Chromosome 13
-
In the study of Pang et al. (2018) uses a scatter simulated annealing algorithm to minimize the total delay and total turnaround time for bi-objective PM scheduling problems at a station [13]. Also, Lin et al. (2019), consider many chromosomes in genetic algorithms to obtain the best PM scheduling.
6p longtimenosee06 27-03-2024 2 2 Download
-
Non-invasive prenatal testing (NIPT) as a screening method for common chromosomal abnormalities such as trisomy 21, 18, and 13 has been widely adopted. In the last five years, the possibility of NIPT to detect common single-gene disorders (SGD) due to de novo mutations or paternal inherited had been reported worldwide.
8p vilarry 12-03-2024 1 1 Download
-
Hereditary chromosomal 9 inversion (p22q13) 9 as a cause for recurrent pregnancy loss: A case report
Chromosomal aberrations are as common as 13.8% in the infertile population. The incidence of pericentric inversion of chromosome 9 is approximately 1–3%. However, although these inversions do not alternate phenotype, there have been conflicting data about their effect as they were correlated with infertility, recurrent pregnancy loss, and deceased children, with no clear evidence of the inversions being the causative factor for these events.
8p vitiki 30-01-2024 7 2 Download
-
Non-invasive prenatal testing (NIPT) is being applied more widely in Vietnam. However, the effects of NIPT on prenatal diagnosis have not been studied much in our country. This study aims to analyze the impact of NIPT on the changes in the number of routine screening tests for chromosomal abnormalities 21, 18, and 13 and the impact of NIPT on invasive prenatal diagnostic procedures and propose strategies to screen for fetal aneuploidy.
7p vimclaren 20-10-2022 5 2 Download
-
Disorders of sex development (DSD) are congenital conditions in which chromosomal, gonadal, or phenotypic sex is atypical. Clinical management of DSD is often difficult and currently only 13% of patients receive an accurate clinical genetic diagnosis.
21p vialfrednobel 29-01-2022 13 0 Download
-
Chapter 13 - Meiosis and sexual life cycles. This chapter presents the following content: Somatic cell and gamete, autosome and sex chromosomes, haploid and diploid; describe the events that characterize each phase of meiosis; describe three events that occur during meiosis I but not mitosis; name and explain the three events that contribute to genetic variation in sexually reproducing organisms.
44p tradaviahe19 29-03-2021 11 1 Download
-
This chapter distinguish between the following terms: somatic cell and gamete, autosome and sex chromosomes, haploid and diploid; describe the events that characterize each phase of meiosis; describe three events that occur during meiosis I but not mitosis; name and explain the three events that contribute to genetic variation in sexually reproducing organisms.
62p tradaviahe14 27-01-2021 12 3 Download
-
13q33–q34 microdeletions are rare chromosomal aberrations associated with a high risk of developmental disability, facial dysmorphism, cardiac defects and other malformation of organs. It is necessary to collect and report evidence of this rare chromosome mutation to improve the prognosis of this rare disease.
6p vimanama2711 28-07-2020 13 2 Download
-
Individuals with 46,XY complete gonadal dysgenesis (CGD) are at high risk of developing gonadal neoplasms. Chromosome 9p monosomy with deletion of the DMRT1 gene, a key transcription factor in testicular development, is one of the known causes of 46,XY CGD. Noninvasive prenatal testing (NIPT) is being increasingly used, and can identify disorders of sexual development (DSDs).
4p caothientrangnguyen 09-05-2020 18 1 Download
-
The present study reports the karyotype, C-banding, and nucleolar organizer regions (NORs) of 6 Sus scrofa (Linnaeus, 1758) males from Anatolia. The karyotype of S. scrofa comprised (2n) 38 chromosomes, the number of chromosomal arms (FN) was 64, and the number of autosomal arms (FNa) was 60. C-positive regions appeared to be restricted to the centromeric regions of autosomes 1, and 13-18, and the entire long arm of the Y chromosome.
