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Homogeneous triploid and tetraploid production through crossing with mixoploid parents in pointed gourd (Trichosanthes dioica Roxb.).
- Published in:
- Euphytica, 2022, v. 218, n. 2, p. 1, doi. 10.1007/s10681-021-02961-2
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- Publication type:
- Article
A Palindromic Motif in the -2084 to -2078 Upstream Region is Essential for ABCA12 Promoter Function in Cultured Human Keratinocytes.
- Published in:
- Scientific Reports, 2014, p. 1, doi. 10.1038/srep06737
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- Publication type:
- Article
Localization of ABCA12 from Golgi apparatus to lamellar granules in human upper epidermal keratinocytes.
- Published in:
- Experimental Dermatology, 2007, v. 16, n. 11, p. 920, doi. 10.1111/j.1600-0625.2007.00614.x
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- Publication type:
- Article
COL7A1 mutation G2037E causes epidermal retention of type VII collagen.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 5, p. 418, doi. 10.1007/s10038-006-0378-5
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- Publication type:
- Article
Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin barrier defects.
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- Human Molecular Genetics, 2008, v. 17, n. 19, p. 3075, doi. 10.1093/hmg/ddn204
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- Publication type:
- Article
BdERECTA controls vasculature patterning and phloem-xylem organization in Brachypodium distachyon.
- Published in:
- BMC Plant Biology, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12870-021-02970-2
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- Publication type:
- Article
Targeted Skipping of a Single Exon Harboring a Premature Termination Codon Mutation: Implications and Potential for Gene Correction Therapy for Selective Dystrophic Epidermolysis Bullosa Patients.
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- Journal of Investigative Dermatology, 2006, v. 126, n. 12, p. 2614, doi. 10.1038/sj.jid.5700435
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- Article
Novel ALDH3A2 Heterozygous Mutations in a Japanese Family with Sjögren–Larsson Syndrome.
- Published in:
- 2006
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- Publication type:
- Letter
Compound Heterozygous Mutations Including a De Novo Missense Mutation in ABCA12 Led to a Case of Harlequin Ichthyosis with Moderate Clinical Severity.
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- Journal of Investigative Dermatology, 2006, v. 126, n. 7, p. 1518, doi. 10.1038/sj.jid.5700295
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- Publication type:
- Article
Fibroblasts Show More Potential as Target Cells than Keratinocytes in COL7A1 Gene Therapy of Dystrophic Epidermolysis Bullosa.
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- Journal of Investigative Dermatology, 2006, v. 126, n. 4, p. 766, doi. 10.1038/sj.jid.5700117
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- Publication type:
- Article
Carbohydrate Binding Specificity of the Recombinant Chitin-binding Domain of Human Macrophage Chitinase.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 11, p. 2402, doi. 10.1271/bbb.67.2402
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- Publication type:
- Article
An Indian family with Sjögren-Larsson syndrome caused by a novel ALDH3A2 mutation.
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- International Journal of Dermatology, 2010, v. 49, n. 9, p. 1031, doi. 10.1111/j.1365-4632.2010.04482.x
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- Publication type:
- Article
Tetraploid Induction by Colchicine Treatment and Crossing with a Diploid Reveals Less-Seeded Fruit Production in Pointed Gourd (Trichosanthes dioica Roxb.).
- Published in:
- Plants (2223-7747), 2020, v. 9, n. 3, p. 370, doi. 10.3390/plants9030370
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- Publication type:
- Article
Compound heterozygous ABCA12 mutations including a novel nonsense mutation underlie harlequin ichthyosis.
- Published in:
- 2007
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- Publication type:
- journal article
Mice that lack the C-terminal region of Reelin exhibit behavioral abnormalities related to neuropsychiatric disorders.
- Published in:
- Scientific Reports, 2016, p. 28636, doi. 10.1038/srep28636
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- Publication type:
- Article
Blocked at the Stomatal Gate, a Key Step of Wheat Stb16q -Mediated Resistance to Zymoseptoria tritici.
- Published in:
- Frontiers in Plant Science, 2022, v. 13, p. 1, doi. 10.3389/fpls.2022.921074
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- Publication type:
- Article
Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer.
- Published in:
- 2005
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- Publication type:
- journal article
Publisher Correction: Spatial modeling of biological patterns shows multiscale organization of Arabidopsis thaliana heterochromatin.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Spatial modeling of biological patterns shows multiscale organization of Arabidopsis thaliana heterochromatin.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-020-79158-5
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- Publication type:
- Article
Altered lignification in mur1-1 a mutant deficient in GDP-L-fucose synthesis with reduced RG-II cross linking.
