*  Chromosome 16 - Wikipedia
Gilbert F (1999). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 16". Genet Test. 3 (2): 243-54. ... Band length in this diagram is proportional to base-pair length. This type of ideogram is generally used in genome browsers (e. ... G-bands of human chromosome 16 in resolution 850 bphs[18] Chr. Arm[19] Band[20] ISCN. start[21] ISCN. stop[21] Basepair. start ... Wikimedia Commons has media related to Human chromosome 16.. *. National Institutes of Health. "Chromosome 16". Genetics Home ...
  https://en.wikipedia.org/wiki/Chromosome_16
*  Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor...
Chromosomes, Human, Pair 11 / genetics. Chromosomes, Human, Pair 16 / genetics. Diuretics / therapeutic use. Drug ... Humans. Hydrochlorothiazide / therapeutic use. Hypertension / drug therapy*, ethnology, genetics*. Male. Middle Aged. ... 9249498 - Myogenic constriction of human coronary arterioles.. 23628418 - Effects of single hyperinflation using a sustained ... 0/Angiotensin II Type 1 Receptor Blockers; 0/Benzimidazoles; 0/Diuretics; 0/Epithelial Sodium Channels; 0/GPR83 protein, human ...
  http://www.biomedsearch.com/nih/Genomic-Association-Analysis-Identifies-Multiple/22566498.html
*  benign deep fibrous histiocytoma 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
MeSH-major] Chromosomes, Human, Pair 16. Chromosomes, Human, Pair 17. Histiocytoma, Benign Fibrous / genetics. Karyotyping / ... Humans Animals + Gender. And for: Male Female + Age. And for these age groups: Newborn: birth to 1 month. Infant: 1 to 23 ... Humans. Male. Radiotherapy, Adjuvant. Vimentin / metabolism. Young Adult. *[Email] Email this result item Email the results to ... Humans. Immunohistochemistry. Microscopy, Electron, Scanning. *MedlinePlus Health Information. consumer health - Breast Cancer. ...
  http://www.bmlsearch.com/?kwr=benign+deep+fibrous+histiocytoma+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  ZFIN Publication: Blake et al., 2000
Chromosome Inversion*. *Chromosomes, Human, Pair 16/genetics*. *Core Binding Factor alpha Subunits ... CBFB is associated with human leukemias through a chromosome 16 inversion and is essential for definitive hematopoiesis during ... This cbfb is highly homologous to human and mouse CBFB/Cbfb genes at both the DNA and protein level. In biochemical analyses, ... cbfbeta binds to human CBFalpha2 and enhances its DNA binding. During zebrafish development, cbfb is expressed in the lateral ...
  http://zfin.org/ZDB-PUB-001221-16
*  acute myeloblastic leukaemia without maturation 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 15. Chromosomes, Human, Pair 17. Leukemia, Myeloid, Acute / genetics. Leukemia, ... MeSH-major] Chromosomes, Human, Pair 10 / genetics. Chromosomes, Human, Pair 17 / genetics. Leukemia, Myeloid, Acute / genetics ...
  http://www.bmlsearch.com/?kwr=acute+myeloblastic+leukaemia+without+maturation+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  Chromosome 16 (human) - Wikipedia
Gilbert F (1999). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 16". Genet Test. 3 (2): 243-54. ... The following is a partial list of genes on human chromosome 16. For complete list, see the link in the infobox on the right. ... The following are some of the gene count estimates of human chromosome 16. Because researchers use different approaches to ... 2004). "The sequence and analysis of duplication-rich human chromosome 16". Nature. 432 (7020): 988-94. doi:10.1038/nature03187 ...
  https://en.wikipedia.org/wiki/Chromosome_16_(human)
*  Find Research Outputs - University of North Carolina at Chapel Hill
Chromosomes, Human, Pair 16 2 Citations Changes in soluble transferrin receptor and hemoglobin concentrations inmalawianmothers ... Kuzawa, C. W., Adair, L. S., Borja, J. & McDade, T. W. Jan 2013 In : American Journal of Human Biology. 25, 1, p. 131-134 4 p. ... Associations of linear growth and relative weight gain during early life with adult health and human capital in countries of ... American Journal of Human Biology. 27, 1, p. 99-105 7 p.. Research output: Research - peer-review › Article ...
  https://uncch.pure.elsevier.com/en/publications/?showAdvanced=false&allConcepts=true&inferConcepts=true&publicationYear=2009&publicationYear=2010&publicationYear=2011&publicationYear=2012&publicationYear=2013&publicationYear=2014&publicationYear=2015&publicationYear=2016&publicationYear=2017&publicationYear=2018&author=c2c0095e-0bd2-44c2-b226-9a09e0ba55a4
*  Human chromosome 16, SEM - Stock Image C009/5639 - Science Photo Library
Humans have 23 pairs of chromosomes. This is chromosome 16, which carries between 850 and 1200 genes. Gene defects on this ... Each chromosome consists of two identical, parallel strands (chromatids, left and right), joined at an area called a centromere ... Chromosomes are a packaged form of the genetic material DNA (deoxyribonucleic acid), and form during cell replication. ... chromosome are related to diseases such as Crohn's disease and thalassaemia, and may also contribute to obesity. Magnification ...
