*  ZFIN Publication: Risinger et al., 1998
Chromosomes/genetics*; Chromosomes, Human, Pair 14/genetics; Chromosomes, Human, Pair 20/genetics; Cloning, Molecular; ... The two zebrafish snap25 loci are located in paralogous linkage groups that seem to correspond to human chromosome 20, which ... and human chromosome 14. Because no additional Snap25 homologue has been reported for any mammal or chicken, snap25.2 may have ... Amino Acid Sequence; Animals; Base Sequence; Chickens/genetics*; Chromosome Mapping (all 27) Amino Acid Sequence; Animals; Base ...
  https://zfin.org/ZDB-PUB-981209-14
*  Chromosome 14 (human) - Wikipedia
Gilbert F (1999). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 14". Genet Test. 3 (4): 379-91. ... The following is a partial list of genes on human chromosome 5. For complete list, see the link in the infobox on the right. ... Kamnasaran D, Cox DW (2002). "Current status of human chromosome 14". J Med Genet. 39 (2): 81-90. doi:10.1136/jmg.39.2.81. PMC ... The following are some of the gene count estimates of human chromosome 14. Because researchers use different approaches to ...
  https://en.wikipedia.org/wiki/Chromosome_14_(human)
*  "Familial and sporadic Alzheimer's disease: neuropathology cannot exclu" by Carol F. Lippa, Ann M. Saunders et al.
... six AD patients with mutations of chromosome 21 (codon 717 of the beta-amyloid percursor protein gene), and 11 sporadic AD (SAD ... Chromosomes, Human, Pair 21; Gene Frequency; Humans; Linkage (Genetics); Middle Aged; Mutation; Neurites; Neurofibrillary ... six AD patients with mutations of chromosome 21 (codon 717 of the beta-amyloid percursor protein gene), and 11 sporadic AD (SAD ... Chromosomes, Human, Pair 14; ...
  https://escholarship.umassmed.edu/neuro_pp/300/
*  Chromosome 14 - Genetics Home Reference
Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 14, one copy inherited from ... Gilbert F. Disease genes and chromosomes: disease maps of the human genome. Chromosome 14. Genet Test. 1999;3(4):379-91. ... Ensembl Human Map View. *. Falk MJ, Curtis CA, Bass NE, Zinn AB, Schwartz S. Maternal uniparental disomy chromosome 14: case ... The DNA Sequence and Analysis of Human Chromosome 14. Nature. 2003 Feb 6;421(6923):601-7. (PDF) ...
  https://ghr.nlm.nih.gov/chromosome/14
*  DECLARATION of Emanuel Petricoin, Ph for Association For Molecular Pathology et al v. United States Patent and Trademark Office...
The human genome comprises about 3 billion nucleotides organized into 23 chromosome pairs. Each chromosome comprises DNA and ... The isolated sequences are no longer located on a human chromosome and therefore are not necessarily assembled in the native ... While a human body does transcribe a gene into mRNA, which is then translated into a protein, the human body does not isolate ... Genes and human genetic sequences are comprised of DNA. The term DNA is an acronym for a chemical compound which is also known ...
  https://docs.justia.com/cases/federal/district-courts/new_york/nysdce/1:2009cv04515/345544/203
*  ZIP9 - Wikipedia
... in the SLC39A9 gene can occur due to genetic deletion of the q24.1-24.3 band of base pairs within the human chromosome 14. This ... ZIP9 influxes zinc ions into the cytosol and its gene is expressed almost in every tissue of human body. The sub-cellular ... Role of human ZIP9 in testosterone-induced prostate and breast cancer cell apoptosis". Endocrinology. 155 (11): 4250-65. doi: ... A study in 2014, elucidated the intermediary role of ZIP9 in causing human breast and prostate cancer, as it induced the ...
  https://en.wikipedia.org/wiki/ZIP9
*  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
*  Expression of the bcl-2 oncogene product and chromosomal translocation t(14;18) in Hodgkin's disease. - Radcliffe Department of...
