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*  Chromosome segregation control by Escherichia coli ObgE GTPase - Foti - 2007 - Molecular Microbiology - Wiley Online Library
Hirano, T. (2005) SMC proteins and chromosome mechanics: from bacteria to humans. Philos Trans R Soc Lond B Biol Sci 360: 507- ... Han, J.S., Kang, S., Lee, H., Kim, H.K., and Hwang, D.S. (2003) Sequential binding of SeqA to paired hemi-methylated GATC ... The defects in chromosome partitioning were accompanied by changes in chromosome organization at oriC and ter, visualized by ... Studies of chromosome organization in bacterial cells show that the chromosome is an exquisitely organized and dynamic ...
  http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2958.2007.05811.x/full
*  Merotelic kinetochore orientation versus chromosome mono-orientation in the origin of lagging chromosomes in human primary...
... that in untreated human primary fibroblasts the frequency of anaphase lagging chromosomes for all the 23 chromosome pairs was ... Merotelic kinetochore orientation versus chromosome mono-orientation in the origin of lagging chromosomes in human primary ... Merotelic kinetochore orientation versus chromosome mono-orientation in the origin of lagging chromosomes in human primary ... Merotelic kinetochore orientation versus chromosome mono-orientation in the origin of lagging chromosomes in human primary ...
  http://jcs.biologists.org/content/115/3/507
*  The region 3′ to Xist mediates X chromosome counting and H3 Lys‐4 dimethylation within the Xist gene | The EMBO Journal
X chromosome inactivation (XCI), which occurs only in female (XX) and not in male (XY) embryos, ensures dosage compensation of ... The location of the primer pairs is represented on the small map below the graph. A 5 kb region around the DXPas34 locus, which ... Interestingly, comparative sequence analysis has identified a 2 kb region of mouse/human conservation (80610-82632 of Genbank ... A counting process senses the X chromosome/autosome ratio and ensures that X chromosome inactivation (XCI) initiates in the ...
  http://emboj.embopress.org/content/23/3/594
*  Errors in chromosome segregation during oogenesis and early embryogenesis - WRAP: Warwick Research Archive Portal
Errors in chromosome segregation occurring during human oogenesis and early embryogenesis are very common. Meiotic chromosome ... The crucial events, including meiotic chromosome pairing and recombination, take place from around 11 weeks until birth. ... New insights into human nondisjunction of chromosome 21 in oocytes. PLoS Genet 2008;4(3):e1000033.. 10. Jones KT. Meiosis in ... Munné S, Cohen J. Chromosome abnormalities in human embryos. Hum Reprod Update 1998a;4(6):842-55.. 42. Munné S, Lee A, ...
  http://wrap.warwick.ac.uk/3796/
*  Linkage of Genetic Markers on Human Chromosomes 20 and 12 to NIDDM in Caucasian Sib Pairs With a History of Diabetic...
Evidence for linkage to NIDDM was found with polymorphic loci that map to the long arms of human chromosomes 20 and 12 in ... 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
*  Chromosome 20 - Wikipedia
G-bands of human chromosome 20 in resolution 850 bphs[19] Chr. Arm[20] Band[21] ISCN. start[22] ISCN. stop[22] Basepair. start ... Band length in this diagram is proportional to base-pair length. This type of ideogram is generally used in genome browsers (e. ... Wikimedia Commons has media related to Human chromosome 20.. *. National Institutes of Health. "Chromosome 20". Genetics Home ... "Human chromosome 20: entries, gene names and cross-references to MIM". UniProt. 2018-02-28. Retrieved 2018-03-16.. ...
  https://en.wikipedia.org/wiki/Chromosome_20
*  De novo deletion of chromosome 20q13.33 in a patient with tracheo-esophageal fistula, cardiac defects and genitourinary...
Chromosome Deletion*. Chromosomes, Human, Pair 20 / genetics*. Genitalia, Male / abnormalities*. Heart Defects, Congenital / ... Humans. Infant, Newborn. Male. Monomeric GTP-Binding Proteins / genetics*. Tracheoesophageal Fistula / genetics*, pathology. ... Human small G proteins, ObgH1, and ObgH2, participate in the maintenance of mitochondria and nucleolar architecturesGenes Cells ... One patient had a submicroscopic de novo deletion of chromosome 20q13.33, part of which did not overlap known regions of copy- ...
