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Genome-wide histone methylation profile for heart failure.
- Published in:
- Genes to Cells, 2009, v. 14, n. 1, p. 69, doi. 10.1111/j.1365-2443.2008.01252.x
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- Article
Conservation and divergence of canonical and non-canonical imprinting in murids.
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- Genome Biology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s13059-023-02869-1
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- Article
Establishment and visual analysis of CBA/J-Pde6b<sup>Y347Y/Y347X</sup> and C3H/HeJ-Pde6b<sup>Y347Y/Y347X</sup> mice.
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- Experimental Animals, 2024, v. 73, n. 2, p. 203, doi. 10.1538/expanim.23-0142
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- Article
Production of Sry knockout mouse using TALEN via oocyte injection.
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- Scientific Reports, 2013, p. 1, doi. 10.1038/srep03136
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- Article
Exploring trophoblast-specific Tead4 enhancers through chromatin conformation capture assays followed by functional screening.
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- Nucleic Acids Research, 2020, v. 48, n. 1, p. 278, doi. 10.1093/nar/gkz1034
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- Article
Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR.
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- Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0640-2
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- Article
POU1F1/Pou1f1 c.143-83A > G Variant Disrupts the Branch Site in Pre-mRNA and Leads to Dwarfism.
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- Endocrinology, 2023, v. 164, n. 2, p. 1, doi. 10.1210/endocr/bqac198
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- Article
Human SRY Expression at the Sex-determining Period is Insufficient to Drive Testis Development in Mice.
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- Endocrinology, 2022, v. 163, n. 1, p. 1, doi. 10.1210/endocr/bqab217
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- Article
Publisher Correction: Calaxin is required for cilia-driven determination of vertebrate laterality.
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- 2019
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- Correction Notice
Calaxin is required for cilia-driven determination of vertebrate laterality.
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- Communications Biology, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42003-019-0462-y
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- Article
Mapping of a responsible region for sex reversal upstream of Sox9 by production of mice with serial deletion in a genomic locus.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35746-0
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- Article
Peptidyl arginine deiminase 2 (Padi2) is expressed in Sertoli cells in a specific manner and regulated by SOX9 during testicular development.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-31376-8
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- Publication type:
- Article
Modeling of Retina and Optic Nerve Ischemia–Reperfusion Injury through Hypoxia–Reoxygenation in Human Induced Pluripotent Stem Cell-Derived Retinal Ganglion Cells.
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- Cells (2073-4409), 2024, v. 13, n. 2, p. 130, doi. 10.3390/cells13020130
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- Article
The p.R92W variant of NR5A1/Nr5a1 induces testicular development of 46,XX gonads in humans, but not in mice: phenotypic comparison of human patients and mutation-induced mice.
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- Biology of Sex Differences, 2016, v. 7, p. 1, doi. 10.1186/s13293-016-0114-6
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- Article
LZTR1 deficiency exerts high metastatic potential by enhancing sensitivity to EMT induction and controlling KLHL12-mediated collagen secretion.
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- Cell Death & Disease, 2023, v. 14, n. 8, p. 1, doi. 10.1038/s41419-023-06072-9
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- Article
Phenotypic Variation in 46,XX Disorders of Sex Development due to the <bold><italic>NR5A1 </italic></bold>p.R92W Variant: A Sibling Case Report and Literature Review.
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- Sexual Development, 2017, v. 11, n. 5/6, p. 284, doi. 10.1159/000485868
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- Article
The Mohawk homeobox transcription factor regulates the differentiation of tendons and volar plates.
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- Journal of Orthopaedic Science, 2014, v. 19, n. 1, p. 172, doi. 10.1007/s00776-013-0485-z
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- Article
Testicular dysgenesis/regression without campomelic dysplasia in patients carrying missense mutations and upstream deletion of SOX9.
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- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 6, p. 550, doi. 10.1002/mgg3.165
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- Article
Efficient production and transmission of CRISPR/Cas9-mediated mutant alleles at the IG-DMR via generation of mosaic mice using a modified 2CC method.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-56676-5
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- Article
Usp26 mutation in mice leads to defective spermatogenesis depending on genetic background.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50318-6
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- Article
Comparative analysis demonstrates cell type-specific conservation of SOX9 targets between mouse and chicken.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-48979-4
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- Article
A Testis-Specific Long Noncoding RNA, Start , Is a Regulator of Steroidogenesis in Mouse Leydig Cells.
- Published in:
- Frontiers in Endocrinology, 2021, v. 11, p. N.PAG, doi. 10.3389/fendo.2021.665874
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- Article
Current strategies for microRNA research.
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- Modern Rheumatology, 2012, v. 22, n. 5, p. 645, doi. 10.3109/s10165-011-0583-8
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- Article
A novel mucopolysaccharidosis type II mouse model with an iduronate-2-sulfatase-P88L mutation.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-34541-w
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- Publication type:
- Article
DNA methylation analysis of human myoblasts during in vitro myogenic differentiation: de novo methylation of promoters of muscle-related genes and its involvement in transcriptional down-regulation.
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- Human Molecular Genetics, 2015, v. 24, n. 2, p. 410, doi. 10.1093/hmg/ddu457
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- Article
Targeted Gene Deletion of miRNAs in Mice by TALEN System.
