*  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
*  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
*  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)
*  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
*  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
*  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
*  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
*  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
*  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
*  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
*  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
*  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
*  HCC38 ATCC ® CRL-2314™ Homo sapiens mammary gland; breast/d
Every chromosome pair had a least one rearrangement. No normal X chromosomes were observed and Y chromosomes were absent by QM ... This is a hyper-triploid human cell line with a modal chromosome number of 75. Homogeneously staining regions and dicentric ... No normal X chromosomes were observed and Y chromosomes were absent by QM staining. Normal copies of chromosomes 2,6,11,13,16 ... a chromosome break in 3/30, a chromatid break in 5/30, a ring chromosome in 1/30, and double minutes in 11/30 (1-5 copies). ...
  https://www.atcc.org/en/Products/Cells_and_Microorganisms/By_Disease__Model/Paired_set_normal_and_diseased_tissue/CRL-2314.aspx?p=1&rel=%7B0%7D
*  Trisomies | definition of trisomies by Medical dictionary
They are organized in pairs. Humans have 23 pairs of chromosomes. In a trisomy syndrome, an extra chromosome is present so that ... There are 46 chromosomes in each human somatic cell organized in 23 pairs, of which 22 pairs are similar in appearance but ... The state of an individual or cell with an extra chromosome instead of the normal pair of homologous chromosomes; in humans, ... The state of an individual or cell with an extra chromosome instead of the normal pair of homologous chromosomes; in humans, ...
  https://medical-dictionary.thefreedictionary.com/trisomies
*  tmp1084 | Retrovirus | Molecular Biology
Eighteen of the 23 pairs of modern human chromosomes are virtually identical to chimpanzee chromosomes, with the most ... All known human-specific LTRs belong to the HERV-K (human ERV) family, the most active family in the human genome. It is likely ... to human evolution. To date, human-specific LTRs have been detected in the genomes and transcriptomes of various human cancer ... the human and chimpanzee karyotypes being a telomeric fusion of chimpanzee chromosomes 12 and 13 to form human chromosome 2, ...
  https://fr.scribd.com/document/64697728/tmp1084
*  Array-MLPA analysis of chromosome X monosomy mosaicism. | Open-i
The average copy number on chromosome X was 0.71. (B) G-bandi ... Array-MLPA analysis of chromosome X monosomy mosaicism. (A) A ... Chromosomes, Human, Pair 13. *Chromosomes, Human, Pair 18. *Chromosomes, Human, Pair 21 ... Background: Chromosome abnormalities, especially trisomy of chromosome 21, 13, or 18 as well as sex chromosome aneuploidy, are ... Background: Chromosome abnormalities, especially trisomy of chromosome 21, 13, or 18 as well as sex chromosome aneuploidy, are ...
  https://openi.nlm.nih.gov/detailedresult.php?img=PMC3111339_1471-2350-12-68-4&req=4
*  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
*  Letters to Lior: 2014
There are 23 pairs of human chromosomes. In Trisomy 18 (Edwards syndrome), there is an extra chromosome with the 18th pair. ... I guess now and its probably only human, the questions now start and I seem to torment myself;. Was I a good enough mommy to ... Trisomy 18 occurs in 1 in 3,000 live births.It is three times more common in girls than boys. Unfortunately, most babies with ... Trisomy 18 severely affects all organ systems of the body.The majority of children who are born with Edward's syndrome do not ...
  http://lior-mylight.blogspot.com/2014/
*  Letters to Lior: October 2012
There are 23 pairs of human chromosomes. In Trisomy 18 (Edwards syndrome), there is an extra chromosome with the 18th pair. ... daddy was having a gawk around and found a pair of sunglasses that fit you. This kind of thing may seem so trivial and such a ... Trisomy 18 occurs in 1 in 3,000 live births.It is three times more common in girls than boys. Unfortunately, most babies with ... Trisomy 18 severely affects all organ systems of the body.The majority of children who are born with Edward's syndrome do not ...
  http://lior-mylight.blogspot.com/2012/10/
*  Letters to Lior: January 2015
There are 23 pairs of human chromosomes. In Trisomy 18 (Edwards syndrome), there is an extra chromosome with the 18th pair. ... Trisomy 18 occurs in 1 in 3,000 live births.It is three times more common in girls than boys. Unfortunately, most babies with ... Trisomy 18 severely affects all organ systems of the body.The majority of children who are born with Edward's syndrome do not ... Before birth Lior was diagnosed with Full Trisomy 18. Below is an explanation to help you better understand. Most T18 mommies ...
  http://lior-mylight.blogspot.com/2015/01/
*  Letters to Lior: December 2011
There are 23 pairs of human chromosomes. In Trisomy 18 (Edwards syndrome), there is an extra chromosome with the 18th pair. ... But we cant blame them, we are all human and if you are not in a position that our family is in, nothing will ever be perfect. ... Trisomy 18 occurs in 1 in 3,000 live births.It is three times more common in girls than boys. Unfortunately, most babies with ... Trisomy 18 severely affects all organ systems of the body.The majority of children who are born with Edward's syndrome do not ...
  http://lior-mylight.blogspot.com/2011/12/