Inheritance pattern

Lecture Introduction to Software engineering - Lesson 14: Reuse and design patterns. This lesson provides students with content about: software reuse; potential benefits of reuse; potential disadvantages of reuse; evaluating software; design for change - replacement of components; inheritance and abstract class; strategy pattern - structure;... Please refer to the detailed content of the lecture!

43p codabach1016 03-05-2024 3 0   Download

Left-sided lesions (LSLs) account for an important fraction of severe congenital cardiovascular malformations (CVMs). The genetic contributions to LSLs are complex, and the mutations that cause these malformations span several diverse biological signaling pathways: TGFB, NOTCH, SHH, and more.

10p vioraclene 31-03-2024 8 2   Download

Recent studies have suggested that individual variants do not sufficiently explain the variable expressivity of phenotypes observed in complex disorders. For example, the 16p12.1 deletion is associated with developmental delay and neuropsychiatric features in affected individuals, but is inherited in > 90% of cases from a mildly-affected parent.

21p vibransone 28-03-2024 8 2   Download

Normal cell BRCA1 epimutations have been associated with increased risk of triple-negative breast cancer (TNBC). However, the fraction of TNBCs that may have BRCA1 epimutations as their underlying cause is unknown. Neither are the time of occurrence and the potential inheritance patterns of BRCA1 epimutations established.

15p vicwell 29-02-2024 6 1   Download

Part 2 book "Mayo clinic neurology board review - Basic sciences and psychiatry for initial certification" includes content: Cellular signaling, cellular processes, cellular injury and death, neuropharmacology, sleep pathophysiology, patterns of inheritance in neurogenetic disease, chromosomal syndromes, electroencephalography, nerve conduction studies and needle electromyography, cerebrospinal fluid, evoked potentials, neuroimaging,... and other contents.

206p muasambanhan07 20-02-2024 4 0   Download

Factor XII deficiency can be related to either homozygous or compound heterozygous pathogenic variants in the F12 gene. The disease is commonly known as Hageman trait and is inherited in both autosomal recessive or dominant patterns.

4p vitiki 30-01-2024 4 2   Download

Part 1 book "Veterinary genetics and reproductive physiology" includes content: The genetic material, mendelian genetics, simple mendelian patterns of inheritance, cytogenetics, the sex chromosomes and sex differentiation, blood groups and blood typing, inbreeding, cross breeding and heterosis, selection and eradication schemes.

67p muasambanhan02 18-12-2023 4 0   Download

Part 1 book "Genetics in medicine" includes content: Introduction, introduction to the human genome, the human genome, human genetic diversity - mutation and polymorphism, principles of clinical cytogenetics and genome analysis, the chromosomal and genomic basis of disease - disorders of the autosomes and sex chromosomes, patterns of single gene inheritance, complex inheritance of common multifactorial disorders, genetic variation in populations, identifying the genetic basis for human disease.

197p oursky09 08-11-2023 7 3   Download

Part 1 book "Essentials of biology" includes content: The chemical basis of life, the organic molecules of life, inside the cell; the dynamic cell, energy for life, energy for cells, cellular reproduction, meiosis and the genetic basis of sexual reproduction, patterns of inheritance, DNA biology, biotechnology and genomics, genetic counseling,.... and other contents.

390p oursky07 23-10-2023 12 3   Download

Part 1 book "Genetics in medicine" includes content: Introduction to the human genome; the human genome, human genetic diversity - mutation and polymorphism; principles of clinical cytogenetics and genome analysis; the chromosomal and genomic basis of disease: disorders of the autosomes and sex chromosomes; patterns of single gene inheritance,.... and other contents.

197p oursky05 20-09-2023 4 1   Download

Part 1 book "Emery’s elements of medical genetics" includes content: The history and impact of genetics in medicine, the cellular and molecular basis of inheritance, chromosomes and cell division, finding the cause of monogenic disorders by identifying disease genes, laboratory techniques for diagnosis of monogenic disorders, patterns of inheritance, population and mathematical genetics, risk calculation, developmental genetics.

223p oursky03 21-08-2023 4 2   Download

Lafora disease is a rare genetic disorder involving glycogen metabolism disorder. It is inherited by autosomal recessive pattern presenting as a progressive myoclonus epilepsy and neurologic deterioration beginning in adolescence. It is characterized by Lafora bodies in tissues such as brain, skin, muscle, and liver.

5p vigamora 23-05-2023 4 2   Download

Triple A syndrome is a very uncommon disease marked by a triad of adrenocorticotrophic hormone (ACTH)—resistant features: adrenal insufficiency, alacrimia, and achalasia. It presents in several clinical forms with undetermined incidence and shows an autosomal pattern of inheritance.

5p vigamora 23-05-2023 7 2   Download

Triploid organisms have three sets of chromosomes. In Atlantic salmon, hydrostatic pressure treatment of newly fertilized eggs has been extensively used to produce triploids which are functionally sterile due to their unpaired chromosomes. These fish often perform poorly on commercial farms, sometimes without explanation. Inheritance patterns in individuals subjected to pressure treatment have not been investigated in Atlantic salmon thus far.

11p vihagrid 30-01-2023 12 3   Download

Part 1 of ebook "Modern Biology" provide readers with content about: foundations of biology; cell biology; cell structure and function; homeostasis and cell transport; genetics and biotechnology; inheritance patterns and human genetics; evolution; ecology; microbes, protists, and fungi;...

563p hanlinhchi 11-11-2022 13 4   Download

The patterns of gene expression on highly differentiated sex chromosomes differ drastically from those on autosomes, due to sex-specific patterns of selection and inheritance. As a result, X chromosomes are often enriched in female-biased genes (feminization) and Z chromosomes in male-biased genes (masculinization).

17p vigalileogalilei 27-02-2022 11 1   Download

Differences in DNA methylation can arise as epialleles, which are loci that differ in chromatin state and are inherited over generations. Epialleles offer an additional source of variation that can affect phenotypic diversity beyond changes to nucleotide sequence. Previous research has looked at the rate at which spontaneous epialleles arise but it is currently unknown how they are maintained across generations.

16p vialfrednobel 29-01-2022 11 0   Download

Genomic regions of autozygosity (ROA) arise when an individual is homozygous for haplotypes inherited identical-by-descent from ancestors shared by both parents. Over the past decade, they have gained importance for understanding evolutionary history and the genetic basis of complex diseases and traits. However, methods to infer ROA in dense genotype data have not evolved in step with advances in genome technology that now enable us to rapidly create large high-resolution genotype datasets, limiting our ability to investigate their constituent ROA patterns.

33p vilarryellison 29-10-2021 5 1   Download

Significant human diseases/phenotypes exist which require both an environmental trigger event and a genetic predisposition before the disease/phenotype emerges, e.g. Carbamazepine with the rare SNP allele of rs3909184 causing Stevens Johnson syndrome, and aminoglycosides with rs267606617 causing sensory neural deafness. The underlying genotypes are fully penetrant only when the correct environmental trigger(s) occur, otherwise they are silent and harmless.

7p vilarryellison 29-10-2021 7 1   Download

Chloroplasts have their own genomes, independent from nuclear genomes, that play vital roles in growth, which is a major targeted trait for genetic improvement in Populus. Angiosperm chloroplast genomes are maternally inherited, but the chloroplast’ variation pattern of poplar at the single-base level during the transmission from mother to offspring remains unknown.

15p vibeauty 23-10-2021 14 1   Download