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- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0076004
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- Article
The AERO System: A 3D-Like Approach for Recording Gene Expression Patterns in the Whole Mouse Embryo.
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- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0075754
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- Article
Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12.
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- Nature Genetics, 2003, v. 35, n. 1, p. 97, doi. 10.1038/ng1233
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- Article
SOX9 is colocalized with paraspeckle protein NONO in cultured murine sertoli cells and features structural characteristics of intrinsically disordered proteins.
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- Molecular Reproduction & Development, 2020, v. 87, n. 11, p. 1124, doi. 10.1002/mrd.23425
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- Article
Epigenetic analysis of the Dlk1–Gtl2 imprinteddomain on mouse chromosome 12: implications for imprinting controlfrom comparison with Igf2–H19.
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- Human Molecular Genetics, 2002, v. 11, n. 1, p. 77, doi. 10.1093/hmg/11.1.77
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- Article
The cell cycle control gene ZAC /PLAGL1 is imprinted--a strong candidate gene for transient neonatal diabetes.
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- Human Molecular Genetics, 2000, v. 9, n. 3, p. 453, doi. 10.1093/hmg/9.3.453
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- Article
Transcription factor Mohawk controls tenogenic differentiation of bone marrow mesenchymal stem cells in vitro and in vivo.
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- Journal of Orthopaedic Research, 2015, v. 33, n. 1, p. 1, doi. 10.1002/jor.22750
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- Article
Identification of transforming activity of free fatty acid receptor 2 by retroviral expression screening.
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- Cancer Science, 2010, v. 101, n. 1, p. 54, doi. 10.1111/j.1349-7006.2009.01348.x
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- Article
Identification of the transforming activity of Indian hedgehog by retroviral expression screening.
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- Cancer Science, 2010, v. 101, n. 1, p. 60, doi. 10.1111/j.1349-7006.2009.01355.x
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- Article
Chromosome copy number analysis in screening for prognosis-related genomic regions in colorectal carcinoma.
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- Cancer Science, 2008, v. 99, n. 9, p. 1835, doi. 10.1111/j.1349-7006.2008.00881.x
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- Article
Experimental trial for diagnosis of pancreatic ductal carcinoma based on gene expression profiles of pancreatic ductal cells.
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- Cancer Science, 2005, v. 96, n. 7, p. 387, doi. 10.1111/j.1349-7006.2005.00064.x
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- Article
Sox8 is expressed at similar levels in gonads of both sexes during the sex determining period in turtles.
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- Developmental Dynamics, 2004, v. 231, n. 2, p. 387
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- Article
Identical NR5A1 Missense Mutations in Two Unrelated 46,XX Individuals with Testicular Tissues.
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- Human Mutation, 2017, v. 38, n. 1, p. 39, doi. 10.1002/humu.23116
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- Article
Cover Image, Volume 38, Issue 1.
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- Human Mutation, 2017, v. 38, n. 1, p. i, doi. 10.1002/humu.23151
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- Article
Identification of the transforming EML4–ALK fusion gene in non-small-cell lung cancer.
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- Nature, 2007, v. 448, n. 7153, p. 561, doi. 10.1038/nature05945
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- Article
Contribution of transcription factor, SP1, to the promotion of HB- EGF expression in defense mechanism against the treatment of irinotecan in ovarian clear cell carcinoma.
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- Cancer Medicine, 2014, v. 3, n. 5, p. 1159, doi. 10.1002/cam4.301
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- Article
Loss of NSD2 causes dysregulation of synaptic genes and altered H3K36 dimethylation in mice.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1308234
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- Article
Mouse microRNA profiles determined with a new and sensitive cloning method.
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- Nucleic Acids Research, 2006, v. 34, n. 17, p. e115, doi. 10.1093/nar/gkl653
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- Article
In vivo and in vitro disease modeling with CRISPR/Cas9.
- Published in:
- Briefings in Functional Genomics, 2017, v. 16, n. 1, p. 13, doi. 10.1093/bfgp/elw031
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- Article
Identification of the first promoter-specific gain-of-function SOX9 missense variant (p.E50K) in a patient with 46,XX ovotesticular disorder of sex development.
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 4, p. 1067, doi. 10.1002/ajmg.a.62063
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- Article
Complex genomic rearrangement in the SOX9 5′ region in a patient with Pierre Robin sequence and hypoplastic left scapula.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 7, p. 1529, doi. 10.1002/ajmg.a.35308
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- Article
Deletion of a Seminal Gene Cluster Reinforces a Crucial Role of SVS2 in Male Fertility.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 18, p. 4557, doi. 10.3390/ijms20184557
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- Article
Tmsb10 triggers fetal Leydig differentiation by suppressing the RAS/ERK pathway.
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- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03941-5
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- Article
Distinctive features of single nucleotide alterations in induced pluripotent stem cells with different types of DNA repair deficiency disorders.
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- Scientific Reports, 2016, p. 26342, doi. 10.1038/srep26342
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- Article
Generation of mutant mice via the CRISPR/Cas9 system using FokI-dCas9.
- Published in:
- Scientific Reports, 2015, p. 11221, doi. 10.1038/srep11221
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- Article