Scientific Accuracy of Holy Qur'an: The Muslim Holy Book, The Book of Guidance, The Koran, Al-Quran Majid
That He did create in pairs, male and female, From a seed when lodged (in its place); Holy Quran (53:45-46) ... "The staging of human embryos was not proposed until the 1940s, and the stages used nowadays were not adopted worldwide until a ... "The idea that development results from a genetic plan contained in the chromosomes of the zygote was not discovered until the ... and he sent down for you eight head of cattle in pairs: He makes you, in the wombs of your mothers, in stages, one after ...
Zur genetik des Parkinson-syndroms<...
Chromosomes, Human, Pair 1 Medicine & Life Sciences 14% * alpha-Synuclein Medicine & Life Sciences 14% ... A second gene locus for an autosomal dominantly inherited Parkinsonian syndrome was recently localized on chromosome 1 (PARK6 ... A second gene locus for an autosomal dominantly inherited Parkinsonian syndrome was recently localized on chromosome 1 (PARK6 ... A second gene locus for an autosomal dominantly inherited Parkinsonian syndrome was recently localized on chromosome 1 (PARK6 ...
Linkage analysis of chromosome 4 in families with familial pancreatic cancer<...
Chromosomes, Human, Pair 4 Medicine & Life Sciences 100% * Pancreatic Neoplasms Medicine & Life Sciences 70% ... Linkage analysis of chromosome 4 in families with familial pancreatic cancer. Alison P. Klein, Mariza De Andrade, Ralph H. ... Linkage analysis of chromosome 4 in families with familial pancreatic cancer. / Klein, Alison P.; De Andrade, Mariza; Hruban, ... Linkage analysis of chromosome 4 in families with familial pancreatic cancer. In: Cancer Biology and Therapy. 2007 ; Vol. 6, No ...
Elizabeth Stephan's research topics | Palmetto Profiles
Publications | Max Planck Institute
... and an MLS of 2.53 in all 87 affected sib-pair families. An area on chromosome 16p near the telomere was the next most ... Bastiaansen, M. C. M., Van Berkum, J. J. A., & Hagoort, P. (2002). Event-related theta power increases in the human EEG during ... using a task in which listeners blended pseudo-word pairs such as ranga-serupa. An assimilated blend of this pair would be ... lexical prosody could serve as a minimal distinguishing feature between pairs of words. However, most pairs of English words ...
Disruption of the E2 Gene Is a Common and Early Event in the Natural History of Cervical Human Papillomavirus Infection: A...
HPV18 primer pairs were validated using primary human foreskin keratinocytes transfected with episomal HPV18 (28). All four ... which contains multiple copies of the HPV16 genome arranged in the host chromosomes as head-to-tail, tandemly repeated arrays, ... Integration of human papillomavirus type 16 DNA into the human genome leads to increased stability of E6 and E7 mRNAs: ... Integration of human papillomavirus type 16 into the human genome correlates with a selective growth advantage of cells. J ...
Michiaki Hamada - 研究成果 - 早稲田大学
Chromosomes, Human, Pair 21 21% * Immune System 19% 4 被引用数 (Scopus) ... Landscape of semi-extractable RNAs across five human cell lines. Zeng, C., Chujo, T., Hirose, T. & Hamada, M., 2023 8月 25, In: ... Impact of human gene annotations on RNA-seq differential expression analysis. Hamaguchi, Y., Zeng, C. & Hamada, M., 2021 12月, ... Possible roles for the hominoid-specific dscr4 gene in human cells. Saber, M. M., Karimiavargani, M., Uzawa, T., Hettiarachchi ...
Ciencias de la Salud - Resultados de investigación - Universidad Nacional Mayor de San Marcos
Chromosomes, Human, Pair 14 17% 20 Citas (Scopus) * Characterizing the construction materials of a historic building and ... Challenges in the early diagnosis of oral cancer in rural populations in Peru during the COVID-19 pandemic. Chumpitaz-Cerrate, ... Characteristics associated with poor COVID-19 outcomes in individuals with systemic lupus erythematosus: data from the COVID-19 ...
John Rice - Research output - Research Profiles at Washington University School of Medicine
Chromosomes, Human, Pair 8 49% * Chromosomes, Human, Pair 4 49% * Chromosomes, Human, Pair 1 44% ... Corbett, J., Gu, C. C., Rice, J. P., Reich, T., Province, M. A. & Rao, D. C., 2004, In: Human heredity. 57, 1, p. 21-27 7 p.. ... Zeegers, M. P. A., Rice, J. P., Rijsdijk, F. V., Abecasis, G. R. & Sham, P. C., 2003, In: Human heredity. 55, 2-3, p. 125-131 7 ... Suggestive linkage on chromosome 1 for a quantitative alcohol-related phenotype. Dick, D. M., Nurnberger, J., Edenberg, H. J., ...
Dolce, A.<...
