| P50 | author | Danlei Zhou | Q93078420 |
| P2093 | author name string | Chack-Yung Yu | |
| | Aiqin Luo | |
| | Michalea Lai | |
| P2860 | cites work | The G11 gene located in the major histocompatibility complex encodes a novel nuclear serine/threonine protein kinase | Q22007987 |
| | Human transcription elongation factor NELF: identification of novel subunits and reconstitution of the functionally active complex | Q24296462 |
| | Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region | Q24301622 |
| | Human helicase gene SKI2W in the HLA class III region exhibits striking structural similarities to the yeast antiviral gene SKI2 and to the human gene KIAA0052: emergence of a new gene family | Q24318692 |
| | The human RD protein is closely related to nuclear RNA-binding proteins and has been highly conserved | Q24321954 |
| | cDNA cloning and characterization of the protein encoded by RD, a gene located in the class III region of the human major histocompatibility complex | Q24528145 |
| | Evidence that negative elongation factor represses transcription elongation through binding to a DRB sensitivity-inducing factor/RNA polymerase II complex and RNA. | Q24537283 |
| | The human DEVH-box protein Ski2w from the HLA is localized in nucleoli and ribosomes | Q24548228 |
| | A landscape of driver mutations in melanoma | Q24603357 |
| | Tricho-Hepato-Enteric Syndrome mutation update: Mutations spectrum of TTC37 and SKIV2L, clinical analysis and future prospects. | Q52661406 |
| | Novel mutations in SKIV2L and TTC37 genes in Malaysian children with trichohepatoenteric syndrome. | Q53128682 |
| | Combined Immunodeficiency in Patients With Trichohepatoenteric Syndrome. | Q54957612 |
| | miR-1236-3p inhibits invasion and metastasis in gastric cancer by targeting MTA2. | Q55293830 |
| | Expanding phenotypic and allelic heterogeneity of tricho-hepato-enteric syndrome | Q57754836 |
| | Genetic variants in the SKIV2L gene in exudative age-related macular degeneration in the Japanese population | Q57755447 |
| | Helicase-Dependent RNA Decay Illuminated by a Cryo-EM Structure of a Human Nuclear RNA Exosome-MTR4 Complex | Q58050020 |
| | Trichohepatoenteric syndrome: A rare mutation in SKIV2L gene in the first Balkan reported case | Q58594827 |
| | Correction: 2'-O-methylation of the mRNA cap protects RNAs from decapping and degradation by DXO | Q58794056 |
| | Structure of activated transcription complex Pol II–DSIF–PAF–SPT6 | Q59070952 |
| | Structure of paused transcription complex Pol II-DSIF-NELF | Q59087446 |
| | Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression | Q60643583 |
| | Opposite Profiles of Complement in Antiphospholipid Syndrome (APS) and Systemic Lupus Erythematosus (SLE) Among Patients With Antiphospholipid Antibodies (aPL) | Q64248332 |
| | Tricho-hepatic-enteric syndrome (THES) without intractable diarrhoea. | Q65950468 |
| | Comparative Structure and Function Analysis of the RIG-I-Like Receptors: RIG-I and MDA5 | Q66679118 |
| | Intractable diarrhea in early infancy | Q72033558 |
| | RNA helicases: modulators of RNA structure | Q75292926 |
| | Tricho-hepato-enteric syndrome: a case of hemochromatosis with intractable diarrhea, dysmorphic features, and hair abnormality | Q79605148 |
| | Role of RDBP and SKIV2L variants in the major histocompatibility complex class III region in polypoidal choroidal vasculopathy etiology | Q84127916 |
| | Associations of the C2-CFB-RDBP-SKIV2L locus with age-related macular degeneration and polypoidal choroidal vasculopathy | Q85763850 |
| | miR-1236-3p represses the cell migration and invasion abilities by targeting ZEB1 in high-grade serous ovarian carcinoma | Q87365891 |
| | Pharmacological Targeting of STK19 Inhibits Oncogenic NRAS-Driven Melanomagenesis | Q91321632 |
| | Unexplained diarrhoea and failure to thrive in 2 siblings with unusual facies and abnormal scalp hair shafts: a new syndrome | Q24677050 |
| | Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune Diseases | Q26766486 |
| | Syndromic diarrhea/Tricho-hepato-enteric syndrome | Q26825160 |
| | Threading the barrel of the RNA exosome | Q26851853 |
| | Structure and function of the 5′→3′ exoribonuclease Rat1 and its activating partner Rai1 | Q27653658 |
| | Dxo1 is a new type of eukaryotic enzyme with both decapping and 5′-3′ exoribonuclease activity | Q27672794 |
| | A Mammalian Pre-mRNA 5′ End Capping Quality Control Mechanism and an Unexpected Link of Capping to Pre-mRNA Processing | Q27676995 |
