About: The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22?q24) by somatic cell hybrid analysis and in situ hybridization

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About: The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22?q24) by somatic cell hybrid analysis and in situ hybridization Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1986 (uk) im März 1986 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q58020746-A9DF4E1C-6245-40C8-9822-D660AB9F9692
publication date	1986-03-01 00:00:00Z (xsd:dateTime)
exact match	wds:Q58020746-512734F7-08C0-4FC1-BCE3-47263700C5C3
exact match	https://scigraph.springernature.com/pub.10.1007/bf00291881
cites work	wds:Q58020746-0C7FEDF5-ACD6-4A9B-86D3-2D09B9EA956F wds:Q58020746-11E267A8-A039-4B2C-A9A9-A19E3A6C1191 wds:Q58020746-1300E4E9-4D02-4317-95CC-628C8362B7AA wds:Q58020746-1736AD86-881D-4D3B-AB79-45F6E71BFB1F wds:Q58020746-3585260F-A442-4FBA-ADA1-C240E269CD8A wds:Q58020746-3C00FEA1-3903-4065-9517-E689FB986792 wds:Q58020746-3F9CF288-F4C8-4385-980E-4DBE8B89E92F wds:Q58020746-4EC2A2E7-4594-4E3A-A79F-8C9B57490516 wds:Q58020746-51D51E2E-7494-4B17-BE19-095E5693D9DF wds:Q58020746-5E08D53F-4F58-484A-B941-20E31AFF170C wds:Q58020746-61DBEE0D-2E6A-4287-8227-A817DD135C9A wds:Q58020746-6E24DD82-0CE2-4E8A-BC00-E46C830CE60B wds:Q58020746-86683528-CEF6-4D7A-A712-C72DB722AF27 wds:Q58020746-A67BB599-610C-4559-805A-2A752562FABD wds:Q58020746-C4DE04C8-39BF-4AB7-99B7-3F67140F8E1E wds:Q58020746-C624ACDF-044D-4107-8346-C563AB7D6448 wds:Q58020746-C750C117-7C06-4FC7-BA7F-A74F8CB2F917 wds:Q58020746-D984BCE4-0FC8-4767-A244-FF0EF142F2F3 wds:Q58020746-DC23392B-8C5C-435F-82E4-4AE0CBDD468B wds:Q58020746-F07CC83E-5D2E-4BF2-ABBD-1E05EDBF0265 wds:Q58020746-FD75EC18-1544-435D-9F3B-A73169C17D81
cites work	A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity Isolation and characterization of the rat tyrosine aminotransferase gene Report of the Committee on Comparative Mapping Gel electrophoresis of restriction fragments Assignment of first random restriction fragment length polymorphism (RFLP) locus ((D14S1) to a region of human chromosome 14. Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization Isolation of cDNA clones coding for rat tyrosine aminotransferase Intrachromosomal gene mapping in man: assignment of nucleoside phosphorylase to region 14cen leads to 14q21 by interspecific hybridization of cells with a t(X;14) (p22;q21) translocation Random X inactivation resulting in mosaic nullisomy of region Xp21.1----p21.3 associated with heterozygosity for ornithine transcarbamylase deficiency and for chronic granulomatous disease Assignment of the major histocompatibility complex to a region of the short arm of human chromosome 6 Transcriptional activation of the rat liver tyrosine aminotransferase gene by cAMP. Isolation, characterization and chromosomal mapping of the mouse tyrosine aminotransferase gene. Insulin selectively slows the degradation rate of tyrosine aminotransferase Activation of human alpha 1-antitrypsin gene in rat hepatoma x human fetal liver cell hybrids depends on presence of human chromosome 14. Insulin-cholera toxin binding unit conjugate: A hybrid molecule with insulin biological activity and cholera toxin binding specificity Purification and properties of human liver tyrosine aminotransferase Richner-Hanhart's Syndrome: Ultrastructural Abnormalities of Epidermal Keratinization Indicating a Causal Relationship to High Intracellular Tyrosine Levels Successful dietary control of tyrosinemia II The role of the insulin receptor in mediating the insulin-stimulated growth response in Reuber H-35 cells Development of tyrosine aminotransferase and para-hydroxyphenylpyruvate dioxygenase activities in fetal and neonatal human liver Induction of cytosolic tyrosine aminotransferase by dexamethasone in organ culture of fetal human liver
author name string	wds:Q58020746-5EE3626D-68C5-44CE-ABA7-75C965A3FE26 wds:Q58020746-9D071310-3B44-4E3A-B941-7047A2E7342B
author name string	T L Yang-Feng U Francke
rdfs:label	The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22?q24) by somatic cell hybrid analysis and in situ hybridization (en) The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (nl)
skos:prefLabel	The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22?q24) by somatic cell hybrid analysis and in situ hybridization (en) The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (nl)
name	The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22?q24) by somatic cell hybrid analysis and in situ hybridization (en) The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (nl)
author	wds:Q58020746-2A52DF81-40CA-4F53-B097-9C5E986384BA
author	David Barton
title	wds:Q58020746-5040A445-616C-4977-9D76-2BD5F3F03CA2
title	The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22----q24) by somatic cell hybrid analysis and in situ hybridization (en)
page(s)	wds:Q58020746-62764B86-BF8B-4572-8370-1CFF3454C89C
page(s)	221-224
instance of	wds:Q58020746-C53AF085-D2C0-4174-9BC9-748F0E6B1329
instance of	scholarly article
PubMed ID	wds:Q58020746-4A7DDF47-05D5-44B6-9050-F27020EF575F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2870017
PubMed ID	2870017
published in	wds:Q58020746-E3C8FA0E-98BF-43F6-BE42-4D1CC89F6FDF
published in	Human Genetics
issue	wds:Q58020746-FCBE39C6-4475-46AE-9330-73D453BC39CE
volume	wds:Q58020746-4AAE842F-1ABD-477C-A547-F2956944EA48
issue	3
volume	72
DOI	wds:Q58020746-359C1299-99A4-4748-8AFD-C9FB395F01BF
DOI	http://dx.doi.org/10.1007/BF00291881
DOI	10.1007/BF00291881
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58020746
is cites work of	Novel use of a chimpanzee pseudogene for chromosomal mapping of human cytochrome c oxidase subunit IV Comparative map for mice and humans Blast-1 possesses a glycosyl-phosphatidylinositol (GPI) membrane anchor, is related to LFA-3 and OX-45, and maps to chromosome 1q21-23 Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13 DLX2 (TES1), a homeobox gene of the Distal-less family, assigned to conserved regions on human and mouse chromosomes 2 Identification of a cDNA encoding a parathyroid hormone-like peptide from a human tumor associated with humoral hypercalcemia of malignancy A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library Richner-Hanhart syndrome (tyrosinemia type II). Case report and literature review Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1----q22.3 in a patient with tyrosinemia type II. Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations. Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis Comparison of nonerythroid alpha-spectrin genes reveals strict homology among diverse species Comparative map for mice and humans Re-localization of Actsk-1 to mouse chromosome 8, a new region of homology with human chromosome 1 Plantar keratoderma: a manifestation of tyrosinemia type II (Richner-Hanhart syndrome).

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