Yu XF, Zou J, Bao ZJ, Dong J (November 2011). "miR-93 suppresses proliferation and colony formation of human colon cancer stem ... Chromosomes & Cancer. 48 (7): 615-23. doi:10.1002/gcc.20669. PMID 19396864. S2CID 22482567. Mascaux C, Laes JF, Anthoine G, ... "MicroRNA profiles in allograft tissues and paired urines associate with chronic allograft dysfunction with IF/TA". American ... Petillo D, Kort EJ, Anema J, Furge KA, Yang XJ, Teh BT (July 2009). "MicroRNA profiling of human kidney cancer subtypes". ...

Articles with short description, Short description matches Wikidata, Genes on human chromosome 13). ... Homo sapiens CFAP97D2 gene (XM_017020910.2) is a 68,395 base pair gene that encodes mRNA transcripts ranging from 952 ... It is located on Chromosome 13 and found at locus 13q34 on the plus strand. CFAP97D2 is on Chromosome 13. This gene encodes 166 ... "Human BLAT Search". genome.ucsc.edu. Retrieved 2022-12-16. "CFAP97D2 CFAP97 domain containing 2 [Homo sapiens (human)] - Gene ...

The resulting karyotype in humans leaves only 45 chromosomes, since two chromosomes have fused together. This has no direct ... meaning that given two healthy pairs of chromosomes, one of each pair "sticks" and blends together homogeneously. A gene fusion ... The most common translocation in humans involves chromosomes 13 and 14 and is seen in about 0.97 / 1000 newborns. Carriers of ... The designation t(A;B)(p1;q2) is used to denote a translocation between chromosome A and chromosome B. The information in the ...

Murray P. Cox and Marta Mirazón Lahr, "Y-Chromosome Diversity Is Inversely Associated With Language Affiliation in Paired ... Reduced Y-Chromosome, but Not Mitochondrial DNA, Diversity in Human Populations from West New Guinea Am J Hum Genet 72:281-302 ... Y-chromosome haplogroup M, Y-chromosome haplogroup O, and Y-chromosome haplogroup S across the mountain highlands; meanwhile, D ... Asian Human Rights Commission - and - Human Rights and Peace for Papua. September 2013. ISBN 978-962-8314-621. Archived (PDF) ...

v t e (Articles with short description, Short description matches Wikidata, Genes on human chromosome 6, Wikipedia articles ... a modular protein structure consisting of a pair of C2H2 zinc fingers with an acidic-rich region and a serine/threonine-rich ... "Localization of the zinc finger DNA-binding protein HIV-EP1/MBP-1/PRDII-BF1 to human chromosome 6p22.3-p24". Genomics. 9 (4): ... "Entrez Gene: HIVEP1 human immunodeficiency virus type I enhancer binding protein 1". Omichinski JG, Clore GM, Robien M, et al ...

Some humans also hunt aardvarks for meat. Aardvarks can dig fast or run in zigzag fashion to elude enemies, but if all else ... Aardvarks pair only during the breeding season; after a gestation period of seven months, one cub weighing around 1.7-1.9 ... Genetically speaking, the aardvark is a living fossil, as its chromosomes are highly conserved, reflecting much of the early ... The Dagombas believe this animal can transfigure into and interact with humans. The ancient Egyptian god Set is usually ...

Four copies of this gene are found on chromosome Y within palindromic duplications; one pair of genes is part of the P2 ... Yen PH, Chai NN, Salido EC (1997). "The human DAZ genes, a putative male infertility factor on the Y chromosome, are highly ... Fox MS, Reijo Pera RA (2002). "Male infertility, genetic analysis of the DAZ genes on the human Y chromosome and genetic ... 1996). "The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified ...

Genes on human chromosome 2, Cytokines). ... "Osteoporotic fractures are associated with an 86-base pair ... The interleukin-1 receptor antagonist protein (IL-1RN) is a protein that in humans is encoded by the IL1RN gene. IL-1RN was ... Anakinra differs from native human IL-1Ra in that it has the addition of a single methionine residue at its amino terminus ... Patterson D, Jones C, Hart I, Bleskan J, Berger R, Geyer D, Eisenberg SP, Smith MF, Arend WP (January 1993). "The human ...

In 2008, a genome sequencing project discovered that large portions of the human X and Y chromosomes are arranged as ... Because a DNA sequence is double stranded, the base pairs are read, (not just the bases on one strand), to determine a ... A palindromic structure allows the Y chromosome to repair itself by bending over at the middle if one side is damaged. ... Since a double helix is formed by two paired antiparallel strands of nucleotides that run in opposite directions, and the ...