In a smaller number of cases this expression of bcl-2 could be explained by the presence of the translocation t(14;18). ... The reciprocal chromosomal translocation t(14;18), leading to overexpression of this oncogene, can be found in the majority of ... 14;18) translocation. We were particularly interested to determine whether nodular paragranuloma (lymphocyte-predominant, ... Chromosomes, Human, Pair 18, Gene Expression, Hodgkin Disease, Humans, Immunoenzyme Techniques, Polymerase Chain Reaction, ...
  https://www.rdm.ox.ac.uk/publications/486737
*  Radiation hybrid mapping - Wikipedia
If two given DNA markers are far apart on the initial chromosome, then it is likely that they will appear in distinct fragments ... First of all, desired chromosomes are broken into several segments with X-rays, after which they are implanted in rodent cells ... Radiation hybrid mapping (also known as RH mapping) is a technique for mapping mammalian chromosomes. Radiation hybrid mapping ... which clone the chromosomes. Then these clones are analyzed for the presence of certain DNA markers. ...
  https://en.wikipedia.org/wiki/Radiation_hybrid_mapping
*  Monosomy 14 - Wikipedia
Monosomy is a form of aneuploidy with the presence of only one chromosome (instead of the typical two in humans) from a pair, ... CantĂș ES, Thomas IT, Frias JL (September 1989). "Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child ... which affects chromosome 14. Fetuses with monosomy 14 are not viable. Only mosaic cases exist and these usually present with ... ISBN 0-683-03445-6. McConnell V, Derham R, McManus D, Morrison PJ (July 2004). "Mosaic monosomy 14: clinical features and ...
  https://en.wikipedia.org/wiki/Monosomy_14
*  Karyotype - Wikipedia
Humans have one pair fewer chromosomes than the great apes. Human chromosome 2 appears to have resulted from the fusion of two ... The normal human karyotypes contain 22 pairs of autosomal chromosomes and one pair of sex chromosomes (allosomes). Normal ... Closer to home, the great apes have 24x2 chromosomes whereas humans have 23x2. Human chromosome 2 was formed by a merger of ... The karyotype of humans includes only 46 chromosomes. Rather interestingly, the great apes have 48 chromosomes. Human ...
  https://en.wikipedia.org/wiki/Karyotype
*  Fragaria vesca - Wikipedia
All strawberry (Fragaria) species have a base haploid count of seven chromosomes; Fragaria vesca is diploid, having two pairs ... Evidence from archaeological excavations suggests that Fragaria vesca has been consumed by humans since the Stone Age. The ... of these chromosomes for a total of 14. ... 14-15 weeks in climate-controlled greenhouses) ease of ...
  https://en.wikipedia.org/wiki/Fragaria_vesca
*  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
*  Active RNA polymerases: mobile or immobile molecular machines? - Oxford Neuroscience
We test this using chromosome conformation capture and human genes switched on rapidly and synchronously by tumour necrosis ... Base Pairing, Cells, Cultured, Chromosomes, Human, Pair 14, DNA-Directed RNA Polymerases, Enzyme Activation, Humans, In Situ ... We test this using chromosome conformation capture and human genes switched on rapidly and synchronously by tumour necrosis ...
  https://www.neuroscience.ox.ac.uk/publications/65905
*  PAX1 - Wikipedia
... a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ ... Paired box protein Pax-1 is a protein that in humans is encoded by the PAX1 gene. This gene is a member of the paired box (PAX ... 1989). "Conservation of the paired domain in metazoans and its structure in three isolated human genes". EMBO J. 8 (4): 1183-90 ... 2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. 414 (6866): 865-71. doi:10.1038/414865a. ...
  https://en.wikipedia.org/wiki/PAX1
*  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 ... 1992) demonstrated that genes for 12-lipoxygenase and 15-lipoxygenase are located on human chromosome 17, whereas the most ... Consequently, human ALOX15 is now referred to as arachidonate-15-lipoxygenase-1, 15-lipoxygenase-1, 15-LOX-1, 15-LO-1, human 12 ... The distribution of Alox15 in sub-human primates and, in particular, rodents differs significantly from that of human ALOX15; ...
