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Terroir Influence on Polyphenol Metabolism from Grape Canes: A Spatial Metabolomic Study at Parcel Scale.
- Published in:
- Molecules, 2023, v. 28, n. 11, p. 4555, doi. 10.3390/molecules28114555
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- Publication type:
- Article
The Arabidopsis DUF239 gene family encodes Neprosin‐like proteins that are widely expressed in seed endosperm.
- Published in:
- Plant Genome, 2023, v. 16, n. 1, p. 1, doi. 10.1002/tpg2.20290
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- Publication type:
- Article
The Arabidopsis protein farnesylation era1 mutant displays an altered hormonal-dependent nitrate regulation of root architecture.
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- Plant Growth Regulation, 2023, v. 99, n. 2, p. 283, doi. 10.1007/s10725-022-00907-9
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- Article
Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder.
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- Clinical Genetics, 2022, v. 101, n. 3, p. 364, doi. 10.1111/cge.14099
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- Publication type:
- Article
Novel interstitial 2q12.3q13 microdeletion predisposes to developmental delay and behavioral problems.
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- Neurogenetics, 2021, v. 22, n. 3, p. 195, doi. 10.1007/s10048-021-00653-6
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- Publication type:
- Article
Whole genome copy number analysis in search of new prognostic biomarkers in first line treatment of mantle cell lymphoma. A study by the LYSA group.
- Published in:
- Hematological Oncology, 2020, v. 38, n. 4, p. 446, doi. 10.1002/hon.2750
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- Article
Pseudodicentric Chromosome Originating from Autosomes 9 and 21 in a Male Patient with Oligozoospermia.
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- Cytogenetic & Genome Research, 2019, v. 159, n. 4, p. 201, doi. 10.1159/000504820
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- Article
Identification of mobile retrocopies during genetic testing: Consequences for routine diagnosis.
- Published in:
- Human Mutation, 2019, v. 40, n. 11, p. 1993, doi. 10.1002/humu.23845
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- Publication type:
- Article
Improved gene co-expression network quality through expression dataset down-sampling and network aggregation.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50885-8
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- Article
Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non-homologous Robertsonian translocation. Should we still perform prenatal diagnosis?
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- 2019
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- Publication type:
- journal article
11q24.2q24.3 microdeletion in two families presenting features of Jacobsen syndrome, without intellectual disability: Role of FLI1, ETS1, and SENCR long noncoding RNA.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 6, p. 993, doi. 10.1002/ajmg.a.61113
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- Publication type:
- Article
Familial autosomal dominant severe ankyloglossia with tooth abnormalities.
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- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 7, p. 1614, doi. 10.1002/ajmg.a.38690
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- Publication type:
- Article
Comparison of Tumor- and Bone Marrow-Derived Mesenchymal Stromal/Stem Cells from Patients with High-Grade Osteosarcoma.
- Published in:
- International Journal of Molecular Sciences, 2018, v. 19, n. 3, p. 707, doi. 10.3390/ijms19030707
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- Publication type:
- Article
CHASE-Containing Histidine Kinase Receptors in Apple Tree: From a Common Receptor Structure to Divergent Cytokinin Binding Properties and Specific Functions.
- Published in:
- Frontiers in Plant Science, 2017, p. 1, doi. 10.3389/fpls.2017.01614
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- Publication type:
- Article
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.
- Published in:
- Planta: An International Journal of Plant Biology, 2017, v. 246, n. 1, p. 45, doi. 10.1007/s00425-017-2681-0
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- Publication type:
- Article
Folivory elicits a strong defense reaction in Catharanthus roseus: metabolomic and transcriptomic analyses reveal distinct local and systemic responses.
- Published in:
- Scientific Reports, 2017, p. 40453, doi. 10.1038/srep40453
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- Publication type:
- Article
Mandibular dysostosis without microphthalmia caused by OTX2 deletion.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 9, p. 2466, doi. 10.1002/ajmg.a.37837
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- Publication type:
- Article
Characterization of a spermidine hydroxycinnamoyltransferase in Malus domestica highlights the evolutionary conservation of trihydroxycinnamoyl spermidines in pollen coat of core Eudicotyledons.
