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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
*  Sex Chromosomes: Genetics, Abnormalities, and Disorders
A human somatic cell has two sex chromosomes: XY in male and XX in female. A human germ cell has one sex chromosome: X or Y in ... Most XX men who lack a Y chromosome do still have a copy of the SRY gene on one of their X chromosomes (moved there by ... Combination of a Y-sperm and an egg will produce a male.Usually, a woman has two X chromosomes (XX) and a man one X and one Y ( ... Chapter 1. Sex Chromosomes, Gender Differences and Disease, pp. 1-24 (Lopes AM, Sargent CA, Affara NA, Amorim A, Instituto de ...
  https://www.novapublishers.com/catalog/product_info.php?products_id=9697
*  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/
*  HUMARA assay - Wikipedia
... short for Human Androgen receptor) that is located on X chromosome. Considering the fact that once one X chromosome is ... The fact that most-but not all-genes on X chromosome undergo inactivation, this feature becomes an important one. 2-) Human ... of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome ... The method is based on X chromosome inactivation and it takes the advantage of having different methylation status of a gene ...
  https://en.wikipedia.org/wiki/HUMARA_assay
*  New Chromosome Research Undermines Human-Chimp Similarity Claims
So, the human Y chromosome looks just as different from a chimp as the other human chromosomes do from a chicken. And to ... the human and chimp Y chromosomes were constructed entirely differently. On the human Y chromosome, there were found four major ... male-specific Y chromosome].'1 As far as looking at specific genes, the chimp and human Y chromosomes had a dramatic difference ... New Chromosome Research Undermines Human-Chimp Similarity Claims. Institution for Creation Research ^ , Apr 1, 2010 , Jeffrey ...
  http://www.freerepublic.com/focus/f-news/2565348/posts?page=10
*  Centromere - Wikipedia
"Chromosomes, Chromosome Anomalies". *Gilbert F (1999). "Disease genes and chromosomes: disease maps of the human genome. ... The human genome includes six acrocentric chromosomes: 13, 14, 15, 21, 22 and the Y chromosome. In an acrocentric chromosome ... A chromosome is metacentric if its two arms are roughly equal in length. In a normal human karyotype, five chromosomes are ... Humans do not possess telocentric chromosomes. If the chromosome's centromere is located closer to its end than to its center, ...
  https://en.wikipedia.org/wiki/Centromere
*  New Chromosome Research Undermines Human-Chimp Similarity Claims | The Institute for Creation Research
So, the human Y chromosome looks just as different from a chimp as the other human chromosomes do from a chicken. And to ... the human and chimp Y chromosomes were constructed entirely differently. On the human Y chromosome, there were found four major ... Human-Chimp Genetic Similarity: Is the Evolutionary Dogma Valid? * New Human-Chimp Chromosome 2 Data Challenge Common Ancestry ... within the chimpanzee Y chromosome had less than 10 percent similarity with the same class in the human Y chromosome, and vice ...
  http://www.icr.org/article/5292/
*  The c-myc gene paradox in Burkitt's lymphoma chromosomal translocation. - Radcliffe Department of Medicine
Animals, Base Sequence, Burkitt Lymphoma, Cell Transformation, Neoplastic, Chromosomes, Human, 6-12 and X, Genetic Variation, ...
  https://www.rdm.ox.ac.uk/publications/601859
*  Genealogy of an ancient protein family: the Sirtuins, a family of disordered members | BMC Evolutionary Biology | Full Text
3D structures of human SIRT2, SIRT3, and SIRT5 revealed the overall conformation of the conserved core domain but they were ... Aim of this work is to understand what structural properties are shared among members of this family in humans as well as in ... Recently, we modeled the 3D-structure of human SIRT1, the most studied member of this family, that unexpectedly emerged as a ... The presence of disorder in human SIRT1 and the propensity of these proteins in promoting molecular interactions make it ...
  https://bmcevolbiol.biomedcentral.com/articles/10.1186/1471-2148-13-60
*  Contribution of Antibody-based Protein Profiling to the Human Chromosome-centric Proteome Project (C-HPP)
A gene-centric Human Proteome Project has been proposed to characterize the human protein-coding genes in a chromosome-centered ... Contribution of Antibody-based Protein Profiling to the Human Chromosome-centric Proteome Project (C-HPP). Fagerberg, Linn ... each gene with regards to protein evidence is visualized in a chromosome-centric manner as part of a new version of the Human ... We estimate that there is good evidence for protein existence for 69% (n = 13985) of the human protein-coding genes, while 23% ...