  http://www.sciencephoto.com/media/158251/view
*  Autosomal dominant polycystic kidney disease: molecular analysis. - Radcliffe Department of Medicine
... a disease associated chromosome translocation was instrumental in its identification. Study of the PKD1 gene has been ... complicated because most of the gene lies in a genomic region reiterated elsewhere on the same chromosome. The duplicate area ... Base Sequence, Chromosome Mapping, Chromosomes, Human, Pair 16, Humans, Molecular Sequence Data, Polycystic Kidney, Autosomal ... a disease associated chromosome translocation was instrumental in its identification. Study of the PKD1 gene has been ...
  https://www.rdm.ox.ac.uk/publications/56750
*  Chromosome 16 - Genetics Home Reference
Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 16, one copy inherited from ... Gilbert F. Disease genes and chromosomes: disease maps of the human genome. Chromosome 16. Genet Test. 1999;3(2):243-54. ... The sequence and analysis of duplication-rich human chromosome 16. Nature. 2004 Dec 23;432(7020):988-94. (PDF) ... The sequence and analysis of duplication-rich human chromosome 16. Nature. 2004 Dec 23;432(7020):988-94. ...
  https://ghr.nlm.nih.gov/chromosome/16
*  A large deletion in the human alpha-globin cluster caused by a replication error is associated with an unexpectedly mild...
We have characterized a newly identified 16.6 kb deletion which removes a significant proportion of the human alpha-globin ... Adult, Cells, Cultured, Child, Chromatin, Chromosomes, Human, Pair 16, DNA Replication, Female, Gene Deletion, Gene Expression ... A large deletion in the human alpha-globin cluster caused by a replication error is associated with an unexpectedly mild ... A large deletion in the human alpha-globin cluster caused by a replication error is associated with an unexpectedly mild ...
  https://www.rdm.ox.ac.uk/publications/124787
*  "2: "The Mapping of Chromosome 16"" by Norman A. Doggett, Raymond L. Stallings et al.
Among the 23 pairs of human chromosomes, one pair, chromosome 16, is identified by fluorescence in-situ hybridization. ... Thousands of yellow fluorescent probes derived from the clone library have hybridized to both copies of chromosome 16. The high ... the evaluation of our chromosome-16-specific library of cloned fragments. ... Human chromosome 16 is the main focus of the mapping efforts at Los Alamos. The large photomicrograph on these opening pages ...
  https://digitalcommons.imsa.edu/bioinfo_genomics/3/
*  Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease--a contiguous gene syndrome. -...
... lie immediately adjacent to each other on chromosome 16p. Renal cysts are often found in TSC, but a specific renal phenotype, ... Adolescent, Adult, Aged, Base Sequence, Child, Child, Preschool, Chromosomes, Human, Pair 16, DNA Primers, Electrophoresis, Gel ... lie immediately adjacent to each other on chromosome 16p. Renal cysts are often found in TSC, but a specific renal phenotype, ... Pulsed-Field, Gene Deletion, Humans, Infant, Middle Aged, Molecular Sequence Data, Polycystic Kidney, Autosomal Dominant, ...
  https://www.rdm.ox.ac.uk/publications/58464
*  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 ... Chromosomes, Human, Pair 3, Eye Diseases, Female, Genetic Linkage, Growth Disorders, Humans, Kidney, Laurence-Moon Syndrome, ...
  https://www.rdm.ox.ac.uk/publications/826713
*  KIAA0895L - Wikipedia
Its genomic DNA consists of 8,379 base pairs. KIAA0895L is located between EXOC3L and E2F4 on the right, and NOL3 and HSF4 on ... Uncharacterized protein KIAA0895-like also known as LOC653319, is a protein that in humans is encoded by the KIAA0895L gene. ... The promoter for KIAA0895L is located on chromosome 16 and spans 67217367-67218383bp. KIAA0895L was first documented by the ... December 2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. ...
  https://en.wikipedia.org/wiki/KIAA0895L
*  Jane Grimwood - Wikipedia
"320 million base pairs . . . comprising more than 10% of the human genome." They discovered that chromosome 19 has the highest ... "GNN - Two More Human Chromosomes Are Complete". www.genomenewsnetwork.org. Retrieved 2017-03-02. Grimwood, Jane; Gordon, Laurie ... gene density of any human chromosome, and were able to link certain genes on the chromosome to genetic diseases including ... 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
*  Biotechnology Project Ideas
One such sequence used in human DNA fingerprinting is the Alu repeat (a 300 base pair repetitive sequence of DNA) on chromosome ... Not surprising as the Human Proteome Project has not received the kind of press that the Human Genome Project did. Nonetheless ... During evolutionary time, up to 1 million copies of the Alu repeat have become randomly inserted throughout the human genome. ...
  https://www.sciencebuddies.org/science-fair-projects/project-ideas/biotechnology?p=3
*  Human ARHGDIG, a GDP-dissociation inhibitor for Rho proteins: genomic structure, sequence, expression analysis, and mapping to...
