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
Endotoxin-tolerant Mice Have Mutations in Toll-like Receptor 4 (Tlr4) | JEM
Human PAPPA had previously been mapped to chromosome 9q33.1, a region known to be homologous to a portion of mouse chromosome 4 ... 1992) Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coliusing an F-factor-based ... comparative mapping of ESTs and genes that had been assigned to regions of human chromosome 9 syntenic with mouse chromosome 4 ... was recently identified as a direct downstream element of the human Toll signaling pathway ((36)). Human Toll and IL-1R ...http://jem.rupress.org/content/189/4/615
Chromosomal Dynamics in Meiosis | Centro de Investigaciones Biológicas - CIB
Differential cohesin loading marks paired and unpaired regions of platypus sex chromosomes at prophase I. Sci. Rep. 7(1):4217. ... and infertility in humans. A key protagonist in this control is the cohesin complex, which are composed essentially by four ... MOLECULAR BASIS OF ANEUPLOIDY IN CANCER:CHROMOSOME SEGREGATION CONTROL AND CHROMOSOME STABILITY. FUNDACIÓN DE INVESTIGACIÓN ... Chromosome segregation control in mammalian meiosis: Cohesins and cohesin-regulators. Head: José Luis Barbero Esteban ...http://cib.csic.es/research/cellular-and-molecular-biology/chromosomal-dynamics-meiosis
HKU Scholars Hub: Common genetic determinants of vitamin D insufficiency: A genome-wide association study
Chromosomes, Human, Pair 11. en_US. dc.subject.mesh. Chromosomes, Human, Pair 4. en_US. ...http://hub.hku.hk/handle/10722/183386
Funduscopic appearance of patients with Wolfram syndrom | Open-i
Chromosomes, Human, Pair 4/genetics. *DNA Mutational Analysis. *Female. *Frameshift Mutation/genetics ... Health and Human Services • 8600 Rockville Pike,Bethesda,MD 20894 Privacy • Accessibility • Freedom of Information Act • ... Health and Human Services • 8600 Rockville Pike,Bethesda,MD 20894 Privacy • Accessibility • Freedom of Information Act • ... Open-i® and the Open i logo are service marks of U.S. Department of Health and Human Services. ...https://openi.nlm.nih.gov/detailedresult.php?img=PMC2483297_mv-v14-1353-f1&req=4
Chromosome 4 (human) - Wikipedia
"Disease genes and chromosomes: disease maps of the human genome. Chromosome 4". Genet Test. 7 (4): 351-72. doi:10.1089/ ... See also: Category:Genes on human chromosome 4. The following is a partial list of genes on human chromosome 4. For complete ... The following are some of the gene count estimates of human chromosome 4. Because researchers use different approaches to ... 2005). "Generation and annotation of the DNA sequences of human chromosomes 2 and 4". Nature. 434 (7034): 724-31. Bibcode: ...https://en.wikipedia.org/wiki/Chromosome_4_(human)
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The...
U.S. Department of Health & Human Services National Institutes of Health National Center for Advancing Translational Sciences ... A (CAG)n repeat longer than the normal range was observed on HD chromosomes from all 75 disease families examined, comprising a ... A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The ... trapped exons from the target area contains a polymorphic trinucleotide repeat that is expanded and unstable on HD chromosomes ...https://publications.ncats.nih.gov/publications/8458085
Find Research Outputs - Fujita Health University
Chromosomes, Human, Pair 18 Genome-Wide Association Study Chromosomes, Human, Pair 4 ... Human tyrosine hydroxylase in Parkinson's disease and in related disorders. Nagatsu, T., Nakashima, A., Ichinose, H. & ... Japan Glaucoma Society Omics Group (JGS-OG) & NEIGHBORHOOD Consortium, 15-04-2018, In : Human molecular genetics. 27, 8, p. ... High rates of human fecal carriage of mcr-1-positive multidrug-resistant enterobacteriaceae emerge in China in association with ...https://pure.fujita-hu.ac.jp/en/publications/?format=&page=6
Chromosomes, Human, Pair 4 Proteins View all 132 research output Powered by Pure, Scopus & Elsevier Fingerprint Engine™ © 2018 ... Bosnakovski, D., Choi, S. H., Strasser, J. M., Toso, E. A., Walters, M. A. & Kyba, M., Feb 1 2014, In : Skeletal Muscle. 4, 1, ... 4, p. 392-399 8 p.. Research output: Contribution to journal › Article ...https://experts.umn.edu/en/persons/michael-kyba
TMEM33 - Wikipedia
