「Chromosomal」の共起表現一覧(1語右で並び替え)
該当件数 : 95件
| ly rare human genetic disorder, caused by a | chromosomal aberration in which the long ("q") arm of o |
| Similarly in mammalian cell lines | chromosomal aberrations have a tendency to increase ove |
| Chromosomal aberrations and increased transcriptional e | |
| Chronic: CrVI can produce | chromosomal aberrations and is a human carcinogen via i |
| aberrant expression is also associated with | chromosomal abnormalities in humans. |
| Chromosomal abnormalities are found in more than half o | |
| Chromosomal abnormalities can lead to a delay in switch | |
| ling the simultaneous assessment of several | chromosomal abnormalities or patients. |
| at are used today in the early diagnosis of | chromosomal abnormalities in mid-trimester pregnant wom |
| iring abnormalities in individuals carrying | chromosomal abnormalities, either in number or in the c |
| ;q22) translocation is a rare but recurrent | chromosomal abnormality associated with therapy-related |
| Trisomy 16 is a | chromosomal abnormality in which there are three copies |
| hter is diagnosed with Turner's Syndrome, a | chromosomal abnormality that keeps her from going throu |
| ies such as the presence of a micropenis, a | chromosomal abnormality (45, X/46, XY), or of accelerat |
| In some cases, the condition results from a | chromosomal abnormality, such as a large deletion or tr |
| differences in morphological, behavioural, | chromosomal and DNA sequence characters. |
| The exact type of her | chromosomal anomaly was never revealed. |
| If the mother's copy of the | chromosomal arm is deleted, Angelman syndrome results. |
| If the father's copy of the | chromosomal arm is deleted, Prader-Willi syndrome resul |
| were the first researchers to describe the | chromosomal basis of sex. |
| She deduced the | chromosomal basis of sex depended on the presence or ab |
| Thanks to a unique | chromosomal been genetically isolated in 1986 and in 19 |
| 100 papers and scientific monographs about | chromosomal behaviour in citogenetics and more than 80 |
| rms a bridge at anaphase leading to another | chromosomal break. |
| It is the most common | chromosomal cause of miscarriage during the first trime |
| Chromosomal CGH is capable of detecting loss, gain and | |
| methylation, relative mRNA quantification, | chromosomal characterisation of cell lines and tissue s |
| importance and the importance of structural | chromosomal characteristics for gene regulation in plan |
| chromatids exchange genetic material during | chromosomal crossover during meiosis (sister chromatids |
| xons (represented by colored boxes) through | chromosomal crossover, resulting in the creation of two |
| ode between the chromosomes, in contrast to | chromosomal crossover, because genetic information is l |
| itional task of genetic mapping by studying | chromosomal crossovers after meiosis. |
| ffian bodies) but are also a feature of the | chromosomal disorder Down syndrome. |
| Trisomy 22 is a | chromosomal disorder in which there are three copies of |
| Penta X syndrome is a very rare | chromosomal disorder where the karotype of the patient |
| Trisomy 9 is a | chromosomal disorder caused by having three copies (tri |
| Peter the Wild Boy was suspected to be the | chromosomal disorder Pitt-Hopkins Syndrome, a condition |
| Chromosomal disorders | |
| of genetic material, the F episome may take | chromosomal DNA with it. |
| (CAD, caspase-activated DNase) that cleaves | chromosomal DNA in a caspase-dependent manner. |
| tor molecules, each carrying a piece of the | chromosomal DNA of the organism, prior to the insertion |
| gene expression without modification of the | chromosomal DNA and is referred to as a "transient knoc |
| Genomic deoxyribonucleic acid is | chromosomal DNA, in contrast to extrachromosomal DNAs l |
| he CAD:ICAD complex, allowing CAD to cleave | chromosomal DNA. |
| Centromeres are the differentiated | chromosomal domains that specify the mitotic behavior o |
| Chromosomal evaluation may be performed. | |
| responsible for nucleosome structure of the | chromosomal fiber in eukaryotes. |
