*  PAX7 - Wikipedia
Schäfer BW, Mattei MG (July 1993). "The human paired domain gene PAX7 (Hup1) maps to chromosome 1p35-1p36.2". Genomics. 17 (1 ... Paired box protein Pax-7 is a protein that in humans is encoded by the PAX7 gene. Pax-7 plays a role in neural crest ... Pilz AJ, Povey S, Gruss P, Abbott CM (March 1993). "Mapping of the human homologs of the murine paired-box-containing genes". ... PAX7 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH) PAX7 human gene location in the UCSC ...
  https://en.wikipedia.org/wiki/PAX7
*  June 13 - Today in Science History - Scientists born on June 13th, died, and events
French geneticist who made the first positive identification (1959) linking a human disorder to a chromosome aberration. The ... Lejeune discovered the existence of an extra chromosome on the 21st pair. On 26 Jan 1959, J r me Lejeune, with Marthe Gauthier ... It doesn't happen as often as it should, because scientists are human and change is sometimes painful. But it happens every day ... American surgeon, a pioneer of modern immunology who performed the world's first successful human bone marrow transplant (1968 ...
  https://todayinsci.com/6/6_13.htm
*  QTL Methodology in Behavior Genetics | Springer for Research & Development
Drigalenko, E. (1998). How sib pairs reveal linkage. American Journal of Human Genetics, 63, 1242-1245.PubMedGoogle Scholar ... 1999). Quantitative trait locus for specific language and reading deficits on chromosome 6p. American Journal of Human Genetics ... Wright, F. A. (1997). The phenotypic difference discards sib-pair QTL linkage information. American Journal of Human Genetics, ... 1997). Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. American Journal of Human ...
  https://rd.springer.com/chapter/10.1007/978-0-387-76727-7_3
*  Artificial chromosome - Patent # 6716608 - PatentGenius
... preparing a CEPH artificial yeast chromosome library containing a human genome, identifying clones having a repetitive human ... telomere sequences are added to the ends of its chromosome. ... An artificial mammalian chromosome, more specifically, a clone ... containing a specific DNA sequence called the repetitive alphoid sequence that repeats over a few hundred kilo base pairs in ... A stable chromosome can thus be prepared in a yeast cell. If such a chromosome is capable of replicating in a human cell, it ...
  http://www.patentgenius.com/patent/6716608.html
*  PAX4 - Wikipedia
Paired box gene 4, also known as PAX4, is a protein which in humans is encoded by the PAX4 gene. This gene is a member of the ... "Assignment of the human PAX4 gene to chromosome band 7q32 by fluorescence in situ hybridization". Cytogenetics and Cell ... Pilz AJ, Povey S, Gruss P, Abbott CM (1993). "Mapping of the human homologs of the murine paired-box-containing genes". ... Members of this gene family typically contain a paired box domain, an octapeptide, and a paired-type homeodomain. These genes ...
  https://en.wikipedia.org/wiki/PAX4
*  PAX1 - Wikipedia
... a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ ... Paired box protein Pax-1 is a protein that in humans is encoded by the PAX1 gene. This gene is a member of the paired box (PAX ... 1989). "Conservation of the paired domain in metazoans and its structure in three isolated human genes". EMBO J. 8 (4): 1183-90 ... 2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. 414 (6866): 865-71. doi:10.1038/414865a. ...
  https://en.wikipedia.org/wiki/PAX1
*  lifeissues.net | Playing God by Manipulating Man: The Facts and Frauds of Human Cloning
When does a human being begin to exist'. Proponents of both abortion and of human cloning want you to think that a human being ... The most devastating scientific myth in both the abortion and in the human cloning debates concerns the question, ' ... Diploid refers to the presence of two sets of homologous chromosomes: 23 pairs, making a total of 46. This is characteristic of ... The 46 chromosomes consist of 44 autosomes and two sex chromosomes: X and Y. In the male the sex chromosomes are XY; in the ...
  http://www.lifeissues.net/writers/irv/irv_22manipulatingman3.html
*  DNA - Human Genome | ENCOGNITIVE.COM
Human Genome. The human genome is the genome of Homo sapiens, which is composed of 24 distinct pairs of chromosomes (22 ... Chromosomes. There are 24 distinct human chromosomes: 22 autosomal chromosomes, plus the sex-determining X and Y chromosomes. ... The Y-Chromosome. Human sex is determined by the X and Y chromosomes. A female has 2 X-Chromosomes and a male has an X and a Y- ... The four bases pair in a set manner: Adenine (A) pairs with thymine (T), while cytosine (C) pairs with guanine (G). These pairs ...