Humans have 23 pairs of chromosomes, while chimpanzees, gorillas and orangutans have 24. Human chromosome 2 is a fusion of two ... human to human) was set to be 1. The ID between humans and gorillas was determined to be 1.09, that between humans and ... Human evolutionary genetics studies how one human genome differs from another human genome, the evolutionary past that gave ... These findings hint at the seemingly important role of human-specific insertions in the recent evolution of humans. Human ...

The breaks can lead to mutations that reposition a chromosome and can even lead to the entire loss of a chromosome. The ... These loops can consist of hundreds of base pairs, but the length depends on how tightly the DNA is wound, as well as how much ... Due to research done using BLAST (biotechnology), it is believed that the yeast RSC complex is even more similar to the human ... SWI/SNF is recruited first, prior to two homologous chromosomes bind, and then RSC is recruited to help complete the repair. A ...

The UQCC3 gene is located on the q arm of chromosome 11 in position 12.3 and spans 2,036 base pairs. The gene produces a 10.1 ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 11, CS1 Chinese-language sources ... "A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stability". Human Molecular ... "A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stability". Human Molecular ...

Brown RM, Dahl HH, Brown GK (Feb 1989). "X-chromosome localization of the functional gene for the E1 alpha subunit of the human ... which range from 61 to 174 base pairs, and introns, whose sizes range from 600 base pairs to 5.7 kilobase pairs. The splice ... Articles with short description, Short description matches Wikidata, Genes on human chromosome X, Mitochondrial proteins). ... The protein encoded by the human PDHA1 gene is part of the pyruvate dehydrogenase multienzyme complex. The entire human complex ...

"one mutation in every 30 million base pairs" Karmin; et al. (2015). "A recent bottleneck of Y chromosome diversity coincides ... In human genetics, a human Y-chromosome DNA haplogroup is a haplogroup defined by mutations in the non-recombining portions of ... 2016). "The Divergence of Neandertal and Modern Human Y Chromosomes". The American Journal of Human Genetics. 98 (4): 728-34. ... Y-chromosome DNA (Y-DNA) haplogroups are the major branches on the human paternal family tree. Each haplogroup has many ...

... is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome ... "Chromosome 19: Chromosome summary - Homo sapiens". Ensembl Release 88. 2017-03-29. Retrieved 2017-05-19. "Human chromosome 19: ... Gilbert F (1997). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 19". Genet Test. 1 (2): 145-9. ... 2010.pdf Wikimedia Commons has media related to Human chromosome 19. National Institutes of Health. "Chromosome 19". Genetics ...

miR-16 and miR-15a are clustered within a 0.5 kbp region in Chromosome 13 (13q14) in humans, a chromosomal region shown to be ... Lewis BP, Burge CB, Bartel DP (2005). "Conserved seed pairing, often flanked by adenosines, indicates that thousands of human ... Eis PS, Tam W, Sun L, Chadburn A, Li Z, Gomez MF, Lund E, Dahlberg JE (2004). "Accumulation of miR-155 and BIC RNA in human B- ... miR16 has been shown to bind to a nine base pair to a complementary sequence in the 3' UTR region of BCL2, which is an anti- ...

... of the Y chromosome during meiosis. Additionally, 10-25% of human X chromosome genes, and 3-7% of mouse X chromosome genes ... with females possessing five pairs of X chromosomes as the homogametic sex, and males possessing five X and five Y chromosomes ... Specifically, platypus X1 shares homology with the chicken Z chromosome, and both share homology with the human chromosome 9. ... expressed X chromosome. Thus, human females have the same number of expressed X-linked genes per cell as do human males (XY), ...

Genes on human chromosome 17, All stub articles, Human chromosome 17 gene stubs). ... The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. The type I ... Keratin, type I cytoskeletal 23 is a protein that in humans is encoded by the KRT23 gene. The protein encoded by this gene is a ... Hesse M, Magin TM, Weber K (2002). "Genes for intermediate filament proteins and the draft sequence of the human genome: novel ...

It shows 22 homologous autosomal chromosome pairs, both the female (XX) and male (XY) versions of the two sex chromosomes, as ... symbols and abbreviated terms used in the description of human chromosome and chromosome abnormalities. Abbreviations include a ... or has more than two chromosomes of a pair (trisomy, tetrasomy, etc.). Aneuploidy can be full, involving a whole chromosome ... Known disorders in humans include Wolf-Hirschhorn syndrome, which is caused by partial deletion of the short arm of chromosome ...

In humans, this gene is located on chromosome 1 p34.3. The human mRNA transcript is 2527 base pairs and the final protein ... The human protein has two isoforms and no paralogs. The second isoform is 645 amino acids long and is identical to the first ... In humans, these SH3 domains have a common amino acid sequence Asp-Glu-Leu. This sequence motif is also conserved in other ... Human Reproduction. 27 (3): 921-9. doi:10.1093/humrep/der440. PMID 22238114. Nahed BV, Seker A, Guclu B, Ozturk AK, Finberg K, ...

