| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/0888-7543(95)80168-L |
| P953 | full work available at URL | https://api.elsevier.com/content/article/PII:088875439580168L?httpAccept=text/xml |
| https://api.elsevier.com/content/article/PII:088875439580168L?httpAccept=text/plain | ||
| P698 | PubMed publication ID | 7607673 |
| P2093 | author name string | A. K. Srivastava | |
| D. Schlessinger | |||
| K. Wein | |||
| T. Featherstone | |||
| P2860 | cites work | Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome | Q24558860 |
| Fabry disease: six gene rearrangements and an exonic point mutation in the alpha-galactosidase gene | Q24626162 | ||
| A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity | Q26778490 | ||
| Identification of mutations in the COL4A5 collagen gene in Alport syndrome | Q28115794 | ||
| De novo mutation in the COL4A5 gene converting glycine 325 to glutamic acid in Alport syndrome | Q28184707 | ||
| Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumors | Q28261788 | ||
| Characterization of the 3' half of the human type IV collagen alpha 5 gene that is affected in the Alport syndrome | Q28269253 | ||
| Human protein kinase C Iota gene (PRKCI) is closely linked to the BTK gene in Xq21.3 | Q28293269 | ||
| Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization | Q29616823 | ||
| Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia | Q30195143 | ||
| Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts | Q30997778 | ||
| Construction of a yeast artificial chromosome contig encompassing the human alpha 5(IV) collagen gene (COL4A5). | Q30997898 | ||
| A second-generation linkage map of the human genome | Q33192755 | ||
| Construction and characterization of a yeast artificial chromosome library for Xpter-Xq27.3: a systematic determination of cocloning rate and X-chromosome representation | Q33209831 | ||
| Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification | Q33230932 | ||
| Yeast artificial chromosomes spanning 8 megabases and 10-15 centimorgans of human cytogenetic band Xq26. | Q33273509 | ||
| Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus | Q33648165 | ||
| The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases | Q34355151 | ||
| Isolation of single-copy human genes from a library of yeast artificial chromosome clones | Q34450414 | ||
| Yeast artificial chromosomes containing human Xq24-Xq28 DNA: library construction and representation of probe sequences | Q34709870 | ||
| Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction | Q34993293 | ||
| Construction of yeast artificial chromosome libraries with large inserts using fractionation by pulsed-field gel electrophoresis | Q35225775 | ||
| A rodent-human hybrid containing Xq24-qter translocated to a hamster chromosome expresses the Xq27 folate-sensitive fragile site | Q36418655 | ||
| Regional localization of 18 human X-linked DNA sequences | Q36458340 | ||
| A 6.5-Mb yeast artificial chromosome contig incorporating 33 DNA markers on the human X chromosome at Xq22. | Q36750605 | ||
| Anhidrotic ectodermal dysplasia gene region cloned in yeast artificial chromosomes | Q36763324 | ||
| Ribosomal DNA clusters in pulsed-field gel electrophoretic analysis of human acrocentric chromosomes | Q36769686 | ||
| Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28. | Q36935731 | ||
| Extrachromosomal maintenance and amplification of yeast artificial chromosome DNA in mouse cells | Q41534917 | ||
| Expression of the fragile (X) chromosome in an interspecific somatic cell hybrid | Q43445313 | ||
| Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes | Q45333368 | ||
| X-linked megalocornea: close linkage to DXS87 and DXS94. | Q46551971 | ||
| Physical linkage of expressed sequence tags (ESTs) to polymorphic markers on the X chromosome | Q48081346 | ||
| Ring chromosome 15: phenotype, Ag-NOR analysis, secondary aneuploidy, and associated chromosome instability | Q52300738 | ||
| X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus | Q55670712 | ||
| Simplified template preparation and improved direct sequencing using Taq polymerase | Q57232817 | ||
| Report of the committee on the genetic constitution of the X chromosome | Q57405682 | ||
| OSP: a computer program for choosing PCR and DNA sequencing primers | Q67909636 | ||
| Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders | Q69805341 | ||
| Aberrant splicing of the COL4A5 gene in patients with Alport syndrome | Q71996165 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 502-509 | |
| P577 | publication date | 1995-04-01 | |
| 1995-04-10 | |||
| P1433 | published in | Genomics | Q5533503 |
| P1476 | title | YAC contigs mapping the human COL4A5 and COL4A6 genes and DXS118 within Xq21.3–q22 | |
| P478 | volume | 26 |
| Q48056032 | 4.5-Mb YAC STS contig at 50-kb resolution, spanning Xq25 deletions in two patients with lymphoproliferative syndrome |
| Q40480903 | Bifunctional promoter of type IV collagen COL4A5 and COL4A6 genes regulates the expression of alpha5 and alpha6 chains in a distinct cell-specific fashion |
| Q36858016 | Construction of a pilot human YAC library in a recombination-defective yeast strain |
| Q74231196 | Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome |
| Q22010558 | Molecular cloning and characterization of TRPC5 (HTRP5), the human homologue of a mouse brain receptor-activated capacitative Ca2+ entry channel |
| Q35765036 | Somatic deletion of the 5' ends of both the COL4A5 and COL4A6 genes in a sporadic leiomyoma of the esophagus |
| Q28296180 | Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy |
| Q36850917 | X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content |
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