  http://encognitive.com/node/1184
*  PAX6 - Wikipedia
Paired box protein Pax-6, also known as aniridia type II protein (AN2) or oculorhombin, is a protein that in humans is encoded ... van Heyningen V, Little PF (1995). "Report of the fourth international workshop on human chromosome 11 mapping 1994". Cytogenet ... The characteristic paired DNA binding domain of Pax6 utilizes two DNA-binding domains, the paired domain (PD), and the paired- ... The paired domain and paired-type homeodomain each have DNA binding activities, while the P/S/T-rich domain possesses a ...
  https://en.wikipedia.org/wiki/PAX6
*  CRX (gene) - Wikipedia
Critical differences during human and mouse eye development". Human Molecular Genetics. 10 (15): 1571-9. doi:10.1093/hmg/10.15. ... "Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion". Nature Genetics. 6 (2 ... a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes". Neuron. 19 (5): ... Cone-rod homeobox protein is a protein that in humans is encoded by the CRX gene. The protein encoded by this gene is a ...
  https://en.wikipedia.org/wiki/CRX_(gene)
*  Antievolution.org - Antievolution.org Discussion Board -Topic::The Origin of 'Information' via natural causes
Humans and other Anthropoids share very similar chromosome structure and genomic sequence as seen in the 98.5% homology at the ... that are located on different chromosomes with hallmarks of retroposition (Table 1). Twenty-four young paralogous pairs ... SCN11A is localized to human chromosome 3 (3p21-24) close to the other TTX-R sodium channel genes SCN5A and SCN10A. An ... New genes in humans and our primate relatives add a new component to the understanding of genetic divergence between humans and ...
  http://www.antievolution.org/cgi-bin/ikonboard/ikonboard.cgi?s=5071d649b5e9c721
*  Antievolution.org - Antievolution.org Discussion Board -Topic::The Origin of 'Information' via natural causes
... both bcntp97 and the h-type bcnt genes are found on bovine chromosome 18, a synteny region of human chromosome 16 on which ... that are located on different chromosomes with hallmarks of retroposition (Table 1). Twenty-four young paralogous pairs ... Birth of 'human-specific' genes during primate evolution.. Nahon JL.. Quote Humans and other Anthropoids share very similar ... SCN11A is localized to human chromosome 3 (3p21-24) close to the other TTX-R sodium channel genes SCN5A and SCN10A. An ...
  http://www.antievolution.org/cgi-bin/ikonboard/ikonboard.cgi?s=50c2f933e02fe4c0
*  PCSK7 - Wikipedia
Proprotein convertase subtilisin/kexin type 7 is an enzyme that in humans is encoded by the PCSK7 gene. The protein encoded by ... 1999). "Molecular analysis of an unstable genomic region at chromosome band 11q23 reveals a disruption of the gene encoding the ... 1997). "Identification of the paired basic convertases implicated in HIV gp160 processing based on in vitro assays and ... 1996). "A new member of the proprotein convertase gene family (LPC) is located at a chromosome translocation breakpoint in ...
  https://en.wikipedia.org/wiki/PCSK7
*  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
*  RSPH6A - Wikipedia
2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs ... The RSPH6A gene maps to a region of chromosome 19 that is linked to primary ciliary dyskinesia-2 (CILD2). GRCh38: Ensembl ... of the axoneme of eukaryotic flagella and are located between the axoneme's outer ring of doublet microtubules and central pair ... 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/RSPH6A
*  COX5B - Wikipedia
The COX5B gene, located on the q arm of chromosome 2 in position 11.2, is made up of 4 exons and is 2,137 base pairs in length ... In humans, cytochrome c oxidase subunit 5B is encoded by the COX5B gene. The enzyme weighs 14 kDa and is composed of 129 amino ... Human COX5B genome location and COX5B gene details page in the UCSC Genome Browser. Mass spectrometry characterization of COX5B ... Cytochrome c oxidase subunit 5B, mitochondrial is an enzyme in humans that is a subunit of the cytochrome c oxidase complex, ...
  https://en.wikipedia.org/wiki/COX5B
*  Bf800d5f72eac060131443307a306d52
In humans bf800d5f72eac060131443307a306d52 ABO genes consist of at least sevenexons, and they are located on chromosome 9. ... For each microbiologicalsample bf800d5f72eac060131443307a306d52 we recommend obtaining a paired biopsy for histopathological ... assuming an average thickness of 16to 20 cells in humans).Therefore, the total epidermal turnover time is approximately 47 days ... assuming an average thickness of 16to 20 cells in humans).Therefore, the total epidermal turnover time is approximately 47 days ...
