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Topic: Chromosome 14 (human)

	Another human chromosome is finished (Site not responding. Last check: 2007-10-16)
		Draft versions of the human genome were published in February 2002, and in the last three years, chromosomes 22, 21, and 20 have been completed.
		By comparing the human genes to genes in other species, including the mouse and the freshwater pufferfish (Tetraodon nigroviridis), the researchers were able to propose biological functions for more than 96 percent of the genes.
		Chromosome 14 contains human versions of two genes in sheep associated with unusually muscular hindquarters, a rare condition known as callipyge (from the Greek for beautiful buttocks).
	www.genomenewsnetwork.org /articles/01_03/human_c14.shtml (349 words)

	Chromosome 14 Ring
		Chromosome 14 Ring is a rare disorder that is characterized by abnormalities of the 14th chromosome.
		Chromosome 14 Ring may also be characterized by other physical abnormalities, including a short neck with excessive skin folds; abnormal skin ridge patterns (dermatoglyphics), such as the presence of a single crease across the palm (simian crease); widely spaced nipples; and abnormalities of skin coloration (pigmentation).
		Chromosome 14 Ring usually appears to be caused by spontaneous or "de novo" errors early during the development of the embryo.
	hw.healthdialog.com /kbase/nord/nord955.htm (1858 words)

	Chromosome 14 - Genetics Home Reference
		Chromosome 14 is one of the 23 pairs of chromosomes in humans.
		Chromosome 14 spans about 105 million base pairs (the building material of DNA) and represents between 3 and 3.5 percent of the total DNA in cells.
		Genes on chromosome 14 are among the estimated 20,000 to 25,000 total genes in the human genome.
	www.ghr.nlm.nih.gov /chromosome=14 (399 words)

	Human Chromosome Map (Site not responding. Last check: 2007-10-16)
		For the first time, scientists have mapped virtually an entire human chromosome, one of the chains of molecules that bear the genetic recipe for human life.
		Chromosome 5 comprises approximately 5% of the human genome or 170 Mb.
		As part of the Human Genome Project, we are constructing a high resolution physical map and cloned DNA contig of this chromosome.
	www.e-dna-tests.info /resources/human-chromosome-map.html (468 words)

	CNN.com - Scientists map fourth human chromosome - Jan. 2, 2003
		Human cells typically have 23 pairs of chromosomes, each pair made up of a chromosome from each parent.
		The researchers describe chromosome 14 and its 87,410,661 pairs of DNA in Thursday's edition of the journal Nature.
		Other diseases with genes present on chromosome 14 are spastic paraplegia, a neurodegenerative condition that leads to weakness or stiffness of the legs; and Usher syndrome, which results in gradual hearing and vision loss.
	www.cnn.com /2003/TECH/science/01/02/chromosome.14 (348 words)

	United Press International: Chromosome 14 sequence completed (Site not responding. Last check: 2007-10-16)
		In all, the researchers identified about 1,050 genes and gene fragments within chromosome 14, more than 60 of which other studies have found are responsible for such conditions as early onset Alzheimer's disease, a severe form of Usher's syndrome and cardiovascular disease.
		"We chose chromosome 14 because we had prepared mapping (substances) for this chromosome in 1998 and 1999 and hence were in good position to establish its sequence," said researcher Jean Weissenbach, of Genoscope, the company that led the mapping effort.
		The work on chromosome 14 was completed as part of the human genome Sequencing Consortium, an international group of researchers attempting to fill in gaps in the data on the human genome.
	www.upi.com /view.cfm?StoryID=20021230-122826-1630r (497 words)

	Current status of human chromosome 14 -- Kamnasaran and Cox 39 (2): 81 -- Journal of Medical Genetics
		300 kb of the translocation breakpoint on chromosome 14.
		A 370-kb cosmid contig of the serpin gene cluster on human chromosome 14q32.1: molecular linkage of the genes encoding alpha 1-antichymotrypsin, protein C inhibitor, kallistatin, alpha 1-antitrypsin, and corticosteroid-binding globulin.
		Maternal uniparental disomy of chromosome 14 confined to an interstitial segment (14q23-14q24.2).
	jmg.bmjjournals.com /cgi/content/full/39/2/81 (7442 words)