  http://www.biomedsearch.com/nih/De-novo-deletion-chromosome-20q1333/21608104.html
*  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
*  "Change-point analysis of paired allele-specific copy number variation " by Yinglei Lai
For a cancer study, it is common to collect data for paired normal and tumor samples. Then, two types of paired data can be ... Chromosomes, Human, Pair 20--genetics; Chromosomes, Human, Pair 21--genetics; DNA, Neoplasm; Neoplasms--genetics; Polymorphism ... For a cancer study, it is common to collect data for paired normal and tumor samples. Then, two types of paired data can be ... Lai, Y. (2012). Change-point analysis of paired allele-specific copy number variation data. Journal of Computational Biology, ...
  https://hsrc.himmelfarb.gwu.edu/biostatscenter_facpubs/36/
*  Chromosome 20 (human) - Wikipedia
The following is a partial list of genes on human chromosome 20. For complete list, see the link in the infobox on the right. ... The following are some of the gene count estimates of human chromosome 20. Because researchers use different approaches to ... Gilbert F (1997). "Disease genes and chromosomes: disease maps of the human genome". Genet Test. 1 (3): 225-229. doi:10.1089/ ... 2001). "The DNA sequence and comparative analysis of human chromosome 20". Nature. 414 (6866): 865-871. doi:10.1038/414865a. ...
  https://en.wikipedia.org/wiki/Chromosome_20_(human)
*  Nucleic Acids | Encyclopedia.com
... in humans and most organisms, is the genetic material and represents a collection of instructions (genes) for making the ... For example, humans have twenty-three pairs of chromosomes in the nucleus of each somatic cell . Within the nucleus, the DNA ... Within the approximately 3.2 × 109 base pairs (3.2 Gbps) in human DNA, the Human Genome Project has determined that there are a ... T base pair; while a G-C base pair contains three hydrogen bonds. These interactions possess a specificity that is pivotal to ...
  https://www.encyclopedia.com/science-and-technology/biology-and-genetics/genetics-and-genetic-engineering/nucleic-acids
*  Born Different: What Causes Asperger's Syndrome? | Encyclopedia.com
In human beings genes are arranged into twenty-three pairs of chromosomes. Each chromosome is made up of thousands of genes. ... One theory involves the chromosomes that determine sex. They are called the X and Y chromosomes. Girls have two X chromosomes. ... This means that genes that cause defects can be on the X chromosome. (Genes for traits are very rare on Y chromosomes.) A girl ... A boy, because he has only one X chromosome, would be likely to have the disorder because his Y chromosome cannot protect him. ...
  https://www.encyclopedia.com/science/medical-magazines/born-different-what-causes-aspergers-syndrome
*  heredity facts, information, pictures | Encyclopedia.com articles about heredity
... chromosomes exist in linear and duplicate form. For example, humans have twenty-three pairs of chromosomes, where inheritance ... SEX CHROMOSOMES:. Chromosomes that determine gender. Human females have two X chromosomes (XX), and males have an X and a Y (XY ... The remaining chromosome, the sex chromosome, is either an X or a Y. Females have two Xs (XX), and males have one of each (XY ... He also discovered a unique pair of chromosomes called the sex chromosomes, which determine the sex of offspring. From his ...
  https://www.encyclopedia.com/science-and-technology/biology-and-genetics/genetics-and-genetic-engineering/heredity
*  Genomic Medicine - UC Davis
Cloutier, M., Gauthier, C., Fortin, J. S., Genève, L., Kim, K., Gruenheid, S., Kim, J. & Thibodeau, J., 2015, In : Human ... American Journal of Human Genetics. 96, 3, p. 432-439 8 p.. Research output: Contribution to journal › Article ...
  https://ucdavis.pure.elsevier.com/en/organisations/genomic-medicine
*  OPUS at UTS: Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. - Open...
Chromosomes, Human, Pair 5. en_US. dc.subject.mesh. Chromosomes, Human, Pair 11. en_US. ... Chromosomes, Human, Pair 11. en_US. dc.subject.mesh. Chromosomes, Human, Pair 20. en_US. ...
  https://opus.lib.uts.edu.au/handle/10453/113594
*  Photograph of ethidium bromide stained 3′RACE product | Open-i
Chromosomes, Human, Pair 20*. *Corneal Dystrophies, Hereditary/genetics*. *Eye Proteins/genetics*/metabolism ... 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 • ... Mentions: To identify different mRNA classes transcribed from the VSX1 gene, a 3′RACE experiment was performed on human adult ...
  https://openi.nlm.nih.gov/detailedresult.php?img=PMC2267740_mv-v14-71-f2&req=4
*  Array-CGH chromosome 16 profile. A) Genomic imbalances | Open-i
A) Genomic imbalances on patient BV chromosome 16, with magnification of the deleted region and B) the contained genes. ... Chromosome Disorders/genetics*/pathology/physiopathology. *Chromosomes, Human, Pair 20/genetics*. *Ring Chromosomes* ... Figure 4: Array-CGH chromosome 16 profile. A) Genomic imbalances on patient BV chromosome 16, with magnification of the deleted ... Figure 4: Array-CGH chromosome 16 profile. A) Genomic imbalances on patient BV chromosome 16, with magnification of the deleted ...
