrados

Showing results (11-20 of 22) with videos related to

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FEBS Letters|January 1, 1973
The N-terminal and C-terminal amino acid sequence of badger myoglobinD Tetaert, K Han, M Dautrevaux, et al.
FEBS Letters|November 15, 1973
The beta-chain of badger haemoglobin: amino acid composition of the tryptic peptides and the N-terminal sequence to position 42S Ducastaing, I Hombrados, A Iron, et al.
Biochimica Et Biophysica Acta|March 18, 1976
Primary sequence of the beta-chain of Badger haemoglobinI Hombrados, S Ducastaing, A Iron, et al.
Acta Crystallographica. Section D, Biological Crystallography|October 8, 1998
Expression, purification, crystallization and preliminary X-ray diffraction analysis of human uroporphyrinogen decarboxylaseM Laterrière, B L d'Estaintot, A Dautant, et al.
American Journal of Medical Genetics|June 13, 1997
Novel point mutation in the uroporphyrinogen III synthase gene causes congenital erythropoietic porphyria of a Japanese familyN Takamura, I Hombrados, K Tanigawa, et al.
Biochimica Et Biophysica Acta|June 7, 1974
The primary sequence of badger myoglobinD Tetaert, K K Han, M T Plancot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1995
[Congenital erythropoietic porphyria. Apropos of a fatal case in the neonatal period due to acute hemolysis with hepatic failure]H de Verneuil, F Moreau-Gaudry, C Ged, et al.
Prenatal Diagnosis|January 1, 1996
Prenatal diagnosis in congenital erythropoietic porphyria by metabolic measurement and DNA mutation analysisC Ged, F Moreau-Gaudry, L Taine, et al.
Human Mutation|September 8, 1999
Screening for mutations in the uroporphyrinogen decarboxylase gene using denaturing gradient gel electrophoresis. Identification and characterization of six novel mutations associated with familial PCTL Christiansen, C Ged, I Hombrados, et al.
The Journal of Investigative Dermatology|December 20, 2000
Congenital erythropoietic porphyria: a novel homozygous mutation in a Japanese patientT Rogounovitch, N Takamura, I Hombrados, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
FEBS Letters|January 1, 1973
The N-terminal and C-terminal amino acid sequence of badger myoglobinD Tetaert, K Han, M Dautrevaux, et al.
FEBS Letters|November 15, 1973
The beta-chain of badger haemoglobin: amino acid composition of the tryptic peptides and the N-terminal sequence to position 42S Ducastaing, I Hombrados, A Iron, et al.
Biochimica Et Biophysica Acta|March 18, 1976
Primary sequence of the beta-chain of Badger haemoglobinI Hombrados, S Ducastaing, A Iron, et al.
Acta Crystallographica. Section D, Biological Crystallography|October 8, 1998
Expression, purification, crystallization and preliminary X-ray diffraction analysis of human uroporphyrinogen decarboxylaseM Laterrière, B L d'Estaintot, A Dautant, et al.
American Journal of Medical Genetics|June 13, 1997
Novel point mutation in the uroporphyrinogen III synthase gene causes congenital erythropoietic porphyria of a Japanese familyN Takamura, I Hombrados, K Tanigawa, et al.
Biochimica Et Biophysica Acta|June 7, 1974
The primary sequence of badger myoglobinD Tetaert, K K Han, M T Plancot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1995
[Congenital erythropoietic porphyria. Apropos of a fatal case in the neonatal period due to acute hemolysis with hepatic failure]H de Verneuil, F Moreau-Gaudry, C Ged, et al.
Prenatal Diagnosis|January 1, 1996
Prenatal diagnosis in congenital erythropoietic porphyria by metabolic measurement and DNA mutation analysisC Ged, F Moreau-Gaudry, L Taine, et al.
Human Mutation|September 8, 1999
Screening for mutations in the uroporphyrinogen decarboxylase gene using denaturing gradient gel electrophoresis. Identification and characterization of six novel mutations associated with familial PCTL Christiansen, C Ged, I Hombrados, et al.
The Journal of Investigative Dermatology|December 20, 2000
Congenital erythropoietic porphyria: a novel homozygous mutation in a Japanese patientT Rogounovitch, N Takamura, I Hombrados, et al.
Pageof 3