Analysis of losses of heterozygosity of the candidate tumour suppressor gene DMBT1 in melanoma resection specimens.
... has recently been identified and found to be deleted in several different types of human tumours. In melanomas, the chromosomal ... a candidate tumour suppressor gene located on chromosome 10q25.3-q26.1, ... Chromosomes, Human, Pair 10*. DNA Primers. Genes, Tumor Suppressor*. Humans. Loss of Heterozygosity*. Melanocytes / metabolism ... Previous Document: Increased expression of dipeptidyl peptidase IV in human mesothelial cells by malignant ascites from.... ...http://www.biomedsearch.com/nih/Analysis-losses-heterozygosity-candidate-tumour/12239452.html
ZFIN Publication: Postlethwait et al., 2000
Human, Pair 11/genetics; Chromosomes, Human, Pair 15/genetics; Chromosomes, Human, Pair 17/genetics; Chromosomes, Human, Pair ... Chromosomes, Human, Pair 11/genetics (all 18) Animals; Chromosome Mapping; Chromosomes/genetics*; Chromosomes, Human, Pair 10/ ... Animals; Chromosome Mapping; Chromosomes/genetics*; Chromosomes, Human, Pair 10/genetics; ... and zebrafish chromosomes are mosaically orthologous to several human chromosomes. Is this because of an excess of chromosome ...https://zfin.org/ZDB-PUB-001221-9
Genetic Variants Associated With Warfarin Dose in African-American Individuals: A Genome-Wide Association Study - American...
Keywords: Chromosomes, Human, Pair 10, Polymorphism, Single Nucleotide, Genome-Wide Association Study, Warfarin, United States ... in the CYP2C cluster on chromosome 10 (rs12777823) and warfarin dose requirement that reached genome-wide significance (p = ... They prespecified a genome-wide significance threshold of p < 5 × 10-8 in the discovery cohort and p < 0.0038 in the ... 10-5); analysis of the two cohorts together produced a p value of 4.5 × 10-12. Individuals heterozygous for the rs12777823 A ...http://www.acc.org/latest-in-cardiology/journal-scans/2013/07/19/11/38/genetic-variants-associated-with-warfarin-dose
Chromosome 10 (human) - Wikipedia
The following is a partial list of genes on human chromosome 10. For complete list, see the link in the infobox on the right. ... The following are some of the gene count estimates of human chromosome 10. Because researchers use different approaches to ... Deloukas P, French L, Meitinger T, Moschonas NK (2000). "Report of the third international workshop on human chromosome 10 ... People normally have two copies of this chromosome. Chromosome 10 spans about 133 million base pairs (the building material of ...https://en.wikipedia.org/wiki/Chromosome_10_(human)
Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease. -...
Evidence from linkage studies suggests that a gene (or genes) conferring susceptibility for LOAD resides on chromosome 10. We ... studied 23 positional/functional candidate genes from our linkage region on chromosome 10 (APBB1IP, ALOX5, AD037, SLC18A3, DKK1 ... Chromosomes, Human, Pair 10, DNA, Female, Gene Frequency, Genotype, Humans, Male, Polymorphism, Single Nucleotide ... Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease. ...https://www.psych.ox.ac.uk/publications/622673
lecture 1 - 1 Outline of lecture 1(1(2(3 Chromosome and its structure First Mendels law Second Mendels law 2 Notes for Lecture...
1 Outline of lecture 1. (1) (2) (3) Chromosome and its structure First Mendels law Second Mendels law 2 Notes for Lecture 1 ... DNA in human chromosome 1 = 250 million bp (base pairs) 10 bp = 3.4 nm of DNA double helix. DNA molecule of human chromosome 1 ... 2 Notes for Lecture 1 Eukaryotic chromosome: Terminus, telomere Centromere Chromatid DNA packaging A chromosome contains a ... 1 Outline of lecture 1. (1) Chromosome and its structure (2) First Mendel's law (3) Second Mendel's law ...https://www.coursehero.com/file/5681296/lecture-1/
A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. - Oxford...
