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*  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 ... 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, ... Voullaire L, Slater H, Williamson R, Wilton L. Chromosome analysis of blastomeres from human embryos by using comparative ...
http://wrap.warwick.ac.uk/3796/
*  The Inherited Diseases Group | Laboratóriumi Medicina Intézet
Human Reproduction 2011, 26 p. i253. Szakszon K, Berényi E, Jakab A, Bessenyei B, Balogh E, Köbling T, Szilvássy J,Knegt AC, ... Partial and total microdeletions of the AZF region on chromosome Y are detected by sequence tagged site (STS) analysis. ... Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia. Blood. 2000, 96: 2479- ... In cases with structural chromosome aberrations the identification of precise breakpoints and involved genes using microarray ...
http://lmi.med.unideb.hu/hu/15/04/17/inherited-diseases-group
*  CHAT | Cancer Genetics Web
CGH has been broadly applied to human and mouse malignancies. The use of metaphase chromosomes, however, limits detection of ... A human hybrid neuronal cell line A1 has been generated by somatic fusion between a human fetal cerebral neuron and a human ... A1 human hybrid neurons express messages for various cytokines and cytokine receptors which are similar to parental human CNS ... in human neuronal and non-neuronal cells. Total RNA from human spinal cord, placenta, cultured choriocarcinoma JEG-3 and ...
http://cancer-genetics.org/CHAT.htm
*  Common Terms in Genetics [M.Tevfik DORAK]
Y-chromosome: The male-specific sex chromosome in humans, which is much smaller than the X-chromosome. 95% of the Y-chromosome ... Acrocentric chromosome: A chromosome with its centromere towards one end. Human chromosomes 13,14,15,21,22 are acrocentric. ... Human chromosome 2 is a result of a centric fusion between two ancestral ape chromosomes (gorillas have 24 pairs of chromosomes ... See Flaquer, 2008; Evolution of Sex Chromosomes in Human Molecular Genetics and Map Viewer: Y-chromosome. ...
http://dorakmt.tripod.com/genetics/glossary.html
*  Silver stain - Wikipedia
Human chromosomes 13, 14, 15, 21, and 22 have NORs, which increase the silver stain activity by at least 50 times.[citation ... C. R. Merril, R. C. Switzer, M. L. Van Keuren: Trace polypeptides in cellular extracts and human body fluids detected by two- ... 13, 1992, S. 429-439. PMID 1425556. C. Lelong, M. Chevallet, S. Luche, T. Rabilloud: Silver staining of proteins in 2DE gels. ... 13 (4): 213-20. doi:10.1016/S1054-8807(03)00153-4. PMID 15210137. Barnini S, Dodi C, Campa M (2004). "Enhanced resolution of ...
https://en.wikipedia.org/wiki/Silver_stain
*  Definition of Robertsonian Translocation | Chegg.com
In case of humans, Robertsonian translocations occur between chromosome 14 and chromosomes 13, 15 or 21. ... In humans, chromosome number 13, 14, 15, 21 and 22 are acrocentric. Robertsonian translocations are also termed whole-arm ... Robertsonian translocation is a rare rearrangement which commonly occurs in acrocentric chromosomes. Acrocentric chromosomes ... The total chromosome number is reduced to 45 as two of the acrocentrics have fused to form one (new) chromosome. ...
https://www.chegg.com/homework-help/definitions/robertsonian-translocation-14
*  Satellite chromosome - Wikipedia
In humans, the chromosomes number 13, 14, 15, 21 and 22 are examples of SAT chromosomes. Rieger, R.; Michaelis, A.; Green, M.M ... A satellite chromosome or SAT chromosome has a chromosome segment that is separated from the main body of the chromosome by ... "Human acrocentric chromosomes with transcriptionally silent nucleolar organizer regions associate with nucleoli", The EMBO ... The satellite at metaphase appears to be attached to the rest of the body of chromosomes by a thread of chromatin. There are at ...
https://en.wikipedia.org/wiki/Satellite_chromosome
*  RNA28S1 Gene - GeneCards | RNA28S1 RNA Gene
45S ribosomal DNA (rDNA) arrays, or clusters, are present on human chromosomes 13, 14, 15, 21 and 22, designated RNR1 through ... The GeneCards human gene database index: 2 3 5 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z ... for each of the five human chromosomes to which these loci are localized. This gene is a representative copy of the 28S ... A Portrait of Ribosomal DNA Contacts with Hi-C Reveals 5S and 45S rDNA Anchoring Points in the Folded Human Genome. (PMID: ...
https://www.genecards.org/cgi-bin/carddisp.pl?gene=RNA28S1
*  RNR3 Gene - GeneCards | RNR3 RNA Gene
Human rDNA: evolutionary patterns within the genes and tandem arrays derived from multiple chromosomes. (PMID: 11350117) ... The GeneCards human gene database index: 2 3 5 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z ... 45S ribosomal DNA (rDNA) arrays, or clusters, are present on human chromosomes 13, 14, 15, 21 and 22, designated RNR1 through ... for each of the five human chromosomes to which these loci are localized. This gene represents the 45S ribosomal DNA cluster on ...
https://www.genecards.org/cgi-bin/carddisp.pl?gene=RNR3
*  Transcription enhancer identified near the human C mu immunoglobulin heavy chain gene is unavailable to the translocated c-myc...