  http://www.torontomarathon.com/barrday-200/
*  TBX1 - Wikipedia
The TBX1 gene is located on the long (q) arm of chromosome 22 at position 11.21, from base pair 18,118,779 to base pair ... Packham EA, Brook JD (April 2003). "T-box genes in human disorders". Human Molecular Genetics. 12. 12 Spec No 1 (Spec No 1): ... Human Mutation. 34 (9): 1250-9. doi:10.1002/humu.22354. PMC 3746749 . PMID 23661601. TBX1 protein, human at the US National ... Loss of the TBX1 gene, due to either a mutation in the gene or a deletion of part of chromosome 22, is responsible for many of ...
  https://en.wikipedia.org/wiki/TBX1
*  CD99 - Wikipedia
"Homologous expressed genes in the human sex chromosome pairing region". Nature. 317 (6039): 739-41. doi:10.1038/317739a0. PMID ... CD99 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH) Human CD99 genome location and CD99 ... a gene shared by the human X and Y chromosomes". Cold Spring Harb. Symp. Quant. Biol. 51 (1): 205-12. doi:10.1101/SQB.1986.051. ... Unusually for a gene present on the X chromosome, the CD99 gene does not undergo X inactivation, and it was the first such ...
  https://en.wikipedia.org/wiki/CD99
*  Synteny - Wikipedia
... and Comparative Chromosome Maps of the Human, Mouse, and Rat. Graham Moore group research page - cereal genomics More ... "Molecular characterization of Ph1 as a major chromosome pairing locus in polyploid wheat". Nature. 439: 749-752. doi:10.1038/ ... For example, many of the genes of humans are syntenic with those of other mammals-not only apes but also cows, mice, and so on ... The term is sometimes also used to describe preservation of the precise order of genes on a chromosome passed down from a ...
  https://en.wikipedia.org/wiki/Synteny
*  Tau protein - Wikipedia
In humans, the MAPT gene for encoding tau protein is located on chromosome 17q21, containing 16 exons.[citation needed] The ... "Biopsy-derived adult human brain tau is phosphorylated at many of the same sites as Alzheimer's disease paired helical filament ... For example, PP2A and PP2B are both present in human brain tissue and have the ability to dephosphorylate Ser396. The binding ... Kanemaru K, Takio K, Miura R, Titani K, Ihara Y (May 1992). "Fetal-type phosphorylation of the tau in paired helical filaments ...
  https://en.wikipedia.org/wiki/Tau_protein
*  SOX4 - Wikipedia
Schepers GE, Teasdale RD, Koopman P (2002). "Twenty pairs of sox: extent, homology, and nomenclature of the mouse and human sox ... refinement of the human SOX4 location to 6p22.3 and of SOX20 to chromosome 17p12.3". Cytogenet Cell Genet. 81 (3-4): 294-5. doi ... SOX4 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH) This article incorporates text from ... Transcription factor SOX-4 is a protein that in humans is encoded by the SOX4 gene. This intronless gene encodes a member of ...
  https://en.wikipedia.org/wiki/SOX4
*  Collagen, type VII, alpha 1 - Wikipedia
COL7A1 is located on the short arm of human chromosome 3, in the chromosomal region denoted 3p21.31. The gene is approximately ... COL7A1 is transcribed into an mRNA of 9,287 base pairs. In the skin, the type VII collagen protein is synthesized by ... Collagen alpha-1(VII) chain is a protein that in humans is encoded by the COL7A1 gene. This gene encodes the alpha chain of ... Greenspan DS, Byers MG, Eddy RL, Hoffman GG, Shows TB (1993). "Localization of the human collagen gene COL7A1 to 3p21.3 by ...
  https://en.wikipedia.org/wiki/Collagen,_type_VII,_alpha_1
*  GTF2H2 - Wikipedia
General transcription factor IIH subunit 2 is a protein that in humans is encoded by the GTF2H2 gene. This gene is part of a ... It is reported to be different by either two or four base pairs; however, no sequence data is currently available for the ... 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements ... Drapkin R, Le Roy G, Cho H, Akoulitchev S, Reinberg D (1996). "Human cyclin-dependent kinase-activating kinase exists in three ...
  https://en.wikipedia.org/wiki/GTF2H2
*  Membrane proteins Bqt3 and -4 anchor telomeres to the nuclear envelope to ensure chromosomal bouquet formation | JCB
HIM-8 binds to the X chromosome pairing center and mediates chromosome-specific meiotic synapsis. Cell. 123:1051-1063. doi: ... Human aneuploidy: incidence, origin, and etiology. Environ. Mol. Mutagen. 28:167-175. doi:10.1002/(SICI)1098-2280(1996)28:3,167 ... each specifically binding to one or two chromosomes, mediates pairing of homologous chromosomes in meiosis (Phillips et al., ... Dynamics of homologous chromosome pairing during meiotic prophase in fission yeast. Dev. Cell. 6:329-341. doi:10.1016/S1534- ...
  http://jcb.rupress.org/content/187/3/413/