Pages that link to "Q34521369"

The following pages link to Genome-wide identification of pseudogenes capable of disease-causing gene conversion. (Q34521369):

Displaying 37 items.

• N-acetyltransferase 8, a positional candidate for blood pressure and renal regulation: resequencing, association and in silico study (Q21261430) (← links)
• The human ortholog of the rodent testis-specific ABC transporter Abca17 is a ubiquitously expressed pseudogene (ABCA17P) and shares a common 5' end with ABCA3 (Q21263011) (← links)
• Pseudogenes (Q21296636) (← links)
• Pseudogenes in the ENCODE regions: consensus annotation, analysis of transcription, and evolution (Q22065739) (← links)
• The AZFc region of the Y chromosome: at the crossroads between genetic diversity and male infertility (Q24634263) (← links)
• PGK deficiency (Q28283311) (← links)
• pseudoMap: an innovative and comprehensive resource for identification of siRNA-mediated mechanisms in human transcribed pseudogenes (Q28709088) (← links)
• Segmental duplications in the human genome reveal details of pseudogene formation (Q28748496) (← links)
• Comprehensive analysis of the pseudogenes of glycolytic enzymes in vertebrates: the anomalously high number of GAPDH pseudogenes highlights a recent burst of retrotrans-positional activity (Q28750314) (← links)
• A computational approach for identifying pseudogenes in the ENCODE regions (Q28763301) (← links)
• The evolution of gene duplications: classifying and distinguishing between models (Q29619358) (← links)
• Integrating multiple immunogenetic data sources for feature extraction and mining somatic hypermutation patterns: the case of "towards analysis" in chronic lymphocytic leukaemia (Q31107783) (← links)
• The human ABC transporter pseudogene family: Evidence for transcription and gene-pseudogene interference (Q33327749) (← links)
• A pattern analysis of gene conversion literature (Q33633991) (← links)
• Mutations in spliceosomal proteins and retina degeneration (Q33739682) (← links)
• Identification of gene mutations in autosomal dominant polycystic kidney disease through targeted resequencing (Q34181261) (← links)
• Molecular trajectories leading to the alternative fates of duplicate genes (Q34311996) (← links)
• Genetic Diversity of the Allodeterminant alr2 in Hydractinia symbiolongicarpus (Q35026057) (← links)
• Interlocus gene conversion explains at least 2.7% of single nucleotide variants in human segmental duplications. (Q35664475) (← links)
• Interlocus gene conversion events introduce deleterious mutations into at least 1% of human genes associated with inherited disease (Q35791522) (← links)
• Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state (Q35946576) (← links)
• Pseudogenes and their composers: delving in the 'debris' of human genome (Q38125345) (← links)
• A gene duplication affecting expression of the ovine ASIP gene is responsible for white and black sheep (Q41334841) (← links)
• Microdeletion/duplication at the Xq28 IP locus causes a de novo IKBKG/NEMO/IKKgamma exon4_10 deletion in families with Incontinentia Pigmenti (Q45088124) (← links)
• Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical next-generation sequencing. (Q46090356) (← links)
• Genomic disorders 20 years on-mechanisms for clinical manifestations (Q46300376) (← links)
• Three novel collagen VI chains with high homology to the alpha3 chain (Q46752689) (← links)
• Purifying selection against gene conversions between the polyamine transport (TPO) genes of Saccharomyces species (Q46850654) (← links)
• Purifying selection against gene conversions in the folate receptor genes of primates (Q46976145) (← links)
• An analysis of effects of heterozygosity in dairy cattle for bovine tuberculosis resistance (Q48169327) (← links)
• Frequent nonallelic gene conversion on the human lineage and its effect on the divergence of gene duplicates (Q50016299) (← links)
• Transcript annotation prioritization and screening system (TrAPSS) for mutation screening. (Q50138334) (← links)
• Gene conversions in the growth hormone gene family of primates: stronger homogenizing effects in the Hominidae lineage. (Q52838228) (← links)
• Long non-coding RNAs in cancer: implications for personalized therapy (Q62083228) (← links)
• Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing (Q88098249) (← links)
• Overcoming challenges and dogmas to understand the functions of pseudogenes (Q92060000) (← links)
• CRISPR-Directed Therapeutic Correction at the NCF1 Locus Is Challenged by Frequent Incidence of Chromosomal Deletions (Q95266321) (← links)