We report here the identification of an enhancer element adjacent to the human C mu gene on normal chromosome 14, but this ... If similar enhancers exist in humans they may lead to increased transcription of the translocated c-myc gene and thus ... has been implicated in the aetiology of this human B-cell malignancy. Burkitt lymphoma cells possess specific chromosomal ... enhancer does not remain on the abnormal chromosome 14 to which the c-myc gene has been translocated in the Burkitt lymphoma ...
https://www.rdm.ox.ac.uk/publications/601894
*  Albinism: modern molecular diagnosis | British Journal of Ophthalmology
The P polypeptide is the product of the pink eye dilution locus (named from the mouse) and the counterpart on human chromosome ... Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are both due to a microdeletion on the human chromosome 15q11-13. The P ... 1992) Assignment of the human TYRP (brown) locus to chromosome region 9p23 by nonradioactive in situ hybridization. Genomics 13 ... 1994) A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12- ...
http://bjo.bmj.com/content/82/2/189.full
*  Different types of Genetic mutations | Genetic Education
A ring chromosome is generally observed in the long metacentric chromosomes. Telomeres of each chromosome have specific ... In humans 13, 14, 15, 21, 22 and Y chromosomes are acrocentric. When translocation between two acrocentric chromosomes occurs, ... Ring chromosome: when both ends of a chromosome are fused together, it creates a ring-like structure and so-called as ring ... Acrocentric chromosomes are small short chromosome with one long q-arm and a short or very smaller p-arm. ...
http://geneticeducation.co.in/different-types-of-genetic-mutations/
*  An Analysis Of The Phenomenon Of Codon Bias
Human chromosomes 13,14,15,21,22 are acrocentric.. This proposition can be illustrated with an analogy. This is done by making ... A more detailed example of this error is given in Table One of two copies of a replicated chromosome during mitosis. The ... Society Institute in Cavalli-Sforza et al concluded in their enormous effort to work out the genetic relationships among human ...
https://luvemyw.joeshammas.com/an-analysis-of-the-phenomenon-of-codon-bias-36151bs.html
*  Chromosome abnormality - Wikipedia
Known disorders in humans include Wolf-Hirschhorn syndrome, which is caused by partial deletion of the short arm of chromosome ... It can be from an atypical number of chromosomes or a structural abnormality in one or more chromosomes. Chromosome mutation ... An example of trisomy in humans is Down syndrome, which is a developmental disorder caused by an extra copy of chromosome 21; ... Acquired chromosome abnormalities[edit]. Most cancers, if not all, could cause chromosome abnormalities,[12] with either the ...
https://en.wikipedia.org/wiki/Chromosome_abnormalities
*  Understanding Genetics
Humans have 23 different chromosomes. They get a set of 23 from mom and a set of 23 from dad for a total of 46. The chromosomes ... In the other 5% of cases, the extra chromosome gets stuck to another chromosome. So, for example, chromosome 14 and chromosome ... To understand how chromosomes can get stuck together, we need to focus a bit more on a chromosome. A chromosome consists of two ... Chromosome 21 is one of these better tolerated chromosomes. Many times having a third copy of chromosome 21 leads to ...
http://genetics.thetech.org/ask-a-geneticist/inherited-down-syndrome
*  User:Z3218657 - CellBiology
In humans, Chromosomes 13, 14, 15, 21, 22 can be found. 2. Identify and add a link to your page of a recent cell biology ... 1. Which chromosomes contribute to the nucleolus? The Nucleolus contains nucleolar organizers which are parts of chromosomes ... Chloroform is a suspected human carcinogen. Aggravation of Pre-existing Conditions: Persons with pre-existing skin disorders or ... Cytochrome C is encoded by the CYCS gene located on chromosome 7. ...
https://cellbiology.med.unsw.edu.au/cellbiology/index.php/User:Z3218657
*  SLC15A1 - Solute carrier family 15 member 1 - Homo sapiens (Human) - SLC15A1 gene & protein
Human chromosome 13: entries, gene names and cross-references to MIM. *MIM cross-references. Online Mendelian Inheritance in ... List of human entries with polymorphisms or disease mutations. *Human polymorphisms and disease mutations. Index of human ... "Genetic variants of the human dipeptide transporter PEPT1.". Anderle P., Nielsen C.U., Pinsonneault J., Krog P.L., Brodin B., ... "Genetic variants of the human dipeptide transporter PEPT1.". Anderle P., Nielsen C.U., Pinsonneault J., Krog P.L., Brodin B., ...
