*  Isolated trisomy 15: a clonal chromosome abnormality in bone marrow with doubtful hematologic significance.
... trisomy 15 (with or without -Y), who did not have any morphologic or clinical features of hematologic disease at initial ... Chromosome Deletion. Chromosomes, Human, Pair 15 / genetics*. Chromosomes, Human, Y / genetics. Female. Humans. In Situ ... a clonal chromosome abnormality in bone marrow with doubtful hematologic significance. ... Clonal trisomy 15 in isolation or in combination with -Y is an uncommon cytogenetic finding that does not seem to be associated ...
  http://www.biomedsearch.com/nih/Isolated-trisomy-15-clonal-chromosome/18285273.html
*  Assessment of hyperphagia in Prader-Willi syndrome.
Chromosome Mapping. Chromosomes, Human, Pair 15. Factor Analysis, Statistical. Female. Humans. Hyperphagia / epidemiology*. ... Vanderbilt Kennedy Center for Research on Human Development, 230 Appleton Place, Peabody Box 40, Vanderbilt University, ... Title: Obesity (Silver Spring, Md.) Volume: 15 ISSN: 1930-7381 ISO Abbreviation: Obesity (Silver Spring) Publication Date: 2007 ...
  http://www.biomedsearch.com/nih/Assessment-hyperphagia-in-Prader-Willi/17636101.html
*  Forest plots for risk variants in the three newly ident | Open-i
Chromosomes, Human, Pair 1. *Chromosomes, Human, Pair 15. *Chromosomes, Human, Pair 5 ... Health and Human Services • 8600 Rockville Pike,Bethesda,MD 20894 Privacy • Accessibility • Freedom of Information Act • ... Health and Human Services • 8600 Rockville Pike,Bethesda,MD 20894 Privacy • Accessibility • Freedom of Information Act • ... Open-i® and the Open i logo are service marks of U.S. Department of Health and Human Services. ...
  https://openi.nlm.nih.gov/detailedresult.php?img=PMC4127632_nihms609586f1&req=4
*  acute promyelocytic leukemia childhood 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
MeSH-major] Chromosomes, Human, Pair 4. Chromosomes, Human, Pair 5. Leukemia, Promyelocytic, Acute / genetics. Leukemia, ... Chromosomes, Human, Pair 17. Humans. Prognosis. Translocation, Genetic. *Genetic Alliance. consumer health - Acute ... Chromosomes, Human, Pair 8. Core Binding Factor Alpha 2 Subunit / genetics. Female. Humans. Infant. Kaplan-Meier Estimate. Male ... Chromosomes, Human, Pair 9. Cytogenetics. Humans. In Situ Hybridization, Fluorescence. Infant. Molecular Sequence Data. Reverse ...
  http://www.bmlsearch.com/?kwr=acute+promyelocytic+leukemia+childhood+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  FEV1 by CHRNA3 genotype (rs1051730) in the AAT Genetic | Open-i
Chromosomes, Human, Pair 15/genetics. *Female. *Humans. *Male. *Middle Aged. *Polymorphism, Single Nucleotide ... Health and Human Services • 8600 Rockville Pike,Bethesda,MD 20894 Privacy • Accessibility • Freedom of Information Act • ... Health and Human Services • 8600 Rockville Pike,Bethesda,MD 20894 Privacy • Accessibility • Freedom of Information Act • ... Open-i® and the Open i logo are service marks of U.S. Department of Health and Human Services. ...
  https://openi.nlm.nih.gov/detailedresult.php?img=PMC3306733_1465-9921-13-16-1&req=4
*  Chromosome 15 (human) - Wikipedia
Gilbert F (1999). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 15". Genet Test. 3 (3): 309-322 ... The human leukocyte antigen gene for β2-microglobulin is found at chromosome 15. The following are some of the gene count ... The following is a partial list of genes on human chromosome 15. For complete list, see the link in the infobox on the right. ... The program...recounts how one scientist determined how the deletion of a key sequence of DNA on human chromosome 15 could lead ...
  https://en.wikipedia.org/wiki/Chromosome_15_(human)
*  Angelman syndrome in Denmark. birth incidence, genetic findings, and age at diagnosis - Danish National Research Database
Chromosome Deletion; Chromosome Duplication; Chromosomes, Human, Pair 15; Denmark; Female; Humans; Incidence; Male Main ... Five patients had paternal uniparental disomy (pUPD) of chromosome 15, and four had a verified UBE3A mutation. Additional ... is a neurogenetic disorder caused by loss of expression of the maternal imprinted gene UBE3A on chromosome 15q11.2-q13. ...
  http://www.forskningsdatabasen.dk/en/catalog/244254215
*  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 ... MeSH-major] Chromosome Aberrations. Chromosomes, Human, Pair 12. Chromosomes, Human, Pair 7. Leukemia, Myeloid, Acute / ... MeSH-major] Chromosomes, Human, Pair 16 / genetics. Chromosomes, Human, Pair 22 / genetics. Leukemia, Myeloid, Acute / genetics ... MeSH-major] Chromosomes, Human, Pair 10 / genetics. Chromosomes, Human, Pair 17 / genetics. Leukemia, Myeloid, Acute / genetics ...
