Here I’m going to discuss about, how to add the table row values using php and mysql. This concept is very simple, we can fetch the data from database add/sum the column values. The values are inserted into database and fetch the values from database, and find the sum values by using SUM(column-name).
Code Explanation:
First, create the database and table ‘addtable’. The ‘addtable’ table contain three field, id,maths,english respectively.
The id is autoincrement and maths,english contain values like mark. Second fetch the data from database using mysql query:
| S No | Maths | English |
|---|---|---|
| Total |
FULL CODE
| S No | Maths | English |
|---|---|---|
| Total |
If anyone has doubts on this topic then please do let me know by leaving comments or send me an email.
This article covers the microbial transformation of sterols, steroidal
hormones and a few new types of steroids often identified as bufadienolides.
Emphasis has positioned on reporting metabolites that might be of general
interest and on the practical aspects of work within the area
of microbial transformations. The primary chemical transformation carried out by different Acremonium species in numerous steroid compounds
have been oxidations, reductions, hydroxylations in numerous positions, isomerizations, and hydrolysis of the chain in C-17.
Hydrocortisone (173) is an important anabolic, used clinically as anti-inflammatory and antiallergic drug, besides being a raw material for
the synthesis of many steroid hormones. Biotransformation of 173
using Gibberella fujikuroi yielded 11β-hydroxyandrost-4-en-3,17-dione (177, 41%), whereas B.
The products 173 (45%) and 3β,11β,17α,21-tetrahydroxy-5α-pregnan-20-one (178, 31%) were obtained from the bioconversion of 173 using Bacillus cereus (Figure 22) [90].
The review is organized by the kind of lipid modification that occurs on varied nucleophilic groups.
For every modification, we focus on the enzymes that control the modification, the
modified proteins, the capabilities of the modification,
and the instruments or technologies which have been developed to
study the modifications. Each part is unbiased; however,
sure modifications, corresponding to cysteine palmitoylation, depend upon other modifications (cysteine prenylation or N-terminal glycine myristoylation).
Therefore, the sections are ordered in order that that
the incidence and capabilities of assorted modifications are simple to know.
The frequent steroid hormones are estrone (E1), 17β-estradiol
(E2), estriol (E3), 17α-ethinylestradiol (EE2), and testosterone (T).
These steroids are reported to contaminate the environment via
wastewater treatment plants.
The third cationic cyclization is somewhat uncommon as a
outcome of it occurs with non-Markovnikov
regiochemistry and provides a secondary cation at C13 somewhat than the choice tertiary cation at C14.
Blakesleeana, which supplies an route for the monohydroxylation of the (86) at C-11, yielded a 17α-acetoxy-11β-hydroxy-6-methylenepregna-4,6-diene-3,20-dione (87)
(Figure 11) [66]. We are a group of more than 103,000 authors and editors from three,291 establishments
spanning 160 nations, including Nobel Prize winners and a number of the world’s most-cited researchers.
Publishing on IntechOpen allows authors to
earn citations and find new collaborators, that means more individuals see your work not solely from your personal
field of study, however from other related fields too.
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Though the loop between oxidative harm and activation of
inflammatory response continues to be a “chicken and egg puzzle”
the inhibition of one of the two mechanisms can quench
the activation of the other one, leading to a lower inflammation and oxidative injury.
In view of those knowledge and to research
the potential mechanism (s) underlying the anti-inflammatory properties of SCA
and SCB compounds, their potential results in inhibiting the exercise of COX,
a common goal for anti-inflammatory medication, have been evaluated.
Curiously, whereas SCA barely affected COX activity only on the decrease concentration tested (0.1 µM), SCB concentration-dependently (0.1–10 µM) inhibited COX activity.
Generally, stacking steroids collectively results in an increase in unwanted effects, corresponding to
further elevations in ldl cholesterol and liver enzyme activity.
Nevertheless, in Deca Durabolin’s case, stacking
it with different steroids can really help to mitigate adverse effects regarding sexual health due to increased
androgenicity. The cause why males could struggle to get
an erection on Deca Durabolin is because of its deficiency in androgenicity.
Androgenic steroids facilitate nitric oxide manufacturing, which is crucial in supplying blood move to the
penis. Thus, we often see Deca Durabolin compromising circulation on this regard.
Also, Deca Durabolin raises prolactin ranges,
a lactating hormone that may lower arousal or sexual interest.
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However, the outcomes of the current research additionally point out
that each SCA and SCB are able to activate the glucocorticoid receptor, demonstrating an analogous efficiency.
The results of the compounds were, however, lower than that of dexamethasone (0.1 µM), used
as a reference glucocorticoid receptor agonist. Though the one presented is an in vitro
preliminary examine, these results counsel a decrease efficacy of SCA and SCB in activating the glucocorticoid receptors in respect to classical corticosteroids.
As the 2 compounds show additive anti-inflammatory mechanisms (e.g.
antioxidant properties; COX-inhibition), it’s potential to speculate that they preserve a relevant anti-inflammatory exercise in vivo,
however with a greater tolerability profile than glucocorticoids.
This promising situation, nonetheless, should be confirmed in an extra intensive in vivo examine.
The microbiological transformation of sterols is at present the technological foundation for
the economic manufacturing of useful steroid precursors, the so-called synthons, from which a variety of steroid
and indane isoprenoids are obtained by combined chemical and enzymatic routes.
Alongside with whole-cell catalysis, the curiosity of researchers is growing in enzymatic strategies that make it
potential to carry out selective structural modifications of steroids, such as the
introduction of double bonds, the oxidation of steroidal alcohols, or the reduction of steroid carbonyl teams.
However, studies and our own findings recommend
that Deca Durabolin is able to causing masculinization in girls, even in small dosages, when taken continuously over
the long term. Though Deca Durabolin is in all probability
not essentially the most optimum steroid for women (with
Anavar being a extra suitable compound), analysis suggests Deca Durabolin presents a low risk of virilization. In the before picture, he had beforehand taken SARMs (selective androgen receptor modulators); due to
this fact, this wasn’t his first PED cycle.
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