The Prometheus League
Breaking News and Updates
- Abolition Of Work
- Ai
- Alt-right
- Alternative Medicine
- Antifa
- Artificial General Intelligence
- Artificial Intelligence
- Artificial Super Intelligence
- Ascension
- Astronomy
- Atheism
- Atheist
- Atlas Shrugged
- Automation
- Ayn Rand
- Bahamas
- Bankruptcy
- Basic Income Guarantee
- Big Tech
- Bitcoin
- Black Lives Matter
- Blackjack
- Boca Chica Texas
- Brexit
- Caribbean
- Casino
- Casino Affiliate
- Cbd Oil
- Censorship
- Cf
- Chess Engines
- Childfree
- Cloning
- Cloud Computing
- Conscious Evolution
- Corona Virus
- Cosmic Heaven
- Covid-19
- Cryonics
- Cryptocurrency
- Cyberpunk
- Darwinism
- Democrat
- Designer Babies
- DNA
- Donald Trump
- Eczema
- Elon Musk
- Entheogens
- Ethical Egoism
- Eugenic Concepts
- Eugenics
- Euthanasia
- Evolution
- Extropian
- Extropianism
- Extropy
- Fake News
- Federalism
- Federalist
- Fifth Amendment
- Fifth Amendment
- Financial Independence
- First Amendment
- Fiscal Freedom
- Food Supplements
- Fourth Amendment
- Fourth Amendment
- Free Speech
- Freedom
- Freedom of Speech
- Futurism
- Futurist
- Gambling
- Gene Medicine
- Genetic Engineering
- Genome
- Germ Warfare
- Golden Rule
- Government Oppression
- Hedonism
- High Seas
- History
- Hubble Telescope
- Human Genetic Engineering
- Human Genetics
- Human Immortality
- Human Longevity
- Illuminati
- Immortality
- Immortality Medicine
- Intentional Communities
- Jacinda Ardern
- Jitsi
- Jordan Peterson
- Las Vegas
- Liberal
- Libertarian
- Libertarianism
- Liberty
- Life Extension
- Macau
- Marie Byrd Land
- Mars
- Mars Colonization
- Mars Colony
- Memetics
- Micronations
- Mind Uploading
- Minerva Reefs
- Modern Satanism
- Moon Colonization
- Nanotech
- National Vanguard
- NATO
- Neo-eugenics
- Neurohacking
- Neurotechnology
- New Utopia
- New Zealand
- Nihilism
- Nootropics
- NSA
- Oceania
- Offshore
- Olympics
- Online Casino
- Online Gambling
- Pantheism
- Personal Empowerment
- Poker
- Political Correctness
- Politically Incorrect
- Polygamy
- Populism
- Post Human
- Post Humanism
- Posthuman
- Posthumanism
- Private Islands
- Progress
- Proud Boys
- Psoriasis
- Psychedelics
- Putin
- Quantum Computing
- Quantum Physics
- Rationalism
- Republican
- Resource Based Economy
- Robotics
- Rockall
- Ron Paul
- Roulette
- Russia
- Sealand
- Seasteading
- Second Amendment
- Second Amendment
- Seychelles
- Singularitarianism
- Singularity
- Socio-economic Collapse
- Space Exploration
- Space Station
- Space Travel
- Spacex
- Sports Betting
- Sportsbook
- Superintelligence
- Survivalism
- Talmud
- Technology
- Teilhard De Charden
- Terraforming Mars
- The Singularity
- Tms
- Tor Browser
- Trance
- Transhuman
- Transhuman News
- Transhumanism
- Transhumanist
- Transtopian
- Transtopianism
- Ukraine
- Uncategorized
- Vaping
- Victimless Crimes
- Virtual Reality
- Wage Slavery
- War On Drugs
- Waveland
- Ww3
- Yahoo
- Zeitgeist Movement
-
Prometheism
-
Forbidden Fruit
-
The Evolutionary Perspective
Category Archives: Transhuman News
Phoenix police: DNA evidence leads to arrest of man in deaths of 2 women in early 1990s
Posted: January 15, 2015 at 7:44 am
Published January 14, 2015
Phoenix Police Crime Response Unit members inspect the house of a man suspected of at least two 1992 murders of two young women on Wednesday, Jan. 14, 2015 in Phoenix, Ariz. Police arrested 42-year-old Bryan Patrick Miller late Tuesday in the deaths of 22-year-old Angela Brosso and 17-year-old Melanie Bernas. Brosso was killed in November 1992, and Bernas was killed in September 1993. Their remains were found in or near the Arizona canal. Both had disappeared while bicycling in the area. (AP Photo/The Arizona Republic, Tom Tingle) MARICOPA COUNTY OUT; MAGS OUT; NO SALES(The Associated Press)
