Concepedia

Author

Faouzi Baklouti

Centre National de la Recherche ScientifiqueORCID

Also Known As

Baklouti, F., Baklouti, Faouzi, F Baklouti, F. BAKLOUTI, F. Baklouti, Faouzi BAKLOUTI, Faouzi Baklouti, Tanguay, Robert M

82

Publications

1.2K

Citations

21

H-Index

44

Concepts

All Affiliations

Centre National de la Recherche ScientifiqueUniversité Claude Bernard Lyon 1Laboratoire de Biologie et Modélisation de la CelluleCentre de Génétique MoléculaireHôpital Edouard Herriot
FB

About

Faouzi Baklouti is an author at Centre National de la Recherche Scientifique specializing in medicine, gene expression, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

12

15

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2

Natural Sciences

7

7

239

3

Biochemistry

3

3

78

4

Engineering

1

1

10

5

Health Sciences

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Faouzi Baklouti

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39

Publications

1.1K

Citations

21

H-Index

YearCitations

Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46.

R Wilmotte, J Maréchal, Laurette Morlé,

Journal of Clinical Investigation

1993

106

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.

Nicole Alloisio, Laurette Morlé, J Maréchal,

Journal of Clinical Investigation

1991

67

Organization of the Human Protein 4.1 Genomic Locus: New Insights into the Tissue-Specific Alternative Splicing of the Pre-mRNA

Faouzi Baklouti, Shu‐Ching Huang, Tom Vulliamy,

Genomics

1997

66

Multiple cis elements regulate an alternative splicing event at 4.1R pre-mRNA during erythroid differentiation

Mireille Deguillien, Shu‐Ching Huang, Madeleine Morinière,

Blood

2001

61

Asynchronous regulation of splicing events within protein 4.1 pre-mRNA during erythroid differentiation

Faouzi Baklouti, SC Huang, J. Delaunay,

Blood

1996

53

Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis.

J. Delaunay, Nicole Alloisio, Laurette Morlé,

PubMed

1996

43

Elliptocytogenic alpha I/36 spectrin Sfax lacks nine amino acids in helix 3 of repeat 4. Evidence for the activation of a cryptic 5'-splice site in exon 8 of spectrin alpha-gene

Faouzi Baklouti, J Maréchal, R Wilmotte,

Blood

1992

42

Band 3 Chur: a variant associated with band 3‐deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11

Philippe Maillet, Agnès Vallier, Walter H. Reinhart,

British Journal of Haematology

1995

38

Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas)

Nicole Alloisio, Philippe Maillet, Geneviève Carré,

Blood

1996

38

Increased oxygen affinity with normal heterotropic effects in hemoglobin Loire [α88(F9)Ala→Ser]

Faouzi Baklouti, V. Baudin‐Chich, J. Kister,

European Journal of Biochemistry

1988

34

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