Y-chromosome haplotypes and implications for human history in the Pacific". Human Mutation. 17 (4): 271-80. doi:10.1002/humu.23 ... "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 ... and East Indonesia by human Y-chromosome DNA haplogroups based on relevant studies. Oceania Languages of Oceania Demographics ...

"International Human Genome Sequencing Consortium Announces "Working Draft" of Human Genome". National Human Genome Research ... Human Genome Sequencing Consortium (2004). "Finishing the euchromatic sequence of the human genome". Nature. 431 (7011): 931- ... The institute's research in human genetics focuses on the characterisation of human genetic variation in health and disease. ... Explores human gene function by studying the impact of genome variation on cell biology. Large-scale systematic screens are ...

The chapters are numbered for the pairs of human chromosomes, one pair being the X and Y sex chromosomes, so the numbering goes ... The book devotes one chapter to each pair of human chromosomes. Since one (unnumbered) chapter is required to discuss the sex ... the chapters matching the 23 pairs of human chromosomes, and notes that Genome is the third of Ridley's books that "tries to ... Ridley concludes that the Human Genome Project is largely based on the inaccurate belief that there is one single human genome ...

When multiple chromosomes are involved in chromothripsis, fragments of both chromosomes are joined together by paired end ... using genome-wide paired-end sequencing and SNP array analysis have found similar patterns of chromothripsis in various human ... Cells with defective chromosome segregation will form micronuclei which contain whole chromosomes or fragments of chromosomes. ... Through paired end sequencing, 55 chromosomal rearrangements were found in the long arm of chromosome 8 and a significant ...

Genes on human chromosome 8, Wikipedia articles incorporating text from the United States National Library of Medicine). ... The TMEM70 gene has 4 exons and is located on the q arm of chromosome 8 in position 21.11 and spans 6,642 base pairs. The gene ... Transmembrane protein 70 is a protein that in humans is encoded by the TMEM70 gene. It is a transmembrane protein located in ... American Journal of Human Genetics. 85 (5): 628-42. doi:10.1016/j.ajhg.2009.10.014. PMC 2775832. PMID 19913121. Karasik D, Hsu ...

In humans, both genes are located on chromosome 2 in position 2p12. The CD8 co-receptor is predominantly expressed on the ... To function, CD8 forms a dimer, consisting of a pair of CD8 chains. The most common form of CD8 is composed of a CD8-α and CD8- ... Genes on human chromosome 2, Clusters of differentiation, Immunology, T cells). ... PDB: 1cd8​; Leahy DJ, Axel R, Hendrickson WA (March 1992). "Crystal structure of a soluble form of the human T cell coreceptor ...

The human DERL1 gene is located on the long (q) arm of chromosome 8 at region 2 band 4, from base pair 123,013,164 to ... Articles with short description, Short description is different from Wikidata, Genes on human chromosome 8). ... Each protomer in human Derlin-1 tetramer shares a high structural similarity with yeast DER1 protein or other rhomboid members ... Wang J, Hua H, Ran Y, Zhang H, Liu W, Yang Z, Jiang Y (2008). "Derlin-1 is overexpressed in human breast carcinoma and protects ...

Among the 23 pairs of chromosomes, there are 22 pairs of autosomes and one pair of sex chromosomes. Like other mammals, humans ... chromosome 2 was formed from the joining of two other chromosomes, leaving humans with only 23 pairs of chromosomes, compared ... MacAndrew A. "Human Chromosome 2 is a fusion of two ancestral chromosomes". Evolution pages. Archived from the original on 9 ... the eight richest humans are worth the same monetary value as the poorest half of all the human population. Humans commit ...

Glutamate rich protein 5 is a protein in humans encoded by the ERICH5 gene, also known as chromosome 8 open reading frame 47 ( ... The second isoform lacks the third and final exon and is 596 base pairs long. ERICH5 contains one conserved domain, a domain of ... The ERICH5 gene is located on human chromosome 8 at 8q22.2 and spans 29 kb on the plus strand of the DNA. ERICH5 contains three ... Database, GeneCards Human Gene. "ERICH5 Gene - GeneCards , ERIC5 Protein , ERIC5 Antibody". www.genecards.org. Retrieved 2018- ...

Pairs of 1B/2B (ABP) genes are arranged head-to-head on the chromosome into "modules" that have been independently duplicated. ... The human and mouse genomes only contain the first three families, per an 2011 update. Not every family is monophyletic. Rat ... Subfamily 6 was supposed to include human and rat RYD5, now reassigned Scgb1c1. Fel d 1 was supposed to be put into two ... Umland TC, Swaminathan S, Singh G, Warty V, Furey W, Pletcher J, Sax M (August 1994). "Structure of a human Clara cell ...

