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
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 ... Rastan S, Robertson EJ, Rasmussen TP, Mastrangelo MA, Eden A, Pehrson JR, Jaenisch R (1985) X‐chromosome deletions in embryo‐ ...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/
High incidence of t(11;18)(q21;q21) in Helicobacter pylori-negative gastric MALT lymphoma.
Chromosomes, Human, Pair 11*. Chromosomes, Human, Pair 18*. Female. Helicobacter pylori* / isolation & purification. Humans. ... 0/Adaptor Proteins, Signal Transducing; 0/BCL10 protein, human; 0/Carrier Proteins ... BCL10 nuclear expression was observed in 7 of 8 t(11;18)(q21;q21)-positive cases and 4 of 7 t(11;18)(q21;q21)-negative cases, ... We reviewed the clinical data and histology, and we examined t(11;18)(q21;q21) and BCL10 expression pattern in 17 such cases. ...http://www.biomedsearch.com/nih/High-incidence-in-Helicobacter-pylori/12517817.html
Bernstein, M. T.<...
Chromosomes, Human, Pair 18 Physical and Genetic Mapping of a Human Apical Epithelial Na+/H+ Exchanger (NHE3) Isoform to ... Jabs, E. W., Thomas, P. J., Bernstein, M. T., Coss, C., Ferreira, G. C. & Pedersen, P. L., May 1994, In : Human Genetics. 93, 5 ... Chromosome 5p15.3. Brant, S. R., Bernstein, M. T., Wasmuth, J. J., Taylor, E. W., McPherson, J. D., Li, X., Walker, S., ...https://jhu.pure.elsevier.com/en/persons/michael-t-bernstein
Chromosome 18 (human) - Wikipedia
Gilbert F (1997). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 18". Genet Test. 1 (1): 69-71. ... The following is a partial list of genes on human chromosome 18. For complete list, see the link in the infobox on the right. ... The following are some of the gene count estimates of human chromosome 18. Because researchers use different approaches to ... People normally have two copies of this chromosome. Chromosome 18 spans about 80 million base pairs (the building material of ...https://en.wikipedia.org/wiki/Chromosome_18_(human)
RNA sequencing of esophageal adenocarcinomas identifies novel fusion transcripts, including NPC1-MELK, arising from a complex...
Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 3 ... chromosome 12 open reading frame 49 (C12orf49) in 1 of 55 or 1.8%. A genomic analysis indicated that NPC1-MELK arose from a ... chromosome 12 open reading frame 49 (C12orf49) in 1 of 55 or 1.8%. A genomic analysis indicated that NPC1-MELK arose from a ... chromosome 12 open reading frame 49 (C12orf49) in 1 of 55 or 1.8%. A genomic analysis indicated that NPC1-MELK arose from a ...https://jhu.pure.elsevier.com/en/publications/rna-sequencing-of-esophageal-adenocarcinomas-identifies-novel-fus
Edwards' Syndrome - baby, symptoms, average, Definition, Description, Demographics, Causes and symptoms
Humans normally have 23 pairs of chromosomes. Chromosomes are numbered 1-22, and the 23rd pair is composed of the sex ... the human body and consisting of a complex of proteins and DNA. Humans have 46 chromosomes arranged into 23 pairs. Chromosomes ... Karyotyping -A laboratory test used to study an individual's chromosome make-up. Chromosomes are separated from cells, stained ... Using special stains and microscopy, individual chromosomes are identified, and the presence of an extra chromosome 18 is ...http://www.healthofchildren.com/E-F/Edwards-Syndrome.html
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 ... 18) translocation. We were particularly interested to determine whether nodular paragranuloma (lymphocyte-predominant, nodular ... Antibodies, Monoclonal, Chromosomes, Human, Pair 14, Chromosomes, Human, Pair 18, Gene Expression, Hodgkin Disease, Humans, ...https://www.rdm.ox.ac.uk/publications/486737
Bacterial artificial chromosome - Wikipedia
"Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector ... Cosmid End-sequence profiling Fosmid Human artificial chromosome Yeast artificial chromosome O'Connor M, Peifer M, Bender W ( ... BACs can also be utilized to detect genes or large sequences of interest and then used to map them onto the human chromosome ... "Construction of a 750-kb bacterial clone contig and restriction map in the region of human chromosome 21 containing the ...https://en.wikipedia.org/wiki/Bacterial_artificial_chromosome
Consequences of chromsome18q deletions. - PubMed - NCBI
Chromosomes, Human, Pair 18/genetics*. *Genotype. *Humans. *Male. *Phenotype. LinkOut - more resources. Full Text Sources. * ...https://www.ncbi.nlm.nih.gov/pubmed/26235940
ROCK1 - Wikipedia
The human ROCK1 gene is located on human chromosome 18 with specific location of 18q11.1. The location of the base pair starts ... In humans, the main function of ROCK1 is actomyosin contractility. As mentioned before, this contributes to many proximal ... "Q13464 (ROCK1_HUMAN)". "Inhibition of Rho-dependent kinases ROCK I/II activates VEGF-driven retinal neovascularization and ... Therefore, increased expression of RhoA and its downstream effector ROCK1 is often observed in human cancers. These cancers are ...https://en.wikipedia.org/wiki/ROCK1
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type...
