Pages that link to "Q28265563"
Jump to navigation
Jump to search
The following pages link to A novel gene family NBPF: intricate structure generated by gene duplications during primate evolution (Q28265563):
Displayed 50 items.
- The DNA sequence and biological annotation of human chromosome (Q21735919) (← 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)
- Gene copy number variation spanning 60 million years of human and primate evolution (Q24676993) (← 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)
- DUF1220 copy number is associated with schizophrenia risk and severity: implications for understanding autism and schizophrenia as related diseases (Q28271073) (← links)
- Molecular pathogenesis of peripheral neuroblastic tumors (Q28271405) (← links)
- DUF1220-domain copy number implicated in human brain-size pathology and evolution (Q28273301) (← links)
- The case for DUF1220 domain dosage as a primary contributor to anthropoid brain expansion (Q28657770) (← 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)
- ASEQ: fast allele-specific studies from next-generation sequencing data. (Q30936481) (← links)
- A constitutional translocation t(1;17)(p36.2;q11.2) in a neuroblastoma patient disrupts the human NBPF1 and ACCN1 genes (Q33336547) (← links)
- The origins and impact of primate segmental duplications (Q33760962) (← links)
- CpG island hypermethylation in human astrocytomas (Q33766932) (← links)
- Coherent somatic mutation in autoimmune disease (Q33837769) (← links)
- Evolution of genetic and genomic features unique to the human lineage (Q33900428) (← links)
- Chibby interacts with NBPF1 and clusterin, two candidate tumor suppressors linked to neuroblastoma (Q34094380) (← links)
- Array comparative genomic hybridization in male infertility (Q34246420) (← links)
- Detection of gene expression changes at chromosomal rearrangement breakpoints in evolution (Q34247897) (← links)
- DUF1220 protein domains drive proliferation in human neural stem cells and are associated with increased cortical volume in anthropoid primates (Q34426197) (← links)
- Understanding the recent evolution of the human genome: insights from human-chimpanzee genome comparisons (Q34571921) (← links)
- Structural divergence between the human and chimpanzee genomes (Q34576851) (← links)
- 1p36 deletion is a marker for tumour dissemination in microsatellite stable stage II-III colon cancer (Q34610744) (← links)
- Insertion of an HERV(K) LTR in the intron of NBPF3 is not required for its transcriptional activity. (Q34613200) (← links)
- Signals of historical interlocus gene conversion in human segmental duplications (Q35016850) (← links)
- Diminishing return for increased Mappability with longer sequencing reads: implications of the k-mer distributions in the human genome (Q35081386) (← links)
- Recurrent duplication-driven transposition of DNA during hominoid evolution (Q35214947) (← links)
- Evolutionary dynamism of the primate LRRC37 gene family (Q36490025) (← links)
- Potential role of human-specific genes, human-specific microRNAs and human-specific non-coding regulatory RNAs in the pathogenesis of systemic sclerosis and Sjögren's syndrome (Q37165647) (← links)
- Adaptive evolution of young gene duplicates in mammals. (Q37176321) (← links)
- Presence of 1q gain and absence of 7p gain are new predictors of local or metastatic relapse in localized resectable neuroblastoma (Q37284320) (← links)
- Characterizing polymorphic inversions in human genomes by single-cell sequencing. (Q37383344) (← links)
- An exon-based comparative variant analysis pipeline to study the scale and role of frameshift and nonsense mutation in the human-chimpanzee divergence (Q37396179) (← links)
- Using Genome Query Language to uncover genetic variation (Q37400072) (← links)
- Evolutionary and Functional Features of Copy Number Variation in the Cattle Genome (Q37427516) (← links)
- Sequencing primate genomes: what have we learned? (Q37561100) (← links)
- A replication study of schizophrenia-related rare copy number variations in a Han Southern Chinese population. (Q37587151) (← links)
- Human-specific genes may offer a unique window into human cell signaling (Q37606885) (← links)
- Copy number variations and cancer susceptibility (Q37642520) (← links)
- The birth of a human-specific neural gene by incomplete duplication and gene fusion (Q37692482) (← links)
- High resolution measurement of DUF1220 domain copy number from whole genome sequence data (Q38625498) (← links)
- Genomewide Association Scan of a Mortality Associated Endophenotype for a Long and Healthy Life in the Long Life Family Study (Q38886426) (← links)
- Human adaptation and evolution by segmental duplication (Q38943761) (← links)
- Characterization of potential driver mutations involved in human breast cancer by computational approaches (Q39286993) (← links)
- Different transcription activity of HERV-K LTR-containing and LTR-lacking genes of the KIAA1245/NBPF gene subfamily (Q39547767) (← links)
- Prevalence of HPV16 E1-1374^63nt variants in Greek women (Q42237614) (← links)