आनुवंशिक-उत्परिवर्तन हिंदी उपयोग और उदाहरण

BRCA1 और BRCA2 जीनों में निश्चित आनुवंशिक उत्परिवर्तन स्तन कैंसर और डिम्बग्रंथि के कैंसर के जोखिम को बढाते हैं।

कुछ अन्य आनुवंशिक उत्परिवर्तन हैं जिनके ऐल्बिनिज़म से संबंधित होने की बात साबित हुई है।

आनुवंशिक उत्परिवर्तन हो सकते हैं, जो बड़े पैमाने पर नुकसान पैदा करने की उनकी क्षमता को बढ़ा सकते हैं; इस प्रकार संक्रामक रोग विशषज्ञों के निकट अवलोकन का काफी महत्व होता है।

वह इन दोनों रोगों और 20 से अधिक आनुवंशिक बीमारियों के निदान में सहायता के लिए विकसित परीक्षणों के लिए जिम्मेदार आनुवंशिक उत्परिवर्तनों की पहचान करने में शामिल थी।

इस प्रकार डार्विन के सिद्धांत, आनुवंशिक उत्परिवर्तन और मेंडेलियन विरासत के बीच झूठे विरोधाभास इस प्रकार सुलझ गए।

""BRCA1 और BRCA2 जीनों में निश्चित आनुवंशिक उत्परिवर्तन स्तन कैंसर और डिम्बग्रंथि के कैंसर के जोखिम को बढाते हैं।

आनुवंशिक उत्परिवर्तन ।

प्रयुक्त प्रकाश विकास अनियमितताओं को प्रेरित कर सकता है, जैसे कि रेटिना हानि, कम शुक्राणु उत्पादन, आनुवंशिक उत्परिवर्तन.।

एक प्राकृतिक आनुवंशिक उत्परिवर्तन, चांदी के रंग के बजाए सुनहरे (असल में कुछ कुछ पीले जैसा नारंगी) रंग का उत्पादन करती है।

आनुवंशिक-उत्परिवर्तन इसके अंग्रेजी अर्थ का उदाहरण

Several rare neurodegenerative diseases are linked to genetic mutations in the motor proteins, kinesin and dynein, and in those cases it is likely that axonal transport is a key player in mediating pathology.

The modularity and adaptability of developmental systems reduces the number of regulatory changes needed to generate adaptive phenotypic variation, increases the probability that genetic mutation will be viable, and allows organisms to respond flexibly to novel environments.

functional and adaptive) phenotypic variation when challenged by genetic mutation or novel environmental conditions.

They explain how, if bones undergo regulatory change in length and thickness as a result of genetic mutation, the muscles, nerves and vasculature will accommodate to those changes without themselves requiring independent regulatory change.

This not only means that viable phenotypes can easily be generated with little genetic change, but also that genetic mutations are less likely to be lethal, that large phenotypic changes can be favored by selection, and that phenotypic variation is functional and adaptive (i.

Chromosomal anomalies and genetic mutations account for nearly 10–15% of all male infertility cases.

Like Uncanny X-Men, most X-books feature mutants, humans born with extraordinary powers due to a genetic mutation.

However, researchers have not uncovered strong evidence for a single schizogene, and instead believe the genetic risk for schizophrenia is better explained by polygenic combinations of common variants and rare genetic mutations.

Unaffected carriers, or previvors, are those who have not been diagnosed with cancer, but who know that they are likely to develop cancer due to certain genetic mutations that form a known cancer syndrome.

The majority of CMD cases result from a genetic mutation in laminin-α2, a subunit of the laminin-211 protein, which serves as an essential mechanical link between basement membrane and muscle fiber in skeletal and heart muscle.

In broad sense, acquired factors practically include any factor that is not based on a genetic mutation, including any intrauterine exposure to toxins during fetal development, which may present as infertility many years later as an adult.

15 kV AC multiple units Chondrodystrophy (literally, "cartilage maldevelopment") refers to a skeletal disorder caused by one of myriad genetic mutations that can affect the development of cartilage.

These disorders arise because of genetic mutations that prevent the production of certain enzymes used in the lysosomes.