	Type II Gonadotropin-Releasing Hormone Receptor Transcripts in Human Sperm -- van Biljon et al. 67 (6): 1741 -- Biology ...
		The chromosome 1 gene is comprised of exons 1, 2, and
		pseudogene on chromosome 1 and a paralogous gene on chromosome
		Absence of mutations in exon 3 of the GnRH receptor in human gonadotroph adenomas.
	www.biolreprod.org /cgi/content/full/67/6/1741 (5971 words)

	Chromosome 14: Human Genome Landmarks Poster
		These regions reflect the unique patterns of light and dark bands seen on human chromosomes that have been stained to allow viewing through a light microscope.
		Chromosomal regions that vary in staining intensity and are sometimes called heterochromatin (meaning "different color").
		(e.g., on chromosome 21) denote variable regions, called stalks, that connect a very small chromosome arm (a "satellite") to the chromosome.
	www.ornl.gov /hgmis/posters/chromosome/chromo14.html (348 words)

	Human Chromosome 14
		Human Chromosome 14 Completed, January 2003 -- From Genome News Network
		Chromosome 14 - BACs -- University of California, Santa Cruz release
		Chromosome: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X Y
	www.ornl.gov /sci/techresources/Human_Genome/launchpad/chrom14.shtml (460 words)

	Human Genetics - UPD Maternal Chromosome 14 (Site not responding. Last check: 2007-10-16)
		The maternal chromosome is shown on the left.
		Healey, S.;Powell, F.;Battersby, M.;Chenevix-Trench, G.;McGill, J. Distinct phenotype in maternal uniparental disomy of chromosome 14.
		Walgenbach, D.D.;Yang, S.P.;McCaskill, C.;Shaffer, L.G.;Towner, D.R. (1997): Maternal uniparental disomy of chromosome 14 in an infant with mild dysmorphology and confined placental mosaicism..
	www.genes.uchicago.edu /upd/upd14m.html (458 words)

	2D crossover-based maps of human chromosome 14. (Site not responding. Last check: 2007-10-16)
		Initially, markers from a chromosome 14 dataset that had been extensively checked for errors and used by Pandit et al.
		Of the 735 crossovers we identified, 227 are contained within the chromosomes of the densely mapped 8-family CEPH subset used by Genethon.
		The average number of chromosome 14 crossovers per meiosis detected was 1.3 in females and 0.93 in males.
	www.genlink.wustl.edu /repository/abstracts/liu1-ab.html (372 words)

	Chromosome 14 (Site not responding. Last check: 2007-10-16)
		Human Chromosome 14 No endorsement is made or implied by inclusion here.
		Chromosome 14 Back to Chromosome 14 summary Conditions related to genes on chromosome 14 Chromosome...
		14 Ring Important It is possible that the main title of the report Chromosome 14 Ring is not the...
	www.e-dna-tests.info /resources/chromosome-14.html (263 words)

	Maternally inherited duplication of the possible imprinted 14q31 region -- Mignon-Ravix et al. 38 (5): 343 -- Journal ...
		The green signal (YAC 815d5) located on the duplicated chromosome 14 is larger than the one located on the normal chromosome 14.
		Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty.
		Search for imprinted regions on chromosome 14: comparison of maternal and paternal UPD cases with cases of chromosome 14 deletion.
	jmg.bmjjournals.com /cgi/content/full/38/5/343 (2044 words)

	Chromosomal Elements Regulate Gene Activity and Chromatin Structure of the Human Serpin Gene Cluster at 14q32.1 -- ...
		chromosome 14 derived from human diploid fibroblasts (30).
		contrast to the behavior of wild-type human chromosome 14 (39).
		Long-range chromatin reorganization of the human serpin gene cluster at 14q32.1 accompanies gene activation and extinction in microcell hybrids.
	mcb.asm.org /cgi/content/full/23/10/3516 (5311 words)