This undated booking photo provided by the Maricopa County Sheriff's Office shows Bryan Patrick Miller. Authorities say DNA evidence led to the arrest of Miller, 42,in the killings of two young women whose bodies were found in northwest Phoenix in the early 1990s. Police arrested Miller late Tuesday, Jan. 13, 2015 in killings of 22-year-old Angela Brosso and 17-year-old Melanie Bernas. His home was the subject of an overnight search. Brosso was killed in November 1992, and Bernas was killed in September 1993. Their remains were found in or near the Arizona canal. Both had disappeared while bicycling in the area. (AP Photo/Maricopa County Sheriff's Office)(The Associated Press)
Phoenix Police Crime Response Unit members inspect the house of a man suspected of at least two 1992 murders of two young women on Wednesday, Jan. 14, 2015 in Phoenix, Ariz. Police arrested 42-year-old Bryan Patrick Miller late Tuesday in the deaths of 22-year-old Angela Brosso and 17-year-old Melanie Bernas. Brosso was killed in November 1992, and Bernas was killed in September 1993. Their remains were found in or near the Arizona canal. Both had disappeared while bicycling in the area. (AP Photo/The Arizona Republic, Tom Tingle) MARICOPA COUNTY OUT; MAGS OUT; NO SALES(The Associated Press)
Phoenix Police Crime Response Unit members inspect the house of a man suspected of at least two 1992 murders of two young women on Wednesday, Jan. 14, 2015 in Phoenix, Ariz. Police arrested 42-year-old Bryan Patrick Miller late Tuesday in the deaths of 22-year-old Angela Brosso and 17-year-old Melanie Bernas. Brosso was killed in November 1992, and Bernas was killed in September 1993. Their remains were found in or near the Arizona canal. Both had disappeared while bicycling in the area. (AP Photo/The Arizona Republic, Tom Tingle) MARICOPA COUNTY OUT; MAGS OUT; NO SALES(The Associated Press)
PHOENIX Authorities say DNA evidence led to the arrest of a man in the 20-year-old killings of two young women who vanished on bike rides near Phoenix's canal system.
Police arrested 42-year-old Bryan Patrick Miller late Tuesday in the deaths of 22-year-old Angela Brosso and 17-year-old Melanie Bernas.
Brosso was killed in November 1992, and Bernas died in September 1993. Both disappeared while bicycling near the Arizona Canal. Brosso's decapitated body was found in the area, while Bernas' body was discovered floating in the water.
Forensic evidence connected the killings within years, but investigators couldn't identify a suspect. Police say DNA evidence recently collected by undercover officers linked Miller to the killings.
Officers searched his home overnight. It's not clear whether he has a lawyer.
See the rest here:
Phoenix police: DNA evidence leads to arrest of man in deaths of 2 women in early 1990s
Posted in DNA
Comments Off on Phoenix police: DNA evidence leads to arrest of man in deaths of 2 women in early 1990s
DNA 'smart glue' could someday be used to build tissues, organs
Posted: at 7:44 am
DNA molecules provide the "source code" for life in humans, plants, animals and some microbes. But now researchers report an initial study showing that the strands can also act as a glue to hold together 3-D-printed materials that could someday be used to grow tissues and organs in the lab. This first-of-its-kind demonstration of the inexpensive process is described in the brand-new journal ACS Biomaterials Science & Engineering.
Andrew Ellington and colleagues explain that although researchers have used nucleic acids such as DNA to assemble objects, most of these are nano-sized -- so tiny that humans can't see them with the naked eye. Making them into larger, visible objects is cost-prohibitive. Current methods also do not allow for much control or flexibility in the types of materials that are created. Overcoming these challenges could potentially have a big payoff -- the ability to make tissues to repair injuries or even to create organs for the thousands of patients in need of organ transplants. With this in mind, Ellington's group set out to create a larger, more affordable material held together with DNA.