The NDUFAF8 gene is located on the q arm of chromosome 17 in position 25.3 and spans 1,987 base pairs. The gene produces a ... v t e (Articles with short description, Short description matches Wikidata, Human genes, Wikipedia articles incorporating text ... from the United States National Library of Medicine, All stub articles, Human chromosome 17 gene stubs). ... GRCm38: Ensembl release 89: ENSMUSG00000078572 - Ensembl, May 2017 "Human PubMed Reference:". National Center for Biotechnology ...

The gene that encodes the human GJB1 protein is found on the X chromosome, on the long arm at position q13.1, in interval 8, ... from base pair 71,215,212 to base pair 71,225,215. Approximately four hundred type X Charcot-Marie-Tooth causing mutations have ... Genes on human chromosome X, Cis-regulatory RNA elements, Connexins). ... Because GJB1 is located on the X chromosome, GJB1 disease is a type of "X-linked" CMT. Multiple X-linked CMTs have now been ...

Genes on human chromosome 11, Protein pages needing a picture, Genes on human chromosome 12, Genes on human chromosome 6, Cell ... one member of a chromosome pair) have acquired new functions in order to manipulate the host cell's metabolism to the viruses' ... In mice and humans, two more cyclin D proteins have been identified. The three homologues, called cyclin D1, cyclin D2, and ... Given that many human cancers happen in response to errors in cell cycle regulation and in growth factor dependent ...

The ALOX5 gene, which occupies 71.9 kilobase pairs (kb) on chromosome 10 (all other human lipoxygenases are clustered together ... Aberrant expression of LOX5 is seen in various types of human cancer tumors in vivo as well as in various types of human cancer ... Studies with cultured human cells have found that there are a large number of ALOX5 mRNA splice variants due to alternative ... Human ALOX5 is a soluble, monomeric protein consisting of 673 amino acids with a molecular weight of ~78 kDa. Structurally, ...

... encoded by six highly homologous genes that are arranged in tandem and inverted pairs on chromosome 19q13.3 - CGB (1, 2, 3, 5, ... Talwar GP (1997). "Fertility regulating and immunotherapeutic vaccines reaching human trials stage". Human Reproduction Update ... Genes on human chromosome 6, Pages using infobox protein with unknown parameters, Protein pages needing a picture, Genes on ... Human chorionic gonadotropin interacts with the LHCG receptor of the ovary and promotes the maintenance of the corpus luteum ...

PAR1 comprises 2.6 Mbp of the short-arm tips of both X and Y chromosomes in humans and great apes (X and Y are 154 Mbp and 62 ... Pairing (synapsis) of the X and Y chromosomes and crossing over (recombination) between their pseudoautosomal regions appear to ... The function of these pseudoautosomal regions is that they allow the X and Y chromosomes to pair and properly segregate during ... between the pseudoautosomal regions of the X and Y chromosomes can disrupt pairing and recombination, and consequently cause ...

For example, the RH procedure was used to map 14 DNA probes from a region of human chromosome 21 spanning 20 megabase pairs. ... If two given DNA markers are far apart on the initial chromosome, then it is likely that they will appear in distinct fragments ... A radiation hybrid is "a cell or organism that contains fragments of chromosomes from a second organism".: 82 Radiation hybrids ... Radiation hybrid mapping was also used in constructing early physical maps of the human genome. Deloukas, Panos (23 September ...

Paired box gene 9, also known as PAX9, is a protein which in humans is encoded by the PAX9 gene. It is also found in other ... Articles with short description, Short description is different from Wikidata, Genes on human chromosome 14, Wikipedia articles ... In humans, a frameshift mutation in the paired domain of PAX9 was discovered in those affected with oligodontia. Multiple ... "A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia". Human Genetics. 114 (3): 242-9. doi: ...

In these mice, the prophase I stage of meiosis is defective due to the disruption of chromosome pairing. This meiotic failure ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 6). ... "Mammalian MutS homologue 5 is required for chromosome pairing in meiosis". Nature Genetics. 21 (1): 123-7. doi:10.1038/5075. ... "Mammalian MutS homologue 5 is required for chromosome pairing in meiosis". Nature Genetics. 21 (1): 123-7. doi:10.1038/5075. ...

The ATPAF2 gene is located on the p arm of chromosome 17 in position 11.2 and spans 24,110 base pairs. The gene produces a 32.8 ... Genes on human chromosome 17, Wikipedia articles incorporating text from the United States National Library of Medicine, Genes ... Human ATPAF2 genome location and ATPAF2 gene details page in the UCSC Genome Browser. This article incorporates text from the ... ATP synthase mitochondrial F1 complex assembly factor 2 is an enzyme that in humans is encoded by the ATPAF2 gene. This gene ...

