Krisp_9 Mp3 Free Sound Fffects Download
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Apakah benar benar bisa sembuh penyakit HIV ? Semoga saja ya #hulxtech #ai #robot #tech #teknologi #CRISPRCas9 #GeneTerapiHIV #TeknologiPenyembuhan #RevolusiPengobatan #masadepankedokteran
Aqui te van mis inpresiones sobre CRISPR/Cas 9 y su utilidad como posible cura de la infeccion crónica por VIH #curaciondelVIH #crisprcas9 #VIH #VIHnoessinonimodemuerte
В своем тгк уже опубликовала еще советы для запоминания() #учеба #какзапомнитьинформацию #лайфхаки #советы #studying
You can now remove background noise while in a call. Krisp bidirectionally mutes all background noise during your call in real time.
🚨 STOP SCROLL – percée scientifique historique en 60 s. 🧬 Des chercheurs japonais viennent de supprimer le chromosome 21 en trop → 1ʳᵉ correction génétique de la trisomie 21. Regarde jusqu’au bout pour voir CRISPR-Cas9 en action + l’impact psycho-cognitif expliqué sans jargon. 👇 Fais exploser l’engagement : 1. Double-tap si tu crois au pouvoir de la science. 2. Commente : tape “21✅” = victoire médicale, “21❌” = zone rouge éthique → meilleurs avis épinglés + LIVE Q&A demain. 3. Stitch/Duet ton opinion pro santé, je réagis sur ta vidéo. 4. Partage en DM à un(e) ami(e) neuro-curieux(se) – tu le/la fais entrer dans le futur. 🔔 Abonne-toi : série #FutureOfGenes (épisode 1/7) arrive + décryptages bio-psycho chaque semaine. — 🎯 Hashtags multi-couches (SEO + trend + niche) #PourToi #FYP #ScienceTok #CRISPR #Trisomie21 #Genetics
CRISPR-CAS9 has a lot of applications! #science #sciencetok #biology #genetics #chemistry #education #lgbtq
🧪 КАК РАБОТАЕТ «РЕДАКТОР» ДЛЯ ДНК? — CRISPR-Cas9: молекулярные ножницы, которые вырезают дефектный ген и вставляют здоровый фрагмент; — Точность снайпера: ошибка — 1 на 1 000 000 000 000 символов (как найти песчинку в океане!); — CAR T-клетки: перепрограммированные иммунные клетки атакуют рак, как антивирусная программа. 📊 ЦИФРЫ, КОТОРЫЕ ВЗОРВУТ СОЗНАНИЕ: → 3 млрд пар оснований в ДНК — CRISPR находит дефект за часы; → 97% успеха в лечении серповидной анемии в первых испытаниях; → 2,1млн→2,1млн→500 тыс. — падение стоимости генной терапии за 5 лет. 🛠️ ТЕХНОЛОГИИ, КОТОРЫЕ УБИВАЮТ БОЛЕЗНИ: — ИИ-предсказатель: нейросети находят опасные мутации до рождения ребёнка; — Вирусы-курьеры: доставляют «заплатки» для ДНК в нужные клетки; — Биопринтинг: 3D-печать органов с исправленным геномом. 🌟 ПОЧЕМУ ЭТО МЕНЯЕТ ВСЁ? — Смерть от наследственных болезней станет пережитком прошлого; — Персонализированные вакцины от рака создаются за неделю; — Этическая революция: споры о дизайне детей и бессмертии уже начались. #CRISPR #ГеннаяТерапия #МедицинаБудущего #СерповиднаяАнемия #ДНКРедактор
#dúo con @La Hiperactina Hay vídeos tan buenos que más que repetirlos, necesitan difusión! Este es uno! #divulgacioncientifica #cienciaentiktok #crispr #cientifica
تقنية كرسبر CRISPR تعمل على استهداف وفصل الكروموسوم الزائد في الخلية، وهو السبب الجيني الرئيسي لمتلازمة داون. الفكرة تعتمد على قص الحمض النووي بدقة باستخدام إنزيم Cas9، ما يفتح الباب أمام علاج جذري لهذه الحالة. والأهم أن هذه التقنية قد تمهّد لمستقبل يمكن فيه تعديل الجينات لإزالة الأمراض الوراثية أو حتى تحسين الصفات البشرية #fyp #biology #science #foryou #معًا_لمحتوى_علمي_عراقي #الشعب_الصيني_ماله_حل😂😂
shame it costs $2.2 million "CRISPR stands for Clustered Regularly Interspaced Short Palindromic Repeats, short repeated sequences found in prokaryotic DNA, separated by spacer sequences derived from past encounters with, for example, a bacteriophage. Inserted into the bacterial genome, these sequences can later be transcribed into a guide RNA that matches, and base-pairs with, sections of the viral genome if it was encountered again. A nuclease associated with the guide RNA then cleaves the sequence base-paired with the guide RNA. (The nucleases are named Cas for CRISPR-associated.) The essential elements of this system are a guide RNA that homes in on the target sequence and a nuclease that can make a cut in the sequence that is bound by the guide RNA. By engineering guide RNAs complementary to a target gene, it is possible to target the nuclease to cleave within that gene. In the CRISPR/Cas9 system, the Cas9 endonuclease cuts both strands of the gene sequence targeted by the guide RNA. This generates a double-strand break that the cell attempts to repair. As you may remember, double-strand breaks in DNA can be repaired by simple, nonhomologous end joining (NHEJ) or by homologous recombination. When a break is fixed by NHEJ, there is good chance that there will be deletions or insertions that will inactivate the gene they are in. Thus, targeted cleavage of a site by CRISPR/Cas9 can easily and specifically inactivate a gene, making it easy to characterize the gene's function. But, what if you wished to simply mutate the gene at a specific site to study the effect of the mutation? This, too, can be achieved. If a homologous sequence bearing the specific mutation is provided, homologous recombination can repair the break, and at the same time insert the exact mutation desired. It is obvious that if you can insert a mutation as just described, it should be possible to correct a mutation in the genome by cleaving at the appropriate spot and providing the correct sequence as a template for repair by homologous recombination. The simplicity of the system holds great promise for curing genetic diseases. Scientists have also come up with some creative variations on the CRISPR/Cas9 system. For instance, one variant inactivates the nuclease activity of Cas9. The guide RNA in this system pairs with the target sequence, but the Cas9 does not cleave it. Instead, the Cas9 blocks the transcription of the downstream gene (Figure 8.10.2) This method allows specific genes to be turned off without actually altering the DNA sequence. Another variation also uses dCas9, but this time, the Cas9 is fused to a transcriptional activation domain. In this situation, the guide RNA positions the Cas9-activator domain in a place where it can enhance transcription from a specific promoter (Figure 8.10.3). Other variations on this theme attach histone-modifying enzymes or DNA methylases to the inactive Cas9. Again, the guide RNA positions the Cas9 in the desired spot, and the enzyme attached to Cas9 can methylate the DNA or modify the histones in that region." libretexts biochemistry free for all #molecularbiology #crispr #crisprcas9 #geneediting #genetics #biochem #biochemistry