(Third part of algebra from central of Sikander Aqeel)
a2 + b2 (3Th part) = c2
a2 + b2 (earth) = c2
a2 (60 sec) + b2 (60 minu) [earth] = c2
a2 (3600) + b2 (3600) [earth] = c2
a2 + b2 = 7200 = c2
a2 + b2 = 7200 / 84.85 = 84.85
a2 + b2 = 84.85 * 4.3017 part of year = 364.9
a2 + b2 = 365 day of earth from third part of algebra
mRNA CODE
Uracil = C4H4N2O2 = 112.0868 g/mol = (U)
a2 + b2 [3Th part] = c2
a2 + b2 (Hormone) = c2
a2 (Uracil) + b2 (60 minute) [Hormone] = c2
a2 (112.0868) + b2 (60 minute) [Hormone] = c2
a2 (12563.45073424) + b2 (3600) [Hormone] = c2
a2 + b2 = 16163.45 [Hormone] = c2
a2 + b2 = 16163.45 / 127.13 = 127.14
a2 + b2 = 127.14 * 2.644 % 3Th Thyroxine hormone = 336.15816
a2 + b2 = 336.15816 / 3 UUU RNA = 112.05 Uracil
a2 + b2 = 336.15816 * 20 amino acid = 6723.1632
a2 + b2 = 6723.1632 * 4.3017 part of year = 28921.03
a2 + b2 = 28921.03 molecular weight
FOR STOP TO RNA
If started from left side to codon chart then GCU Alanine stop belongs with 29th numbers,
a2 + b2 = 28921.03 / 29 = 997.27
a2 + b2 = 997.27 + 9.23 H7.38 = 1006.5
a2 + b2 = 1006.5 = six Phenylalanine = (C9H11NO2)6
a2 + b2 = 1006.5 = UUU UUU = RNA Stop at the 29th GCU Alanine
So through this theory, the start and stop are not always conform, that different RNA and different shape of body belongs with different start to stop, or why our nature and shape are different, that from reason of different star and stop of RNA, basically the protein makes shape of body and face, for example your weight is 80 kg, and you arrange one more person of 80 kg, now here two person has same weight, but their face and body shape is different from each another, from reason of different start to stop of both from RNA, I am writing a question to you, It will decide you, which is right,
1 = same start/stop = same face and body of people in whole world
2 = different start/stop = different face and body of people in whole world
It is easy to understand in few words, that DNA makes human and RNA makes different shape of body from protein,
HYPOPHOSPHATASIA
Hypophosphatasia (HPP) is a rare genetic disorder characterized by the abnormal development of bones and teeth. These abnormalities occur due to defective mineralization, the process by which bones and teeth take up minerals such as calcium and phosphorus. These minerals are required for proper hardness and strength. Defective mineralization results in bones that are soft and prone to fracture and deformity. Defective mineralization of teeth can lead to premature tooth loss. The specific symptoms can vary greatly from one person to another, sometimes even among members of the same family. There are five major clinical forms of HPP that range from an extremely severe form that can cause stillbirth to a form associated with only premature loss of baby (deciduous) teeth, but no bone abnormalities. Hypophosphatasia is caused by mutations in the tissue nonspecific alkaline phosphatase (ALPL) gene. This gene is also known as the TNSALP gene. Such mutations lead to low levels of the tissue nonspecific alkaline phosphatase enzyme. Depending on the specific form, hypophosphatasia can be inherited in an autosomal recessive or autosomal dominant manner.
EARTH AND RNA
a2 + b2 (3Th part) = c2
a2 + b2 (earth) = c2
a2 (60 sec) + b2 (60 minute) [earth] = c2
a2 (3600) + b2 (3600) [earth] = c2
a2 + b2 = 7200 = c2
a2 + b2 = 7200 / 84.85 = 84.85
a2 + b2 = 84.85 * 4.3017 part of year = 364.9
a2 + b2 = 365 day of earth from third part of algebra
mRNA CODE
HYPOPHOSPHATASIA
Hypophosphatasia (HPP) is a rare genetic disorder characterized by the abnormal development of bones and teeth. These abnormalities occur due to defective mineralization, the process by which bones and teeth take up minerals such as calcium and phosphorus.
Uracil = C4H4N2O2 = 112.0868 g/mol = (U)
Calcium + phosphorus = Ca + P = 71 g/mol
a2 + b2 [3Th part] = c2
a2 + b2 (amino acid) = c2
a2 (Uracil) + b2 (60 minute) [amino acid] = c2
a2 (112.0868) + b2 (60 minute) [amino acid] = c2
a2 (12563.45073424) + b2 (3600) [amino acid] = c2
a2 + b2 = 16163.45 [amino acid] = c2
a2 + b2 = 16163.45 / 127.13 = 127.14
a2 + b2 = 127.14 * 71 (Ca + P) = 9026.94
a2 + b2 = 9026.94 / 3 triple RNA = 3008.98
a2 + b2 = 3008.98 - 1610.7332% (Proline-117.25) = 1398.2468
a2 + b2 = 1398.2468 m/g = CCU CCC CCA CCG RNA
Proline = 1398.2468 % / 157.25 Pro = 8.891 sets in RNA
Proline = CCU CCC CCA CCG
Proline = as used in over age to do strong tissues bones and bones joints,
FOR STOP TO RNA
If started from left side to codon chart
Then start = AUU AUC AUU Isoleucine = 11.559 amino acid,
Then end = CCA CCG Proline = 22 amino acids,
a2 + b2 = 16163.45 / 11.559 amino acids (Start Isoleucine) = 1398.2468
a2 + b2 = 1398.2468 = CCU CCC CCA CCG
a2 + b2 = 1398.2468 = CCU CCC CCA CCG = RNA (End at the 22th CCA CCG Proline)
The first number is Phenylalanine UUU at the left side on chart, and then 11.55th number is AUU AUC AUU Isoleucine to start, and then end is 22th number CCA CCG Proline,
Or to make protein under the Proline + Isoleucine use only 10.441 codes of RNA,
End = 22 – 11.559 start = 10.441 codon RNA
ISOLEUCINE
Required in the formation of hemoglobin, and hemoglobin is most important for feed of bones by blood cells into the bones, or blood cells for strong of bone,
GENETIC TREATMENT
8.891 sets Proline + Isoleucine = strong bones
8.891 sets Proline + Isoleucine + Vitamin-D = extra strong bone,