This 1069 base pair promoter sequence spans 41936535-41937603 on human chromosome 4. The promoter sequence overlaps with the 5 ... In humans, this gene's DNA location is the short arm of chromosome 4, loci position: 4p13. The genomic range is 41937502- ... Transcripts a, b, and c have a 744 base pair long coding range and a particularly long 3' UTR that is 6000 base pairs long. In ... There is an experimentally determined acetylation point is at alanine, amino acid residue 2 in humans. Human TMEM33 has ...https://en.wikipedia.org/wiki/TMEM33
Replication timing - Wikipedia
... whereas all the other pairs of chromosomes replicate in the same temporal pattern. It was also noticed by Mary Lyon  that ... A diagrammatic representation of replication timing in a 70-Mb segment of human chromosome 2. The red horizontal line ... Replication timing and chromosome structure. Figure 5. Nucleus of a female amniotic fluid cell. Top: Both X-chromosome ... Chromosome Res 18: 115-125. *^ Taylor JH (1960) Asynchronous duplication of chromosomes in cultured cells of Chinese hamster. J ...https://en.wikipedia.org/wiki/Replication_timing
acute promyelocytic leukemia childhood 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
Chromosomes, Human, Pair 15. Chromosomes, Human, Pair 8. Core Binding Factor Alpha 2 Subunit / genetics. Female. Humans. Infant ... Chromosomes, Human, Pair 15. Chromosomes, Human, Pair 9. Cytogenetics. Humans. In Situ Hybridization, Fluorescence. Infant. ... Chromosomes, Human, Pair 15. Chromosomes, Human, Pair 17. Humans. Prognosis. Translocation, Genetic ... MeSH-major] Chromosomes, Human, Pair 15. Chromosomes, Human, Pair 17. Leukemia, Promyelocytic, Acute / genetics. Oncogene ...http://www.bmlsearch.com/?kwr=acute+promyelocytic+leukemia+childhood+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
Pediatric diagnosis not made until adulthood: a case of Wolf-Hirschhorn syndrome. - Nuffield Department of Women's &...
Wolf-Hirschhorn syndrome is a well-known clinical entity caused by a terminal deletion of the short arm of chromosome 4 (4p-). ... Adult, Chromosome Deletion, Chromosomes, Human, Pair 4, Female, Humans, Infant, Newborn, Oligonucleotide Array Sequence ... Wolf-Hirschhorn syndrome is a well-known clinical entity caused by a terminal deletion of the short arm of chromosome 4 (4p-). ...https://www.wrh.ox.ac.uk/publications/541204
NAVER Academic > Search...
Aneuploidy, Carcinoma, Small Cell, genetics, Chromosomes, Human, Pair 4, Exons, Gastrointestinal Neoplasms, Gene Amplification ... KIT and platelet-derived growth factor receptor alpha tyrosine kinase gene mutations and KIT amplifications in human solid ... Aged, Carcinoma, Non-Small-Cell Lung, drug therapy, mortality, Female, Humans, Liver Neoplasms, secondary, Lung Neoplasms, Male ... Adult, Arm, Female, Follow-Up Studies, Humans, Leg, Male, Middle Aged, Neoplasm Metastasis, Neoplasm Recurrence, Local, ...https://academic.naver.com/search.naver?field=3&query=Journal+of+Clinical+Oncology+23%EA%B6%8C+1%ED%98%B8
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. - MRC...
... that results from a single point mutation in the fibroblast growth factor receptor 3 gene on chromosome 4p. In this instance, a ... Adult, Child, Chromosomes, Human, Pair 4, Craniosynostoses, Female, Foot Deformities, Congenital, Hand Deformities, Congenital ... that results from a single point mutation in the fibroblast growth factor receptor 3 gene on chromosome 4p. In this instance, a ... Humans, Male, Pedigree, Point Mutation, Protein-Tyrosine Kinases, Radiography, Receptor, Fibroblast Growth Factor, Type 3, ...https://www.imm.ox.ac.uk/publications/827554
Chromosome 4 - Genetics Home Reference - NIH
Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 4, one copy inherited from ... Ensembl Human Map View. *Generation and annotation of the DNA sequences of human chromosomes 2 and 4. Nature. 2005 Apr 7;434( ... Ensembl Human Map View. *. Goldfrank D, Schoenberger E, Gilbert F. Disease genes and chromosomes: disease maps of the human ... Ring chromosomes occur when a chromosome breaks in two places and the ends of the chromosome arms fuse together to form a ...https://ghr.nlm.nih.gov/chromosome/4
DNA Protein Analysis Of Human Chromosome 6, Counts 166,880,988 Base Pairs, Covers Global Diseases | BioWorld
Bulkiest Human Sequence Packs Medical Arsenal DNA Protein Analysis Of Human Chromosome 6, Counts 166,880,988 Base Pairs, Covers ...http://www.bioworld.com/content/dna-protein-analysis-human-chromosome-6-counts-166880988-base-pairs-covers-global-diseases
'chromosomes human 4 5' Protocols and Video...