  http://uu.diva-portal.org/smash/record.jsf?pid=diva2%3A614201&c=19&searchType=SIMPLE&language=en&query=&af=%5B%5D&aq=%5B%5B%7B%22personId%22%3A%22authority-person%3A11074%22%7D%5D%5D&aq2=%5B%5B%5D%5D&aqe=%5B%5D&noOfRows=50&sortOrder=author_sort_asc&sortOrder2=title_sort_asc&onlyFullText=false&sf=all
*  A major quantitative trait locus on chromosome 3 controls colitis severity in IL-10-deficient mice | PNAS
... it would map to either human Chr. 5q (APC) or 18q (DCC and SMAD). Evidence for a human 5q colitis linkage has been reported (33 ... chromosome;. B6,. C57BL/6J;. C3H,. C3H/HeJBir;. QTL,. quantitative trait locus/loci;. Cdcs,. cytokine deficiency-induced ... illustrates why detection of human inflammatory bowel disease linkages has proven to be so difficult. A human ortholog of the ... The human ortholog for the Cdcs1 locus, if one existed, would be expected on either Chr. 4q or 1p rather than the Crohn's ...
  http://www.pnas.org/content/98/24/13820
*  E2F4 (E2F transcription factor 4, p107/p130-binding)
LINC, a human complex that is related to pRB-containing complexes in invertebrates regulates the expression of G2/M genes.. ... 16q22.1 [Link to chromosome band 16q22]. Location_base_pair. Starts at 67192165 and ends at 67198918 bp from pter ( according ... Summary: Deletion of chromosome arm 16q22 or LOH (Dorion-Bonnet et al., 1995; Iida et al., 1997; Cleton-Jansen et al., 2001); ... Phosphorylation dynamics during early differentiation of human embryonic stem cells.. Van Hoof D, Munoz J, Braam SR, Pinkse MW ...
  http://atlasgeneticsoncology.org/Genes/GC_E2F4.html
*  GLOD4 - Wikipedia
Guo JY, Xu J, Mao Q, Fu LL, Gu JR, De Zhu J (Jan 2003). "The promoter analysis of the human C17orf25 gene, a novel chromosome ... "Entrez Gene: C17orf25 chromosome 17 open reading frame 25". Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, ... Glyoxalase domain-containing protein 4 is an enzyme that in humans is encoded by the GLOD4 gene. GRCh38: Ensembl release 89: ... 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/GLOD4
*  LIG1 - Wikipedia
1992). "Assignment of the gene encoding DNA ligase I to human chromosome 19q13.2-13.3". Genomics. 12 (1): 164-6. doi:10.1016/ ... 1993). "Fluorescence in situ hybridization mapping of human chromosome 19: cytogenetic band location of 540 cosmids and 70 ... 1990). "Human DNA ligase I cDNA: cloning and functional expression in Saccharomyces cerevisiae". Proc. Natl. Acad. Sci. U.S.A. ... DNA ligase 1 is an enzyme that in humans is encoded by the LIG1 gene. DNA ligases are important tools for DNA replication and ...
  https://en.wikipedia.org/wiki/LIG1
*  GABRB3 - Wikipedia
... characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7". ... characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7". ... paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer". Human Molecular ... The GABRB3 gene is located on the long arm of chromosome 15, within the q12 region in the human genome. It is located in a gene ...
  https://en.wikipedia.org/wiki/GABRB3
*  SERPINA2 - Wikipedia
"Molecular linkage of the human alpha 1-antitrypsin and corticosteroid-binding globulin genes on chromosome 14q32.1". Mammalian ... "Update of the human and mouse SERPIN gene superfamily". Human Genomics. 7 (1): 22. doi:10.1186/1479-7364-7-22. PMC 3880077 . ... Serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 2 is a protein that in humans is encoded by ... These studies with SERPINA2 in humans have concluded that recent positive selection is favoured by the loss of SERPINA2 ...
