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*  Avian sex chromosome dimorphism | Biology Letters
The idea of morphological reduction of W is also enhanced by our perspective of the gradual shortening of human Y chromosome [5 ... The avian Z chromosome is remarkably preserved across taxa [4]. Usually, it is 4-6th in size among all the chromosomes and has ... 2006 Comparison of the chicken and zebra finch Z chromosomes shows evolutionary rearrangements. Chromosome Res. 14, 805-815. ... 2008 Molecular cloning of zebra finch W chromosome repetitive sequences: Evolution of the avian W chromosome. Chromosoma 117, ...
http://rsbl.royalsocietypublishing.org/content/8/4/636
*  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- ... 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 ... Our results are consistent with a role for ObgE in chromosome partitioning, with defects in chromosome segregation observed ...
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...
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 ... 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
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 ... Rastan S, Robertson EJ, Rasmussen TP, Mastrangelo MA, Eden A, Pehrson JR, Jaenisch R (1985) X‐chromosome deletions in embryo‐ ... Panning B, Dausman J, Jaenisch R, Avner P, Brockdorff N, Turner BM (1997) X chromosome inactivation is mediated by Xist RNA ...
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 ... 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/
*  BioNews - What next for preimplantation genetic screening (PGS)?
Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos. Prenat Diagn ... which just looks at the chromosomes) or SNP arrays (single nucleotide polymorphism - which can look at the chromosomes and ... Reader in Human Genetics and Embryology, UCL Centre for PGD, Institute for Women's Health, University College London; Chair of ... The UK's Human Fertilisation and Embryology Authority (HFEA) has reviewed the regulation of PGS and now no longer require ...
http://www.bionews.org.uk/page_45447.asp
*  Chromosomes, Human, Pair 17 - Semantic Scholar
Chromosome 17 spans more than 81 million base pairs and represents between 2.5 and 3% of the total DNA in normal diploid cells. ... The designation for each member of the seventeenth largest human autosomal chromosome pair. ... Chromosomes, Human, Pair 17. Known as: Chromosome 17 The designation for each member of the seventeenth largest human autosomal ... Chromosome 17 trisomy. Chromosome 17, deletion 17q23 q24. Chromosome 17, trisomy 17p. Chromosome 17q21.31 Deletion Syndrome ...
https://www.semanticscholar.org/topic/Chromosomes%2C-Human%2C-Pair-17/77805
*  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
*  A lookup of the Danio rerio genome assembly making use of the coding sequence of the CIRH1A cDNA as the query discovered a...
... area of zebrafish chromosome eighteen flanking cirh1a maps to a 20 Mb stretch of human chromosome 16q that is made up of CIRH1A ... Zebrafish Cirhin is made up of 685 amino acids, and is 54% equivalent and 72% very similar to the human protein, with ... The encoded 685 amino acid protein is fifty four% similar and seventy two% equivalent to human CIRHIN (Determine 1A). ... Current info have demonstrated that zebrafish are a valuable animal design for studying human liver improvement and disease [21 ...
http://www.sgkinhibitor.com/2016/06/03/a-lookup-of-the-danio-rerio-genome-assembly-making-use-of-the-coding-sequence-of-the-cirh1a-cdna-as-the-query-discovered-a-solitary-homologous-gene-found-on-chromosome-18/
*  Construction and characterization of three region-specific microdissection libraries for human chromosome 18 | SpringerLink
Three region-specific libraries for the entire human chromosome 18 were constructed using microdissection and MboI linker- ... Human Chromosome Blot Hybridization Insert Size Density Marker Southern Blot Hybridization This is a preview of subscription ... Three region-specific libraries for the entire human chromosome 18 were constructed using microdissection and MboI linker- ... Construction and characterization of three region-specific microdissection libraries for human chromosome 18. ...
https://link.springer.com/article/10.1007/BF02369909
*  Highly variable regions of DNA flank the human alpha globin genes - Radcliffe Department of Medicine
... highly polymorphic areas provides a large number of individual genetic markers for the alpha globin gene cluster on chromosome ... If, as seems likely, such regions occur frequently throughout the human genome they should be of considerable value in the ... polymorphisms which are due to DNA rearrangements have been identified within two highly variable regions flanking the human ... Chromosomes, Human, 16-18 DNA/*analysis DNA Restriction Enzymes/metabolism Deoxyribonuclease BamHI Genetic Markers Globins/* ...
