The cell is the basic structural, functional and biological unit of all known living organisms. Cells are the smallest unit of life that can replicate independently, and are often called the "building blocks of life". The study of cells is called cell biology.
The cell is the basic structural, functional and biological unit of all known living organisms. Cells are the smallest unit of life that can replicate independently, and are often called the "building blocks of life". The study of cells is called cell biology.
The study of the cell cycle focuses on mechanisms that regulate the timing and frequency of DNA duplication and cell division. As a biological concept, the cell cycle is defined as the period between successive divisions of a cell. During this period, the contents of the cell must be accurately replicated.
The cell cycle is regulated by cyclins and cyclin-dependent kinases.
How long is one cell cycle?
Depends. Eg. Skin cells every 24 hours. Some bacteria every 2 hours. Some cells every 3 months. Cancer cells very short. Nerve cells never.
Programmed cell death:
Each cell type will only do so many cell cycles then die. (Apoptosis)
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
DERIVATION OF MODIFIED BERNOULLI EQUATION WITH VISCOUS EFFECTS AND TERMINAL V...Wasswaderrick3
In this book, we use conservation of energy techniques on a fluid element to derive the Modified Bernoulli equation of flow with viscous or friction effects. We derive the general equation of flow/ velocity and then from this we derive the Pouiselle flow equation, the transition flow equation and the turbulent flow equation. In the situations where there are no viscous effects , the equation reduces to the Bernoulli equation. From experimental results, we are able to include other terms in the Bernoulli equation. We also look at cases where pressure gradients exist. We use the Modified Bernoulli equation to derive equations of flow rate for pipes of different cross sectional areas connected together. We also extend our techniques of energy conservation to a sphere falling in a viscous medium under the effect of gravity. We demonstrate Stokes equation of terminal velocity and turbulent flow equation. We look at a way of calculating the time taken for a body to fall in a viscous medium. We also look at the general equation of terminal velocity.
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
5. Prophase - The first stage of mitosis.
The chromosomes condense and become visible.
The centrioles form and move toward opposite ends of the cell ("the poles").
The nuclear membrane dissolves.
The mitotic spindle forms (from the centrioles in animal cells)
Spindle fibers from each centriole attach to each sister chromatid at the
kinetochore
6. • Metaphase
• The Centrioles complete their migration to
the poles.
• The chromosomes line up in the middle of
the cell ("the equator") : Metaphase Plate.
7. • Anaphase
• Spindles attached to kinetochores begin to
shorten.
• This exerts a force on the sister chromatids that
pulls them apart.
• Spindle fibers continue to shorten, pulling
chromatids to opposite poles.
• This ensures that each daughter cell gets
identical sets of chromosomes
8. • Telophase
• The chromosomes decondense.
• The nuclear envelope forms.
• The Mitotic spindles break down.
• Starts the Cytokinesis process.
9. Cytokinesis
• In animal cells:
• A cleavage furrow forms in the center of the cell. Under the membrane: Contractil
Rings. The cell stretches, thins out and separates into two ones.
• In plant cells is different because plant cells have cell walls.
• There is no cleavage furrow.
• During telophase, vesicles from the Golgi apparatus form a wall: Cell plate
which grows from the Center to the edge of the cell and divides the cytoplasm in two.
10. Cytokinesis
• In animal cells:
• A cleavage furrow forms in the center of the cell. Under the membrane: Contractil
Rings. The cell stretches, thins out and separates into two ones.
• In plant cells is different because plant cells have cell walls.
• There is no cleavage furrow.
• During telophase, vesicles from the Golgi apparatus form a wall: Cell plate
which grows from the Center to the edge of the cell and divides the cytoplasm in two.