  http://www.bmlsearch.com/?kwr=acute+myelogenous+leukemia+without+maturation+fab+m1+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  Robertsonian translocation - Wikipedia
In humans, Robertsonian translocations generally occur in the five acrocentric chromosome pairs, namely 13, 14, 15, 21 and 22. ... or non-homologous chromosomes (i.e. two different chromosomes, not belonging to a homologous pair). A feature of chromosomes ... This type of translocation is cytologically visible, and can reduce chromosome number (from 23 to 22 pairs, in humans) if the ... In humans, when a Robertsonian translocation joins the long arm of chromosome 21 with the long arm of chromosomes 14 or 15, the ...
  https://en.wikipedia.org/wiki/Robertsonian_translocation
*  VNTR polymorphism in the hepatic lipase gene (LIPC). - Radcliffe Department of Medicine
Base Sequence, Chromosomes, Human, Pair 15, European Continental Ancestry Group, Humans, Lipase, Liver, Molecular Sequence Data ...
  https://www.rdm.ox.ac.uk/publications/165114
*  Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families. - Radcliffe Department of Medicine
Body Height, Body Mass Index, Chromosome Mapping, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 15, Chromosomes, Human ... Pair 16, Chromosomes, Human, Pair 3, Eye Diseases, Female, Genetic Linkage, Growth Disorders, Humans, Kidney, Laurence-Moon ...
  https://www.rdm.ox.ac.uk/publications/826713
*  Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes. - PubMed - NCBI
Chromosome Deletion*. *Chromosomes, Human, Pair 15. *Cohort Studies. *DNA Copy Number Variations ... identified from this study are shown in solid lines with base pair positions of BPs confirmed by aCGH. These base pair ... have maternal-only expression in mouse and humans, and this imprinted expression is limited to certain tissue-specific regions ...
  https://www.ncbi.nlm.nih.gov/pubmed/22045295
*  Longer leukocyte telomere length is associated with smaller hippocampal volume among non-demented APOE ε3/ε3 subjects
They consist of tandemly repeated non-coding short nucleotide sequences (TTAGGG in all vertebrates), in humans spanning over ... Telomeres are the outermost parts of linear chromosomes. ... the last 2 to 15 kilobase pairs of the chromosome. Due to the ...
  http://umu.diva-portal.org/smash/record.jsf?pid=diva2:516681
*  https://www.medicalnewstoday.com/articles/182287.php
All human genes come in pairs, except for those related to sex characteristics. One copy is from the father, called the ... In PWS, it is thought that the paternal genes on chromosome 15 are either missing or faulty. ... It remains unclear which genes are involved, but the abnormality is found on chromosome 15. ... People with PWS have seven genes on chromosome 15 that are deleted or unexpressed. ...
  https://www.medicalnewstoday.com/articles/182287.php
*  OCA2 - Wikipedia
... specifically from base pair 28,000,020 to base pair 28,344,457 on chromosome 15. OCA2 provides instructions for making the ... OCA2 encodes the human homologue of the mouse p (pink-eyed dilution) gene. The human OCA2 gene is located on the long arm (q) ... "Blue-eyed humans have a single, common ancestor". News. University of Copenhagen. 2008-01-30. Retrieved 2008-11-06. Eiberg H, ... A mutation in the HERC2 gene adjacent to OCA2, affecting OCA2's expression in the human iris, is found common to nearly all ...
  https://en.wikipedia.org/wiki/OCA2
*  CHST14 - Wikipedia
In humans, CHST14 is positioned on the long arm (q) of chromosome 15 at position 15.1, from base pair 40,470,961 to base pair ... Human CHST14 genome location and CHST14 gene details page in the UCSC Genome Browser. Otsuki T, Ota T, Nishikawa T, Hayashi K, ... Carbohydrate sulfotransferase 14 is an enzyme that in humans is encoded by the CHST14 gene. CHST14, a protein-coding gene, ... August 2010). "Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndrome". Human Mutation. 31 (8): 966-74. ...
  https://en.wikipedia.org/wiki/CHST14
*  SLC24A5 - Wikipedia
The SLC24A5 gene, in humans, is located on the long (q) arm of chromosome 15 on position 21.1, from base pair 46,200,461 to ... base pair 46,221,881. NCKX5 is 43 kDa protein that is partially localized to the trans-Golgi network in melanocytes. Removal of ... Jablonski NG, Chaplin G (July 2000). "The evolution of human skin coloration" (PDF). Journal of Human Evolution. 39 (1): 57-106 ... SLC24A5 appears to have played a key role in the evolution of light skin in humans of European ancestry. The gene's function in ...