Using FISH, we have mapped the gene to chromosome band 16p13.3. This band is rich in deletion mutants of genes involved in ... several human diseases, notably polycystic kidney disease, alpha-thalassemia, tuberous sclerosis, mental retardation, and ... Base Sequence Chromosome Mapping Chromosomes, Human, Pair 16/*genetics Cloning, Molecular GTP-Binding Proteins/*genetics Gene ... Human ARHGDIG, a GDP-dissociation inhibitor for Rho proteins: genomic structure, sequence, expression analysis, and mapping to ...
  https://www.rdm.ox.ac.uk/publications/483542
*  Regulation of human embryonic globin genes zeta 2 and epsilon in stably transformed mouse erythroleukemia cells. - Radcliffe...
Previous work has suggested that the promoter regions of the human embryonic zeta 2 and epsilon globin genes contain negative ... Adenine Phosphoribosyltransferase, Animals, Blotting, Southern, Cell Line, Transformed, Chromosomes, Human, Pair 16, DNA, ... Regulation of human embryonic globin genes zeta 2 and epsilon in stably transformed mouse erythroleukemia cells. ... Regulation of human embryonic globin genes zeta 2 and epsilon in stably transformed mouse erythroleukemia cells. ...
  https://www.rdm.ox.ac.uk/publications/32480
*  Opposite effects on facial morphology due to gene dosage sensitivity. - Oxford Big Data Institute
Chromosomes, Human, Pair 17, Chromosomes, Human, Pair 4, Chromosomes, Human, Pair 7, DNA Copy Number Variations, European ... Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 16, ... Humans, Imaging, Three-Dimensional, Male, Phenotype, Sequence ... Adolescent, Adult, African Continental Ancestry Group, Case-Control Studies, Child, Child, Preschool, Chromosome Disorders, ...
  https://www.bdi.ox.ac.uk/publications/541198
*  mitochondrial DNA - Everything2.com
... the vast majority of it is in chromosomes in the nucleus; but a small amount is in each mitochondrio... ... base pair. multiregional. Nuclear Detonation Sensors. chromosome. antigen. cell. genome. Human Genome Project. DNA. Carolina ... There are two places in a cell where DNA is stored: the vast majority of it is in chromosomes in the nucleus; but a small ... Humans have 37 genes in their mitochondria, in a total of only 16 569 base pairs. Compare this to the genome in the chromosomes ...
  https://everything2.com/title/mitochondrial+DNA
*  DNA - New World Encyclopedia
For instance, the largest human chromosome, chromosome number 1, is 220 million base pairs long.[17] ... The set of chromosomes in a cell makes up its genome. The human genome has approximately 3 billion base pairs of DNA arranged ... The GC base pair is therefore stronger than the AT base pair. As a result, it is both the percentage of GC base pairs and the ... and in human cells the different chromosomes even occupy separate areas in the nucleus called "chromosome territories."[105] ...
  http://www.newworldencyclopedia.org/entry/DNA
*  TMEM8A - Wikipedia
The human gene TMEM8A is found on chromosome 16 at the band 16p13.3. The span of this gene on chromosome 16 spans from base ... pair 420,773 to 437,113 making this gene 16,340 base pairs in length. This gene is found on the minus strand of the chromosome ... There are two paralogs for TMEM8A found in humans, C9orf127 and TMEM8C. Both of these paralogs are found on Chromosome 9. The ... December 2004). "The sequence and analysis of duplication-rich human chromosome 16". Nature. 432 (7020): 988-94. doi:10.1038/ ...
  https://en.wikipedia.org/wiki/TMEM8A
*  Identification and analysis of over 2000 ribosomal protein pseudogenes in the human genome. - Semantic Scholar
Interestingly, on chromosome 16, an RPL26 processed pseudogene was found in the intron region of a functional RPS2 gene. The ... from random insertions with the numbers on each chromosome, consequently, proportional to its size. In contrast to RP genes, ... In total, we found 2090 processed pseudogenes and 16 duplications of RP genes. In relation to the matching parent protein, each ... we have comprehensively identified pseudogenes of these proteins in the human genome. Our assignments are available at http:// ...
  https://www.semanticscholar.org/paper/Identification-and-analysis-of-over-2000-ribosomal-Zhang-Harrison/a903046ce97c41a96a95e83da12202d47c41d447
*  PLOS Genetics: U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line
Each orange line represents a single mate-pair as a link between one end of a read and its mate-pair. Between the breakpoints ... The outer ring represents the chromosomes displaying tick marks every 100 bases. The green plot shows base-coverage for each ... U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line. Figure 6. Reads spanning ... This suggests an interchromosomal translocation between chromosomes 2 and 16 resulting in a loss of the genomic material ...
  http://journals.plos.org/plosgenetics/article/figure?id=10.1371/journal.pgen.1000832.g006