... called group B in the human chromosome classification. This group consists of chromosome pairs 4 and 5. ... Chromosomes, Human, 4-5: The large, submetacentric human chromosomes, ...https://www.jove.com/keyword/chromosomes+human+4+5
The Average Human Has 60 New Genetic Mutations - Slashdot
This number was less than expected, leading the researchers to believe human evolution happens more slowly than p... ... Each parent contributes 23 chromosomes, and which chromosome gets contributed is random. The chances of any two children all ... The Average Human Has 60 New Genetic Mutations 246 Posted by samzenpus on Friday June 17, 2011 @11:49AM. from the magnetic- ... Just because that is the way the human brain likes to work doesn't mean that it's a universal truth. Species do not exist as a ...https://science.slashdot.org/story/11/06/17/1425243/the-average-human-has-60-new-genetic-mutations?sdsrc=prev
NAVER Academic > Search...
Alleles, Base Pairing, Base Sequence, Case-Control Studies, Chromosomes, Human, Pair 4, genetics, Consensus Sequence, Female, ... Adult, Aged, Autopsy, Chromosome Deletion, Chromosomes, Human, Pair 17, genetics, Diabetes Mellitus, Epilepsy, complications, ... Australia, Body Height, genetics, Chromosomes, Human, Databases, Genetic, Female, Genetic Variation, Genome, Human, Humans, ... Genome partitioning of genetic variation for height from 11,214 sibling pairs.. Peter M Visscher et al. American Journal of ...https://academic.naver.com/search.naver?field=3&query=American+Journal+of+Human+Genetics+81%EA%B6%8C+5%ED%98%B8
THREE OF A KIND: December 2011
... humans have 23 pairs of chromosomes). In some cases, a child inherits achondroplasia from a parent who also has the condition. ... Achondroplasia is caused by an abnormal gene located on one of the chromosome 4 pair ( ... 12/31/2011 4 comments: Email ThisBlogThis!Share to TwitterShare to FacebookShare to Pinterest. ... 12/26/2011 4 comments: Email ThisBlogThis!Share to TwitterShare to FacebookShare to Pinterest. ...http://chmielewskifamily.blogspot.com/2011/12/
THREE OF A KIND: What is Achondroplasia?
... humans have 23 pairs of chromosomes). In some cases, a child inherits achondroplasia from a parent who also has the condition. ... Achondroplasia is caused by an abnormal gene located on one of the chromosome 4 pair ( ...http://chmielewskifamily.blogspot.com/2011/12/what-is-achondroplasia.html
PSMB4 proteasome subunit beta 4 [Homo sapiens (human)] - Gene - NCBI
... the paired chromosomes separate at the centromeres, and move to the opposite sides of the cell. The movement of the chromosomes ... Cloning and expression of a human pro(tea)some beta-subunit cDNA: a homologue of the yeast PRE4-subunit essential for ... The metaphase plate is formed when the spindle fibers align the chromosomes along the middle of the cell. Such an organization ... Cellular response to hypoxia, organism-specific biosystemOxygen plays a central role in the functioning of human cells: it is ...https://www.ncbi.nlm.nih.gov/gene/5692
Common genetic determinants of vitamin D insufficiency: a genome-wide association study. - The Kennedy Institute of Rheumatology
Canada, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 4, Cohort Studies, Dietary Supplements, Europe, European ... Kennedy Institute joins global Human Cell Atlas initiative * Professor Michael Dustin reviews innovative work for Nature ... Continental Ancestry Group, Genetic Predisposition to Disease, Genome-Wide Association Study, Heterozygote, Homozygote, Humans ...https://www.kennedy.ox.ac.uk/publications/66229
Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum. - PubMed - NCBI
Chromosomes, Human, Pair 19. *Chromosomes, Human, Pair 4. *Cohort Studies. *Female. *Gene Expression ... Chromosomes are arranged along the X-axis. Log10-scaled p-values are shown on the Y-axis. The loci with positions with p , 5 × ... Fejzo MS1,2, Sazonova OV3, Sathirapongsasuti JF3, Hallgrímsdóttir IB3,4, Vacic V3, MacGibbon KW5, Schoenberg FP6, Mancuso N7, ... 4. Amgen Inc., South San Francisco, CA, 94080, USA.. 5. Hyperemesis Education and Research Foundation, Damascus, OR, 97089, USA ...https://www.ncbi.nlm.nih.gov/pubmed/29563502