Pages that link to "Q35704490"
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The following pages link to The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans (Q35704490):
Displaying 50 items.
- A complex genomic rearrangement involving the endothelin 3 locus causes dermal hyperpigmentation in the chicken (Q21563372) (← links)
- Quantifying the mechanisms of domain gain in animal proteins (Q21999552) (← links)
- Mechanisms of change in gene copy number (Q22122003) (← links)
- Mechanisms underlying structural variant formation in genomic disorders (Q26765934) (← links)
- Managing Single-Stranded DNA during Replication Stress in Fission Yeast (Q26782193) (← links)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics (Q27022289) (← links)
- Structural variation mutagenesis of the human genome: Impact on disease and evolution (Q27691419) (← links)
- A mechanism of gene amplification driven by small DNA fragments (Q27930879) (← links)
- Complex chromosomal rearrangements mediated by break-induced replication involve structure-selective endonucleases (Q27932385) (← links)
- Replication stress in Mammalian cells and its consequences for mitosis (Q28087011) (← links)
- RAD51 mutants cause replication defects and chromosomal instability (Q28115721) (← links)
- Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation (Q28253227) (← links)
- GJB1/Connexin 32 whole gene deletions in patients with X-linked Charcot-Marie-Tooth disease (Q28284701) (← links)
- Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders (Q28392162) (← links)
- Somatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjects (Q28394993) (← links)
- Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans (Q28481587) (← links)
- In with the old, in with the new: the promiscuity of the duplication process engenders diverse pathways for novel gene creation (Q28727624) (← links)
- X-linked acrogigantism syndrome: clinical profile and therapeutic responses (Q30370618) (← links)
- The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy. (Q30379223) (← links)
- Polymorphism in the exon 4 of β-lactoglobulin variant B precursor gene and its association with milk traits and protein structure in Chinese Holstein (Q30404771) (← links)
- PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations (Q30415792) (← links)
- Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms (Q30416550) (← links)
- Characterizing complex structural variation in germline and somatic genomes (Q30423222) (← links)
- Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome (Q30434301) (← links)
- Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort (Q31149204) (← links)
- Short template switch events explain mutation clusters in the human genome (Q33365166) (← links)
- Structural haplotypes and recent evolution of the human 17q21.31 region (Q33608188) (← links)
- Repair of DNA double-strand breaks by templated nucleotide sequence insertions derived from distant regions of the genome (Q33694621) (← links)
- Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS (Q33708568) (← links)
- Is homologous recombination really an error-free process? (Q33736829) (← links)
- Inversion variants in the human genome: role in disease and genome architecture (Q33762256) (← links)
- Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci (Q33792938) (← links)
- Chimeric transcripts resulting from complex duplications in chromosome Xq28 (Q33837412) (← links)
- Evolution in health and medicine Sackler colloquium: Genomic disorders: a window into human gene and genome evolution (Q33844453) (← links)
- Ontogenetic de novo copy number variations (CNVs) as a source of genetic individuality: studies on two families with MZD twins for schizophrenia (Q33844724) (← links)
- What drives recombination hotspots to repeat DNA in humans? (Q33856640) (← links)
- The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance (Q33881358) (← links)
- Dynamics and processes of copy number instability in human gamma-globin genes (Q33929439) (← links)
- Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines (Q33960440) (← links)
- Copy number variation in human health, disease, and evolution (Q34019142) (← links)
- Genome-wide signatures of 'rearrangement hotspots' within segmental duplications in humans (Q34110429) (← links)
- Identification of copy number variation hotspots in human populations (Q34169422) (← links)
- Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements (Q34217081) (← links)
- Screening of Duchenne muscular dystrophy (DMD) mutations and investigating its mutational mechanism in Chinese patients (Q34227098) (← links)
- De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder. (Q34431180) (← links)
- Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D (Q34471005) (← links)
- Controlled somatic and germline copy number variation in the mouse model (Q34479642) (← links)
- SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints. (Q34501235) (← links)
- Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability (Q34544478) (← links)
- Genome wide analysis of chromosomal alterations in oral squamous cell carcinomas revealed over expression of MGAM and ADAM9. (Q34583947) (← links)