5p vitamix 15-02-2019 12 0 Download
-
This chapter distinguish between the following terms: somatic cell and gamete, autosome and sex chromosomes, haploid and diploid; describe the events that characterize each phase of meiosis; describe three events that occur during meiosis I but not mitosis; name and explain the three events that contribute to genetic variation in sexually reproducing organisms.
43p nomoney10 04-05-2017 45 3 Download
-
This chapter include objectives: Evaluate the effects of continuous variation, pleiotropic genes, lack of complete dominance, environmental modifications of genes, and epistasis on disease; understand the importance of crossing over in terms of gene assortment and construction of genetic maps; describe the many genetic disorders discussed in the text, their symptoms, relative frequency in specialized populations, and their genetic basis;...
33p tangtuy07 02-04-2016 41 2 Download
-
Chapter 13 - Chromosomal rearrangements and changes in chromosome number. This chapter presents the following content: Rearrangements of DNA sequences, transposable genetic elements, rearrangements and evolution: a speculative comprehensive example, changes in chromosome number, emergent technologies: beyond the karyotype.
89p tangtuy04 12-03-2016 51 5 Download
-
Chapter 13 - Meiosis and sexual life cycles. This chapter distinguish between the following terms: somatic cell and gamete, autosome and sex chromosomes, haploid and diploid; describe the events that characterize each phase of meiosis; describe three events that occur during meiosis I but not mitosis; name and explain the three events that contribute to genetic variation in sexually reproducing organisms.
53p tangtuy02 08-03-2016 58 3 Download
-
Idiopathic Parkinson’s disease (PD) is an age-dependent, neurodegenerative disorder and is predominantly sporadic. Only 20–30% of patients have a positive family history for PD with a complex mode of inheritance. In a few extended families, the disease is inherited as an autosomal dominant trait. Linkage to chromosome 4 was reported in a large Italian kindred multiply affected by an early-onset form of PD (1). However, this finding was not replicated in a sample of 94 Caucasian families by Scott et al. (2), or in 13 multigenerational families by Gasser et al. (3)....
288p maket1311 16-10-2012 55 5 Download
-
The most frequent chromosomal abnormality in CLL is deletion of 13q14, being monoallelic in 76% of cases, and biallelic in 24% [13, 14, 24]. This deletion, also detected in MBL [11] occurs at a much lower frequency in multiple myeloma, DLBCL, mature T-cell lymphomas, and in several solid tumors [25-29]. A minimal deleted region (MDR) has been defined in a large number of CLL cases with monoallelic 13q14 deletion. This region contains the long non-coding RNA deleted in leukemia (DLEU)-2, and the first exon of the DLEU1 gene [30, 31].
302p wawawawawa 26-07-2012 51 4 Download
-
Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: a case report...
4p thulanh26 08-12-2011 47 2 Download
-
Parkinson’s disease is the second most common neurodegenerative disorder. The pathological hallmark of the disease is degeneration of midbrain dopaminergic neurons. Genetic association studies have linked 13 human chromosomal loci to Parkinson’s disease. Identification of gene(s), as part of the etiology of Parkinson’s disease, within the large number of genes residing in these loci can be achieved through several approaches, including screening methods, and considering appropriate criteria.
5p toshiba23 18-11-2011 54 3 Download
-
Tuyển tập các báo cáo nghiên cứu về sinh học được đăng trên tạp chí sinh học thế giới đề tài: A higher resolution radiation hybrid map of bovine chromosome 13
0p toshiba19 15-11-2011 41 1 Download
-
Table 79-3 Representative Oncogenes at Chromosomal Translocations Gene (Chromosome) Translocation Malignancy ABL BCR (22q11) (9q34.1)– (9;22)(q34;q11) Chronic myelogenous leukemia ATF1 EWS (22q12) (12q13)– (12;22)(q13;q12) Malignant melanoma of soft parts (MMSP) BCL1 IgH (14q32) (11q13.3)– (11;14)(q13;q32) Mantle lymphoma cell BCL2 IgH (14q32) (18q21.
5p konheokonmummim 03-12-2010 66 3 Download