  https://en.wikipedia.org/wiki/SLC24A5
*  Genetic polymorphisms in 15q25 and 19q13 loci, cotinine levels, and risk of lung cancer in EPIC. - Oxford Big Data Institute
Chromosomes, Human, Pair 19, Humans, Adenocarcinoma, Carcinoma, Large Cell, Carcinoma, Squamous Cell, Lung Neoplasms, Cotinine ... Chromosomes, Human, Pair 15, ...
  https://www.bdi.ox.ac.uk/publications/175151
*  Forex mall ru
In humans so far, five chromosome pairs (6, 7, 11, 14, 15) (Donlon et al. ... The R pair is ligated to restriction- digested cDNA used for preparing the tester and driver amplicons, the J pair is ligated ... and the N pair Page 291 286 Wallrapp forex pair correlation chart Gress is ligated to the difference product 1 for the second ... Fore locations of bglA and serA on the Escherichia coli K-12 chromosome. 1B). Dually related to the notion of proxy signatures ...
  http://retzepti.ru/forex-mall-ru.html
*  2002 Release: Draft Sequence of Mouse Genome - National Human Genome Research Institute (NHGRI)
The human genome is 3.1 billion base pairs spread out over 23 pairs of chromosomes (22 autosomes and the X and the Y sex ... The mouse genome is contained in 20 chromosome pairs and the current results suggest that it is about 2.7 billion base pairs in ... chromosomes).. Analysis of the genome assembly indicates roughly the same number of genes for the mouse as the human. So far ... For most human illnesses, from cancer to autoimmune disease, important insights have come from the study of mouse models. ...
  https://www.genome.gov/10002983/2002-release-draft-sequence-of-mouse-genome/
*  Mothers against decapentaplegic homolog 3 - Wikipedia
The human SMAD3 gene is located on chromosome 15 on the cytogenic band at 15q22.33. The gene is composed of 9 exons over ... 129,339 base pairs. It is one of several human homologues of a gene that was originally discovered in the fruit fly Drosophila ... Lu S, Lee J, Revelo M, Wang X, Lu S, Dong Z (October 2007). "Smad3 is overexpressed in advanced human prostate cancer and ... Lu S, Lee J, Revelo M, Wang X, Lu S, Dong Z (October 2007). "Smad3 is overexpressed in advanced human prostate cancer and ...
  https://en.wikipedia.org/wiki/Mothers_against_decapentaplegic_homolog_3
*  Genuises.. get in here | goTitans | a Tennessee Titans Fan Forum
28) 23 pairs of chromosomes in the human body. 31) 6 balls to an over in cricket, I'm not sure you would know that.... hope ... 28) 23 pairs of chromosomes in the human body. 31) 6 balls to an over in cricket, I'm not sure you would know that.... hope ... 15 P in a R T ?? 15 3 W on a T 3 wheels on a tricycle 16 100 C in a R ??. 17 11 P in a F (S) T 11 players in a football (soccer ... 14) 15 players on a rugby team. 19) 13 is unlucky for some. 20) 8 tentacles on an octopus. ...
  https://gotitans.com/threads/genuises-get-in-here.24631/
*  Epigenome-wide association study of total serum immunoglobulin E in children: a life course approach | SpringerLink
We further removed probes within 10 base pairs of a known SNP (UCSC Human Feb. 2009 [GRCh37/hg19] Assembly) with a minor allele ... At the probe level, low-quality probes with detection P values , 0.05, probes on sex chromosomes, SNP-associated probes, non- ... Total serum IgE levels showed a right-skewed distribution, with a mean ± SD of 146.4 ± 310.2 kU/L. Of the 217 children pairs ... Systematic identification of genetic influences on methylation across the human life course. Genome Biol. 2016;17:61.CrossRef ...
  https://link.springer.com/article/10.1186/s13148-018-0488-x
*  ALOX15 - Wikipedia
In humans, it is encoded by the ALOX15 gene located on chromosome 17p13.3. This 11 kilobase pair gene consists of 14 exons and ... The distribution of Alox15 in sub-human primates and, in particular, rodents differs significantly from that of human ALOX15; ... Both human ALOX15 and ALOX15B genes are located on chromosome 17; their product proteins have an amino acid sequence identity ... human ALOX15 forms ω-6 peroxy intermediates; in PUFAs that do have this third double bound, human ALOX15 makes the ω-6 peroxy ...
  https://en.wikipedia.org/wiki/ALOX15
*  Biology Unit 2 - Revision Cards in GCSE Biology
Chromosomes -The cell's nucleus contains chromosomes made from long DNA molecules.- Human body cells have 23 pairs of ... the characteristic controlled by a dominant allele develops if the allele is present on one or both chromosomes in a pair ... the characteristic controlled by a recessive allele develops only if the allele is present on both chromosomes in a pair. ... DNA, genes and chromosomes. DNA - carry the genetic code that determines the characteristics of a living thing. ...
  https://getrevising.co.uk/revision-cards/biology_unit_2_4