Chromosomes, Human, Pair 18 19% * Acetazolamide 18% 2 Scopus citations * Electroclinical Features in MECP2 Duplication Syndrome ...
Structure and mapping of the G protein γ3 subunit gene and a divergently transcribed novel gene, Gng3lg - Fingerprint -...
Department of Evolutionary and Environmental Biology - Research output - University of Haifa
Chromosomes, Human, Pair 2 19% * Mosquito larvae (Culiseta longiareolata) prey upon and compete with toad tadpoles (Bufo ... Chromosome 4 controls potential water use efficiency (δ13C) in barley. Handley, L. L., Nevo, E., Raven, J. A., Martinez- ... Nevo, E., 1993, In: Quaternary International. 19, C, p. 13-19 7 p.. Research output: Contribution to journal › Article › peer- ... Izhaki, I., Nov 1993, In: Journal of Chemical Ecology. 19, 11, p. 2605-2615 11 p.. Research output: Contribution to journal › ...
Immunohistochemical and molecular genetics study of a granular cell astrocytoma: A case report of malignant transformation to a...
New thinking on regulation of sex chromosomes in fruit flies | ScienceDaily
While chromosomes in most animals come in pairs, that is not the case with all sex chromosomes. Males, typically being the ones ... Fruit flies have been indispensible to our understanding of genetics and biological processes in all animals, including humans ... The Single X Chromosome of Male Fruit Flies Can Be Just as Active as the Two X Chromosomes of Females Thanks to Two Sticky ... of genes on most of the single X chromosomes is doubled to match the expression of the two X chromosomes in female cells. ...
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive...
Chromosomes, Human, Pair 19 Medicine & Life Sciences 18% * Single Nucleotide Polymorphism Medicine & Life Sciences 11% ... In: Human molecular genetics, Vol. 22, No. 2, dds425, 01.2013, p. 408-415.. Research output: Contribution to journal › Article ... We not only confirmed the association of a PrCa susceptibility locus, rs11672691 on chromosome 19, but also showed an ... We not only confirmed the association of a PrCa susceptibility locus, rs11672691 on chromosome 19, but also showed an ...
The tabby cat - Cat in the Box LLC
In cats and humans, chromosomes come in pairs. We get one from each parent to make a full set. Cats have 19 pairs and there are ... called chromosomes. The genes inside the chromosomes determine many of our traits, from our sex to our eye color. ... We humans had something to do with that. But we did not breed tabby cats for their stripes. Tabby cats came by their stripes ... without any help or design on the part of humans, as a kind of adaptation to their environment. (Read the section, "Why do cats ...
Identity-by-Descent Mapping to Detect Rare Variants Conferring Susceptibility to Multiple Sclerosis<...
Chromosomes, Human, Pair 19 Medicine & Life Sciences 50% * linkage (genetics) Agriculture & Biology 49% ... We identified a genome-wide significant linkage signal on chromosome 19 (LOD = 4.65; p = 1.9×10-6). Network analysis of cases ... We identified a genome-wide significant linkage signal on chromosome 19 (LOD = 4.65; p = 1.9×10-6). Network analysis of cases ... We identified a genome-wide significant linkage signal on chromosome 19 (LOD = 4.65; p = 1.9×10-6). Network analysis of cases ...
Variability in developmental milestones and developmental delay in children with Williams syndrome<...
Chromosomes, Human, Pair 7 Medicine & Life Sciences 22% * damages Social Sciences 19% ... N2 - Williams syndrome (WS) results from damage (varying in extent between individuals) to chromosome 7. Symptoms include ... AB - Williams syndrome (WS) results from damage (varying in extent between individuals) to chromosome 7. Symptoms include ... Williams syndrome (WS) results from damage (varying in extent between individuals) to chromosome 7. Symptoms include ...
Human histamine n-methyltransferase gene: structural characterization and chromosomal localization<...
Chromosomes, Human, Pair 2 Medicine & Life Sciences 19% * Length Chemical Compounds 17% ... We localized HNMTlo chromosome 2 by performing the PCR with template DNA from NIGMS Human/Rodent Somatic Cell Hybrid Mapping ... We localized HNMTlo chromosome 2 by performing the PCR with template DNA from NIGMS Human/Rodent Somatic Cell Hybrid Mapping ... We localized HNMTlo chromosome 2 by performing the PCR with template DNA from NIGMS Human/Rodent Somatic Cell Hybrid Mapping ...
The cloning and expression of a sodium channel β1-subunit cDNA from human brain<...
Chromosomes, Human, Pair 19 Medicine & Life Sciences 38% * Voltage-Gated Sodium Channels Medicine & Life Sciences 38% ... The cloning and expression of a sodium channel β1-subunit cDNA from human brain. Human molecular genetics. 1993 Jun;2(6):745- ... The cloning and expression of a sodium channel β1-subunit cDNA from human brain. In: Human molecular genetics. 1993 ; Vol. 2, ... we have isolated a cDNA encoding the human brain β1-subunit and assigned the corresponding gene to chromosome 19. We have also ...