Chromosomes, Human, Pair 18/genetics. *CpG Islands/genetics. *DNA Methylation/genetics. *Epigenesis, Genetic ... f) Similar as panel e, AON-mediated exon skipping of SMCHD1 exon 29 in normal human myoblasts 2333 and 2435. The mutation in ... e) AON-mediated exon skipping of SMCHD1 exon 36 in normal human myoblasts 2333 and 2435. The mutation in family Rf1014 results ... a) Short hairpin RNAs against different regions of SMCHD1 are effective in reducing the production of SMCHD1 in normal human ...https://www.ncbi.nlm.nih.gov/pubmed/23143600
Haplogroup S1a (Y-DNA) - Wikipedia
Cox MP, Mirazón Lahr M (2006). "Y-chromosome diversity is inversely associated with language affiliation in paired Austronesian ... Haplogroup S1a is a human Y-DNA haplogroup, defined by SNPs Z41335, Z41336, Z41337, Z41338, Z41339, Z41340, and Z41341. S1a is ... European Journal of Human Genetics. 23. doi:10.1038/ejhg.2014.106. Kayser M, Choi Y, Van Oven M, Mona S, Brauer S, Trent RJ, ... "Improved phylogenetic resolution and rapid diversification of Y-chromosome haplogroup K-M526 in Southeast Asia". Eur J Hum ...https://en.wikipedia.org/wiki/Haplogroup_S1a_(Y-DNA)
Haplogroup S-M230 - Wikipedia
... genealogy Haplogroup Haplotype Human Y-chromosome DNA haplogroup Molecular phylogenetics Paragroup Subclade Y-chromosome ... "Y-chromosome diversity is inversely associated with language affiliation in paired Austronesian- and Papuan-speaking ... "Reduced Y-Chromosome, but Not Mitochondrial DNA, Diversity in Human Populations from West New Guinea". The American Journal of ... Haplogroup S-M230, also known as S1a1b (and previously as S* or K2b1a4), is a Y-chromosome DNA haplogroup. It is by far the ...https://en.wikipedia.org/wiki/Haplogroup_S-M230
Y-DNA haplogroups in populations of Oceania - Wikipedia
Y-chromosome haplotypes and implications for human history in the Pacific". Human Mutation. 17 (4): 271-80. doi:10.1002/humu.23 ... Cox, Murray P.; Mirazón Lahr, Marta (2006). "Y-chromosome diversity is inversely associated with language affiliation in paired ... by human Y-chromosome DNA haplogroups based on relevant studies. Oceania Languages of Oceania Demographics of Oceania List of ... "Reduced Y-Chromosome, but Not Mitochondrial DNA, Diversity in Human Populations from West New Guinea". The American Journal of ...https://en.wikipedia.org/wiki/Y-DNA_haplogroups_in_populations_of_Oceania
Marta Mirazón Lahr - Wikipedia
"Y-chromosome diversity is inversely associated with language affiliation in paired Austronesian- and Papuan-speaking ... She and Robert Foley were the first to propose a 'southern route' for humans out of Africa, and for human diversity to be the ... Lahr's research is in human evolution, and ranges across human and hominin morphology, prehistory and genetics. Her early work ... Lahr, M. M. & Foley, R. (1998). "Towards a theory of modern human origins: Geography, demography, and diversity in recent human ...https://en.wikipedia.org/wiki/Marta_Miraz%C3%B3n_Lahr
Haplogroup M-P256 - Wikipedia
Cox, Murray P.; Mirazón Lahr, Marta (2006). "Y-chromosome diversity is inversely associated with language affiliation in paired ... genetic genealogy Haplogroup Haplotype Human Y-chromosome DNA haplogroup molecular phylogeny Paragroup Subclade Y-chromosome ... "Reduced Y-Chromosome, but Not Mitochondrial DNA, Diversity in Human Populations from West New Guinea". The American Journal of ... Haplogroup M, also known as M-P256 and Haplogroup K2b1b (previously K2b1d) is a Y-chromosome DNA haplogroup. M-P256 is a ...https://en.wikipedia.org/wiki/Haplogroup_M-P256
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
Biparietal diameter at 11 to 13 weeks' gestation in fetuses with holoprosencephaly. - Nuffield Department of Obstetrics and...