The researchers developed DNA-coated nanoparticles made of either polystyrene or polyacrylamide. DNA binding adhered these inexpensive nanoparticles to each other, forming gel-like materials that they could extrude from a 3-D printer. The materials were easy to see and could be manipulated without a microscope. The DNA adhesive also allowed the researchers to control how these gels came together. They showed that human cells could grow in the gels, which is the first step toward the ultimate goal of using the materials as scaffolds for growing tissues.
Story Source:
The above story is based on materials provided by American Chemical Society. Note: Materials may be edited for content and length.
Read the original here:
DNA 'smart glue' could someday be used to build tissues, organs
Posted in DNA
Comments Off on DNA 'smart glue' could someday be used to build tissues, organs
Finding the Telltale Genome – Video
Posted: at 7:43 am
Finding the Telltale Genome
Whenever a cell divides, its genetic code is copied into the new cell. But sometimes an imperfect copy is made, and the result is called a mutation. Most of the time, this does nothing; sometimes...
By: World Science Festival
Here is the original post:
Finding the Telltale Genome - Video
Posted in Genome
Comments Off on Finding the Telltale Genome – Video
The Number One of Enterobacteria Deciphered
Posted: at 7:43 am
14.01.2015 - (idw) Leibniz-Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH
Genome of the Escherichia coli type strain finally sequenced DNA includes potentially pathogenic segments The colon bacillus Escherichia coli is one of the best studied model organisms in the life sciences. However, the reference organism for this species, its so-called type strain, has been overlooked in microbial genomics until now. In the Genomic Encyclopedia of Bacteria and Archaea (GEBA) project, the DNA of type strain DSM 30083T has now been sequenced and compared to that of close relatives of the strain. This study not only allows an entirely new view of the numerous E. coli strains that play relevant roles in medicine and biotechnology, including the EHEC pathogen and Shigella, but they also yielded a generally applicable method for determining the subspecies of any bacterial species. The research was conducted at the Leibniz Institute DSMZ German Collection of Microorganisms and Cell Cultures GmbH, Braunschweig, Germany, and at the Joint Genome Institute, Walnut Creek, CA, USA.
The colon bacterium Escherichia (E.) coli to microbiologists and biotechnologists is like a pet bacterium and looks back on an exciting history. Initially described as "Bacterium coli commune" by bacteriologist Theodor Escherich in 1886, its original isolate was lost at the beginning of the 1920s. It was not until 1941 that it was isolated again, this time by Fritz Kaufmann at the State Serum Institute in Copenhagen, Denmark, who also deposited it in in several collections of microbial strains and provided a scientific description. Today, E. coli is likely the best understood microorganism in the world and serves as an important indicator for the quality of drinking and recreational waters.
"It seems strange that the number one, the type strain of a bacterium that has entire scientific conferences dedicated to it as a model organism, had not been fully sequenced until now", said Christine Rohde, Head of the E. coli strain collection at DSMZ, Braunschweig, Germany. "Initially, scientists primarily sequenced the genomes of pathogenic strains of E. coli, or of genetically modified strains of biotechnological relevance. In addition, physicians and hygienists in their daily practice use serotypes that are quickly determined by antibody tests in order to differentiate between different strains of E. coli. As Markus Gker, a bioinformatics scientist at DSMZ added: Complete bacterial genomes are of fundamental importance for diagnostics in humans, for biotechnology, and for the search for antimicrobial agents. Today, this is truer than ever, as some strains of E. coli have developed into dangerous pathogens such as EHEC or EAHEC. The E. coli type strain was sequenced as part of the GEBA project that focuses on type strains exhibiting an unusual physiology or occupying a key place in the phylogenetic tree. This is the only microorganism in the project that was included based on its importance as a model organism.
A genome with pathogenic potential
There are major physiological and genomic differences between the E. coli type strain and the harmless laboratory strain K-12. Due to its serotype, the type strain had been grouped into the biological containment level 2, and its genome sequence now confirmed its pathogenic potential, said Jrn Petersen, an expert of plasmid biology at the DSMZ. Unlike laboratory strain K-12, the E. coli type strain harbors an additional circular plasmid of 131,289 base pairs in its genome of 5,038,133 base pairs; this plasmid exhibits a sequence identity of 99% with plasmids from pathogenic E. coli isolates. These strains cause, e.g., colibacillosis in poultry and meningitis in newborns, with the horizontally transferable plasmid being responsible for their virulence, explained Petersen.