An SGM Plus profile consists of a list of 10 number pairs, one number pair for each of 10 genetic markers, along with two ... The Human Genetics Commission has reported that the random match probability is in the region of 1 in a trillion. However it ... For example, D21S11 is on chromosome 21. SGM Plus also uses the amelogenin (amelo) sex-indicating test. SGM Plus differs from ... Each number pair denotes the two allele values for the marker - one value is inherited from each of the subject's parents. If ...

... the species has 112 pairs of chromosomes. The cited authority, Georgi, is in reference to the work of a German botanist named ... or dispersed by humans. The establishment of the seed in the appropriate ecological conditions for N. tetragona to thrive and ... Retrieved 14 February 2021. Raskoti, B. B.; Bhatt, G. D.; Ale, R. (2015-09-24). "Nymphaea tetragona (Nymphaeaceae) a new record ... treatment in combination with antibiotics for fighting against the bacterial resistance of a Salmonella infection in humans and ...

v t e (Articles lacking in-text citations from January 2020, All articles lacking in-text citations, Genes on human chromosome ... which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational ... MicroRNA 3173 is a protein that in humans is encoded by the MIR3173 gene. microRNAs (miRNAs) are short (20-24 nt) non-coding ... GRCh38: Ensembl release 89: ENSG00000264607 - Ensembl, May 2017 "Human PubMed Reference:". National Center for Biotechnology ...

Chromosome 16 open reading frame 95 (C16orf95) is a gene which in humans encodes the protein C16orf95. It has orthologs in ... The longest transcript contains 1156 base pairs and 7 exons. Compared to variant 1, the second transcript variant lacks exons 4 ... "C16orf95 chromosome 16 open reading frame 95 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2016-05-03 ... C16orf95 is a Homo sapiens gene oriented on the minus strand of chromosome 16. It is located on the cytogenic band 16q24.2 and ...

... karyotypes that include mixed XX and XY chromosome pairs (46XX/46XY, 46XX/47XXY or 45X/XY mosaic). Clinically, medicine ... African Commission on Human and Peoples' Rights; Council of Europe Commissioner for Human Rights; Inter-American Commission on ... from the Y chromosome to the X chromosome during meiosis. The SRY is then activated in only certain areas, causing development ... Commissioner for Human Rights (April 2015), Human rights and intersex people, Issue Paper, archived from the original on 2016- ...

MIT Press ISBN 9780262046756 Jablonka, E.; Lamb, M. (1988). "Meiotic pairing constraints and the activity of sex chromosomes ... extended models of human cultural transmission to the non-human animal world, to show that cultural evolution has played an ... They suggest that consciousness is found not only in humans but also in such animals as octopuses and bees, as well as ... The fourth dimension is symbolic inheritance, which is unique to humans, and in which traditions are passed on "through our ...

... (Chromosome 2, Open Reading Frame 72) is a gene in humans (Homo sapiens) that encodes a protein currently named after ... on the long arm of the chromosome. C2orf72's mRNA transcript is reported to be about 3,629 base pairs long. It appears to have ... "C2orf72 chromosome 2 open reading frame 72 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2021-08-02. " ... Genes on human chromosome 2, Articles with short description, Short description is different from Wikidata, Genes, Lipids, ...

... embryos do not have sex chromosomes, and unlike humans, sex is not determined genetically. Sex is determined by ... In the UK, a row of schoolchildren walking in pairs, or two by two is known as "crocodile". The French clothing company Lacoste ... Mating always takes place in water, where the pair can be observed mating several times. Females can build or dig several trial ... The larger species of crocodiles are very dangerous to humans, mainly because of their ability to strike before the person can ...

MEN-mediated Cdk dephosphorylation is necessary for chromosome decondensation. In vertebrates, chromosome decondensation is ... An important regulator and effector of telophase is cdc48 (homologous to yeast cdc48 is human p97, both structurally and ... Cytokinesis typically begins before late telophase and, when complete, segregates the two daughter nuclei between a pair of ... As chromosomes reach the cell poles, a nuclear envelope is re-assembled around each set of chromatids, the nucleoli reappear, ...

Down Syndrome is a genetic disorder caused by trisomy of human chromosome 21. The current hypothesis regarding congenital heart ... and this study was among the first to utilize these concepts in a paired fashion to determine information about the underlying ... is that three copies of functional genomic elements on chromosome 21 and genetic variation of chromosome 21 and non-chromosome ... A study of the human immune system in 2015 uses the same general concepts to identify several loci involved in the development ...