scholarly article | Q13442814 |
P819 | ADS bibcode | 1986PNAS...83.6573S |
P356 | DOI | 10.1073/PNAS.83.17.6573 |
P932 | PMC publication ID | 386546 |
P698 | PubMed publication ID | 3462714 |
P5875 | ResearchGate publication ID | 19693053 |
P50 | author | Jeremy A. Squire | Q39802515 |
P2093 | author name string | A Goddard | |
T P Dryja | |||
M Musarella | |||
T Hofmann | |||
H F Willard | |||
B L Gallie | |||
J Dunn | |||
R A Phillips | |||
A J Becker | |||
P2860 | cites work | DNA sequencing with chain-terminating inhibitors | Q22066207 |
Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes | Q24298720 | ||
A human T cell-specific cDNA clone encodes a protein having extensive homology to immunoglobulin chains | Q24301420 | ||
Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 | ||
Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I | Q27860885 | ||
Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing | Q27860941 | ||
Esterase D: a new human polymorphism | Q28245471 | ||
A cDNA cloning vector that permits expression of cDNA inserts in mammalian cells | Q29614815 | ||
Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus. | Q33671171 | ||
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma | Q34264957 | ||
A general theory of carcinogenesis | Q34744320 | ||
A sialic acid-specific O-acetylesterase in human erythrocytes: possible identity with esterase D, the genetic marker of retinoblastomas and Wilson disease | Q35589883 | ||
Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus | Q36593024 | ||
pEMBL: a new family of single stranded plasmids | Q36597299 | ||
Homogeneously staining chromosomal regions contain amplified copies of an abundantly expressed cellular oncogene (c-myc) in malignant neuroendocrine cells from a human colon carcinoma | Q37606881 | ||
Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus | Q37680904 | ||
Purification and substrate specificity of polymorphic forms of esterase D from human erythrocytes | Q40637629 | ||
Accuracy of detection of the retinoblastoma gene by esterase D linkage | Q44602163 | ||
Retinoblastoma and Subband Deletion of Chromosome 13 | Q45128520 | ||
Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients | Q52830301 | ||
Retinoblastoma: host resistance and 13q- chromosomal deletion. | Q52875579 | ||
Patient with 13 Chromosome Deletion: Evidence That the Retinoblastoma Gene Is a Recessive Cancer Gene | Q55062498 | ||
Retinoblastoma: Importance of recessive mutations in tumorigenesis | Q58348248 | ||
Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism | Q59053447 | ||
Chromosomal deletion and retinoblastoma | Q67839651 | ||
Retinoblastoma and chromosome abnormality. Partial deletion of the long arm of chromosome 13 | Q68837050 | ||
Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders | Q69805341 | ||
Deletions of the esterase D locus from a survey of 200 retinoblastoma patients | Q69996001 | ||
Electrophoretic separations of large DNA molecules by periodic inversion of the electric field | Q70022520 | ||
Model Hereditary Cancers of Man | Q70187705 | ||
17 A rapid alkaline extraction method for the isolation of plasmid DNA | Q70284325 | ||
Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3) | Q70673831 | ||
Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D | Q71656765 | ||
P433 | issue | 17 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | retinoblastoma | Q500695 |
P304 | page(s) | 6573-7 | |
P577 | publication date | 1986-09-01 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13 | |
P478 | volume | 83 |
Q24631236 | A gene encoding 22 highly related zinc fingers is expressed in lymphoid cell lines |
Q41445534 | A null allele of esterase D is a marker for genetic events in retinoblastoma formation |
Q45280068 | Allelic loss on 13q in esophageal squamous cell carcinomas from northern China |
Q36028754 | An assessment of the usefulness of electrophoretic variants of esterase-D in the antenatal diagnosis of retinoblastoma in the United Kingdom |
Q33268330 | Characterization of a Zinc Finger Gene Disrupted by the t(15;17) in Acute Promyelocytic Leukemia |
Q41632381 | Chromosomal sublocalization of the 2;13 translocation breakpoint in alveolar rhabdomyosarcoma |
Q24314094 | Crystal structure of human esterase D: a potential genetic marker of retinoblastoma |
Q69901151 | Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus |
Q34453650 | Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma |
Q34384790 | Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling. |
Q52065255 | Genetic and cytogenetic analysis of patients showing reduced esterase-D levels and mental retardation from a survey of 500 individuals with retinoblastoma. |
Q24296960 | Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma |
Q36788845 | Infrequent genomic rearrangement and normal expression of the putative RB1 gene in retinoblastoma tumors |
Q41225785 | Inherited mental disorders |
Q35197191 | Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene |
Q43652805 | Localization of the pig gene ESD to chromosome 13 by in situ hybridization |
Q41658140 | Microsequencing of proteins recorded in human two-dimensional gel protein databases |
Q34322097 | Molecular analysis of esterase D polymorphism |
Q70228509 | Molecular and cytogenetic analysis of chromosomal arms 2q and 13q in alveolar rhabdomyosarcoma |
Q36752741 | Molecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptibility locus |
Q41406097 | Molecular evidence that the esterase-D gene lies proximal to the retinoblastoma susceptibility locus in chromosome region 13q14. |
Q39701871 | Molecular genetic approaches to the analysis of human ophthalmic disease |
Q39553062 | Ocular and orbital tumors. |
Q34636589 | Pharmacokinetics and molecular detoxication |
Q58348180 | Preferential germline mutation of the paternal allele in retinoblastoma |
Q55261668 | Retinoblastoma--clinical and genetic aspects: a review. |