Found: 40
Select item for more details and to access through your institution.
Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-72418-8
- By:
- Publication type:
- Article
IL-3 produced by T cells is crucial for basophil extravasation in hapten-induced allergic contact dermatitis.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1151468
- By:
- Publication type:
- Article
IL-3 produced by T cells is crucial for basophil extravasation in hapten-induced allergic contact dermatitis.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1151468
- By:
- Publication type:
- Article
The cell proliferation antigen Ki-67 organises heterochromatin.
- Published in:
- eLife, 2016, p. 1, doi. 10.7554/eLife.13722
- By:
- Publication type:
- Article
Development of HPV16 mouse and dog models for more accurate prediction of human vaccine efficacy.
- Published in:
- Laboratory Animal Research, 2023, v. 39, n. 1, p. 1, doi. 10.1186/s42826-023-00166-3
- By:
- Publication type:
- Article
The COL6A5-p.Glu2272* mutation induces chronic itch in mice.
- Published in:
- Mammalian Genome, 2024, v. 35, n. 2, p. 122, doi. 10.1007/s00335-024-10032-9
- By:
- Publication type:
- Article
Modeling human disease in rodents by CRISPR/Cas9 genome editing.
- Published in:
- Mammalian Genome, 2017, v. 28, n. 7/8, p. 291, doi. 10.1007/s00335-017-9703-x
- By:
- Publication type:
- Article
Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project.
- Published in:
- Mammalian Genome, 2012, v. 23, n. 9/10, p. 600, doi. 10.1007/s00335-012-9418-y
- By:
- Publication type:
- Article
The mammalian gene function resource: the international knockout mouse consortium.
- Published in:
- Mammalian Genome, 2012, v. 23, n. 9/10, p. 580, doi. 10.1007/s00335-012-9422-2
- By:
- Publication type:
- Article
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.
- Published in:
- Biomedicines, 2022, v. 10, n. 12, p. 3148, doi. 10.3390/biomedicines10123148
- By:
- Publication type:
- Article
Transgenic mouse models expressing human and macaque prion protein exhibit similar prion susceptibility on a strain-dependent manner.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-52155-z
- By:
- Publication type:
- Article
The Human SCN10A<sup>G1662S</sup> Point Mutation Established in Mice Impacts on Mechanical, Heat, and Cool Sensitivity.
- Published in:
- Frontiers in Pharmacology, 2021, v. 12, p. 1, doi. 10.3389/fphar.2021.780132
- By:
- Publication type:
- Article
Increased On-Target Rate and Risk of Concatemerization after CRISPR-Enhanced Targeting in ES Cells.
- Published in:
- Genes, 2023, v. 14, n. 2, p. 401, doi. 10.3390/genes14020401
- By:
- Publication type:
- Article
The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia.
- Published in:
- Journal of Anatomy, 2019, v. 235, n. 3, p. 637, doi. 10.1111/joa.13013
- By:
- Publication type:
- Article
Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders.
- Published in:
- Frontiers in Neuroscience, 2023, p. 1, doi. 10.3389/fnins.2023.1148683
- By:
- Publication type:
- Article
A Novel Rat Tetraspan Protein in Cells of the Oligodendrocyte Lineage.
- Published in:
- Journal of Neurochemistry, 1999, v. 73, n. 6, p. 2600, doi. 10.1046/j.1471-4159.1999.0732600.x
- By:
- Publication type:
- Article
Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction.
- Published in:
- BMC Cell Biology, 2016, v. 17, p. 1, doi. 10.1186/s12860-016-0108-6
- By:
- Publication type:
- Article
Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes.
- Published in:
- PLoS Genetics, 2016, v. 12, n. 2, p. 1, doi. 10.1371/journal.pgen.1005709
- By:
- Publication type:
- Article
The Human SCN9A <sup> R 185 H </sup> Point Mutation Induces Pain Hypersensitivity and Spontaneous Pain in Mice.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.913990
- By:
- Publication type:
- Article
The Rogdi knockout mouse is a model for Kohlschütter–Tönz syndrome.