Sophisticated computer-aided phylogenetic analysis
Thanks to the complete genome sequence of the E. coli type strain, the Braunschweig scientists were able to examine whether the huge number of previously sequenced isolates of E. coli actually belong to the same species, using modern taxonomic techniques in the process. To this end, we analyzed more than 250 strains of E. coli and also verified their published taxonomic classification in subgroups, the 'phylotypes'. This bioinformatics-based analysis was performed with the state-of-the-art GGDC method. This technique is analogous to classical DNA-DNA hybridization in the laboratory, but yields significantly more exact results," as Markus Gker explained.
Original article:
Meier-Kolthoff JP et al. (2014). Complete genome sequence of DSM 30083T, the type strain (U5/41T) of Escherichia coli, and a proposal for delineating subspecies in microbial taxonomy. Stand Genomic Sci 9: 2 http://www.standardsingenomics.com/content/pdf/1944-3277-9-2.pdf
See the original post:
The Number One of Enterobacteria Deciphered
Posted in Genome
Comments Off on The Number One of Enterobacteria Deciphered
Cats Claw Their Way into Genomics
Posted: at 7:43 am
The genetic sequencing of cats has now officially taken off
The first cat genome sequence from an Abyssinian named Cinnamon was reported in 2007. Credit:Valerius Geng via Wikimedia Commons
Cats may have beaten dogs on the Internet but felines have been a rare breed in genetics labs compared with their canine counterparts. Now, at last, cats are clawing their way into genomics.
At a meeting this week in San Diego, California, a close-knit group of geneticists unveiled the first results from an effort to sequence the genomes of 99 domestic cats. The work will benefit both humans and felines, the researchers say, by mapping the mutations underlying conditions that afflict the two species, such as kidney disease.
Its a great time to be in cat genomics, says William Murphy, a geneticist at Texas A&M University in College Station who is involved in the effort. Plummeting costs for DNA sequencing now make it possible to do genomics cheaply and cat genomics, long under-funded compared with similar efforts in dogs, is benefiting, he says. Were finally at the point where we can do all sorts of things we wanted to do 5 or 10years ago.
The first cat genome sequence from an Abyssinian named Cinnamon was reported in 2007. But the sequence contained significant gaps and errors, which slowed efforts to map genes. A high-quality version of Cinnamons genome was not publisheduntil late 2014. Domestic dogs, meanwhile, have become a darling of geneticists: their full genomewas reported in 2005, and the sequence has been continually improved. Hundreds of genes underlying canine diseases and traits are estimated to have been discovered, compared with as few as a dozen for cats.
The discrepancy can be traced back to the early 2000s. After the completion of the human, mouse and rat genomes, the US National Institutes of Health organized a commission to decide on their next target; the dog genome was selected for high-quality sequencing, whereas cats were put on hold.
That got some cat geneticists backs up. The truth is there were more powerful people interested in dogs, says Stephen OBrien, director of the Theodosius Dobzhansky Center for Genome Bioinformatics in StPetersburg, Russia, who led the initial cat-sequencing efforts.
But canine researchers were able to make a compelling case. Pet dogs suffer from many of the same conditions as humans, from narcolepsy to arthritis. And the intensely inbred nature of dog breeds made it relatively easy to identify disease-causing genes: because there is little genetic variation within any particular breed, the genes that cause disease in affected individuals stand out.
Dogs had other advantages, too. The existence of kennel clubs, which maintain breed standards and are full of enthusiastic pet owners and veterinary surgeons, helped dog geneticists to recruit subjects for study. Given the resources they had, they were discovering new genetic diseases in breeds almost daily, says Niels Pedersen, a veterinary scientist at the University of California, Davis.
Follow this link:
Cats Claw Their Way into Genomics
Posted in Genome
Comments Off on Cats Claw Their Way into Genomics
Human Longevity, Inc. Signs Agreement with Genentech for Whole Genome Sequencing and Analysis of Samples
Posted: at 7:43 am
LA JOLLA, Calif., Jan. 14, 2015 /PRNewswire/ -- Human Longevity, Inc. (HLI), the human health information technology and health care company, today announced a multi-year agreement with Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), to conduct whole genome sequencing of tens of thousands of de-identified samples from Genentech. HLI, using proprietary tools and unique expertise, will sequence genomes to 30x coverage and analyze the data. Financial details of the agreement were not disclosed.