	Publications: Molecular Anthropolgy
		Y chromosome STR haplotypes and the genetic structure of U.S. populations of African, European, and Hispanic ancestry.
		Alu insertion polymorphisms and the genetic structure of human populations from the Caucasus.
		Human mtDNA and Y-chromosome variation is correlated with matrilocal vs. patrilocal residence.
	www.eva.mpg.de /genetics/files/pubs_stoneking.html (1361 words)

	Chromosome 14 - Genetics Home Reference
		Chromosome 14 likely contains between 700 and 1,200 genes.
		Ideograms show a chromosome's relative size and its banding pattern.
		Another human chromosome is finished (Genome News Network, January 10,
	ghr.nlm.nih.gov /chromosome=14 (399 words)

	Nature web focus: The Human Genome (Site not responding. Last check: 2007-10-16)
		A comprehensive genetic map of the human genome based on 5,264 microsatellites
		Estimate of human gene number provided by genome-wide analysis using Tetraodon nigroviridis DNA sequence
		Experimental annotation of the human genome using microarray technology
	www.nature.com /nature/focus/humangenome/14.html (52 words)

	Human Genetics - UPD Paternal Chromosome 14 (Site not responding. Last check: 2007-10-16)
		The paternal chromosome is shown on the left.
		Ledbetter, D.H. and Engel, E. (1995): Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis.
		Morison, I.M. and Reeve, A.E.(1998): A catalogue of imprinted genes and parent-of-origin effects in humans and animals.
	www.genes.uchicago.edu /upd/upd14p.html (129 words)

	Human to Mouse Homology Region Map, Chromosome 14
		Human to Mouse Homology Region Map, Chromosome 14
		Gene order has been changed from that shown in the chromosome committee reports or online databases, as required by high-resolution human physical mapping data; these data also indicate a probable difference between human and mouse organization, e.g.
		The asterisk character ('') is used to indicate a different region of homology on the same mouse chromosome*.
	www3.ncbi.nlm.nih.gov /Omim/Homology/human14.html (298 words)

	Novel Imprinted DLK1/GTL2 Domain on Human Chromosome 14 Contains Motifs that Mimic Those Implicated in IGF2/H19 ...
		Human tissues were obtained from the NIH-supported Birth Defects Research Laboratory at the University of Washington.
		Ledbetter, D.H. and Engel, E. Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis.
		Miyoshi, N. Identification of an imprinted gene, Meg3/Gtl2, and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q.
	www.genome.org /cgi/content/full/10/11/1711 (5045 words)

	Chromosome 14 - References - Genetics Home Reference
		These sources were used to develop the Genetics Home Reference chromosome summary on chromosome 14.
		Gilbert F. Disease genes and chromosomes: disease maps of the human genome.
		Further delineation of the chromosome 14q terminal deletion syndrome.
	ghr.nlm.nih.gov /chromosome=14/show/References (135 words)

	The Sanger Institute: Human Genome Project
		The human genome research programme at The Sanger Institute encompasses mapping, sequencing, and structural and functional interpretation.
		The Sanger Institute is engaged upon collaborative projects to sequence all or part of chromosomes 1, 6, 9, 10, 11, 13, 20, 22 and X.
		You may search individual or combined chromosome project information using our combined search form.
	www.sanger.ac.uk /HGP (170 words)

	HUMAN CHROMOSOME #14 (Site not responding. Last check: 2007-10-16)
		Localization of the human bona fide calmodulin genes CALM1, CALM2, and CLAM 3 to chromosomes 14q24-q31, 2p21.1-p21.3, and 19q13.2-q13.3.
		Powell SJ, Slynn G, Thomas C, Hopkins B, Briggs I, Graham A. Human bradykinin B2 receptor: Nucleotide dequence analysis and assignment to chromosome 14.
		Human somatostatin receptor genes: Localization of SSTR5 to human chromosomes 14, 17, and 22, and identification of simple tandem repeat polymorphisms.
	www.il-st-acad-sci.org /genecats/hsa14.html (223 words)

