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X-Linked Late-Onset Sensorineural Deafness Caused by a Deletion Involving OA1 and a Novel Gene Containing WD-40 Repeats
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archopht.1976.03910040593001openalex-snapshot
X-Linked Ocular Albinism
inferredcites →https://doi.org/10.1002/(sici)1097-0134(199707)28:3<405::aid-prot10>3.0.co;2-lopenalex-snapshot
Pfam: A comprehensive database of protein domain families based on seed alignments
inferredcites →https://doi.org/10.1002/ajmg.1320190421openalex-snapshot
X‐linked inheritance of ocular albinism with late‐onset sensorineural deafness
inferredcites →https://doi.org/10.1002/yea.320101014openalex-snapshot
II . Yeast sequencing reports. Analysis of a 70kb region on the right arm of yeast chromosome II
inferredcites →https://doi.org/10.1006/geno.1993.1495openalex-snapshot
X-Linked Ocular Albinism and Sensorineural Deafness: Linkage to Xp22.3
inferredcites →https://doi.org/10.1007/s003359900926openalex-snapshot
Mapping of the murine Tbl1 gene reveals a new rearrangement between mouse and human X Chromosomes
inferredcites →https://doi.org/10.1016/0003-2697(90)90595-zopenalex-snapshot
Molecular cloning: A laboratory manual
inferredcites →https://doi.org/10.1016/0092-8674(95)90367-4openalex-snapshot
A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy
inferredcites →https://doi.org/10.1016/0168-9525(94)90131-7openalex-snapshot
Fishing for complements: finding genes by direct selection
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1038/353529a0openalex-snapshot
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
inferredcites →https://doi.org/10.1038/371297a0openalex-snapshot
The ancient regulatory-protein family of WD-repeat proteins
inferredcites →https://doi.org/10.1038/379369a0openalex-snapshot
Crystal structure of a GA protein βγdimer at 2.1 Å resolution
inferredcites →https://doi.org/10.1038/ng0593-19openalex-snapshot
Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting
inferredcites →https://doi.org/10.1038/ng0595-13openalex-snapshot
Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome
inferredcites →https://doi.org/10.1038/ng0793-272openalex-snapshot
A high resolution deletion map of human chromosome Xp22
inferredcites →https://doi.org/10.1038/ng1197-285openalex-snapshot
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
inferredcites →https://doi.org/10.1073/pnas.83.7.2162openalex-snapshot
Repetitive segmental structure of the transducin beta subunit: homology with the CDC4 gene and identification of related mRNAs.
inferredcites →https://doi.org/10.1086/301776openalex-snapshot
OA1 Mutations and Deletions in X-Linked Ocular Albinism
inferredcites →https://doi.org/10.1093/hmg/2.7.947openalex-snapshot
The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions
inferredcites →https://doi.org/10.1093/hmg/3.4.547openalex-snapshot
A gene from the Xp22.3 region shares homology with voltage-gated chloride channels
inferredcites →https://doi.org/10.1093/hmg/3.4.647openalex-snapshot
A submicroscopic deletion in a patient with isolated X-linked ocular albinism (OA1)
inferredcites →https://doi.org/10.1093/hmg/3.6.879openalex-snapshot
A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human
inferredcites →https://doi.org/10.1093/hmg/4.10.1821openalex-snapshot
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3–Xp21.3
inferredcites →https://doi.org/10.1093/hmg/4.3.373openalex-snapshot
Cloning of a human homologue of the Xenopus Iaevis APX gene from the ocular albinism type 1 critical region
inferredcites →https://doi.org/10.1093/hmg/5.9.1383openalex-snapshot
A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22
inferredcites →https://doi.org/10.1093/ije/18.4.911openalex-snapshot
The Prevalence of Hearing Impairment and Reported Hearing Disability among Adults in Great Britain
inferredcites →https://doi.org/10.1093/nar/16.5.1829openalex-snapshot
‘DNA Strider’: a ‘C’ program for the fast analysis of DNA and protein sequences on the Apple Macintosh family of computers
inferredcites →https://doi.org/10.1093/nar/18.14.4191openalex-snapshot
X chromosome inactivation of the human TIMP gene
inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
inferredcites →https://doi.org/10.1093/nar/25.17.3389openalex-snapshot
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
inferredcites →https://doi.org/10.1101/gr.6.2.71openalex-snapshot
Around the genomes: the Drosophila genome project.