https://www.uniprot.org/uniprot/P46059
*  Human Heredity: Principles and Issues / Edition 9 by Michael Cummings | 9780538498821 | Paperback | Barnes & Noble®
HUMAN HEREDITY presents the concepts of human genetics in clear, concise language and provides relevant examples that you can ... 4. Pedigree Analysis in Human Genetics. 5. The Inheritance of Complex Traits. 6. Cytogenetics: Karyotypes and Chromosome ... Human Heredity: Principles and Issues / Edition 9. HUMAN HEREDITY presents the concepts of human genetics in clear, concise ... Empowerment Series: Understanding Human Behavior and the Social Zastrow and Kirst-Ashman's UNDERSTANDING HUMAN BEHAVIOR AND THE ...
https://www.barnesandnoble.com/w/human-heredity-michael-cummings/1116753782?ean=9780538498821
*  High-Resolution Whole Genome BAC Rearrays - Human, Mouse, Rat
The clone array is available from BACPAC (bacpac.chori.org) in chromosome-specific plates (clones have been rearrayed at BACPAC ... Download human data. hs.clone.txt 958.58K Tue Jan 27 16:24:28 2004 Clone List. List of clones in the rearray ... If you have obtained your rearray from BACPAC, you should use the chromosome-specific rearray plate mappings. ... when the field is a number the clone is on the same chromosome as the neighbourhood, but not overlapping, and the number is the ...
http://mkweb.bcgsc.ca/bacarray/?view=download
*  Rhesus macaque - Wikipedia
The PRAME family has 26 members on human chromosome 1. In the macaque, it has eight, and has been very simple and stable for ... coming to rely on handouts or refuse from humans.[5] They adapt well to human presence, and form larger troops in human- ... So, macaque, chimpanzee, and human chromosomes are mosaics of each other.[citation needed] ... The X chromosome has three times more rearrangements than other chromosomes. The macaque gained 1,358 genes by duplication.[ ...
http://www.let.rug.nl/~gosse/termpedia2/termpedia.php?language=dutch_general&density=7&link_color=000000&termpedia_system=perl_db&url=http%3A%2F%2Fen.wikipedia.org%2Fwiki%2FRhesus_monkey
*  HNF4 and HNF1 as well as a panel of hepatic functions are extinguished and reexpressed in parallel in chromosomally reduced rat...
... of two independent lineages containing only 8-11 human chromosomes show pleiotropic extinction of thirteen out of fifteen ... correlates with loss of human chromosome 2. The extinguished cells and their reexpressing derivatives have been examined for ... well as a panel of hepatic functions are extinguished and reexpressed in parallel in chromosomally reduced rat hepatoma-human ... well as a panel of hepatic functions are extinguished and reexpressed in parallel in chromosomally reduced rat hepatoma-human ...
http://jcb.rupress.org/content/121/4/887
*  Macaca mulatta - Wikipedia, a enciclopedia libre
"Banding patterns of the chromosomes of the Rhesus monkey (Macaca mulatta)". Journal of Human Evolution 3 (4): 291-295. doi: ... in human blood reacting with anti-rhesus sera and with human isoantibodies". J Exp Med 74 (4): 309-320. PMC 2135190. PMID ... In: Mitruka, B. M., Rawnsley, H. M., Vadehra, D. V., (eds.) Animals for medical research: models for the study of human disease ... "DNA sequence of Rhesus macaque has evolutionary, medical implications" (Nota de prensa). Human Genome Sequencing Center. 13 ...
https://gl.wikipedia.org/wiki/Macaca_mulatta
*  Chromosome abnormalities - The Full Wiki
Known disorders in humans include Wolf-Hirschhorn syndrome, which is caused by partial deletion of the short arm of chromosome ... In a Robertsonian translocation, an entire chromosome has attached to another at the Centromere - in humans these only occur ... When the chromosome's structure is altered. This can take several forms:. *Deletions: A portion of the chromosome is missing or ... A chromosome anomaly, abnormality or aberration reflects an atypical number of chromosomes or a structural abnormality in one ...
http://www.thefullwiki.org/Chromosome_abnormalities
*  nucleus facts, information, pictures | Encyclopedia.com articles about nucleus
The human genome contains 180 rRNA genes located on the tips of five different chromosomes (chromosomes 13, 14, 15, 21, and 22 ... Chromosomes fill much of the nuclear interior, with each chromosome occupying its own neighborhood. In differentiated human ... Boveri rightly predicted that humans inherit traits on the chromosomes.. During nuclear assembly, membranes reattach to ... The DNA in each chromosome is highly contorted, looping back and forth within its territory. Chromosomes appear capable of ...
https://www.encyclopedia.com/science-and-technology/physics/physics/nucleus
*  WikiPremed MCAT Course - Human Genetics
Human Y-chromosome DNA haplogroups. Human Y-chromosome DNA haplogroups are large groups of haplotypes defined by differences in ... XYY syndrome is an aneuploidy of the sex chromosomes in which a human male receives an extra Y chromosome. ... Y-chromosomal Adam is the patrilineal human most recent common ancestor from whom all Y chromosomes in living men are descended ... Robertsonian translocation is a common form of chromosomal rearrangement that occurs in the five acrocentric human chromosome ...
https://www.wikipremed.com/mcat_course.php?code=040406