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- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0184820
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- Publication type:
- Article
Design of a comprehensive microfluidic and microscopic toolbox for the ultra-wide spatio-temporal study of plant protoplasts development and physiology.
- Published in:
- Plant Methods, 2019, v. 15, n. 1, p. N.PAG, doi. 10.1186/s13007-019-0459-z
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- Publication type:
- Article
Combining laser-assisted microdissection (LAM) and RNA-seq allows to perform a comprehensive transcriptomic analysis of epidermal cells of Arabidopsis embryo.
- Published in:
- Plant Methods, 2018, v. 14, p. 1, doi. 10.1186/s13007-018-0275-x
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- Publication type:
- Article
Characteristics and Genetic Control of Rhizome Coloration in Red Rhizome Lotus.
- Published in:
- Horticulture Journal, 2022, v. 91, n. 3, p. 366, doi. 10.2503/hortj.UTD-350
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- Publication type:
- Article
Humanization of autoantigen.
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- Nature Medicine, 2007, v. 13, n. 3, p. 378, doi. 10.1038/nm1496
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- Publication type:
- Article
AKT Has an Anti-Apoptotic Role in ABCA12-Deficient Keratinocytes.
- Published in:
- 2011
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- Publication type:
- Letter
ABCA12 Is a Major Causative Gene for Non-Bullous Congenital Ichthyosiform Erythroderma.
- Published in:
- 2009
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- Publication type:
- Letter
Prevalent and Rare Mutations in the Gene Encoding Filaggrin in Japanese Patients with Ichthyosis Vulgaris and Atopic Dermatitis.
- Published in:
- 2009
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- Publication type:
- Letter
Mild Recessive Bullous Congenital Ichthyosiform Erythroderma due to a Previously Unidentified Homozygous Keratin 10 Nonsense Mutation.
- Published in:
- Journal of Investigative Dermatology, 2008, v. 128, n. 7, p. 1648, doi. 10.1038/sj.jid.5701257
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- Publication type:
- Article
Specific Filaggrin Mutations Cause Ichthyosis Vulgaris and Are Significantly Associated with Atopic Dermatitis in Japan.
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- Journal of Investigative Dermatology, 2008, v. 128, n. 6, p. 1436, doi. 10.1038/sj.jid.5701205
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- Publication type:
- Article
Novel ABCA12 Mutations Identified in Two Cases of Non-Bullous Congenital Ichthyosiform Erythroderma Associated with Multiple Skin Malignant Neoplasia.
- Published in:
- 2007
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- Publication type:
- Letter
Keratin 1 Gene Mutation Detected in Epidermal Nevus with Epidermolytic Hyperkeratosis.
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- Journal of Investigative Dermatology, 2007, v. 127, n. 6, p. 1371, doi. 10.1038/sj.jid.5700712
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- Publication type:
- Article
Possible Involvement of Exon 31 Alternative Splicing in Phenotype and Severity of Epidermolysis Bullosa Caused by Mutations in PLEC1.
- Published in:
- 2007
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- Publication type:
- Letter
A Novel GJB2 Mutation p.Asn54His in a Patient with Palmoplantar Keratoderma, Sensorineural Hearing Loss and Knuckle Pads.
- Published in:
- 2007
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- Publication type:
- Letter
DNA-Based Prenatal Diagnosis of Harlequin Ichthyosis and Characterization of ABCA12 Mutation Consequences.
- Published in:
- Journal of Investigative Dermatology, 2007, v. 127, n. 3, p. 568, doi. 10.1038/sj.jid.5700617
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- Publication type:
- Article
Novel duplication mutation in the patatin domain of adipose triglyceride lipase (PNPLA2) in neutral lipid storage disease with severe myopathy.
- Published in:
- Muscle & Nerve, 2007, v. 36, n. 6, p. 856, doi. 10.1002/mus.20869
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- Publication type:
- Article
ERO1α is a novel endogenous marker of hypoxia in human cancer cell lines.
- Published in:
- 2019
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- Publication type:
- journal article
Nuclear Architecture and Chromatin Dynamics in Interphase Nuclei of Arabidopsis thaliana.
- Published in:
- Cytogenetic & Genome Research, 2014, v. 143, n. 1-3, p. 28, doi. 10.1159/000363724
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- Publication type:
- Article
Effects of Total Asphyxia on the Development of Synaptic Junctions in the Brains of Mice.
- Published in:
- Pediatrics International, 1992, v. 34, n. 1, p. 1, doi. 10.1111/j.1442-200X.1992.tb00916.x
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- Publication type:
- Article