inferredcites →https://doi.org/10.1128/mcb.13.8.4953openalex-snapshot
Saccharomyces cerevisiae cdc15 mutants arrested at a late stage in anaphase are rescued by Xenopus cDNAs encoding N-ras or a protein with beta-transducin repeats.
inferredcites →https://doi.org/10.1128/mcb.13.8.4953-4966.1993openalex-snapshot
Saccharomyces cerevisiae cdc15 Mutants Arrested at a Late Stage in Anaphase Are Rescued by Xenopus cDNAs Encoding N -ras or a Protein with β-Transducin Repeats†
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Genetic Hypomelanoses: Generalized Hypopigmentation
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Sequence‐Based, in situ detection of chromosomal abnormalities at high resolution
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A male infant with a 9.6 Mb terminal Xp deletion including the OA1 locus: Limit of viability of Xp deletions in males
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Congenital nasal pyriform aperture stenosis and ocular albinism co‐occurring in a sibship with a maternally‐inherited 97 kb Xp22.2 microdeletion
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Ocular albinism with infertility and late‐onset sensorineural hearing loss
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New insights into ocular albinism type 1 (OA1): Mutations and polymorphisms of the OA1 gene
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Molecular Cloning, Expression Analysis, and Chromosome Mapping of WDR6, a Novel Human WD-Repeat Gene
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Human Genome and Diseases:¶WD-repeat proteins: structure characteristics, biological function, and their involvement in human diseases
inferred← citeshttps://doi.org/10.1007/s10038-005-0237-9openalex-snapshot
Molecular analysis of TBL1Y, a Y-linked homologue of TBL1X related with X-linked late-onset sensorineural deafness
inferred← citeshttps://doi.org/10.1007/s10930-018-9785-7openalex-snapshot
WD40 Repeat Proteins: Signalling Scaffold with Diverse Functions
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Corepressors in Mediating Repression by Nuclear Receptors
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Corepressors in Mediating Repression by Nuclear Receptors
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Overexpression of MIP2, a novel WD-repeat protein, promotes proliferation of H9c2 cells
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The multiple genetic causes of central hypothyroidism
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Hepatic Deficiency in Transcriptional Cofactor TBL1 Promotes Liver Steatosis and Hypertriglyceridemia
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CRN2 binds to TIMP4 and MMP14 and promotes perivascular invasion of glioblastoma cells
inferred← citeshttps://doi.org/10.1016/j.exphem.2022.09.006openalex-snapshot
TBL1X: At the crossroads of transcriptional and posttranscriptional regulation
inferred← citeshttps://doi.org/10.1016/j.gep.2024.119355openalex-snapshot
Embryonic expression patterns of TBL1 family in zebrafish
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A LisH-domain protein interaction map reveals a Lis1-ARIH2-dynein regulatory axis
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The Structure of Sif2p, a WD Repeat Protein Functioning in the SET3 Corepressor Complex
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The Dimerization Mechanism of LIS1 and its Implication for Proteins Containing the LisH Motif
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Sexual orientation, fraternal birth order, and the maternal immune hypothesis: A review
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A Corepressor/Coactivator Exchange Complex Required for Transcriptional Activation by Nuclear Receptors and Other Regulated Transcription Factors
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Cloning and characterization of WDR17, a novel WD repeat-containing gene on chromosome 4q34
inferred← citeshttps://doi.org/10.1016/s0301-472x(00)00539-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0378-1119(01)00483-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0888-7543(03)00151-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1097-2765(02)00468-9openalex-snapshot
The N-CoR-HDAC3 Nuclear Receptor Corepressor Complex Inhibits the JNK Pathway through the Integral Subunit GPS2
inferred← citeshttps://doi.org/10.1016/s1472-6483(10)61095-4openalex-snapshot
Reprogramming of epigenetic inheritance by somatic cell nuclear transfer
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inferred← citeshttps://doi.org/10.1038/ng900openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41380-020-0667-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41467-026-73227-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1385/nmm:8:4:547openalex-snapshot
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inferred← citeshttps://doi.org/10.2353/jmoldx.2007.060198openalex-snapshot
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inferred← citeshttps://doi.org/10.3410/f.1032947.374585openalex-snapshot
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inferred← citeshttps://doi.org/10.3803/enm.2021.1150openalex-snapshot
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