"We are excited to be working with Genentech so that patient samples can be analyzed according to more precise genetic categories," said J. Craig Venter, Ph.D., HLI CEO and Co-Founder. "At HLI we have built unprecedented capabilities for whole genome sequencing and interpretation to enable a wide array of advances in health care. The application of our capabilities to discover new diagnostics and targeted therapies is one of the most relevant today."
HLI is focused on building the world's most comprehensive integrated human genotype and phenotype database, the HLI Knowledgebase. To achieve that, HLI has established the largest human genome sequencing center in the world, and is sequencing and analyzing complete, 30x coverage genomes using Illumina's HiSeq X Ten sequencing machines. HLI also utilizes Illumina HiSeq 2500 and Pac Bio RS II instruments.
"Genentech's goal is to harness the power of widespread whole genome sequencing to identify new therapeutic targets and diagnostic biomarkers," said James Sabry, senior vice president and global head of Genentech partnering. "We are pleased to join forces with HLI and leverage their expertise in DNA sequencing and analysis along with scientific expertise to accelerate our drug discovery efforts and ultimately bring to market promising new therapies for patients with serious medical conditions."
HLI and Genentech take the privacy and protection of individual's personal information very seriously. All sample and patient data elements are de-identified to remove all personally identifiable information.
About Human Longevity, Inc.HLI, a privately held company headquartered in San Diego, CA was founded in 2013 by pioneers in the fields of genomics and stem cell therapy. Using advances in genomic sequencing, the human microbiome, proteomics, informatics, computing, and cell therapy technologies, HLI is building the world's most comprehensive knowledge base of human genotypes and phenotypes as a basis for a variety of opportunities to help solve aging related disease and human biological decline. HLI will be licensing access to its Knowledgebase to pharmaceutical and biotech companies, academic institutions and medical centers, governments, insurers and physicians, and developing new diagnostics and therapeutics as part of their product offerings. For more information please visit, http://www.humanlongevity.com
Logo- http://photos.prnewswire.com/prnh/20140304/LA76169LOGO
SOURCE Human Longevity, Inc.
RELATED LINKS http://www.humanlongevity.com
See the original post here:
Human Longevity, Inc. Signs Agreement with Genentech for Whole Genome Sequencing and Analysis of Samples
Posted in Human Longevity
Comments Off on Human Longevity, Inc. Signs Agreement with Genentech for Whole Genome Sequencing and Analysis of Samples
Defeat Eczema – Video
Posted: at 7:43 am
Defeat Eczema
Defeat Eczema Link: http://goweb.pw/h Defeat Eczema, Defeat Eczema ebook, Defeat Eczema complaints, Defeat Eczema Review, reviews on Defeat Eczema , Defeat E...
By: Julius Sammons
More here:
Defeat Eczema - Video
Posted in Eczema
Comments Off on Defeat Eczema – Video
How To Get Rid Of Eczema – Eczema Treatment (2015) – Video
Posted: at 7:43 am
How To Get Rid Of Eczema - Eczema Treatment (2015)
Defeat Eczema Today You can visit - http://tinyurl.com/defeat-eczema-today-2015 Defeat Eczema Today Review Defeat Eczema Today by Ellie Caroll is a natural t...
By: Sarah Allen
Read more here:
How To Get Rid Of Eczema - Eczema Treatment (2015) - Video
Posted in Eczema
Comments Off on How To Get Rid Of Eczema – Eczema Treatment (2015) – Video
Mutations linked to repair of chromosome ends may make emphysema more likely in smokers
Posted: at 7:42 am
Mutations in a gene that helps repair damaged chromosome ends may make smokers -- especially female smokers -- more susceptible to emphysema, according to results of a new study led by Johns Hopkins Kimmel Cancer Center researchers.
The mutations are one of a few genetic factors directly linked to chronic obstructive pulmonary disease (COPD), including emphysema, since the 1960s, says Mary Armanios, M.D., associate professor of oncology at the Johns Hopkins University School of Medicine.
Specifically, the alteration occurs in the telomerase reverse transcriptase (TERT) gene, which helps produce an enzyme called telomerase. Telomerase maintains and repairs the "caps" that protect the ends of chromosomes from degradation during cell division. Telomeres gradually shorten with age and act as a sort of cellular clock in cells. Mutations in TERT lead to excessively shortened telomeres.