Located on the negative strand of human DNA, TMEM143 spans 31,882 base pairs on human chromosome 19 (19q13.33), neighbored by ... human)]". NCBI. "Tmem143 (human)". NCBI. "TMEM143 Gene". GeneCards. "TMEM143 - Normal human tissue expression profiling". NCBI ... There are no known paralogs for the human TMEM143 sequence. Possible human expression of TMEM143 protein occurs in Jurkat cells ... Chromosome 14 open reading frame 28 (C14orf28), Chromosome 14 open reading frame 28 (TRIN71), and Cytoplasmic polyadenylation ...

December 1999). "Y-Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age". ... "Y-chromosome diversity is inversely associated with language affiliation in paired Austronesian- and Papuan-speaking ... November 2000). "Y chromosome sequence variation and the history of human populations". Nature Genetics. 26 (3): 358-361. doi: ... 1 July 2001). "Hierarchical Patterns of Global Human Y-Chromosome Diversity". Molecular Biology and Evolution. 18 (7): 1189- ...

... 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), ...

Human AVPR1A is situated on chromosome 12q14-15, and the promoter region does not have repeat sequences homologous to those ... associates with pair-bonding behavior in humans". Proceedings of the National Academy of Sciences of the United States of ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 12, Wikipedia articles needing ... human AVPR2, rat Avpr2, and human oxytocin receptor (OXTR), respectively. AVPR1A is a G-protein coupled receptor (GPCR) with 7 ...

Genes on human chromosome 10, All stub articles, Human chromosome 10 gene stubs). ... The gene is located on the long arm of chromosome 10 (10q21.2) on the 'plus' strand. It spans 195,261 base pairs in length. It ... Human ARID5B genome location and ARID5B gene details page in the UCSC Genome Browser. Yuan YC, Whitson RH, Liu Q, Itakura K, ... AT-rich interactive domain-containing protein 5B is a protein that in humans is encoded by the ARID5B gene. Alternative names ...

September 1999). "Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q". Genomics ... "The assignment of chemokine-chemokine receptor pairs: TARC and MIP-1 beta are not ligands for human CC-chemokine receptor 8". ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 16, Cytokines). ... In humans the gene for CCL17 is located on chromosome 16 along with other chemokines including CCL22 and CX3CL1. GRCh38: ...

Articles with short description, Short description matches Wikidata, Genes on human chromosome 11, All stub articles, ... a high-affinity ligand-receptor pair". Cell. 116 (6): 883-895. doi:10.1016/S0092-8674(04)00216-8. PMID 15035989. S2CID 18687651 ... "Molecular cloning and characterization of human Frizzled-4 on chromosome 11q14-q21". Biochemical and Biophysical Research ... Frizzled-4 (Fz-4) is a protein that in humans is encoded by the FZD4 gene. Fz-4 has also been designated as CD344 (cluster of ...

Articles with short description, Short description is different from Wikidata, Genes on human chromosome X). ... The first ninety base pairs compose the five prime untranslated region and the last 1913 base pairs compose the three prime ... The isoelectric point of EFHC2 is estimated to be 7.13 in humans. Relative to other proteins expressed in humans, EFHC2 has ... EFHC2 is located on the negative strand (sense strand) of the X chromosome at p11.3. EFHC2 is one of a few, select number of ...

These ten chromosomes form five unique pairs of XY in males and XX in females, i.e. males are X1Y1X2Y2X3Y3X4Y4X5Y5. One of the ... Although powerful enough to kill smaller animals such as dogs, the venom is not lethal to humans, but the pain is so ... "In the platypus a meiotic chain of ten sex chromosomes shares genes with the bird Z and mammal X chromosomes". Nature. 432 ( ... Shaw even took a pair of scissors to the dried skin to check for stitches. The common name "platypus" literally means 'flat- ...

v t e (Genes on human chromosome 12, Keratins, All stub articles, Human chromosome 12 gene stubs). ... chromosomal location emphasizes difference from other keratin pairs". New Biol. 2 (5): 464-78. PMID 1705144. Romano V, Hatzfeld ... Waseem A, Gough AC, Spurr NK, Lane EB (1990). "Localization of the gene for human simple epithelial keratin 18 to chromosome 12 ... 1990). "Localisation of a cDNA clone for human cytokeratin 18 to chromosome 17p11-p12 by in situ hybridisation". Hum. Genet. 85 ...