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La Revue Du Praticien
|
October 1, 1992
[Health policies and sickle cell disease]
I S Zohoun, G Mérault, P Reinette, et al.
FEBS Letters
|
February 1, 1975
Haemoglobin G Norfolk alpha 85 (F6) Asp leads to Asn. Structural characterization by sequenator analysis and functional properties of a new variant with high oxygen affinity
M Cohen-Solal, B Manesse, J Thillet, et al.
FEBS Letters
|
June 15, 1973
Haemoglobin Saint Louis beta28 (B10) leucine leads to glutamine. A new unstable haemoglobin only present in a ferri form
M Cohen-Solal, M Seligmann, J Thillet, et al.
Frontiers in Psychology
|
December 10, 2021
Is Pupil Activity Associated With the Strength of Memory Signal for Words in a Continuous Recognition Memory Paradigm?
Jorge Oliveira, Marta Fernandes, Pedro J Rosa, et al.
Biochimica Et Biophysica Acta
|
July 24, 1980
Oxidation properties of two hemoglobin variants with their mutation localized in the heme pocket: Hb Castilla beta 32 (B14) Leu replaced by Arg and Hb Toulouse beta 66 (E10) Lys replaced by Glu, and abnormal functional properties of Hb Castilla
J Thillet, M C Garel, R Bierme, et al.
Hemoglobin
|
January 1, 1991
Sickle cell anemia in the Tunisian population: haplotyping and HB F expression
S Abbes, S Fattoum, M Vidaud, et al.
Acta Haematologica
|
January 1, 1987
Characterization approach of 'silent' beta-chain hemoglobin variants
C Lacombe, J Riou, C Godard, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles
|
November 29, 1976
[Biochemical characterization of a circulating thymic factor]
J F Bach, M Dardenne, J M Pleau, et al.
Gastroenterology
|
November 1, 1990
Long-term 6-mercaptopurine treatment in adolescents with Crohn's disease
J Markowitz, J Rosa, K Grancher, et al.
Biochemical and Biophysical Research Communications
|
January 30, 1978
Protein-protein interactions:possible location of hemoglobin-haptoglobin contacts
A Tsapis, C Mihaesco, A Alfsen, et al.
Page
of 43
Search research articles
Search
Showing results (111-120 of 424) with videos related to
Sort By:
Page
of 43
La Revue Du Praticien
|
October 1, 1992
[Health policies and sickle cell disease]
I S Zohoun, G Mérault, P Reinette, et al.
FEBS Letters
|
February 1, 1975
Haemoglobin G Norfolk alpha 85 (F6) Asp leads to Asn. Structural characterization by sequenator analysis and functional properties of a new variant with high oxygen affinity
M Cohen-Solal, B Manesse, J Thillet, et al.
FEBS Letters
|
June 15, 1973
Haemoglobin Saint Louis beta28 (B10) leucine leads to glutamine. A new unstable haemoglobin only present in a ferri form
M Cohen-Solal, M Seligmann, J Thillet, et al.
Frontiers in Psychology
|
December 10, 2021
Is Pupil Activity Associated With the Strength of Memory Signal for Words in a Continuous Recognition Memory Paradigm?
Jorge Oliveira, Marta Fernandes, Pedro J Rosa, et al.
Biochimica Et Biophysica Acta
|
July 24, 1980
Oxidation properties of two hemoglobin variants with their mutation localized in the heme pocket: Hb Castilla beta 32 (B14) Leu replaced by Arg and Hb Toulouse beta 66 (E10) Lys replaced by Glu, and abnormal functional properties of Hb Castilla
J Thillet, M C Garel, R Bierme, et al.
Hemoglobin
|
January 1, 1991
Sickle cell anemia in the Tunisian population: haplotyping and HB F expression
S Abbes, S Fattoum, M Vidaud, et al.
Acta Haematologica
|
January 1, 1987
Characterization approach of 'silent' beta-chain hemoglobin variants
C Lacombe, J Riou, C Godard, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles
|
November 29, 1976
[Biochemical characterization of a circulating thymic factor]
J F Bach, M Dardenne, J M Pleau, et al.
Gastroenterology
|
November 1, 1990
Long-term 6-mercaptopurine treatment in adolescents with Crohn's disease
J Markowitz, J Rosa, K Grancher, et al.
Biochemical and Biophysical Research Communications
|
January 30, 1978
Protein-protein interactions:possible location of hemoglobin-haptoglobin contacts
A Tsapis, C Mihaesco, A Alfsen, et al.
Page
of 43