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201. [Two-year follow-up cohort studies on triplets: development of children and mother-child relationship].

202. [Follow-up of mothers of triplets 2 years after delivery. Results of a longitudinal study].

203. Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase. Functional consequences of substitutions of His10, His187 and Arg89.

205. Structural modeling of the human erythrocyte bisphosphoglycerate mutase.

206. Assessment at 1 year of the psychological consequences of having triplets.

207. Towards a transgenic mouse model of sickle cell disease: hemoglobin SAD.

208. Crystallization and preliminary X-ray diffraction studies of the human erythrocyte bisphosphoglycerate mutase.

209. Changes of polymerization and conformation of hemoglobin S induced by thiol reagents.

210. Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutase.

211. Human bisphosphoglycerate mutase expressed in E coli: purification, characterization and structure studies.

212. Psychosocial consequences of caesarean childbirth: a four-year follow-up study.

213. Towards a mouse model for sickle cell disease: HB SAD.

214. [Maternal consequences of cesarean delivery. Results of a 4-year follow-up].

215. Natural and artificial mutants of the human 2,3-bisphosphoglycerate as a tool for the evaluation of structure-function relationships.

216. Fate of alpha-hemoglobin chains and erythrocyte defects in beta-thalassemia.

217. Molecular cloning and sequencing of the human erythrocyte 2,3-bisphosphoglycerate mutase cDNA: revised amino acid sequence.

218. Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34----7q22.

219. Antisickling effect of cystamine and its action on the biosynthesis of hemoglobin.

220. Contact inhibition within hemoglobin S polymer by thiol reagents.

221. Functional studies of Hb Malmö beta97 (FG4) His leads to Gln.

222. [An acquired S hemoglobin in the adult].

223. [Evaluation of three commercial kits for the estimation of total glycolysed hemoglobin: Hb Al (author's transl)].

224. [Use of a new rheometer for the study of the filtrability of a suspension of sickled red cells as a function of PO2].

225. Hemoglobin Dakar = Hb Grady: demonstration by a new approach to the analysis of the tryptic core region of the alpha chain and oxygen equilibrium properties.

226. Sickle cell hemoglobin fiber formation strongly inhibited by the Stanleyville II mutation (alpha 78 Asn leads to Lys).

227. Abnormal functional properties of Hb Hope alpha C2A beta2 (H14) Gly-Asp: a low oxygen affinity hemoglobin with decreased DPG effect.

229. Haemoglobin Strasbourg alpha2beta2 23 (B5) Val replaced by Asp: revised structure anf functional properties.

230. Hemoglobin J Cairo: beta 65 (E9) Lys leads to Gln, A new hemoglobin variant discovered in an Egyptian family.

231. Binding of 21 thiol reagents to human hemoglobin in solution and in intact cells.

232. Effects of the alpha 20 mutation on the polymerization of Hb S.

233. [Epidural analgesia. Women's viewpoint].

234. Hemoglobin Castilla beta 32 (B14) Leu leads to Arg; a new unstable variant producing severe hemolytic disease.

235. Molecular cloning of the human 2,3-bisphosphoglycerate mutase cDNA and revised amino acid sequence.

236. [Early discharge of women after delivery. Results of an opinion survey among patients and unit personnel].

237. A method for isolation of abnormal haemoglobins with high oxygen affinity due to a frozen quaternary r-structure: application to Hb Creteil alpha 2 A beta 2 (F5) 89 ASN.

238. Filterability of sickle cells as a function of pO2: role of physico-chemical factors.

239. [Consequences of peridural analgesia for the Cesarean experience and initial mother-child relations].

240. Hb Henri Mondor: beta26 (B8) Glu leads to Val: a variant with a substitution localized at the same position as that of HbE beta26 Glu leads to Lys.

241. [A new case of hemoglobin G Georgia (author's transl)].

242. Isoelectric focusing of human hemoglobin: its application to screening, to the characterization of 70 variants, and to the study of modified fractions of normal hemoglobins.

243. Beta-chain contact sites in the haemoglobin S polymer.

244. [Clinical and biochemical studies of a new case of Hb J Baltimore (alpha 2A beta2 16 Gly yields Asp) isolated in France (author's transl)].

246. Haemoglobin Lyon (beta17-18 (A 14-15) Lys-Val leads to O). Determination by sequenator analysis.

247. [Prenatal prevention and women behaviour (author's transl)].

248. Hemoglobin C Ziguinchor alphaA2 beta62 (A3) Glu leads to Val beta58 (E2) Pro leads to Arg: the second sickling variant with amino acid substitutions in 2 residues of the beta polypeptide chain.

249. Hb A1c: a review on its structure, biosynthesis, clinical significance and methods of assay.

250. One- and two-dimensional NMR investigations of the heme pocket in free alpha(CO) chains from human hemoglobin.

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