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Blood
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June 1, 1989
Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families
A F Roux, F Morlé, D Guetarni, et al.
British Journal of Clinical Pharmacology
|
June 1, 1983
Pharmacokinetics of tinidazole in chronic renal failure and in patients on haemodialysis
B L Flouvat, C Imbert, D M Dubois, et al.
Human Molecular Genetics
|
February 1, 1994
Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complex
A F Roux, J Rommens, C McDowell, et al.
Blood
|
April 1, 1988
Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state
N Alloisio, L Morlé, B Pothier, et al.
Human Genetics
|
October 1, 1990
Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele
D Guetarni, A F Roux, N Alloisio, et al.
Blood
|
August 1, 1989
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain
L Morlé, F Morlé, A F Roux, et al.
The Journal of Clinical Investigation
|
August 1, 1990
Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe)
L Morlé, A F Roux, N Alloisio, et al.
The Journal of Clinical Investigation
|
June 1, 1991
Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans
N Alloisio, L Morlé, J Maréchal, et al.
Clinical Genetics
|
September 8, 2011
Audiological findings in 100 USH2 patients
C Abadie, C Blanchet, D Baux, et al.
Journal of Medical Genetics
|
May 9, 2006
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%
A-F Roux, V Faugère, S Le Guédard, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Blood
|
June 1, 1989
Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families
A F Roux, F Morlé, D Guetarni, et al.
British Journal of Clinical Pharmacology
|
June 1, 1983
Pharmacokinetics of tinidazole in chronic renal failure and in patients on haemodialysis
B L Flouvat, C Imbert, D M Dubois, et al.
Human Molecular Genetics
|
February 1, 1994
Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complex
A F Roux, J Rommens, C McDowell, et al.
Blood
|
April 1, 1988
Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state
N Alloisio, L Morlé, B Pothier, et al.
Human Genetics
|
October 1, 1990
Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele
D Guetarni, A F Roux, N Alloisio, et al.
Blood
|
August 1, 1989
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain
L Morlé, F Morlé, A F Roux, et al.
The Journal of Clinical Investigation
|
August 1, 1990
Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe)
L Morlé, A F Roux, N Alloisio, et al.
The Journal of Clinical Investigation
|
June 1, 1991
Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans
N Alloisio, L Morlé, J Maréchal, et al.
Clinical Genetics
|
September 8, 2011
Audiological findings in 100 USH2 patients
C Abadie, C Blanchet, D Baux, et al.
Journal of Medical Genetics
|
May 9, 2006
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%
A-F Roux, V Faugère, S Le Guédard, et al.
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of 3