DR. BARUAH HEART CITY

                                                                                                   

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Unlimited poweR     of                  GenetiC EngineerinG

Inventor’s mouth.

Consequences of my research.

Introduction.

Mysteries in genetic sciences.

What is coronary artery disease?

Misconceptions in cardio-vascular sciences.

Foundation on which building of Baruah Applied Human.

Revolution in medical sciences rocked by Dr.D.R. Baruah,FRCSGlas.

Unfolding the mysteries in human genetic sciences.

Mysteries in human genetic sciences.

How does the mutation expresses in particular disease form?

Selection of patients for gene analysis

Eradication of heart disease & rarest of the rare diseases- Human genetic studies through sequencing of m-RNA.

Signal Transduction plays a major role during pre-bypass and post-bypass events.

How bypass surgery triggers signal transduction & phenotypically expressed.

Mutation

Selection of genes causing heart & other diseases.

Hypoxia, reactive oxygen species, intracellular calcium & Baruah syndrome.

Re-sequencing of the following genes to identify the mysteries.

First time on this planet– Genovac.

Baruah applied human genetic engineering- a choice of treatment for Cancer.

TGA-A New Method of Treatment of Complex Congenital Heart Disease.

Endocardial Cushion defect.

Genetic Engineering–To cure the rarest of the rare autoimmune.

First time on the Planet–Manifestation of Baruah Syndrome–Moyamoya

The rarest of the rare genetic disorder–Takayasu.

Isolated congenital Right Ventricular Hypertrophy.

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Applied Human Genetic Engineering - Vol.II

UNFOLDING THE MYSTERIES OF GENETIC SCIENCES IN INCURABLE DISEASES LIKE CORONARY ARTERY DISEASES, CANCER, & RAREST OF THE RARE DISEASES LIKE MOYAMOYA, SLE, TAKAYASU ETC.

CITY OF HUMAN GENOME A INSITUTE OF APPLIED HUMAN GENETIC ENGINEERING

              

Mysteries in human genetic scienceS

 

          Unfortunately, all genetic research ended up with publication, but no application. Genetic scientist are found to be more theoretical and we have not observed its application so far applying it to human race to cure the dreaded diseases like coronary artery disease and cancer. It is not digestible fact if the genetic engineering has applied to cure the dreaded disease like CAD then one can ask a question, why this disease has become an epidemic on this planet and why wrong treatment like coronary artery bypass surgery, stenting, angioplasty, are undertaken? Therefore, it has been proven that till now, not a single step has gone ahead in genetic sciences to find out the genes responsible for causing the coronary artery disease, hypertension, diabetes, cancer etc. and how to engineer those mistaken genes to cure these diseases permanently. Till now, so far we have observed the results of genetics for curing various diseases on this planet is zero.

          Splicing is the process where intron & exon alignment has to play an important role which will express normally in disease form during the process of translation. Intron goes into nucleus with DNA and exon follow m-RNA at the level of maturity in cytoplasm and this is the time, genetic encoding takes place and accordingly, it is expressed when the conditions are favourable. In some cases, it remains dormant, not expressed, when environment is not favourable for genetic code. Favourable & unfavourable conditions are being described in terms of degree of active immune system, if the immune system is not very active, that means conditions are favourable for that expression of the disease. During our experimentation, we were surprised to see how mutation of these particular genes are seen and how it is been de-mutated after injecting the Baruah biological molecules. Baruah biological molecules are subsequently used as tools for demutation of genes which are isolated from plants of north eastern region of India. We have described in earlier chapters how we have carried out the experimentation ex-vivo & in vivo with these molecules, We found that Baruah biological molecules are tools on this planet to cure these diseases permanently. The details of the genetic procedures of genetic engineering are given in following chapters. In the past, there is none in the genetic science who has carried out this type of work.. Had there been, I would not have taken up time consuming, laborious & expensive genetic sciences for my research being myself a cardiac surgeon.

          What surprises me is the decoding. De-mutation leads to decoding of mistaken gene by replacing with correct nucleoide, thereby synthesizing correct amino acids for circulation, which removes the errors and reverse the metabolic pathways and cures the disease permanently. It has been thought and suggested by genetic scientists, characteristic of m-RNA are changeable, therefore, one can expect decoding can be reversed , so is the metabolic pathways and diseased can be expressed again. However, in our case reverse decoding is not possible because of re-synthesis of amino acid molecules, which is active and permanent.

Our post long-term experience of Baruah genetic engineering has suggested permanent de-mutation, which are not reversed.

These conditions have been correlated with clinical situation where following findings are obtained:-

    Feeling of well being and disappearance of signs & symptoms of the disease

   Disappearnace of plaques from peripheral & central arteries within average 5-8 days take place

   Excessive Intracellular calcium is remarkably reduced allowing the mitochondria for normal respiration and synthesis of ATP.

  Cellular de-ageing and coincide of biological & real age .and of the organs reaches what it was 20 years earlier.

   Heart, liver & kidney regain their normal function

         Our animal experiments have suggested that mutation for heart diseases is not under the influence of change of life style, and food habits. It is due to change of mental status, stress & strain. This happens at the age between 13-16, when human physiology changes, leading to pathological conditions under certain environment, those who are under change of mental status and degree of mental stress. These two conditions have greater effect on mutations which get expressed in diseased form in about 15-20years bringing the errors, reversing the metabolic pathways and ultimately expressed in diseased form of respective type.

          These diseases can be stopped by de-mutation, thereby decoding the mistaken gene, that is genotypic effect will be expressed in phenotypic disease-free form permanently.

          We are capable of preventing these diseases by using Baruah biological molecules which stops initiation of mutation at the age between 13 and 16 and question of decoding of mistaken genes does not arise.. Therefore, I conclude that coronary artery disease can be eradicated completely by using the method of Baruah applied human genetic engineering, where Baruah biological molecules can be used as tools.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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