We performed a chromosome 10-specific association study with 1,412 gene-based single-nucleotide polymorphisms (SNPs), to ... Although significant associations with several biological candidate genes on chromosome 10 have been reported, these findings ... has been observed on chromosome 10, which implicates a wide region and at least one disease-susceptibility locus. ... Alleles, Alzheimer Disease, Chromosomes, Human, Pair 10, European Continental Ancestry Group, Genetic Linkage, Genetic Markers ...https://www.neuroscience.ox.ac.uk/publications/622692
Linkage of Genetic Markers on Human Chromosomes 20 and 12 to NIDDM in Caucasian Sib Pairs With a History of Diabetic...
Linkage of Genetic Markers on Human Chromosomes 20 and 12 to NIDDM in Caucasian Sib Pairs With a History of Diabetic ... Linkage of Genetic Markers on Human Chromosomes 20 and 12 to NIDDM in Caucasian Sib Pairs With a History of Diabetic ... Linkage of Genetic Markers on Human Chromosomes 20 and 12 to NIDDM in Caucasian Sib Pairs With a History of Diabetic ... Linkage of Genetic Markers on Human Chromosomes 20 and 12 to NIDDM in Caucasian Sib Pairs With a History of Diabetic ...http://diabetes.diabetesjournals.org/content/46/5/882
acute myelogenous leukemia without maturation fab m1 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
Chromosomes, Human, Pair 11 / genetics. Chromosomes, Human, Pair 5 / genetics. Chromosomes, Human, Pair 7 / genetics. Gene ... twenty ten [shown] Results per page: 5. 10. 20. 50. 100. 200. 500. [expand/collapse] show these sections expanded by default: ... MeSH-major] Chromosome Aberrations. Chromosomes, Human, Pair 12. Chromosomes, Human, Pair 7. Leukemia, Myeloid, Acute / ... MeSH-major] Chromosomes, Human, Pair 15. Chromosomes, Human, Pair 17. Leukemia, Myeloid, Acute / genetics. Leukemia, ...http://www.bmlsearch.com/?kwr=acute+myelogenous+leukemia+without+maturation+fab+m1+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
C10 - Wikipedia
... human), one of the 23 pairs of human chromosomes Bill C-10 (disambiguation), the official numbering for several Canadian bills ... Committee of Ten, Economic committee established in 2008 comprising 2 representatives each from Northern, Southern, Eastern, ... was a section of the South African Police responsible for assassinating opponents of Apartheid during the 1980s Chromosome 10 ( ... C10, C.X or C-10 may refer to: ... C-10), a United States Navy cruiser which operated in the ...https://en.wikipedia.org/wiki/C10
Computational and Statistical Genetics - Wikipedia
In humans, we have 23 pairs of chromosomes. Another example is maize which is also a diploid with 10 pairs of chromosomes. ... For diploid organisms such as humans and maize, each organism has two copies of a chromosome - one each from the two parents. ... However, with current technology, it is difficult to separate the two chromosomes within a pair and the assays produce the ... Variations in human genome have been long known to make us susceptible to many diseases. We are hurtling towards the era of ...https://en.wikipedia.org/wiki/Computational_and_Statistical_Genetics
Arachidonate 5-lipoxygenase - Wikipedia
The ALOX5 gene, which occupies 71.9 kilobase pairs (kb) on chromosome 10 (all other human lipoxygenases are clustered together ... Aberrant expression of LOX5 is seen in various types of human cancer tumors in vivo as well as in various types of human cancer ... Studies with cultured human cells have found that there are a large number of ALOX5 mRNA splice variants due to Alternative ... Human ALOX5 is a soluble, monomeric protein consisting of 673 amino acids with a molecular weight of ~78 kDa. Structurally, ...https://en.wikipedia.org/wiki/Arachidonate_5-lipoxygenase
A major gene affecting age-related hearing loss in C57BL/6J mice." by K R. Johnson, L C. Erway et al.
