Pages that link to "Q28261261"
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The following pages link to Human lineage-specific amplification, selection, and neuronal expression of DUF1220 domains (Q28261261):
Displaying 50 items.
- DUF1220 dosage is linearly associated with increasing severity of the three primary symptoms of autism (Q21563351) (← links)
- DUF1220 domains, cognitive disease, and human brain evolution (Q22337096) (← links)
- Evolutionary history and genome organization of DUF1220 protein domains (Q24610261) (← links)
- Copy number variation at 1q21.1 associated with neuroblastoma (Q24642330) (← links)
- Reconstructing phylogenies and phenotypes: a molecular view of human evolution (Q24646554) (← links)
- Gene copy number variation spanning 60 million years of human and primate evolution (Q24676993) (← links)
- Comparative primate genomics: emerging patterns of genome content and dynamics (Q27006713) (← links)
- New genes contribute to genetic and phenotypic novelties in human evolution (Q27026809) (← links)
- DUF1220 copy number is linearly associated with increased cognitive function as measured by total IQ and mathematical aptitude scores (Q28249286) (← links)
- Replicated linear association between DUF1220 copy number and severity of social impairment in autism (Q28258666) (← links)
- Exploring the role of copy number variants in human adaptation (Q28263929) (← links)
- DUF1220 copy number is associated with schizophrenia risk and severity: implications for understanding autism and schizophrenia as related diseases (Q28271073) (← links)
- DUF1220-domain copy number implicated in human brain-size pathology and evolution (Q28273301) (← links)
- Evolutionary conservation in genes underlying human psychiatric disorders (Q28657468) (← links)
- The case for DUF1220 domain dosage as a primary contributor to anthropoid brain expansion (Q28657770) (← links)
- Explaining human uniqueness: genome interactions with environment, behaviour and culture (Q28750822) (← links)
- The population genetics of structural variation (Q28752151) (← links)
- A natural history of the human mind: tracing evolutionary changes in brain and cognition (Q28754363) (← links)
- Karl Pribram, The James Arthur lectures, and what makes us human (Q28764730) (← links)
- Generation of mice lacking DUF1220 protein domains: effects on fecundity and hyperactivity (Q30392455) (← links)
- NBPF1, a tumor suppressor candidate in neuroblastoma, exerts growth inhibitory effects by inducing a G1 cell cycle arrest. (Q30651336) (← links)
- Analysis of the largest tandemly repeated DNA families in the human genome (Q30851540) (← links)
- Integrating Diverse Types of Genomic Data to Identify Genes that Underlie Adverse Pregnancy Phenotypes (Q31030572) (← links)
- A constitutional translocation t(1;17)(p36.2;q11.2) in a neuroblastoma patient disrupts the human NBPF1 and ACCN1 genes (Q33336547) (← links)
- High divergence in primate-specific duplicated regions: human and chimpanzee chorionic gonadotropin beta genes (Q33349625) (← links)
- The origins and impact of primate segmental duplications (Q33760962) (← links)
- Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeats (Q33778575) (← links)
- Rare copy number deletions predict individual variation in intelligence (Q33813542) (← links)
- Evolution in health and medicine Sackler colloquium: Genomic disorders: a window into human gene and genome evolution (Q33844453) (← links)
- Evolution of genetic and genomic features unique to the human lineage (Q33900428) (← links)
- The evolution of human segmental duplications and the core duplicon hypothesis (Q33965283) (← links)
- Takusan: a large gene family that regulates synaptic activity (Q33986620) (← links)
- Copy number variation in human health, disease, and evolution (Q34019142) (← links)
- The human brain: rewired and running hot (Q34026994) (← links)
- Accelerated recruitment of new brain development genes into the human genome (Q34058009) (← links)
- Rapid sequence and expression divergence suggest selection for novel function in primate-specific KRAB-ZNF genes (Q34310586) (← links)
- Primate genome architecture influences structural variation mechanisms and functional consequences (Q34369514) (← links)
- The ethics of using transgenic non-human primates to study what makes us human (Q34369649) (← links)
- Cortical evolution: judge the brain by its cover (Q34381990) (← links)
- DUF1220 protein domains drive proliferation in human neural stem cells and are associated with increased cortical volume in anthropoid primates (Q34426197) (← links)
- No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort. (Q34576211) (← links)
- Structural divergence between the human and chimpanzee genomes (Q34576851) (← links)
- Cell-cycle control and cortical development (Q34630030) (← links)
- The current excitement about copy-number variation: how it relates to gene duplications and protein families (Q34782604) (← links)
- Mode of genetic inheritance modifies the association of head circumference and autism-related symptoms: a cross-sectional study (Q34994932) (← links)
- Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome (Q35178106) (← links)
- Frequent recent origination of brain genes shaped the evolution of foraging behavior in Drosophila (Q35244063) (← links)
- A nucleolar protein, H19 opposite tumor suppressor (HOTS), is a tumor growth inhibitor encoded by a human imprinted H19 antisense transcript. (Q35288950) (← links)
- Copy number variation in the speciation of pigs: a possible prominent role for olfactory receptors (Q35551381) (← links)
- Haplotype phasing and inheritance of copy number variants in nuclear families (Q35597451) (← links)