SMART: THEG domain annotation
... weassigned the human THEG gene (THEG) to human chromosome 19ptel p13 byfluorescence in situ hybridization. Moreover, we ... which is approximately 14 kb pairs in size, contains eight exons,and comparison of the two cDNA sequences with the genomic ... Both human and mouse THEG are specifically expressed in the nucleus of haploid male germ cells and are involved in the ... Alternative splicing, chromosome assignment and subcellular localizationof the testicular haploid expressed gene (THEG). ...
Characterizing the Genetic Architecture of Parkinson's Disease in Latinos<...
Chromosomes, Human, Pair 14 Medicina y ciencias biológicas 17% * Chromosomes, Human, Pair 6 Medicina y ciencias biológicas 17% ... a locus on chromosome 14, containing the gene STXBP6, achieved significance in a joint test of ancestries and in the Native ... a locus on chromosome 14, containing the gene STXBP6, achieved significance in a joint test of ancestries and in the Native ... a locus on chromosome 14, containing the gene STXBP6, achieved significance in a joint test of ancestries and in the Native ...
Åke Lundwall - Fingerprint - Lund University
Y chromosome
Human Y chromosome. In humans, the Y chromosome spans about 58 million base pairs (the building blocks of DNA) and represents ... Stevens proposed that chromosomes always existed in pairs and that the Y chromosome was the pair of the X chromosome discovered ... The DNA in the human Y chromosome is composed of about 59 million base pairs.[5] The Y chromosome is passed only from father to ... Y chromosome The Y chromosome is one of two sex chromosomes (allosomes) in mammals, including humans, and many other animals. ...
Despite flash, males are simple creatures
One pair of these is called the sex chromosome. In this case, the females have two X chromosomes (XX) and males, XY. ... In flies and humans, thousands of genes made up of DNA are packaged into tiny units called chromosomes. Each parent contributes ... In humans, one of the X chromosomes gets inactivated in females, though research is finding this inactivation isnt always ... Many genes are found on the X chromosome, whereas few are associated with the Y chromosome. For female fruit flies, the X- ...
A High-Density Whole-Genome Association Study Reveals That APOE Is the Major Susceptibility Gene for Sporadic Late-Onset...
SNP rs4420638 on chromosome 19, located 14 kilobase pairs distal to the APOE e4 variant, significantly distinguished between AD ... with an OR significantly greater than any other locus in the human genome. It also supports the feasibility of the ultra-high- ... initial genome scans using microsatellite markers in late-onset AD failed to identify this locus on chromosome 19. Recently ... empirical support for the suggestion that the APOE locus is the major susceptibility gene for late-onset AD in the human genome ...
Cat with down syndrome - Breeds of Cat
Cats cant have down syndrome because of the less number chromosome than a human. Where a human has 23 pairs of chromosomes, a ... cats have no down syndrome because they do have not a similar chromosome to a human. For example, a human has 23 chromosomes, ... Usually, a healthy child has 23 pairs of chromosomes in each cell. There a down syndrome affected child has three copies of the ... Down syndrome can occur from the additional chromosomal copies of 21pairs since the cat has not had 21 pairs of chromosomes, so ...
Hiroshi Nishihara - 研究成果 - Keio University
Chromosomes, Human, Pair 3 100% * Renal Cell Carcinoma 73% * Mutation 64% * Chromosomes 30% ... Derivative Chromosome 3 Loss from t(3;6)(q12;q14) Followed by Differential VHL Mutations Underlie Multifocal ccRCC. Mizutani, K ... DOCK2 is involved in the host genetics and biology of severe COVID-19. The Biobank Japan Project, 2022 9月 22, In: Nature. 609, ... Early symptoms preceding post-infectious irritable bowel syndrome following COVID-19: a retrospective observational study ...
Convergent recombination suppression suggests role of sexual selection in guppy sex chromosome formation | Nature Communications
The dominant model of sex chromosome evolution posits that recombination is suppressed between emerging X and Y chromosomes in ... We show that although the nascent Y chromosome encompasses nearly half of the linkage group, there has been no perceptible ... It has been suggested that sex chromosomes arise as a result of sexual conflict, resulting in selection against recombination ... These results provide empirical support for longstanding models of sex chromosome catalysis, and suggest an important role for ...
Tandon School of Engineering - Research output - NYU Scholars
A human nuclear shuttling protein that interacts with human immunodeficiency virus type 1 matrix is packaged into virions. ... A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-36. Wiggs, J. L., Andersen, J. S., Pralea, A. M. ... Janssen, C. P., Boyle, L. N., Kun, A. L., Ju, W. & Chuang, L. L., Jul 3 2019, In: International Journal of Human-Computer ... A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36. Andersen, J. S., Pralea, A. M., Delbono, E ...