| | The yeast ski complex: crystal structure and RNA channeling to the exosome complex | Q27685388 |
| | Innate immune recognition | Q27860721 |
| | Saccharomyces cerevisiae RAI1 (YGL246c) is homologous to human DOM3Z and encodes a protein that binds the nuclear exoribonuclease Rat1p | Q27930913 |
| | The yeast antiviral proteins Ski2p, Ski3p, and Ski8p exist as a complex in vivo | Q27931202 |
| | Identification of a quality-control mechanism for mRNA 5'-end capping | Q27933732 |
| | The 3' to 5' degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3' to 5' exonucleases of the exosome complex | Q27934144 |
| | Evidence that the SKI antiviral system of Saccharomyces cerevisiae acts by blocking expression of viral mRNA. | Q27936790 |
| | The yeast Ski complex is a hetero-tetramer | Q27938845 |
| | NELF, a multisubunit complex containing RD, cooperates with DSIF to repress RNA polymerase II elongation | Q28141291 |
| | Organizations and gene duplications of the human and mouse MHC complement gene clusters | Q28145348 |
| | Interferon-inducible gene expression signature in peripheral blood cells of patients with severe lupus | Q28212039 |
| | Characterisation of the novel gene G11 lying adjacent to the complement C4A gene in the human major histocompatibility complex | Q28243879 |
| | Genomic organization of the human DDX13 gene located between RD and RP1 in the class III MHC complex | Q28246627 |
| | Structure and genetics of the partially duplicated gene RP located immediately upstream of the complement C4A and the C4B genes in the HLA class III region. Molecular cloning, exon-intron structure, composite retroposon, and breakpoint of gene dupli | Q28250748 |
| | The complete exon-intron structure of a human complement component C4A gene. DNA sequences, polymorphism, and linkage to the 21-hydroxylase gene | Q28263424 |
| | Structure of the human RD gene: a highly conserved gene in the class III region of the major histocompatibility complex | Q28264256 |
| | A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B | Q28270356 |
| | Four ubiquitously expressed genes, RD (D6S45)-SKI2W (SKIV2L)-DOM3Z-RP1 (D6S60E), are present between complement component genes factor B and C4 in the class III region of the HLA | Q28287601 |
| | A Previously Undetected MHC Gene with an Unusual Periodic Structure | Q28296754 |
| | Cell-specific expression of the human complement protein factor B gene: evidence for the role of two distinct 5'-flanking elements | Q28302180 |
| | Dynamics of human immunodeficiency virus transcription: P-TEFb phosphorylates RD and dissociates negative effectors from the transactivation response element | Q28646726 |
| | Complement: a key system for immune surveillance and homeostasis | Q29615484 |
| | Innate immunity | Q29618949 |
| | Genome evolution in the allotetraploid frog Xenopus laevis | Q30275672 |
| | miR-1236 regulates hypoxia-induced epithelial-mesenchymal transition and cell migration/invasion through repressing SENP1 and HDAC3. | Q51525226 |
| | Targeted next-generation sequencing identification of a novel missense mutation of the SKIV2L gene in a patient with trichohepatoenteric syndrome. | Q51632670 |
| | p38-MK2 signaling axis regulates RNA metabolism after UV-light-induced DNA damage. | Q51764434 |
| | Eukaryotic RNA 5'-End NAD+ Capping and DeNADding. | Q52653653 |
| | 5' End Nicotinamide Adenine Dinucleotide Cap in Human Cells Promotes RNA Decay through DXO-Mediated deNADding. | Q38914420 |
| | Overexpression of the RD RNA binding protein in hepatitis C virus-related hepatocellular carcinoma | Q39344738 |
| | Identification of Variants in Genes Associated with Single-gene Inflammatory Bowel Disease by Whole-exome Sequencing. | Q39478165 |
| | Multiomic Analysis of the UV-Induced DNA Damage Response | Q39762223 |
| | Targeted p21(WAF1/CIP1) activation by miR-1236 inhibits cell proliferation and correlates with favorable survival in renal cell carcinoma | Q40483674 |
| | The Exosome Is Recruited to RNA Substrates through Specific Adaptor Proteins | Q40596532 |
| | Structural studies on the RNA-recognition motif of NELF E, a cellular negative transcription elongation factor involved in the regulation of HIV transcription | Q41079588 |
| | Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis | Q41192731 |
| | Chemical genetic discovery of PARP targets reveals a role for PARP-1 in transcription elongation | Q41218811 |
| | Genomic analysis identifies new drivers and progression pathways in skin basal cell carcinoma | Q42490053 |