  https://openi.nlm.nih.gov/detailedresult.php?img=PMC2967536_1471-2350-11-146-4&req=4
*  How Sex is Determined by Genetics
Two X chromosomes produce a female, and one X and one Y chromosome produce a male. When a baby is conceived, it receives one X ... chromosome from the mother and either an X or a Y chromosome from the father. ... Gender or sex is determined in humans genetically by one pair of chromosomes out of a total of 23 pairs. ... The human organism contains threadlike, gene-bearing chromosomes, twenty three pairs of them. These chromosomes contain the ...
  https://www.brighthub.com/science/genetics/articles/7083.aspx
*  Meiosis | edHelper.com
Humans have forty-six chromosomes, arranged in twenty-three pairs. But human egg and sperm cells only have twenty-three ... For example, most cells of fruit flies have eight chromosomes, arranged as four similar pairs. But the egg or sperm cells of a ... Cells formed through meiosis have only half the number of chromosomes or genetic material of the parent cell. ... chromosomes. How does this happen?. Paragraphs 4 to 9:. For the complete story with questions: click here for printable. Weekly ...
  https://www.edhelper.com/ReadingComprehension_54_49.html
*  Inbreeding and origin of races - creation.com
The information in twenty three chromosome pairs of a human is a sophisticated DNA program with an inheritance property. Even a ... evidence for a faster evolutionary rate of mtDNA lineages than Y chromosomes, American J. Human Genetics 72:1370-1388, 2003. ... Evidence for a faster evolutionary rate of mtDNA lineages than Y chromosomes, American J. Human Genetics 72:1370-1388, 2003. ... Quintana-Murci, L., Human variation chalked up to natural selection: study, PhysOrg.com, 4 February 2008. Return to text. ...
  https://creation.com/inbreeding-and-origin-of-races
*  Glossary of Terms
In humans, there are twenty-three pairs of chromosomes in the sex chromosomes, in this case, female. A few girls with Rett ... Autosome: any of the first twenty-two pairs of chromosomes; all chromosomes are autosomes, except for the sex chromosomes, X ... Human genome: the information content of one set of human chromosomes.. Hydrotherapy: water therapy, such as provided in a ... Sex chromosomes: those chromosomes that determine gender; the X and Y chromosomes. ...
  https://www.rettsyndrome.org/about-rett-syndrome/glossary-of-terms
*  Calico cat - Wikipedia
As with humans, female cats have paired sex chromosomes, XX, and male cats have XY sex chromosomes. The female cat, therefore, ... Such a combination of chromosomes could produce tortoiseshell or calico markings in the male, in the same way as XX chromosomes ... a male calico would have to have a rare condition where they have three sex chromosomes (two X chromosomes and one Y chromosome ... with one color linked to the maternal X chromosome and a second color linked to the paternal X chromosome. Because males only ...
  https://en.wikipedia.org/wiki/Calico_cat
*  hemophilia facts, information, pictures | Encyclopedia.com articles about hemophilia
All normal human cells contain twenty-three pairs of chromosomes. Half of the chromosomes come from the father, and half from ... One pair of chromosomes is the sex chromosomes. These two chromosomes determine sexual characteristics, along with other ... Two types of sex chromosomes exist: an X chromosome and a Y chromosome. Men have one X and one Y chromosome. Women have two X ... All humans have two chromosomes determining their gender: females have XX, males have XY. Because the trait is carried only on ...
  https://www.encyclopedia.com/medicine/diseases-and-conditions/pathology/hemophilia
*  Thale Cress, Arabidopsis thaliana - Flowers - NatureGate
It has a simple genome with only five pairs of chromosomes (e.g. a human has twenty-three pairs). This insignificant weed can ...
  http://www.luontoportti.com/suomi/en/kukkakasvit/thale-cress
*  Glossary - Fibrolamellar Cancer Foundation
Normal human cells contain twenty-three pairs of chromosomes. One of each pair is inherited separately from a person's father ... Chromosome. Part of a cell that contains genetic information. Except for sperm and eggs, all human cells contain 46 chromosomes ... Each human cell has about 80,000 genes, but most of these are not active in a given type of cell. ... This is usually the first testing of a treatment on humans after extensive laboratory work. Recruitment for Phase I trials are ...
  https://fibrofoundation.org/help-support/glossary/