S. Cure

发表

The DNA sequence and analysis of human chromosome 14

Patrick Wincker, Jean Weissenbach, Leroy Hood, 2023, Nature.

Tracing ancestors and relatives of Escherichia coli B, and the derivation of B strains REL606 and BL21(DE3).

R. Lenski, F. Studier, Jihyun F. Kim, 2009, Journal of molecular biology.

Cost of skeletal-related events in European patients with solid tumours and bone metastases: data from a prospective multinational observational study

V. Lorusso, I. Durán, D. Lüftner, 2013, Journal of medical economics.

A retrospective database study comparing treatment outcomes and cost associated with choice of fixed-dose inhaled corticosteroid/long-acting β2-agonists for asthma maintenance treatment in Germany

C. Vogelmeier, S. Aballéa, A. Wirén, 2008, International journal of clinical practice.

Novel point mutations, deletions, and polymorphisms in the cathepsin C gene in nine families from Europe and North Africa with Papillon-Lefèvre syndrome.

J. Prud'homme, J. Fischer, B. Bouadjar, 2001, The Journal of investigative dermatology.

An autosomal-recessive form of cutis laxa is due to homozygous elastin mutations, and the phenotype may be modified by a heterozygous fibulin 5 polymorphism.

A. Mégarbané, R. de Cid, J. Sass, 2009, The Journal of investigative dermatology.

Determination of the growth rate in human fibroblasts in cell culture.

A. Boué, S. Cure, 1976, Methods in cell biology.

L-2-Hydroxyglutaric aciduria: Identification of ten novel mutations in the L2HGDH gene

H. Omran, M. Topcu, J. Sass, 2008, Journal of Inherited Metabolic Disease.

Growth characteristics of human embryonic cell lines with chromosomal anomalies.

J. Boué, A. Boué, S. Cure, 1974, Biomedicine / [publiee pour l'A.A.I.C.I.G.].

Specific TGM1 mutation profiles in bathing suit and self-improving collodion ichthyoses: phenotypic and genotypic data from 9 patients with dynamic phenotypes of autosomal recessive congenital ichthyosis.

C. Derbois, J. Fischer, C. Blanchet‐Bardon, 2012, Archives of dermatology.

In vitro cultivation of cells from aneuploid human embryos. Initiation of cell lines and longevity of the cultures

J. Boué, A. Boué, S. Cure, 1975, In Vitro.

Innovative Therapeutic Perspectives in Neuromuscular Diseases

S. Braun, S. Cure, 2012 .

Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity.

J. Weissenbach, J. Prud'homme, J. Fischer, 2000, American journal of human genetics.

A simple method for the determination of the growth rate in human fibroblast cell cultures

A. Boué, S. Cure, 2005, Experientia.

Clinical and genetic studies of 3 large, consanguineous, Algerian families with Mal de Meleda.

J. Prud'homme, J. Fischer, B. Bouadjar, 2000, Archives of dermatology.

PCN115 Cost of Skeletal-Related Events (SREs) in Patients with Bone Metastases to solid Tumours Based on the Health Resource Utilisation (HRU) Collected in a Prospective European Multinational Observational Study

I. Durán, D. Lüftner, A. Bahl, 2011 .

Novel mutations in the gene encoding secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related protein-1 (SLURP-1) and description of five ancestral haplotypes in patients with Mal de Meleda.

J. Prud'homme, D. Hohl, C. Munro, 2003, The Journal of investigative dermatology.

Tracing ancestors and relatives of Escherichia coli B, and the derivation of B strains REL606 and BL21(DE3).

F. Studier, Jihyun F. Kim, P. Daegelen, 2009, Journal of molecular biology.