... selection was then used to produce congenic lines of C57BL/6J that contain different CAST-derived segments of chromosome 10. ... Both qualitative and quantitative linkage analyses gave the same genetic map position for the AHL gene (Ahl on chromosome 10, ... Animal, Auditory-Threshold: ph, Chromosome-Mapping, Chromosomes-Human-Pair-10, Cochlea: pa, Evoked-Potentials-Auditory-Brain- ... Both qualitative and quantitative linkage analyses gave the same genetic map position for the AHL gene (Ahl on chromosome 10, ...https://mouseion.jax.org/stfb1990_1999/1017/
humans, too, have their share of oddly paired chromosomes. experts estimate that about 10 to 30 percent of human eggs or fusion ... METHODS: Ten patients were studied with chronic fat malabsorption, calcium oxalate stones, and hyperoxaluria thought to be ... Human sIgA was found to facilitate biofilm formation by normal human gut flora and by Escherichia coli on cultured human ... To prove that the model correlates with human infections, Rosen led an analysis of human urine samples sent from a clinic at ...http://members.tripod.com/mueller_ranges/links/compendium/biofilms.html
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2. - Radcliffe...
In Stage 2, we selected the lead genetic variants at loci with association P,5×10(-6) and performed in silico association ... 10(-9)). The associated locus is in an intergenic region between TCF7L2 and HABP2. In a further analysis in an independent ... Chromosomes, Human, Pair 10, Computer Simulation, DNA, Intergenic, European Continental Ancestry Group, Female, Genetic ... Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2. ...https://www.rdm.ox.ac.uk/publications/584198
Gene Report for G00001955 - Genes2Cognition Neuroscience Research Programme
Human cortex PSD consensus. 748. L00000069. G2C. Homo sapiens. BAYES-COLLINS-HUMAN-PSD-FULL. Human cortex biopsy PSD full list ... OTTHUMG00000071527 (Vega human gene). Gene. ENSG00000105402 (Ensembl human gene). 8775 (Entrez Gene). 1108 (G2Cdb plasticity & ... Human clathrin. Human orthologues of mouse clathrin coated vesicle genes adapted from Collins et al (2006). 150. ... Human PSD. Human orthologues of mouse PSD adapted from Collins et al (2006). 1080. ...http://www.genes2cognition.org/db/Gene/G00001955
Switch to Europe/Worldwide website
Spanning nearly 135 million base pairs and encoding nearly 1,200 genes, chromosome 10 makes up approximately 4.5% of the human ... The gene that encodes Tect3 contains approximately 31,560 bases and maps to human chromosome 10q24.1. ... Human 721_B; WB Suggested Anti-TCTN3 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:312500. Positive Control: 721_B cell ... Sample Tissue:Human Fetal Heart. Antibody Dilution: 1.0ug/ml.; TCTN3 antibody - middle region (ARP44677_P050) in Hum. Fetal ...https://www.acris-antibodies.com/target/tectonic-3-antibody.htm?ab_applications=ICC%2FIF
2008: Year in Review | NSF - National Science Foundation
Ancient 'Nutcracker Man' Challenges Ideas on Evolution of Human Diet. Tiny marks on the teeth of an ancient human ancestor, ... At 2.5 billion base pairs covering 10 chromosomes, the corn genome's size is comparable to that of the human and is one of the ... reptilian and mammalian lineages that may hold clues to speciation during evolution and also to human disease prevention. ... conformable monitor to detect electrical signals traveling across the undulating surface of the human brain.. August 6, 2008. ...https://www.nsf.gov/discoveries/disc_summ.jsp?cntn_id=114372&org=BCS
Wellcome Sanger Institute - Wikipedia
The Institute was engaged in collaborations to sequence 8 of the 23 human pairs of chromosomes (1, 6, 9, 10, 13, 20, 22, and X ... Logan, D. W.; Sandal, M.; Gardner, P. P.; Manske, M.; Bateman, A. (2010). "Ten Simple Rules for Editing Wikipedia". PLOS ... "International Human Genome Sequencing Consortium Announces "Working Draft" of Human Genome". National Human Genome Research ... Human Genome Sequencing Consortium (2004). "Finishing the euchromatic sequence of the human genome". Nature. 431 (7011): 931- ...https://en.wikipedia.org/wiki/Wellcome_Sanger_Institute
