Konopka et al., 2009 - Google Patents
Human-specific transcriptional regulation of CNS development genes by FOXP2Konopka et al., 2009
View HTML- Document ID
- 18079723528076477445
- Author
- Konopka G
- Bomar J
- Winden K
- Coppola G
- Jonsson Z
- Gao F
- Peng S
- Preuss T
- Wohlschlegel J
- Geschwind D
- Publication year
- Publication venue
- Nature
External Links
Snippet
The signalling pathways controlling both the evolution and development of language in the human brain remain unknown. So far, the transcription factor FOXP2 (forkhead box P2) is the only gene implicated in Mendelian forms of human speech and language dysfunction,,. It …
- 101700039417 FOXP2 0 title abstract description 147
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/502—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Hybridisation probes
- C12Q1/6883—Hybridisation probes for diseases caused by alterations of genetic material
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/158—Expression markers
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Konopka et al. | Human-specific transcriptional regulation of CNS development genes by FOXP2 | |
Kim et al. | Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells | |
Jacko et al. | Rbfox splicing factors promote neuronal maturation and axon initial segment assembly | |
Braun et al. | Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome | |
Doorenweerd et al. | Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy | |
Liu et al. | Progressive degeneration of human neural stem cells caused by pathogenic LRRK2 | |
Nakaya et al. | Amyotrophic Lateral Sclerosis associated FUS mutation shortens mitochondria and induces neurotoxicity | |
Deriziotis et al. | De novo TBR1 mutations in sporadic autism disrupt protein functions | |
Sowers et al. | Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction | |
Boulting et al. | Activity-dependent regulome of human GABAergic neurons reveals new patterns of gene regulation and neurological disease heritability | |
Barnard et al. | Mutations and modeling of the chromatin remodeler CHD8 define an emerging autism etiology | |
Gauthier et al. | De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia | |
Couthouis et al. | A yeast functional screen predicts new candidate ALS disease genes | |
Liao et al. | Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy | |
Zhang et al. | Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy | |
Arboleda et al. | Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome | |
Wen et al. | Synaptic dysregulation in a human iPS cell model of mental disorders | |
Chang et al. | The schizophrenia risk gene ZNF804A: clinical associations, biological mechanisms and neuronal functions | |
Yu et al. | Systems-level analysis of cell-specific AQP2 gene expression in renal collecting duct | |
Verma et al. | Rbfox2 function in RNA metabolism is impaired in hypoplastic left heart syndrome patient hearts | |
Katsel et al. | The expression of long noncoding RNA NEAT1 is reduced in schizophrenia and modulates oligodendrocytes transcription | |
Zhao et al. | Quaking I controls a unique cytoplasmic pathway that regulates alternative splicing of myelin-associated glycoprotein | |
Cuttler et al. | Emerging evidence implicating a role for neurexins in neurodegenerative and neuropsychiatric disorders | |
Goold et al. | Down-regulation of the dopamine receptor D2 in mice lacking ataxin 1 | |
Gray et al. | Translational profiling of stress-induced neuroplasticity in the CA3 pyramidal neurons of BDNF Val66Met mice |