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Apertura de un nuevo centro de diagnostico para enfermedades neurológicas y tumorales en Granada

Apertura de un nuevo centro de diagnostico para enfermedades neurológicas y tumorales en Granada
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Andalusian Centre , Centre Of Diagnosis , Centre Or , Andalusian Centre Diagnostic , New Centre , Diagnosis For Positron , Oncological Processes , Diagnosis Pet Tac , Picture Quality , Recently Incorporated , Central Andalucia , அண்டலூசின் மையம் , மையம் அல்லது , புதியது மையம் , படம் தரம் ,

A fly's eye view of evolution


Credit: Georg Bullinger
The fascinating compound eyes of insects consist of hundreds of individual eyes known as facets . In the course of evolution, an enormous variety of eye sizes and shapes has emerged, often representing adaptations to different environmental conditions. Scientists, led by an Emmy Noether research group at the University of Göttingen, together with scientists from the Andalusian Centre for Developmental Biology (CABD) in Seville, have now shown that these differences can be caused by very different changes in the genome of fruit flies. The study was published in the journal
Molecular Biology and Evolution.
Anyone who has seen hoverflies manoeuvring through the air and, quick as a flash, changing direction, has probably witnessed a mating attempt in which the male, with breath-taking accuracy, pursues a fast-moving female. To carry out this specialised visual task, the huge compound eyes of hoverflies consist of up to 6,000 individual facets. Th ....

Micael Reis , Nico Posnien , Emmy Noether , Elisa Buchberger , Department Of Developmental Biology , Johann Friedrich Blumenbach Institute Of Zoology , Andalusian Centre For Developmental Biology , Andalusian Centre , Developmental Biology , Molecular Biology , Friedrich Blumenbach Institute , Cell Biology , Developmental Reproductive Biology , துறை ஆஃப் வளர்ச்சி உயிரியல் , அண்டலூசின் மையம் க்கு வளர்ச்சி உயிரியல் , அண்டலூசின் மையம் , வளர்ச்சி உயிரியல் , மூலக்கூறு உயிரியல் , செல் உயிரியல் , வளர்ச்சி இனப்பெருக்கம் உயிரியல் ,

Researchers use massive sequencing methods to identify rare genetic bone disorder


Researchers use massive sequencing methods to identify rare genetic bone disorder
Researchers of the Cell Biology and Physiology-LABRET group of the University of Malaga (UMA), together with the Networking Biomedical Research Center in Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), have described a new genetic skeletal disorder based on a precision medicine strategy.
By using methods of massive sequencing -of all genes- they have identified the mutations that caused a rare bone disorder, particularly, the mutations in LAMA5 , the gene encoding an extracellular matrix protein around blood vessels in skeletal tissue.
This disorder consists in an extreme bone fragility combined with a lack of mineralization and skeletal deformity associated with joint dislocation and heart diseases, as well as a pulmonary insufficiency that causes perinatal mortality -at the time of birth. ....

Czech Republic , Emily Henderson , Networking Biomedical Research Center , Andalusian Centre For Nanomedicine , Department Of Cell Biology , Biomedical Research Institute Of Malaga , Cell Therapy Network , Masaryk University Czech Republic , University Of Malaga , Andalusian Centre , International Skeletal Dysplasia Registry , Los Angeles , Masaryk University , Study Main Author , Cell Biology , Biomedical Research Institute , செக் குடியரசு , எமிலி ஹென்டர்சன் , நெட்வொர்க்கிங் உயிர் மருத்துவ ஆராய்ச்சி மையம் , துறை ஆஃப் செல் உயிரியல் , உயிர் மருத்துவ ஆராய்ச்சி நிறுவனம் ஆஃப் மலகா , செல் சிகிச்சை வலைப்பின்னல் , பல்கலைக்கழகம் ஆஃப் மலகா , அண்டலூசின் மையம் , சர்வதேச எலும்பு டிஸ்ப்ளாசியா பதிவு , லாஸ் ஏஞ்சல்ஸ் ,