https://www.rdm.ox.ac.uk/publications/483583
*  RBMY1A1 - RNA-binding motif protein, Y chromosome, family 1 member A1 - Homo sapiens (Human) - RBMY1A1 gene & protein
Human chromosome Y. Human chromosome Y: entries, gene names and cross-references to MIM ... sp,P0DJD3,RBY1A_HUMAN RNA-binding motif protein, Y chromosome, family 1 member A1 OS=Homo sapiens OX=9606 GN=RBMY1A1 PE=1 SV=1 ... "Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm.". Elliott D ... "Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm.". Elliott D ...
https://www.uniprot.org/uniprot/P0DJD3
*  CD200 - Wikipedia
1988). "RFLP and mapping of human MOX-1 gene on chromosome 3". Nucleic Acids Res. 16 (18): 9067. doi:10.1093/nar/16.18.9067. ... 2005). "Down-regulation of basophil function by human CD200 and human herpesvirus-8 CD200". J. Immunol. 175 (7): 4441-9. doi: ... "Human PubMed Reference:". "Mouse PubMed Reference:". "P41217 (OX2G_HUMAN)". Uniprot. Retrieved 16 May 2013. "Entrez Gene: CD200 ... OX-2 membrane glycoprotein, also named CD200 (Cluster of Differentiation 200) is a human protein encoded by the CD200 gene. The ...
https://en.wikipedia.org/wiki/CD200
*  FGF18 - Wikipedia
... to human chromosome 5q34 by use of radiation hybrid mapping and fluorescence in situ hybridization". Cytogenet. Cell Genet. 90 ... Hu MC, Wang YP, Qiu WR (1999). "Human fibroblast growth factor-18 stimulates fibroblast cell proliferation and is mapped to ... 2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci ... 2003). "The Secreted Protein Discovery Initiative (SPDI), a Large-Scale Effort to Identify Novel Human Secreted and ...
https://en.wikipedia.org/wiki/FGF18
*  Expression of NFE2L3 in cancer - Summary - The Human Protein Atlas
Chromosome. External id. - DATA AVAILABILITY -. Has protein data. - DATA RELIABILITY -. Reliability score tissue (IHC). ... HUMAN PROTEIN ATLAS INFORMATION. RNA categoryi. RNA category is based on mRNA expression levels in the analyzed samples (RNA ... The Human Protein Atlas project is funded. by the Knut & Alice Wallenberg foundation. ... Note that samples used for immunohistochemistry by the Human Protein Atlas do not correspond to samples in the TCGA dataset. ...
http://www.proteinatlas.org/ENSG00000050344-NFE2L3/pathology
*  Antievolution.org - Antievolution.org Discussion Board -Topic::The Origin of 'Information' via natural causes
... a synteny region of human chromosome 16 on which human BCNT is localized. Complete nucleotide sequencing of the BAC clone ... Evidence of more retrogenes in the human genome. Nucleic Acids Res. 2003 Aug 1;31(15):4385-90.. The human genome contains many ... Whereas the pseudogene is localized on chromosome 26, both bcntp97 and the h-type bcnt genes are found on bovine chromosome 18 ... Leptin Receptor Isoform 219.1: An Example of Protein Evolution by LINE-1 Mediated Human Specific Retrotransposition of a Coding ...
http://www.antievolution.org/cgi-bin/ikonboard/ikonboard.cgi?s=50c40d619bf541ec
*  Antievolution.org - Antievolution.org Discussion Board -Topic::The Origin of 'Information' via natural causes
Humans and other Anthropoids share very similar chromosome structure and genomic sequence as seen in the 98.5% homology at the ... SCN11A is localized to human chromosome 3 (3p21-24) close to the other TTX-R sodium channel genes SCN5A and SCN10A. An ... Evidence of more retrogenes in the human genome. Nucleic Acids Res. 2003 Aug 1;31(15):4385-90.. The human genome contains many ... New genes in humans and our primate relatives add a new component to the understanding of genetic divergence between humans and ...
http://www.antievolution.org/cgi-bin/ikonboard/ikonboard.cgi?s=50c2f933e02fe4c0
*  AE BB DB Explorer
Humans and other Anthropoids share very similar chromosome structure and genomic sequence as seen in the 98.5% homology at the ... SCN11A is localized to human chromosome 3 (3p21-24) close to the other TTX-R sodium channel genes SCN5A and SCN10A. An ... Evidence of more retrogenes in the human genome. Nucleic Acids Res. 2003 Aug 1;31(15):4385-90.. The human genome contains many ... Whereas the pseudogene is localized on chromosome 26, both bcntp97 and the h-type bcnt genes are found on bovine chromosome 18 ...
