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Kristupo vasaros festivalis pradeda fortepijono rečitalių ciklą Bernardinų sode


Lukaszas Byrdy
Organizatorių nuotr.
Paulina Dūmanaitė ir Joris Sodeika
Organizatorių nuotr.
Pernai ypač didelio klausytojų susidomėjimo sulaukęs Kristupo vasaros festivalio organizuotas fortepijono rečitalių ciklas Bernardinų sode bus tęsiamas ir šiais metais. Juose skambės ne tik gražiausios Frederiko Chopino melodijos, bet ir visi Johanneso Brahmso „Vengriški šokiai“, sakoma pranešime.
Tradiciškai prieš koncertus vyks „Gatvės gyvos“ organizuojamos ekskursijos, kurios supažindins su įspūdingomis Bernardinų sodo transformacijomis ir leis visai kitu rakursu pažvelgti į šią žaliąją Vilniaus oazę.
Ciklą rugpjūčio 4 d. pradės Jorio Sodeikos ir Paulinos Dūmanaitės fortepijoninis duetas. Pianistai keturiomis rankomis atliks vengriškus šokius. Atlikėjai ragina apsia ....

Vilniaus Apskritis , Gabriele Agila , Institute Vilnius , Theater Academy , Republic Embassy , Last Year , Green Vilnius , Cycle August , Start Sodeika , Polish Philharmonic , Professor Barbara , Polish Republic Embassy , Polish Institute Vilnius , திரையரங்கம் கலைக்கழகம் , கடந்த ஆண்டு , ப்ரொஃபெஸர் பார்பரா ,

Organoids Reveal Common Mechanism Underlying Rare Disorders | Cell And Molecular Biology


Organoids Reveal Common Mechanism Underlying Rare Disorders
Genetic testing has shown that mutations in a gene called HUWE1 are connected to rare syndromes that cause developmental problems, including stunted growth and difficulties with movement. Some patients are so severely impacted that they never learn to speak. There is no cure for these HUWE1-associated diseases. While genetic sequencing can t always show scientists how to treat these disorders, knowing that they are caused by genetic errors can sometimes be a comfort to families. Molecular techniques have now also enabled researchers to examine the physiological impact of those genetic errors.
Many parents are afraid that the cause of their child s condition stems from something they could have avoided. A lot of parents have thought this for years before the child is referred and given a genetic diagnosis, which often adds an extra burden to their situation. Once they know that damage to a gene is the cause, many ....

Norwegian University Of Science , Olavs Hospital , Professor Barbara , Cell Reports Medicine , Norwegian University , Cell Reports , நோர்வே பல்கலைக்கழகம் ஆஃப் அறிவியல் , ப்ரொஃபெஸர் பார்பரா , செல் அறிக்கைகள் மருந்து , நோர்வே பல்கலைக்கழகம் , செல் அறிக்கைகள் ,