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- Journal of Experimental Botany, 2015, v. 66, n. 22, p. 7271, doi. 10.1093/jxb/erv423
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- Publication type:
- Article
Patients with isolated oligo/hypodontia caused by RUNX2 duplication.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 6, p. 1386, doi. 10.1002/ajmg.a.37052
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- Publication type:
- Article
Disruption of the SEMA3 D Gene in a Patient with Congenital Heart Defects.
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- Human Mutation, 2015, v. 36, n. 1, p. 30, doi. 10.1002/humu.22702
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- Publication type:
- Article
Congenital Heart Defects in Patients with Deletions Upstream of SOX9.
- Published in:
- Human Mutation, 2013, v. 34, n. 12, p. 1628, doi. 10.1002/humu.22449
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- Publication type:
- Article
Exudative retinopathy, cerebral calcifications, duodenal atresia, preaxial polydactyly, micropenis, microcephaly and short stature: A new syndrome?
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 8, p. 1829, doi. 10.1002/ajmg.a.36021
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- Publication type:
- Article
Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas.
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- European Journal of Human Genetics, 2013, v. 21, n. 7, p. 784, doi. 10.1038/ejhg.2012.252
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- Publication type:
- Article
Characterization of the Early Events Leading to Totipotency in an Arabidopsis Protoplast Liquid Culture by Temporal Transcript Profiling.
- Published in:
- Plant Cell, 2013, v. 25, n. 7, p. 2444, doi. 10.1105/tpc.113.109538
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- Publication type:
- Article
Molecular characterization of 1q44 microdeletion in 11 patients reveals three candidate genes for intellectual disability and seizures.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 7, p. 1633, doi. 10.1002/ajmg.a.35423
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- Publication type:
- Article
De novo duplication and deletions at 7q in a three-generation family.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 6, p. 1493, doi. 10.1002/ajmg.a.35332
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- Publication type:
- Article
Serpentine fibula-polycystic kidney syndrome caused by truncating mutations in NOTCH2.
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- Human Mutation, 2011, v. 32, n. 11, p. 1239, doi. 10.1002/humu.21563
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- Publication type:
- Article
Molecular Characterization of an Aux/IAA of Catharanthus roseus.
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- Journal of Plant Growth Regulation, 2011, v. 30, n. 2, p. 235, doi. 10.1007/s00344-010-9187-3
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- Publication type:
- Article
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis.
- Published in:
- Nature Genetics, 2011, v. 43, n. 4, p. 306, doi. 10.1038/ng.778
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- Publication type:
- Article
Two distinct intracellular Ca2+-release components act in opposite ways in the regulation of the auxin-dependent MIA biosynthesis in Catharanthus roseus cells.
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- Journal of Experimental Botany, 2009, v. 60, n. 4, p. 1387, doi. 10.1093/jxb/erp017
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- Publication type:
- Article
The regulatory PII protein controls arginine biosynthesis in Arabidopsis
- Published in:
- FEBS Letters, 2006, v. 580, n. 8, p. 2015, doi. 10.1016/j.febslet.2006.02.075
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- Publication type:
- Article
Electrophysiological characterization of tomato hypocotyl putative action potentials induced by cotyledon heating.
- Published in:
- Physiologia Plantarum, 2002, v. 115, n. 2, p. 197, doi. 10.1034/j.1399-3054.2002.1150204.x
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- Publication type:
- Article
Plasmalemma ATPase activity modifications induced by traumatisms in Bidens pilosa.
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- Journal of Experimental Botany, 1996, v. 47, n. 6, p. 831, doi. 10.1093/jxb/47.6.831
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- Article
Is cytoplasmic pH involved in the regulation of cell cycle in plants?
- Published in:
- Physiologia Plantarum, 1994, v. 92, n. 2, p. 261, doi. 10.1111/j.1399-3054.1994.tb05335.x
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- Publication type:
- Article