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Annemieke Aartsma-Rus is the winner of an Ammodo Science Award for fundamental research 2021 in the Biomedical Sciences domain.nnAartsma-Rus has made an important contribution to research in Duchenne muscular dystrophy. Patients with this serious hereditary muscle disease lack the protein dystrophin, because the gene code for dystrophin is unreadable. Thanks in part to the fundamental pioneering work of Aartsma-Rus, an exon skipping therapy is now available in the USA and Japan that can make the

Ammodo Science Award 2021 | Annemieke Aartsma-Rus

⏲ 1 min 57 sec ✓ 02-Sep-2021

Amoeba Sisters

Mutations (Updated)

⏲ 7 minutes 14 seconds 👁 1.3M

Amoeba Sisters

DNA vs RNA (Updated)

⏲ 6 minutes 31 seconds 👁 1.8M

GenePro is the first ever, medical grade protein powder made only of pure chains of amino acids- no fillers, flavors, or clumpy chunks!nnLearn more and use the code vimeo10 at checkout to save 10% here:nhttps://dirobi.com/collections/all-products-1/products/musclegen-performance-nutrition-genepro-medical-grade-protein

Intro to Gene Pro Protein Powder

⏲ 96 sec ✓ 16-Apr-2021

Beverly Biology

Translation Protein Synthesis (updated)

⏲ 19 minutes 56 seconds 👁 15.7K

REDMEDBD

Protein synthesis animation

⏲ 19 minutes 13 seconds 👁 1.1M

Building New Live BeingsnFrancois Taddei, INSERM, Faculte Necker-Enfants MaladesnnResearchers from the Craig Venter Institute have recently managed to synthesize the entire genomic DNA of the bacterium Mycoplasma genitalium . This is a major step towards the construction of a live being de novo. Indeed, although we still do not understand how life appeared and what the first living organisms looked like during evolution, one may wonder what would be the minimal biological components required to

Building New Live Beings - Francois Taddei, INSERM, Faculte Necker-Enfants Malades

⏲ 18 min 52 sec ✓ 07-Dec-2011

MooMooMath and Science

Decode from DNA to mRNA to tRNA to amino acids

⏲ 2 minutes 33 seconds 👁 290.7K

Nucleus Biology

DNA and RNA - Transcription

⏲ 5 minutes 52 seconds 👁 175.6K

Speaker:nSandra Pankow, PhDnThe Scripps Research InstitutennINTRODUCTION: Cystic Fibrosis is a disease caused by mutations in the cystic fibrosis ion transport regulator gene (CFTR). The most common mutation, deletion of Phe at position 508 (DF508), results in a loss of function phenotype that causes a large number of clinical symptoms including chronic respiratory infections. At the protein level, the DF508 mutation causes the protein to misfold which results in rapid degradation of the protein

Using Mass Spectrometry and Proteomics to Understand the Mechanism Involved in Cystic Fibrosis

⏲ 39 min 37 sec ✓ 24-Sep-2020

Cognito

How are Proteins Made? - Transcription and Translation Explained #66

⏲ 11 minutes 21 seconds 👁 484.6K

HLRCC Foundation

Understanding How Genes Code for Proteins - HLRCC Science Lecture #1

⏲ 16 minutes 48 seconds 👁 311

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