http://antievolution.org/features/aebbexp.php?form_cmd=view_author&form_srcid=theyeti&execute=Submit
*  Where Chromosomes Agree, Stanford researchers Trace Human History
... News Aug 20, 2012 ... There are the marks left by human evolution, the traces of ancient human migrations out of Africa and, scattered throughout, ... It's a clear artifact of ancient waves of human migration.. "It's something novel, to see the signature of the distance from ... Runs of homozygosity, or ROH, are segments of the genome where both chromosomes are identical. Homozygosity is what allows ...
https://www.technologynetworks.com/genomics/news/where-chromosomes-agree-stanford-researchers-trace-human-history-213991
*  Localization of a neural crest transcription factor, Slug, to mouse Chromosome 16 and human Chromosome 8, Mammalian Genome | 10...
... to mouse Chromosome 16 and human Chromosome 8, Mammalian Genome" on DeepDyve, the largest online rental service for scholarly ... Localization of a neural crest transcription factor, Slug, to mouse Chromosome 16 and human Chromosome 8. Rhim, Hyangshuk; ... Localization of a neural crest transcription factor, Slug, to mouse Chromosome 16 and human Chromosome 8. Localization of a ... 872 Mammalian Genome 8, Brief Data Reports Chromosome 16 Localization of a neural crest transcription factor, Slug, to mouse ...
https://www.deepdyve.com/lp/springer_journal/localization-of-a-neural-crest-transcription-factor-slug-to-mouse-0ZPQmlbMNe
*  FA2H - Wikipedia
Fatty acid 2-hydroxylase is a protein that in humans is encoded by the FA2H gene. This gene encodes a protein that catalyzes ... "Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French- ... Alderson, N. L.; Rembiesa, B. M.; Walla, M. D.; Bielawska, A.; Bielawski, J.; Hama, H. (2004). "The Human FA2H Gene Encodes a ... Human Mutation. 31 (4): E1251-E1260. doi:10.1002/humu.21205. PMID 20104589. Dan, P.; Edvardson, S.; Bielawski, J.; Hama, H.; ...
https://en.wikipedia.org/wiki/FA2H
*  Chromosome speciation: Humans, Drosophila, and mosquitoes | PNAS
... and human chromosome 2 represents a fusion of two acrocentric chromosomes present in chimpanzees (chromosomes 12 and 13) and ... Remarkably, the KA/KS ratios are also 1.41 times greater for rearranged chromosomes than for colinear chromosomes in humans ( ... Of 89 chromosomes with KA/KS ratios ≤1, 39 (43.8%) are on rearranged chromosomes, and 50 are on colinear chromosomes. The ... Table 6 shows that genes in rearranged chromosomes 4, 5, and 9, as well as in colinear chromosome 22, have human expression ...
https://www.pnas.org/content/102/suppl_1/6535
*  Piet Borst - Wikipedia
... later also found in human telomeres. Introduction of PFG electrophoresis for the separation of chromosome-sized DNA molecules ... Reid G, Wielinga P, Zelcer N, Van der Heijden I, Kuil A, De Haas M, Wijnholds J, Borst P. The human multidrug resistance ... Bernards A, Michels PA, Lincke CR, Borst P. Growth of chromosome ends in multiplying trypanosomes. Nature. 1983;303:592-7. Van ... Van der Ploeg LH, Cornelissen AW, Barry JD, Borst P. Chromosomes of kinetoplastida. EMBO J. 1984;3:3109-15. Heymans HS, ...
https://en.wikipedia.org/wiki/Piet_Borst
*  VPS4B - Wikipedia
In humans, two paralogs of the yeast protein have been identified. The former share a high degree of aa sequence similarity ... The gene encoding this paralog has been mapped to chromosome 18; the gene for the other resides on chromosome 16. GRCh38: ... Vacuolar protein sorting-associated protein 4B is a protein that in humans is encoded by the VPS4B gene. The protein encoded by ... 2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci ...
https://en.wikipedia.org/wiki/VPS4B
*  DSC1 - Wikipedia
1997). "A YAC contig joining the desmocollin and desmoglein loci on human chromosome 18 and ordering of the desmocollin genes ... 2000). "Clustered cadherin genes: a sequence-ready contig for the desmosomal cadherin locus on human chromosome 18". Genomics. ... coding for human type 1 desmocollin and its assignment to chromosome 18". Genomics. 18 (2): 185-94. doi:10.1006/geno.1993.1453 ... Desmocollin-1 is a protein that in humans is encoded by the DSC1 gene. The protein encoded by this gene is a calcium-dependent ...
https://en.wikipedia.org/wiki/DSC1