  https://en.wikipedia.org/wiki/SERPINA2
*  SCNN1A - Wikipedia
The human gene SCNN1A is located in the short arm of chromosome 12 (12p3). Human SCNN1A includes 13 exons spanning about 29,000 ... Farr TJ, Coddington-Lawson SJ, Snyder PM, McDonald FJ (February 2000). "Human Nedd4 interacts with the human epithelial Na+ ... Farr TJ, Coddington-Lawson SJ, Snyder PM, McDonald FJ (February 2000). "Human Nedd4 interacts with the human epithelial Na+ ... "Localisation of pseudohypoaldosteronism genes to chromosome 16p12.2-13.11 and 12p13.1-pter by homozygosity mapping". Human ...
  https://en.wikipedia.org/wiki/SCNN1A
*  الوحدة الفرعية بيتا للفولليتروبين - ويكيبيديا، الموسوعة الحرة
... and regional assignment of the human follicle-stimulating hormone beta-subunit gene to the short arm of human chromosome 11". ... 1989). "Expression of biologically active human follitropin in Chinese hamster ovary cells". J. Biol. Chem. 264 (9): 4769-75. ... 1999). "Characterization of single-nucleotide polymorphisms in coding regions of human genes". Nat. Genet. 22 (3): 231-8. PMID ... Fox KM، Dias JA، Van Roey P (2001). "Three-dimensional structure of human follicle-stimulating hormone". Mol. Endocrinol. 15 (3 ...
  https://ar.wikipedia.org/wiki/%D9%87%D8%B1%D9%85%D9%88%D9%86_%D9%85%D9%86%D8%A8%D9%87_%D9%84%D9%84%D8%AC%D8%B1%D9%8A%D8%A8_%D8%A8%D9%8A%D8%AA%D8%A7
*  Spinocerebellar ataxia 13; SCA13 | Disease page | IUPHAR/BPS Guide to PHARMACOLOGY
... and mapping of Kv3.3 and Kv3.4 to human chromosomes 19 and 1. Genomics, 12 (2): 190-6. [PMID:1740329] ... 6. Waters MF, Minassian NA, Stevanin G, Figueroa KP, Bannister JP, Nolte D, Mock AF, Evidente VG, Fee DB, Müller U et al.. ( ... Mutat., 31 (2): 191-6. [PMID:19953606] 3. Figueroa KP, Waters MF, Garibyan V, Bird TD, Gomez CM, Ranum LP, Minassian NA, ... 2011) Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13). PLoS ONE, 6 (3): e17811. [PMID:21479265] ...
  http://www.guidetopharmacology.org/GRAC/DiseaseDisplayForward?diseaseId=877
*  Malonyl-CoA decarboxylase deficiency - Wikipedia
This means that the defective gene is located on an autosome (chromosome 16 is an autosome), and two copies of the defective ... By 1999, only seven cases of Malonyl- CoA decarboxylase deficiency had been reported in human in Australia; however, this ... Malonyl-CoA decarboxylase deficiency is caused by mutations in the MLYCD gene, located on chromosome 16q24. The gene encodes ... Annals of Human Genetics. 71 (Pt 6): 705-12. doi:10.1111/j.1469-1809.2007.00373.x. PMID 17535268. Online Mendelian Inheritance ...
  https://en.wikipedia.org/wiki/Malonyl-CoA_decarboxylase_deficiency
*  FSHB - Wikipedia
... and regional assignment of the human follicle-stimulating hormone beta-subunit gene to the short arm of human chromosome 11". ... Shome B, Parlow AF, Liu WK, Nahm HS, Wen T, Ward DN (Sep 1989). "A reevaluation of the amino acid sequence of human follitropin ... Follitropin subunit beta also known as follicle-stimulating hormone beta subunit (FSH-B) is a protein that in humans is encoded ... 2001). "Characterization of human FSH isoforms reveals a nonglycosylated beta-subunit in addition to the conventional ...
  https://en.wikipedia.org/wiki/FSHB
*  De novo deletion of chromosome 11q12.3 in monozygotic twins affected by Poland Syndrome | SpringerLink
Davydov EV, Goode DL, Sirota M, Cooper GM, Sidow A, Batzoglou S: Identifying a high fraction of the human genome to be under ... At twelve years, she presented mild scoliosis without indication for surgical intervention. The second twin had severe ... Identification of a de novo chromosome 11q12.3 deletion in MZ twins with Poland Syndrome. A) Array-CGH profile of chromosome 11 ... Chromosome 11q deletion Congenital abnormalities Monozygotic twins Poland syndrome CNV HRASLS5 HRASLS2 RARRES3 PLA2G16 ...
  https://link.springer.com/article/10.1186%2F1471-2350-15-63