Pages that link to "Q42738063"
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The following pages link to Nuclear factor I X deficiency causes brain malformation and severe skeletal defects (Q42738063):
Displaying 50 items.
- MicroRNA and gene expression patterns in the differentiation of human embryonic stem cells (Q21245471) (← links)
- Nuclear factor I regulates brain fatty acid-binding protein and glial fibrillary acidic protein gene expression in malignant glioma cell lines (Q24338788) (← links)
- Heterozygosity for nuclear factor one x affects hippocampal-dependent behaviour in mice (Q27316759) (← links)
- Absence of the transcription factor Nfib delays the formation of the basilar pontine and other mossy fiber nuclei (Q28507481) (← links)
- Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletions. (Q30472505) (← links)
- The transcription factor Nfix is essential for normal brain development (Q33334247) (← links)
- A novel diffuse gastric cancer susceptibility variant in E-cadherin (CDH1) intron 2: a case control study in an Italian population (Q33334990) (← links)
- NFIX--one gene, two knockouts, multiple effects (Q33382551) (← links)
- A DNA sequence directed mutual transcription regulation of HSF1 and NFIX involves novel heat sensitive protein interactions (Q33425228) (← links)
- The role of nuclear factor I-C in tooth and bone development. (Q33619118) (← links)
- NFI transcription factors interact with FOXA1 to regulate prostate-specific gene expression. (Q33701352) (← links)
- A novel mutation of NFIX causes Sotos-like syndrome (Malan syndrome) complicated with thoracic aortic aneurysm and dissection (Q33747299) (← links)
- A new case of de novo 19p13.2p13.12 deletion in a girl with overgrowth and severe developmental delay (Q33799838) (← links)
- Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome (Q34050951) (← links)
- Global mapping of cell type-specific open chromatin by FAIRE-seq reveals the regulatory role of the NFI family in adipocyte differentiation (Q34058172) (← links)
- Crosstalk between nuclear factor I-C and transforming growth factor-β1 signaling regulates odontoblast differentiation and homeostasis (Q34110780) (← links)
- Nuclear factor I and cerebellar granule neuron development: an intrinsic-extrinsic interplay (Q34252668) (← links)
- DNA methylation shows genome-wide association of NFIX, RAPGEF2 and MSRB3 with gestational age at birth (Q34261777) (← links)
- A promoter-level mammalian expression atlas (Q34412203) (← links)
- The unique transcriptional activation domain of nuclear factor-I-X3 is critical to specifically induce marker gene expression in astrocytes. (Q34606277) (← links)
- Temporal control of a dendritogenesis-linked gene via REST-dependent regulation of nuclear factor I occupancy (Q34675276) (← links)
- The stimulation of HSD17B7 expression by estradiol provides a powerful feed-forward mechanism for estradiol biosynthesis in breast cancer cells (Q34856382) (← links)
- Deletion of Mecom in mouse results in early-onset spinal deformity and osteopenia. (Q35062274) (← links)
- Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature (Q35477955) (← links)
- Nfix expression critically modulates early B lymphopoiesis and myelopoiesis (Q35579282) (← links)
- Nuclear factor one transcription factors: Divergent functions in developmental versus adult stem cell populations (Q36040938) (← links)
- Nuclear factor I isoforms regulate gene expression during the differentiation of human neural progenitors to astrocytes (Q36158401) (← links)
- NFI-C2 temporal-spatial expression and cellular localization pattern during tooth formation (Q36469880) (← links)
- Polycystin-1 regulates skeletogenesis through stimulation of the osteoblast-specific transcription factor RUNX2-II. (Q36585580) (← links)
- Nfib Regulates Transcriptional Networks That Control the Development of Prostatic Hyperplasia (Q36625094) (← links)
- Polycomb repressive complex 2 regulates skeletal growth by suppressing Wnt and TGF-β signalling (Q37031055) (← links)
- Epigenomic enhancer annotation reveals a key role for NFIX in neural stem cell quiescence (Q37138577) (← links)
- Disruption of Nfic causes dissociation of odontoblasts by interfering with the formation of intercellular junctions and aberrant odontoblast differentiation (Q37174040) (← links)
- Nuclear factor I transcription factors regulate IGF binding protein 5 gene transcription in human osteoblasts (Q37254131) (← links)
- 19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome (Q37278734) (← links)
- Nuclear factor I-C is essential for odontogenic cell proliferation and odontoblast differentiation during tooth root development (Q37285177) (← links)
- NFIX regulates neural progenitor cell differentiation during hippocampal morphogenesis (Q37390226) (← links)
- Nuclear factor I-C links platelet-derived growth factor and transforming growth factor beta1 signaling to skin wound healing progression (Q37410414) (← links)
- The gene or not the gene--that is the question: understanding the genetically engineered mouse phenotype (Q37942500) (← links)
- Distinct Molecular Signature of Murine Fetal Liver and Adult Hematopoietic Stem Cells Identify Novel Regulators of Hematopoietic Stem Cell Function (Q38439209) (← links)
- Nfix Regulates Temporal Progression of Muscle Regeneration through Modulation of Myostatin Expression (Q38790394) (← links)
- Transcriptional control of chondrocyte specification and differentiation (Q38803469) (← links)
- Calcineurin regulates nuclear factor I dephosphorylation and activity in malignant glioma cell lines (Q39128188) (← links)
- Cell-type-specific expression of NFIX in the developing and adult cerebellum (Q39160371) (← links)
- A novel microdeletion/microduplication syndrome of 19p13.13. (Q41936568) (← links)
- Nfix is a novel regulator of murine hematopoietic stem and progenitor cell survival (Q42044050) (← links)
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling* (Q42114886) (← links)
- Parkinson-like phenotype in insulin-resistant PED/PEA-15 transgenic mice (Q42416060) (← links)
- Efficient generation of astrocytes from human pluripotent stem cells in defined conditions (Q43637863) (← links)
- Novel isoforms of the bovine Nuclear factor I/X (CCAAT-binding transcription factor) transcript products and their diverse expression profiles (Q44300810) (← links)