	14 (Site not responding. Last check: 2007-10-16)
		This is the entry point for the updated data for the Human Chromosome 14 The other participating groups in the Chromosome 14 Project include the
		The MathWorks Release 14 includes all the products in the MATLAB® and Note: Release 14 with Service Pack 2 is now available as an update to R14.
		The Multi-dimensional Human Embryo is an NICHD funded project to generate three-dimensional image data of the human embryo based on magnetic resonance
	www.ad999.com /?q=14 (937 words)

	Intracellular self/not-self discrimination (Site not responding. Last check: 2007-10-16)
		Recent investigations of the transcriptional activities of the ß-globin region of human chromosome 11
		Alu and other repetitive elements are shown in part of the 100 kilobase segment of human chromosome one containing the two exon gene,
		This was greatly supported by the discovery of multiple "non-coding" transcripts in cDNA libraries prepared from humans and mice.
	mail.queensu.ca /~forsdyke/theorimm4.htm (3184 words)

	bib06
		Bains JS, Shaw CA: "Neurodegenerative disorders in humans: the role of glutathione in oxidative stress-mediated neuronal death." Brain Research.
		Animal model and postmortem human studies." Annals of the New York Academy of Sciences (1997) Sep 26;826:56-74.
		Feuerstein TJ, Seeger W: "Modulation of acetylcholine release in human cortical slices: possible implications for Alzheimer's disease." Pharmacology and Therapeutics (1997) 74(3):333-347.
	www.biologyofhumanaging.com /bib06.htm (2974 words)

	Energy Citations Database (ECD) - Energy and Energy-Related Bibliographic Citations
		Three sets of linkage maps (index, comprehensive microsatellite, and unified) have been constructed for human chromosome 14 based on genotypes from the CEPH reference pedigrees.
		Our maps are anchored by a microsatellite telomere marker sCAW1 (D14S826), developed from a telomere YAC clone TYAC196, which extends the linkage map to the physical terminus of the long arm of chromosome 14.
		Together with previously established cytogenetic map designations for other loci, our maps display links between genetic markers for 10 of 13 cytogenetic bands of chromosome 14 at the 550 genome band resolution.
	www.osti.gov /energycitations/product.biblio.jsp?osti_id=443864 (386 words)

	Molecular Biology databases/Bioinformatics databases-Species Specific databases
		Chr16 TIGR - Human chromosome 16 db at TIGR
		Chr21 at ERI - Human chromosome 21 genomic sequence db from the Eleanor Roosevelt Institute
		ADB - Albinism db (Mutations in human genes causing albinism)
	www.geocities.com /bioinformaticsweb/speciesspecificdatabases.htm (2235 words)

	Chromosome 14 (Site not responding. Last check: 2007-10-16)
		Pandit S.D., Wang J.C., Veile R.A., Mishra, S.K., Warlick C.A., and Donis-Keller H. (1995) Index, comprehensive microsatellite, and unified linkage maps of human chromosome 14 with cytogenetic tie points and a telomere microsatellite marker.
		The cumulative length of the genetic map is indicated at the bottom of the map (in centimorgans; recombination fractions were converted to cM using the Kosambi mapping function).
		Asterisks indicate markers used to construct the index map (shown in Fig.2).
	www.genlink.wustl.edu /repository/figures/14ms_map.html (144 words)

	[No title] (Site not responding. Last check: 2007-10-16)
		(isolated from cultured epidermal cells grown from human foreskin) /chromosome=1 /cytoband=7p15-p12 + 0 777 53874 V00478: Human mRNA fragment encoding cytoplasmic actin.
		Contains ESTs and GSSs + 1e-136 486 52574 AL022718: Human DNA sequence from clone 1052M9 on chromosome Xq25.
		Contains the BING5 gene, exons 11 to 15 of the BING4 gene, the gene for GalT3 (beta3 AL031228: Human DNA sequence from clone 1033B10 on chromosome 6p21.2-21.31.
	www.dkfz-heidelberg.de /abt0840/whuber/rcc/fred.1-892.known+.txt (510 words)

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