Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Martine Aubry"'
Autor:
Martine Aubry, Matthieu de Oliveira
Publikováno v:
In Situ, Vol 25 (2015)
After the First World War, families, local authorities and the whole nation wanted to pay homage to ‘the heroes fallen for France’. From 1919 on war memorials appeared in practically each French commune, with commemorative messages that could var
Externí odkaz:
https://doaj.org/article/448534683981483ea362f42db57d9037
Autor:
Caroline Garcia, Michel Becchi, Martine Bererd, Isabelle Zanella-Cleon, Alain Francina, Martine Aubry, Philippe Lacan, Nicole Couprie, Philippe Joly
Publikováno v:
Hemoglobin. 33:196-205
We present here five new hemoglobin (Hb) variants which have been identified during routine Hb analysis before their genotypic characterization. Four of these result from a classical missense mutation: Hb Canuts [α85(F6)Asp→His (α1)], Hb Ambroise
Publikováno v:
Hemoglobin. 31:159-165
We report here two new beta(0)-thalassemic mutations. In the first case, a deletion of two nucleotides (-CC) at codon 142 was found in a French Caucasian woman. In the second case, an insertion of a single nucleotide (+T) at codon 45 was found in a T
Autor:
Michel Becchi, Nicole Couprie, Isabelle Zanella-Cléon, Nelly Burnichon, Philippe Lacan, Alain Francina, Mohammed Mowafy, Martine Aubry
Publikováno v:
Hemoglobin. 30:155-164
A new hemoglobin (Hb) variant in the heterozygous state, Hb Al-Hammadi Riyadh [codon 75 (GAC→GTC); α75(EF4)Asp→Val (α2)] corresponding to an A→T transversion on the second exon of the α2-globin gene, is described. The variant was characteriz
Publikováno v:
Hemoglobin. 29:225-228
A new mutation of the beta-globin gene initiation codon, ATG--AAG (Met--Tyr), is reported in a man originating from the southeast of France. Typical hematological findings of beta-thalassemia (thal) trait were found. We emphasize the importance of ch
Autor:
Michel Becchi, Philippe Lacan, Nicole Couprie, Martine Aubry, Nelly Burnichon, Isabelle Zanella-Cléon, Alain Francina
Publikováno v:
Hemoglobin. 29:301-305
A new G(gamma) hemoglobin (Hb) variant, Hb F-Bron [gamma20(B2)Val-->Ala] on the first exon of the G(gamma)-globin gene is described. The variant was characterized by DNA sequencing and mass spectrometry (MS). Hematological abnormalities included hypo
Autor:
Michel Becchi, Mathieu Moreau, Alain Francina, Philippe Lacan, Nicole Couprie, Isabelle Zanella-Cléon, Martine Aubry, Jean-Jacques Louis
Publikováno v:
Hemoglobin. 29:69-75
Two new hemoglobin (Hb) variants: Hb Brem-sur-Mer [codon 9 (TC T→TA T); β9(A6)Ser→Tyr] on the first exon of the β-globin gene and Hb Passy [codon 81 (T CC→C CC); α81(F2)Ser→Pro (α2)] on the second exon of the α2-globin gene, are describe
Autor:
Philippe Lacan, Mathieu Moreau, Michel Becchi, Isabelle Zanella-Cleon, Martine Aubry, Jean-Jacques Louis, Nicole Couprie, Alain Francina
Publikováno v:
Hemoglobin. 29:69-75
Autor:
Philippe Lacan, Michel Becchi, Nicole Couprie, Martine Aubry, Martine Ffrench, Alain Francina, Isabelle Zanella-Cléon
Publikováno v:
Hemoglobin. 28:205-212
Two new β‐globin chain variants: Hb Tripoli: codon 26, GAG→GCG [β26(B8)Glu→Ala] and Hb Tizi‐Ouzou: codon 29, GGC→AGC [β29(B11)Gly→Ser] are described on the first exon of the β‐globin gene. The two variants are characterized by DNA s
Publikováno v:
Hemoglobin. 28:59-63
The first new α chain variant here reported, Hb Die [α93(FG5)Val→Ala (α1)], was found during investigations of an anemia prior to surgery for correcting spina bifida. The patient was a 7‐year‐old g...