| | Further assessment of the complement component 2 and factor B region associated with age-related macular degeneration | Q43995283 |
| | A genetic variant in the SKIV2L gene is significantly associated with age-related macular degeneration in a Han Chinese population | Q44654865 |
| | Tricho-hepato-enteric syndrome with novel SKIV2L gene mutations: A case report | Q47133393 |
| | Structural basis for mutually exclusive co-transcriptional nuclear cap-binding complexes with either NELF-E or ARS2. | Q47442873 |
| | NELF interacts with CBC and participates in 3' end processing of replication-dependent histone mRNAs | Q50336087 |
| | Oncogenic Activation of the RNA Binding Protein NELFE and MYC Signaling in Hepatocellular Carcinoma. | Q50897012 |
| | Identification of two independent risk factors for lupus within the MHC in United Kingdom families | Q30837981 |
| | Genomics of the major histocompatibility complex: haplotypes, duplication, retroviruses and disease | Q33630704 |
| | Next-generation sequencing traces human induced pluripotent stem cell lines clonally generated from heterogeneous cancer tissue | Q33716184 |
| | mRNA quality control at the 5' end. | Q33826909 |
| | Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease as | Q33844920 |
| | Identification and characterization of a bidirectional promoter from the intergenic region between the human DDX13 and RD genes | Q33898922 |
| | SVA elements are nonautonomous retrotransposons that cause disease in humans | Q33905356 |
| | Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease | Q33906196 |
| | The human and mouse MHC class III region: a parade of 21 genes at the centromeric segment | Q33953177 |
| | Phenotypic and molecular analysis of mes-3, a maternal-effect gene required for proliferation and viability of the germ line in C. elegans | Q33966270 |
| | Pleiotropic genes for metabolic syndrome and inflammation | Q34005816 |
| | The SKIV2L RNA exosome limits activation of the RIG-I-like receptors | Q34071054 |
| | Features of the two gene pairs RD-SKI2W and DOM3Z-RP1 located between complement component genes factor B and C4 at the MHC class III region | Q34085937 |
| | SVA retrotransposons: Evolution and genetic instability | Q34156329 |
| | Polymorphism of human complement component C4. | Q34192206 |
| | Genetic organization of the human MHC class III region | Q34327331 |
| | Intractable infant diarrhea associated with phenotypic abnormalities and immunodeficiency | Q34329634 |
| | Tricho-hepato-enteric syndrome: further delineation of a distinct syndrome with neonatal hemochromatosis phenotype, intractable diarrhea, and hair anomalies | Q34415467 |
| | Characterisation of the potential function of SVA retrotransposons to modulate gene expression patterns | Q34732755 |
| | RNA polymerase II transcription elongation control | Q34960186 |
| | Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy) | Q35195413 |
| | Dancing with Complement C4 and the RP-C4-CYP21-TNX (RCCX) Modules of the Major Histocompatibility Complex | Q35578276 |
| | Genetics of the central MHC. | Q35876814 |
| | SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome. | Q35877863 |
| | Gene map of the extended human MHC. | Q35968433 |
| | Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration | Q36031664 |
| | Mutational status of naevus-associated melanomas. | Q36095004 |
| | Splicing-dependent expression of microRNAs of mirtron origin in human digestive and excretory system cancer cells. | Q36728209 |
| | Superkiller Mutations in Saccharomyces cerevisiae Suppress Exclusion of M2 Double-Stranded RNA by L-A-HN and Confer Cold Sensitivity in the Presence of M and L-A-HN | Q36943809 |
| | The innate immune system in SLE: type I interferons and dendritic cells | Q36960344 |
| | Defining NELF-E RNA binding in HIV-1 and promoter-proximal pause regions | Q37487966 |
| | Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders | Q37601815 |
| | NELF-E is recruited to DNA double-strand break sites to promote transcriptional repression and repair. | Q38880991 |
| P275 | copyright license | Creative Commons Attribution | Q6905323 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 9 | |
| P921 | main subject | transcription factor | Q407384 |
| | major histocompatibility complex | Q423163 |
| P577 | publication date | 2019-08-30 | |
| P1433 | published in | Cells | Q27724621 |
| P1476 | title | An RNA Metabolism and Surveillance Quartet in the Major Histocompatibility Complex | |
| P478 | volume | 8 | |