Found: 18
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In vivo evaluation of PhiC31 recombinase activity using a self-excision cassette.
- Published in:
- Nucleic Acids Research, 2008, v. 36, n. 20, p. e134, doi. 10.1093/nar/gkn627
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- Article
Sustained in vitro intestinal epithelial culture within a Wnt-dependent stem cell niche.
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- Nature Medicine, 2009, v. 15, n. 6, p. 701, doi. 10.1038/nm.1951
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- Publication type:
- Article
Bmi1 is expressed in vivo in intestinal stem cells.
- Published in:
- Nature Genetics, 2008, v. 40, n. 7, p. 915, doi. 10.1038/ng.165
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- Article
Identification of new candidate genes for spina bifida through exome sequencing.
- Published in:
- Child's Nervous System, 2021, v. 37, n. 8, p. 2589, doi. 10.1007/s00381-021-05153-4
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- Article
Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects.
- Published in:
- 2016
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- Publication type:
- Erratum
Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects.
- Published in:
- Child's Nervous System, 2016, v. 32, n. 6, p. 1061, doi. 10.1007/s00381-016-3087-1
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- Publication type:
- Article
Phenotypic effects of chronic and acute use of methiopropamine in a mouse model.
- Published in:
- International Journal of Legal Medicine, 2019, v. 133, n. 3, p. 811, doi. 10.1007/s00414-018-1891-8
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- Publication type:
- Article
A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy.
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- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1673, doi. 10.1038/ejhg.2015.52
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- Article
BMI1 represses Ink4a/Arf and Hox genes to regulate stem cells in the rodent incisor.
- Published in:
- Nature Cell Biology, 2013, v. 15, n. 7, p. 846, doi. 10.1038/ncb2766
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- Publication type:
- Article
Results of a Gene Panel Approach in a Cohort of Patients with Incomplete Distal Renal Tubular Acidosis and Nephrolithiasis.
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- Kidney & Blood Pressure Research, 2021, v. 46, n. 4, p. 469, doi. 10.1159/000516389
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- Article
The Clinical Chameleon of Autoinflammatory Diseases in Children.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 14, p. N.PAG, doi. 10.3390/cells11142231
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- Article
A genomic rearrangement resulting in a tandem duplication is associated with split hand–split foot malformation 3 (SHFM3) at 10q24.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 16, p. 1959, doi. 10.1093/hmg/ddg212
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- Article
From Churchill to Elephants: The Role of Protective Genes against Cancer.
- Published in:
- Genes, 2024, v. 15, n. 1, p. 118, doi. 10.3390/genes15010118
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- Article
Base-Excision Repair Mutational Signature in Two Sebaceous Carcinomas of the Eyelid.
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- Genes, 2023, v. 14, n. 11, p. 2055, doi. 10.3390/genes14112055
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- Article
Identification by Exome Sequencing of Predisposing Variants in Familial Cases of Autoinflammatory Recurrent Fevers.
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- Genes, 2023, v. 14, n. 7, p. 1310, doi. 10.3390/genes14071310
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- Publication type:
- Article
RADX Gene Variant May Predispose to Familial Asperger Syndrome.
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- Genes, 2023, v. 14, n. 2, p. 301, doi. 10.3390/genes14020301
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- Publication type:
- Article
DNA Methylation in the Diagnosis of Monogenic Diseases.
- Published in:
- Genes, 2020, v. 11, n. 4, p. 355, doi. 10.3390/genes11040355
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- Publication type:
- Article
Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura.
- Published in:
- Journal of Nephrology (JNonline), 2018, v. 31, n. 5, p. 731, doi. 10.1007/s40620-018-0482-6
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- Publication type:
- Article