À propos de Lydie Salvayre

Cher Professeur Notte-- Vous noterez que je continue à buter sur votre patronyme. Allez savoir pourquoi ma mémoire n’a pas enregistré Motte. Allez comprendre le fonctionne du cerveau. Vous en savez quelque chose vous ? Moi non ? Il faudrait demander à Lydie Salvayre. Vous ne pensez pas ? La fille a exercé comme psychiatre. La tronche, la caboche, elle connaît, pendant plus de trente ans, elle a nagé dans les délires et les névroses. Et ? Donc ? De quoi je parle ? J’y viens, cher Professeur. Patience. Faisons à la Française. D’abord, les politesses

Lydie Salvayre, maintenant même

Warren Motte, «Dans le vif du vivant» Lydie Salvayre et Warren Motte, «Une conversation avec Lydie Salvayre» Lydie Salvayre, «Deux artistes» Lydie Salvayre, «Projet en cours» Lydie Salvayre, «Quatre photos» Bernard Wallet, «Lydie Salvayre, écrivain baroque’n’roll» David Lopez, «Almuerz» Marie Cosnay, «Diamant brut» Mahir Guven, «À propos de Lydie Salvayre» Stéphane Bikialo, «Éloge de la fuite» «Ouvrages de Lydie Salvayre»https://digitalcommons.unl.edu/zeabook/1103/thumbnail.jp

The role of TMPRSS6 gene variants in iron-related hematological parameters in Turkish patients with iron deficiency anemia

TMPRSS6 gene mutations can result in iron deficiency anemia (IDA) and cause an increased iron-regulatory hormone, hepcidin, levels. TMPRSS6 encodes a serine protease, matriptase-2, which functions as negative regulatory protein of hepcidin transcription. Thus, TMPRSS6 variations might be risk factors for IDA. The aim of the study was to investigate the association of rs855791, rs4820268, rs5756506, rs2235324, rs2413450, rs2111833, rs228919, and rs733655 SNPs in TMPRSS6 gene with IDA susceptibility and iron-related clinical parameters. The study consisted of 150 IDA patients and 100 healthy controls. We analyzed the genotype distributions by using Real-Time polymerase chain reaction (Real-Time PCR) technique. We did not find any statistically differences for all SNPs between patients and controls (P > 0.05). In IDA patients, variations rs855791 and rs2413450 were associated with increased RBC (P = 0.03) and TIBC (P = 0.04), respectively. Also, increased of TIBC for rs4820268 (P < 0.05). On the other hand, in control group, rs5756506 was associated with two parameters, Hb (P = 0.02) and Hct (P = 0.03). We did not find markedly hepcidin levels in IDA patients compared to controls (P = 0.32). Our findings suggest that TMPRSS6 variations may not be risk factors for IDA. However, TMPRSS6 polymorphisms are associated with increased many iron-related hematological parameters