- Published in:
- Scientific Reports, 2024, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-50870-2
- By:
- Publication type:
- Article
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 23, p. 6736, doi. 10.1093/hmg/ddv380
- By:
- Publication type:
- Article
Repression of Osteoblast Maturation by ERRα Accounts for Bone Loss Induced by Estrogen Deficiency.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054837
- By:
- Publication type:
- Article
Absence of TI-VAMP/Vamp7 Leads to Increased Anxiety in Mice.
- Published in:
- Journal of Neuroscience, 2012, v. 32, n. 6, p. 1962, doi. 10.1523/JNEUROSCI.4436-11.2012
- By:
- Publication type:
- Article
Targeted deletion of kidney glucose-6 phosphatase leads to nephropathy.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Targeted deletion of kidney glucose-6 phosphatase leads to nephropathy.
- Published in:
- Kidney International, 2014, v. 86, n. 4, p. 747, doi. 10.1038/ki.2014.102
- By:
- Publication type:
- Article
Deciphering the Role of Oncogenic MITFE318K in Senescence Delay and Melanoma Progression.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Reg-2 is a motoneuron neurotrophic factor and a signalling intermediate in the CNTF survival pathway.
- Published in:
- Nature Cell Biology, 2000, v. 2, n. 12, p. 906, doi. 10.1038/35046558
- By:
- Publication type:
- Article
Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models.
- Published in:
- Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-020-00405-7
- By:
- Publication type:
- Article
A mu-delta opioid receptor brain atlas reveals neuronal co-occurrence in subcortical networks.
- Published in:
- Brain Structure & Function, 2015, v. 220, n. 2, p. 677, doi. 10.1007/s00429-014-0717-9
- By:
- Publication type:
- Article
Highly-efficient, fluorescent, locus directed cre and FlpO deleter mice on a pure C57BL/6N genetic background.
- Published in:
- Genesis: The Journal of Genetics & Development, 2012, v. 50, n. 6, p. 482, doi. 10.1002/dvg.20826
- By:
- Publication type:
- Article
Improving laboratory animal genetic reporting: LAG-R guidelines.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49439-y
- By:
- Publication type:
- Article
Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome.
- Published in:
- PLoS Genetics, 2021, v. 17, n. 9, p. 1, doi. 10.1371/journal.pgen.1009777
- By:
- Publication type:
- Article
Conditional switching of KIF2A mutation provides new insights into cortical malformation pathogeny.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 5, p. 766, doi. 10.1093/hmg/ddz316
- By:
- Publication type:
- Article
Cbs overdosage is necessary and sufficient to induce cognitive phenotypes in mouse models of Down syndrome and interacts genetically with Dyrk1a.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 9, p. 1561, doi. 10.1093/hmg/ddy447
- By:
- Publication type:
- Article
A new mouse model of ARX dup24 recapitulates the patients behavioral and fine motor alterations.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 12, p. 2138, doi. 10.1093/hmg/ddy122
- By:
- Publication type:
- Article
TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-10081-8
- By:
- Publication type:
- Article
Distinct roles of α‐ and β‐tubulin polyglutamylation in controlling axonal transport and in neurodegeneration.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Distinct roles of α‐ and β‐tubulin polyglutamylation in controlling axonal transport and in neurodegeneration.
- Published in:
- EMBO Journal, 2021, v. 40, n. 17, p. 1, doi. 10.15252/embj.2021108498
- By:
- Publication type:
- Article
Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss.
- Published in:
- EMBO Journal, 2016, v. 35, n. 10, p. 1077, doi. 10.15252/embj.201592559
- By:
- Publication type:
- Article
Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.
- Published in:
- PLoS Genetics, 2017, v. 13, n. 7, p. 1, doi. 10.1371/journal.pgen.1006886
- By:
- Publication type:
- Article