Using genetic data gathered in COPD studies funded by the National Institutes of Health, Armanios and colleagues found TERT mutations in three of 292 smokers with emphysema. The researchers then looked at a sample of 50 Johns Hopkins patients with syndromes linked to telomere shortening. Among 39 nonsmokers, there were no cases of emphysema. Among smokers, seven of 11 patients, including all six female smokers, had emphysema. Armanios says this suggests that female smokers with telomerase-related mutations may be more susceptible to emphysema.
A report on the research was published Dec. 22 in the Journal of Clinical Investigation. Lung disease is the third leading cause of death in the U.S., and the main risk factors are aging and smoking. However, only about 10 percent of smokers develop COPD, according to Armanios. "Not everyone who smokes gets emphysema, so our study is part of a bigger effort to find out why some people get it and others do not," says Armanios, who notes that other studies have shown that young women who smoke may be more susceptible to emphysema.
The researchers had some clues about telomerase genes from earlier studies, including one in which Armanios and her colleagues identified the impact of shortened telomeres in mice as a risk factor for emphysema after being exposed to cigarette smoke. The scientists previously had noted a link between telomerase mutations and a severe hereditary lung disease called idiopathic pulmonary fibrosis.
Patients with emphysema often suffer from other health problems, including osteoporosis, liver disease and cancer. These disorders are common in people with shortened telomeres as well. The new study, says Armanios, "may now give us an explanation for why people with emphysema have these systemic problems. If we know that they have a telomerase mutation, it may help us take care of them in a more sophisticated way and delay the onset of those diseases."
Armanios and colleagues published a study last year showing that telomerase mutations may lead to more complications during lung transplants for people with idiopathic pulmonary fibrosis.
In the current study, only 1 percent of the smokers with severe emphysema carried the TERT mutation, but Armanios says this is comparable to the percentage who carry another known genetic factor related to COPD -- a mutation in the alpha-1 antitrypsin gene.
The researchers only looked at mutations in two telomerase genes but will now search for mutations in other telomere-regulating genes that might also predispose people to lung disease. "There are many genes that regulate the telomere, so it's likely that more than 1 percent could be impacted by these predisposing factors," says Armanios.
Read the original:
Mutations linked to repair of chromosome ends may make emphysema more likely in smokers
Posted in Gene Medicine
Comments Off on Mutations linked to repair of chromosome ends may make emphysema more likely in smokers
'Titin' gene mutations will help identify patients at risk of heart failure
Posted: at 7:42 am
A new study has identified genetic mutations that cause the heart condition dilated cardiomyopathy (DCM), paving the way for more accurate diagnosis.
By sequencing the gene encoding the muscle protein titin in more than 5,000 people, scientists have worked out which variations are linked to disease, providing information that will help screen high-risk patients.
Titin gene mutations were previously associated with DCM, a leading cause of inherited heart failure, but many people have variations in the genetic code that are completely benign.
The new study, published in Science Translational Medicine, sorts the harmful from the harmless mutations, giving doctors a directory to interpret patients' DNA sequences.
The information could also help researchers develop therapies to prevent or treat heart disease caused by titin mutations.
The study was led by researchers at Imperial College London and Royal Brompton & Harefield NHS Foundation Trust.
Around one in 250 people are estimated to have DCM. It causes the heart muscle to become thin and weak, often leading to heart failure.
Mutations in the titin gene that make the protein shorter, or truncated, are the most common cause of DCM, accounting for about a quarter of cases. But truncations in the gene are common - around one in 50 people have one - and most are not harmful, making it difficult to develop a useful genetic test.
The researchers sequenced the titin gene from 5,267 people, including healthy volunteers and patients with DCM, and analysed the levels of titin in samples of heart tissue. The results showed that mutations that cause DCM occur at the far end of the gene sequence. Mutations in healthy individuals tend to occur in parts of the gene that aren't included in the final protein, allowing titin to remain functional.
Professor Stuart Cook, from the Medical Research Council (MRC) Clinical Sciences Centre at Imperial College London, who led the study, said: "These results give us a detailed understanding of the molecular basis for dilated cardiomyopathy. We can use this information to screen patients' relatives to identify those at risk of developing the disease, and help them to manage their condition early."
More here:
'Titin' gene mutations will help identify patients at risk of heart failure
Posted in Gene Medicine
Comments Off on 'Titin' gene mutations will help identify patients at risk of heart failure