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American Journal of Human Genetics|April 17, 1999
The promoters of the survival motor neuron gene (SMN) and its copy (SMNc) share common regulatory elementsA Echaniz-Laguna, P Miniou, D Bartholdi, et al.Cytogenetics and Cell Genetics|January 1, 1997
Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysisP Miniou, D Bourc'his, D Molina Gomes, et al.Nucleic Acids Research|September 11, 1999
Gene targeting restricted to mouse striated muscle lineageP Miniou, D Tiziano, T Frugier, et al.Human Genetics|June 1, 1997
alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissuesP Miniou, M Jeanpierre, D Bourc'his, et al.Human Genetics|August 1, 1995
Three new dinucleotide repeat polymorphisms on human chromosome 9: D9S970, D9S971, and D9S972B S Kimmel, P Miniou, S L Robbins, et al.Genomics|July 15, 1994
Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1L Oliveira, P Miniou, E Viegas-Pequignot, et al.Genomics|July 1, 1995
cDNA, gene structure, and chromosomal localization of human GAR1 (CNCG3L), a homolog of the third subunit of bovine photoreceptor cGMP-gated channelM D Ardell, A K Makhija, L Oliveira, et al.Human Molecular Genetics|April 6, 2000
Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophyT Frugier, F D Tiziano, C Cifuentes-Diaz, et al.Human Molecular Genetics|December 1, 1994
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patientsP Miniou, M Jeanpierre, V Blanquet, et al.American Journal of Human Genetics|January 1, 1997
The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann diseaseL Bürglen, T Seroz, P Miniou, et al.Pageof 2