  https://en.wikipedia.org/wiki/ALOX15
*  Publications | Max Planck Institute for Biophysical Chemistry
Poleev, A.; Fickenscher, H.; Mundlos, S.; Winterpacht, A.; Zabel, B.; Fidler, A.; Gruss, P.; Plachov, D.: PAX8, a human paired ... is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH). Genomics 14 (3), pp. 740 - 744 (1992) ... Jost, M.; Thiel, C.; Weber, K.; Gerke, V.: Mapping of 3 unique CA-2+-binding sites in human annexin-II. European Journal of ... Schnittger, S.; Rao, V. V. N. G.; Deutsch, U.; Gruss, P.; Balling, R.; Hansmann, I.: Pax1, a member of the paired box- ...
  https://www.mpibpc.mpg.de/publications?year=1992
*  Transmembrane protein 251 - Wikipedia
The TMEM251 gene is located on human chromosome 14, at 14q32.12, on the plus strand. The gene size is 1,277 base pairs. It ... The promoter region starts 500 base pairs upstream of the 5' UTR of TMEM251 mRNA transcript and contains part of this 5' UTR. ... "Q8N6I4 - TM251_HUMAN". UniProt. UnitProt. Retrieved 9 May 2015. "Human BLAT Search". UCSC Genome Browser. UCSC. Retrieved 9 May ... EST Profile data shows the tissue expression of TMEM251 in humans. TMEM251 has no paralogs in humans. It does have orthologs ...
  https://en.wikipedia.org/wiki/Transmembrane_protein_251
*  Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways...
Because BMP4 interacts with HH signaling genes in animals, we evaluated gene expression in human embryos and demonstrate ... of low-penetrant variants in BMP4 and HH signaling partners is suggestive of an interaction between the two pathways in humans. ... Using in situ hybridization in human embryos, we demonstrate expression of BMP4 in optic vesicle, developing retina and lens, ... Bone Morphogenetic Protein 4, Bone Morphogenetic Proteins, Chromosome Aberrations, Chromosomes, Human, Pair 14, Cohort Studies ...
  https://www.ndcn.ox.ac.uk/publications/186522
*  Stock Options Profits from Low Cost Gene Sequencing
There is a race going on to lower the cost human gene sequencing to a level of a comprehensive battery of blood tests. The ... called chromosomes. These strands are paired, connected side to side along their lengths. Humans have 23 pairs of chromosomes. ... These strands are paired, connected side to side along their lengths. Humans have 23 pairs of chromosomes. www.Options-Trading- ... The human genome is the sum total of all human genes.Human genes are present on long strands of DNA (complex molecules) called ...
  https://www.slideshare.net/InvestingTips/stock-options-profits-from-low-cost-gene-sequencing
*  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
*  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, ... August 2010). "Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndrome". Human Mutation. 31 (8): 966-74. ... Mikami T, Mizumoto S, Kago N, Kitagawa H, Sugahara K (September 2003). "Specificities of three distinct human chondroitin/ ...
  https://en.wikipedia.org/wiki/CHST14
*  FAM71F2 - Wikipedia
The gene paralog FAM71F1 and the gene LINC01000 directly neighbor FAM71F2 on chromosome 7. The gene spans 30,627 base pairs and ... FAM71F2 gene is located on chromosome 7 in humans (7q32.1), starting at 128,671,636 and ending at 128,702,262 on the positive ... The time of divergence between eight orthologs from the human FAM71F2 is shown in Figure 5. It is not found in birds or in ... Isoform a is the longest of the mRNA transcripts and spans 5,775 base pairs that translates into a 309 amino acids sequence. It ...
  https://en.wikipedia.org/wiki/FAM71F2
*  CCDC47 - Wikipedia
The CCDC47 gene itself is located on the minus strand of human chromosome 17 and contains 13 exon splice sites and 14 distinct ... In regards to the mRNA, translation begins at base pair 337 and ends at 1728. There is a strong stem loop located in the 5' UTR ... Coiled-coil domain 47 (CCDC47) is a gene located on human chromosome 17, specifically locus 17q23.3 which encodes for the ... Percent identity of human CCDC47 to a specific ortholog declines with increasing years of divergence, as expected. Homologous ...
  https://en.wikipedia.org/wiki/CCDC47