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Deep sequencing analysis of the developing mouse brain reveals a novel microRNA.
- Published in:
- BMC Genomics, 2011, v. 12, p. 1, doi. 10.1186/1471-2164-12-176
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- Publication type:
- Article
Deep sequencing analysis of the developing mouse brain reveals a novel microRNA.
- Published in:
- BMC Genomics, 2011, v. 12, n. 1, p. 176, doi. 10.1186/1471-2164-12-176
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- Publication type:
- Article
Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema.
- Published in:
- Science Translational Medicine, 2022, v. 14, n. 634, p. 1, doi. 10.1126/scitranslmed.abm4869
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- Publication type:
- Article
Distribution of Parkinson's disease associated RAB39B in mouse brain tissue.
- Published in:
- Molecular Brain, 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13041-020-00584-7
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- Publication type:
- Article
The Nestin neural enhancer is essential for normal levels of endogenous Nestin in neuroprogenitors but is not required for embryo development.
- Published in:
- PLoS ONE, 2021, v. 16, n. 11, p. 1, doi. 10.1371/journal.pone.0258538
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- Publication type:
- Article
Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy.
- Published in:
- 2016
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- Publication type:
- journal article
Disrupted Excitatory Synaptic Contacts and Altered Neuronal Network Activity Underpins the Neurological Phenotype in PCDH19-Clustering Epilepsy (PCDH19-CE).
- Published in:
- Molecular Neurobiology, 2021, v. 58, n. 5, p. 2005, doi. 10.1007/s12035-020-02242-4
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- Publication type:
- Article
SOX3 is required during the formation of the hypothalamo-pituitary axis.
- Published in:
- Nature Genetics, 2004, v. 36, n. 3, p. 247, doi. 10.1038/ng1309
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- Publication type:
- Article
A reduction in Npas4 expression results in delayed neural differentiation of mouse embryonic stem cells.
- Published in:
- Stem Cell Research & Therapy, 2014, v. 5, n. 3, p. 1, doi. 10.1186/scrt453
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- Publication type:
- Article
SOX3 promotes generation of committed spermatogonia in postnatal mouse testes.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-63290-3
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- Publication type:
- Article
Locally Fixed Alleles: A method to localize gene drive to island populations.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-51994-0
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- Publication type:
- Article
Gain of chromosome 21 increases the propensity for P2RY8::CRLF2 acute lymphoblastic leukemia via increased HMGN1 expression.
- Published in:
- Frontiers in Oncology, 2023, p. 1, doi. 10.3389/fonc.2023.1177871
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- Publication type:
- Article
Spatiotemporal Regulation of Multiple Overlapping Sense and Novel Natural Antisense Transcripts at the Nrgn and Camk2n1 Gene Loci during Mouse Cerebral Corticogenesis.
- Published in:
- Cerebral Cortex, 2011, v. 21, n. 3, p. 683, doi. 10.1093/cercor/bhq141
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- Publication type:
- Article
Congenital Hydrocephalus and Abnormal Subcommissural Organ Development in Sox3 Transgenic Mice.
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- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0029041
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- Publication type:
- Article
Survival and Differentiation of Pituitary Colony-Forming Cells In Vivo.
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- Stem Cells, 2007, v. 25, n. 7, p. 1730, doi. 10.1634/stemcells.2007-0012
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- Publication type:
- Article
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse.
- Published in:
- Nature Genetics, 1998, v. 19, n. 2, p. 125, doi. 10.1038/477
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- Publication type:
- Article
Adrenocorticotropin Deficiency in Combined Pituitary Hormone Deficiency Patients Homozygous for a Novel PROP1 Deletion.
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- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 12, p. 4556, doi. 10.1210/jcem.85.12.7013
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- Publication type:
- Article
Pcdh19 Loss-of-Function Increases Neuronal Migration In Vitro but is Dispensable for Brain Development in Mice.
- Published in:
- Scientific Reports, 2016, p. 26765, doi. 10.1038/srep26765
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- Publication type:
- Article
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
- Published in:
- Clinical Endocrinology, 2005, v. 63, n. 1, p. 10, doi. 10.1111/j.1365-2265.2005.02291.x
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- Publication type:
- Article
Differential modulation of motor cortex excitability in BDNF Met allele carriers following experimentally induced and use-dependent plasticity.
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- European Journal of Neuroscience, 2012, v. 36, n. 5, p. 2640, doi. 10.1111/j.1460-9568.2012.08177.x
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- Publication type:
- Article
Optimized nickase- and nuclease-based prime editing in human and mouse cells.
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- Nucleic Acids Research, 2021, v. 49, n. 18, p. 10785, doi. 10.1093/nar/gkab792
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- Publication type:
- Article
Population genomics of invasive rodents on islands: Genetic consequences of colonization and prospects for localized synthetic gene drive.
- Published in:
- Evolutionary Applications, 2021, v. 14, n. 5, p. 1421, doi. 10.1111/eva.13210
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- Publication type:
- Article
Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouse.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-37855-x
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- Publication type:
- Article
Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERα).
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 11, p. 2042, doi. 10.1093/hmg/ddx094
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- Publication type:
- Article
CRISPR applications for Duchenne muscular dystrophy: From animal models to potential therapies.
- Published in:
- WIREs: Mechanisms of Disease, 2023, v. 15, n. 1, p. 1, doi. 10.1002/wsbm.1580
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- Publication type:
- Article
Identification of an IGSF1-specific deletion in a five-generation pedigree with X-linked Central Hypothyroidism without macroorchidism.
- Published in:
- Clinical Endocrinology, 2016, v. 85, n. 4, p. 609, doi. 10.1111/cen.13094
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- Publication type:
- Article
Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 1, p. 39, doi. 10.1093/hmg/10.1.39
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- Publication type:
- Article
Scalability of genetic biocontrols for eradicating invasive alien mammals.
- Published in:
- NeoBiota, 2022, n. 74, p. 93, doi. 10.3897/neobiota.74.82394
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- Publication type:
- Article