FOXP2
FoxP2 integrates strategy, design, digital and creative advertising into innovative results for its clients. The company is one of the creative agencies in South Africa and boast numerous industry awards, both locally and internationally.
FOXP2
Industry:
Advertising Creative Agency
Founded:
2005-01-01
Address:
Cape Town, NA - South Africa, South Africa
Country:
South Africa
Status:
Active
Contact:
+27 (0)21 424 4802
Email Addresses:
[email protected]
More informations about "FoxP2"
The FOXP2-Driven Network in Developmental Disorders and
Jul 26, 2017 Besides, our FOXP2-driven network contributes to the organization of the microtubule scaffold. In particular, the new FOXP2 target DCDC2 codes for a protein (Figure 5 and Table 2) … See details»
FOXP2 - Wikipedia
The FOXP2 gene has been implicated in several cognitive functions including; general brain development, language, and synaptic plasticity. The FOXP2 gene region acts as a transcription factor for the forkhead box P2 protein. Transcription factors affect other regions, and the forkhead box P2 protein has been suggested to also act as a transcription factor for hundreds of genes. This prolific involvement opens the possibility that the FOXP2 gene is much more extensive tha…See details»
Chromatin decondensation by FOXP2 promotes human …
Forkhead box P2 (FOXP2) is a transcription factor expressed in the human brain that peaks during fetal development, and disruption in its ability to regulate downstream target genes leads to vulnerability to neurodevelopmental disorders. However, ... See details»
Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in …
Jul 7, 2011 Author Summary Foxp2 codes for an intriguing regulatory protein that provides a window into unusual aspects of brain function in multiple species. For example, the gene is … See details»
The FOXP2-Driven Network in Developmental Disorders and ...
Jul 26, 2017 The transcription repressor FOXP2 is a crucial player in nervous system evolution and development of humans and songbirds. In order to provide an additional insight into its functional … See details»
Molecular networks of the FOXP2 transcription factor in …
Jul 14, 2021 The discovery of the FOXP2 transcription factor, and its implication in a rare severe human speech and language disorder, has led to two decades of empirical studies focused on uncovering its roles in the brain using a range of in … See details»
Human Genetics: The Evolving Story of FOXP2 - ScienceDirect
Jan 21, 2019 FOXP2 mutations cause a speech and language disorder, raising interest in potential roles of this gene in human evolution. A new study re-evaluates ge… See details»
What Is the FOXP2 Protein and What Does It Do?
Jun 18, 2025 Learn how the FOXP2 protein acts as a gene regulator, influencing the neural development and fine motor control required for human speech and other functions. See details»
FOXP2 and the neuroanatomy of speech and language - Nature
Feb 1, 2005 The discovery of a mutation in FOXP2 in a family with a speech and language disorder has enabled neuroscientists to trace the neural expression of this gene during embryological … See details»
FOXP2 exhibits projection neuron class specific …
The results demonstrate that Foxp2 is not required for establishing basic developmental organization, molecular phenotypes or efferent connectivity of Foxp2 -expressing neurons in SSC of mice. See details»
FOXP2 - an overview | ScienceDirect Topics
Far from being unique to humans, FOXP2 is one of the most highly conserved of vertebrate genes [10–17]. Nonetheless, against this background, there are indications of accelerated change in … See details»
Foxp-Mediated Suppression of N-Cadherin Regulates …
Apr 26, 2012 Neural stem and progenitor cells are held in a proliferative, neuroepithelial state by cadherin-based adhesions. Rousso et al. identify a crucial role for the Forkhead transcription … See details»
What is FOXP2 related speech & language disorder?
FOXP2 is a gene which has important functions for the development of the brain. A disruption or absence of one gene copy results in difficulties in the acquisition of speech and language. See details»
Mapping of Human FOXP2 Enhancers Reveals Complex Regulation
Mutations of the FOXP2 gene cause a severe speech and language disorder, providing a molecular window into the neurobiology of language. Individuals with FOXP2 mutations have structural and … See details»
The functions of FOXP transcription factors and their regulation by ...
Dec 1, 2023 The forkhead box subfamily P (FOXP) of transcription factors, consisting of FOXP1, FOXP2, FOXP3, and FOXP4, is involved in the regulation of multisystemic functioning. Disruption … See details»
Molecular networks of the FOXP2 transcription factor in the brain
Jul 14, 2021 The discovery of the FOXP2 transcription factor, and its implication in a rare severe human speech and language disorder, has led to two decades of empirical studies focused on … See details»
FOXP2 as a molecular window into speech and language
Mar 23, 2009 Rare mutations of the FOXP2 transcription factor gene cause a monogenic syndrome characterized by impaired speech development and linguistic deficits. Recent genomic … See details»
FOXP2 protein expression summary - The Human Protein Atlas
54:Lymphatic endothelial cells - Lymph vessel development 78:NK-cells & T-cells - Immune system & Transcription 38:Proximal tubular cells - Transmembrane transport 70:Spermatocytes & … See details»
FOXP2 - PMC
The forkhead box P2 gene, designated FOXP2, is the first gene implicated in a speech and language disorder. Since its discovery, many studies have been carried out in an attempt to explain the … See details»
From songbird to humans: The multifaceted roles of FOXP2 in …
Dec 1, 2024 The growing recognition of the critical role of genetic factors, particularly the FOXP2 gene, in speech and language development has spurred significant interest in understanding the … See details»