Adult, Aneuploidy, Case-Control Studies, Cephalometry, Chromosome Disorders, Chromosomes, Human, Pair 13, Chromosomes, Human, ... Pair 18, Crown-Rump Length, Female, Holoprosencephaly, Humans, Nuchal Translucency Measurement, Pregnancy, Pregnancy Trimester ... First, Retrospective Studies, Skull, Trisomy, Trisomy 13 Syndrome, Trisomy 18 Syndrome, Ultrasonography, Prenatal ...https://www.obs-gyn.ox.ac.uk/publications/511633
Mothers against decapentaplegic homolog 4 - Wikipedia
In humans, the SMAD4 gene contains 54 829 base pairs and is located from pair n° 51,030,212 to pair 51,085,041 in the region ... In mammals, SMAD4 is coded by a gene located on chromosome 18. ... Somatic mutations found in human cancers of the MH1 domain of ... Zawel L, Dai JL, Buckhaults P, Zhou S, Kinzler KW, Vogelstein B, Kern SE (Mar 1998). "Human Smad3 and Smad4 are sequence- ... Martin MM, Buckenberger JA, Jiang J, Malana GE, Knoell DL, Feldman DS, Elton TS (Sep 2007). "TGF-beta1 stimulates human AT1 ...https://en.wikipedia.org/wiki/Mothers_against_decapentaplegic_homolog_4
ZFIN Publication: Postlethwait et al., 2000
Human, Pair 10/genetics; Chromosomes, Human, Pair 11/genetics; Chromosomes, Human, Pair 15/genetics; Chromosomes, Human, Pair ... Animals; Chromosome Mapping; Chromosomes/genetics*; Chromosomes, Human, Pair 10/genetics; Chromosomes, Human, Pair 11/genetics ... 17/genetics; Chromosomes, Human, Pair 19/genetics; Chromosomes, Human, Pair 9/genetics; Evolution, Molecular*; Gene Duplication ... and zebrafish chromosomes are mosaically orthologous to several human chromosomes. Is this because of an excess of chromosome ...https://zfin.org/ZDB-PUB-001221-9
Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH. - Semantic Scholar
The extent and nature of the chromosome-18 deletions were studied in detail by array-based comparative genomic hybridization ( ... High-resolution chromosome-18 profiles were obtained for all patients, and a critical region of 5 Mb that was deleted in all ... to a detailed delineation of ring chromosomes. This study clearly demonstrates the power of the arrayCGH technology in high- ... Deletions of the long arm of chromosome 18 occur in approximately 1 in 10,000 live births. Congenital aural atresia (CAA), or ...https://www.semanticscholar.org/paper/Definition-of-a-critical-region-on-chromosome-18-by-Veltman-Jonkers/c351d6bb4f202e2450104bf1394a54e5748f5328
Mmw 21 Study Guide Essay - 1048 Words
1.To map and sequence all of the DNA base pairs in the human chromosomes. 2.To identify all of the genes within the seqeunce. ... These new cells undergo division by meiosis I and form haploid secondary spermatocytes with 23 chromosomes. These haploid cells ... each contains 46 chromosomes. During spermatogenesis, these cells enlarge and become primary spermatocytes. ... What food are rich in ion= greens organ meat, spinach, red meat, broccoli 18. Folic acid= tofu, soy 19. Why do we recommend ...http://www.studymode.com/essays/Mmw-21-Study-Guide-1208239.html