Eukaryotic chromosome fine structure - Wikipedia
The repeats are normally a few hundred base pairs in length. These sequences constitute about 13% of the human genome with the ... The repeats are normally several thousand base pairs in length. These sequences constitute about 21% of the human genome. Both ... Eukaryotic chromosome fine structure refers to the structure of sequences for eukaryotic chromosomes. Some fine sequences are ... They may also be involved in fillers for increasing chromosome size to some minimum threshold level necessary for chromosome ...https://en.wikipedia.org/wiki/Eukaryotic_chromosome_fine_structure
Functional Characterization of Cyclooxygenase-2 Polymorphisms | Journal of Pharmacology and Experimental Therapeutics
The human COX-2 gene, mapped to chromosome 1q25.2-q25.3, is about 8.3 kilobase pairs in size and contains 10 exons (Kosaka et ... Ten nanograms of COX-2 standard, 30 μg of total protein/lane. B, high-pressure liquid chromatography analyses of arachidonic ... The human COX-1 gene, mapped to chromosome 9q32-q33.3, is about 22 kilobase pairs in size and contains 11 exons (Yokoyama and ... Sequencing of the Human COX-2 Gene.. The COX-2 gene was sequenced in 72 individuals (144 chromosomes), and 20 differences from ...http://jpet.aspetjournals.org/content/299/2/468.long
Jane Grimwood - Wikipedia
... of the human genome." They discovered that chromosome 19 has the highest gene density of any human chromosome, and were able to ... She and her team worked on sequencing and analyzing chromosomes 5, 16, and 19 -- "320 million base pairs . . . comprising more ... "GNN - Two More Human Chromosomes Are Complete". www.genomenewsnetwork.org. Retrieved 2017-03-02. Grimwood, Jane; Gordon, Laurie ... Grimwood was an important part of the Human Genome Project effort, working from the Stanford Human Genome Center. Grimwood ...https://en.wikipedia.org/wiki/Jane_Grimwood
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein...
The function of Twinkle is inferred to be critical for lifetime maintenance of human mtDNA integrity. ... Amino Acid Sequence, Cell Compartmentation, Chromosomes, Human, Pair 10, DNA Helicases, DNA Primase, DNA, Mitochondrial, Female ... Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein ... Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein ...https://www.neuroscience.ox.ac.uk/publications/242344
Determining significance of pairwise co-occurrences of events in bursty sequences | BMC Bioinformatics | Full Text
Some pairs are found significant in only one chromosome sequence, e.g., (HMG-IY, ESR1) in chromosome 4, and some pairs in all ... International Human Genome Sequencing Consortium: Initial sequencing and analysis of the human genome. Nature 2001, 409(6822): ... Table 4 shows the number of FL- and FL(r)-specific pairs for each chromosome, and the number of pairs that are found ... while some pairs may only show that tendency in specific genome regions.. Table 5 Significant pairs in chromosome data ...https://bmcbioinformatics.biomedcentral.com/articles/10.1186/1471-2105-9-336
ANKRD26 - Wikipedia
On the positive strand of human chromosome ten, located next to the 5' end of ANKRD26 is MASTL, microtubule associated serine/ ... It has 6816 base pairs in the reference sequence mRNA transcript. LOC100289548 (PUTAETIVE UNCHARACTERIZED PROTEIN C10ORF52-LIKE ... 2004). "The DNA sequence and comparative analysis of human chromosome 10". Nature. 429 (6990): 375-81. doi:10.1038/nature02462 ... In humans ANKRD26 was seen to be most highly expressed in the ear, lymph, esophagus, parathyroid, and placenta, as well as, ...https://en.wikipedia.org/wiki/ANKRD26
Download our free solidary book to support research on VHL disease