276 results on '"Pichon, Olivier"'
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2. The Arabidopsis protein farnesylation era1 mutant displays an altered hormonal-dependent nitrate regulation of root architecture
3. Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variants
4. Protein farnesylation is involved in nitrogen starvation adaptation in Arabidopsis
5. Stilbenoid-Enriched Grape Cane Extracts for the Biocontrol of Grapevine Diseases
6. Novel interstitial 2q12.3q13 microdeletion predisposes to developmental delay and behavioral problems
7. Structural abnormalities of chromosome 8 and fetoplacental discrepancy: A second case report and review of fetal phenotype of 8p inverted duplication deletion syndrome
8. A de novo 2q37.2 deletion encompassing AGAP1 and SH3BP4 in a patient with autism and intellectual disability
9. Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20
10. Variants in MED12L, encoding a subunit of the mediator kinase module, are responsible for intellectual disability associated with transcriptional defect
11. Setting-up a fast and reliable cytokinin biosensor based on a plant histidine kinase receptor expressed in Saccharomyces cerevisiae
12. Conversation biomoléculaire au coin du « Terroir » : quand les polyphénols se font l’écho de la qualité du vignoble
13. ALSV-Based Virus-Induced Gene Silencing in Apple Tree (Malus × domestica L.)
14. Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants
15. Virus-induced gene silencing of the two squalene synthase isoforms of apple tree ( Malus × domestica L.) negatively impacts phytosterol biosynthesis, plastid pigmentation and leaf growth
16. Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders
17. Terroir Influence on Polyphenol Metabolism from Grape Canes: A Spatial Metabolomic Study at Parcel Scale
18. Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders.
19. Assortative mating and parental genetic relatedness drive the pathogenicity of variably expressive variants
20. Improved gene co-expression network quality through expression dataset down-sampling and network aggregation
21. Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome
22. The Arabidopsis DUF239 gene family encodes Neprosin‐like proteins that are widely expressed in seed endosperm
23. Virus-induced gene silencing of the two squalene synthase isoforms of apple tree (Malus × domestica L.) negatively impacts phytosterol biosynthesis, plastid pigmentation and leaf growth
24. Conversation biomoléculaire au coin du « Terroir » : quand les polyphénols se font l’écho de la qualité du vignoble
25. Le terroir viticole
26. Characterization of a spermidine hydroxycinnamoyltransferase in Malus domestica highlights the evolutionary conservation of trihydroxycinnamoyl spermidines in pollen coat of core Eudicotyledons
27. The Arabidopsis protein farnesylation era1 mutant displays an altered hormonal-dependent nitrate regulation of root architecture
28. Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases
29. Unexpected discovery of syndromic epilepsy during the genetic exploration of a case of leukemia.
30. Ranking genome-wide correlation measurements improves microarray and RNA-seq based global and targeted co-expression networks
31. Characterization of the Early Events Leading to Totipotency in an Arabidopsis Protoplast Liquid Culture by Temporal Transcript Profiling
32. The Arabidopsis DUF239 gene family encodes Neprosin‐like proteins that are widely expressed in seed endosperm.
33. The Arabidopsis Abscisic Acid Catabolic Gene CYP707A2 Plays a Key Role in Nitrate Control of Seed Dormancy
34. Two distinct intracellular Ca 2+ -release components act in opposite ways in the regulation of the auxin-dependent MIA biosynthesis in Catharanthus roseus cells
35. Arabidopsis NRP1 and NRP2 Encode Histone Chaperones and Are Required for Maintaining Postembryonic Root Growth
36. Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder
37. Exome sequencing as a first-tier test for copy number variant detection : retrospective evaluation and prospective screening in 2418 cases.
38. Patients with isolated oligo/hypodontia caused by RUNX2 duplication
39. Phenotype–genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature
40. Disruption of the SEMA3D Gene in a Patient with Congenital Heart Defects
41. Optical Genome Mapping Combined with High-Throughput Sequencing Is Effective for the Diagnostic and Prognostic Genomic Classification of Acute Myeloid Leukemia and Myelodysplastic Neoplasms
42. Molecular Characterization of an Aux/IAA of Catharanthus roseus
43. Plasmalemma ATPase activity modifications induced by traumatisms in Bidens pilosa
44. Novel interstitial 2q12.3q13 microdeletion predisposes to developmental delay and behavioral problems
45. Congenital Heart Defects in Patients with Deletions Upstream of SOX9
46. Deciphering the Evolution, Cell Biology and Regulation of Monoterpene Indole Alkaloids
47. RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features
48. Exudative retinopathy, cerebral calcifications, duodenal atresia, preaxial polydactyly, micropenis, microcephaly and short stature: A new syndrome?
49. Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder.
50. Molecular Characterization of 1q44 Microdeletion in 11 Patients Reveals Three Candidate Genes for Intellectual Disability and Seizures
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