| to the tumor suppressor gene FHIT, and the | chromosomal fragile site FRBA3. |
| cation pause site MPS1, and a novel type of | chromosomal imprint, marking one of the sister chromati |
| numerous than those supported by mtDNA or Y | chromosomal information, many such 'smaller' migrations |
| r plant transformation, integrase sites for | chromosomal insertion, lacZα fragment for α complementa |
| These mice exhibit | chromosomal instability, indicating that NHEJ is import |
| somal recessive congenital disorder causing | chromosomal instability, probably as a result of a defe |
| C1) and KCNQ3 (BFNC2) and the third being a | chromosomal inversion (BFNC3). |
| ver system responsible for the Drosophila Y | chromosomal lampbrushloop evolution in some species.[3] |
| Because of its | chromosomal localization and ability to form heterodime |
| locus for juvenile myoclonic epilepsy and a | chromosomal location involved in the genetic transmissi |
| R) before being assigned CXCR6 based on its | chromosomal location (within the chemokine receptor clu |
| The | chromosomal locus containing the SNORD115 gene cluster |
| Gulf war and increased risk of stillbirth, | chromosomal malformations, or congenital syndromes. |
| rge range of outcomes depending on how much | chromosomal material is involved. |
| Comparative genomic hybridization (CGH) or | Chromosomal Microarray Analysis (CMA) is a molecular-cy |
| omparative genomic hybridization (also CMA, | Chromosomal Microarray Analysis, Microarray-based compa |
| a ring, the individual suffers from ring 20 | chromosomal mosaicism. |
| Chromosomal order is 5'-UCP3-UCP2-3'. | |
| This is an example of | chromosomal polymorphism; the variability occurs as a r |
| Chromosomal problems due to a parent's genes are, howev | |
| Most | chromosomal problems happen by chance, have nothing to |
| the formation of | chromosomal rearrangements by exposure to ionizing radi |
| omeres (knobs) of maize, as well as several | chromosomal rearrangements in mammals. |
| Chromosomal rearrangements that generate a fusion gene | |
| is the occurrence of numeric and structural | chromosomal rearrangements as means of generating genet |
| e helped to clarify the events that lead to | chromosomal recombination-the reshuffling of genes that |
| rm a chemokine receptor gene cluster on the | chromosomal region 3p21. |
| family, which is found in a gene cluster at | chromosomal region 19q13.4. |
| s lost in several tumor types and maps to a | chromosomal region (3p14.1) |
| Leptomycin B alkylates and inhibits CRM1 ( | chromosomal region maintenance)/exportin 1 (XPO1), a pr |
| CDC2L2, a nearly identical gene in the same | chromosomal region. |
| Linkage mapping often identifies | chromosomal regions associated with a disease with no e |
| nt in the gene regulation at interphase and | chromosomal segregation in mitosis. |
| d plays an important role in maintenance of | chromosomal segregation and genomic stability. |
| eroid ratios (in terms of 2D:4D) and actual | chromosomal sex dimorphism were found to operate differ |
| approach yields more data (including novel | chromosomal spelling variants, which SNP chips do not d |
| packaging from the raw DNA molecules to the | chromosomal structures seen during metaphase in mitosis |
| Similar | chromosomal structures were described in Chironomus by |
| Of course we might also ask why the Y | chromosomal study appeared in the Frankenberger section |
| cated the gene that causes it and created a | chromosomal test to identify sufferers. |
| This is done by modulating | chromosomal transcription. |
| The 2;5 | chromosomal translocation is associated with approximat |
| identified in a recurrent t(11;18)(q21;q21) | chromosomal translocation associated with a subset of M |
| ways: as a result of gene amplification or | chromosomal translocation. |
| Chromosomal translocations involving this gene have bee | |
| a range of proteins initially described in | chromosomal translocations involving chromosomes 14 and |
| oteins of APL, of the genes involved in the | chromosomal translocations of APL, as well as of major |
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