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Monthly Archives: September 2012
DNA Dynamics Update on Sports Title
Posted: September 30, 2012 at 6:14 pm
LEAMINGTON SPA, UNITED KINGDOM--(Marketwire - Sep 25, 2012) - DNA Dynamics, Inc. ( PINKSHEETS : DNAD ), a global developer and publisher of mobile video games and applications, announces today that it is to unveil the first of its new Sports Game at GDC Online in Austin in October.
The Company recently announced that it had hired Kevin Corti to head up studio operations. Kevin took responsibility on day one for reworking Warheads Battle to turn the 100,000 users into a more profitable part of the DNA Games business. Moreover, Kevin was given the task of developing the two exciting social mobile games that DNA is working on right now.One of these games, a Sports Based Social Mobile Game, is to be announced at GDC Online in Austin, TX this October.
This comes hot on the back of the decision to close down one of its subsidiaries, DNA Interactive Limited, the company responsible for the Naked Gun: ICUP license, as the game just failed to hit the numbers expected.
Talking of the experience of the Naked Gun game, CEO Ed Blincoe had this to say, "We learnt a lot of lessons working with the Naked Gun license, more than we had wanted to. After DNA initially being mis-sold the Naked Gun license by GameCentric Media and a widespread, but misplaced, belief that DNA had received AppBackr funds, the game itself just missed the mark. We were always frustrated when AppBackr's Backers thought we had received their funds -- we didn't receive a dime from AppBackr, though we understand that GameCentric Media may have received some of the pledged funds."
When talking about the quality of the game, Blincoe says: "In industry reviews as well as user reviews, the game was a real hit with an average rating of 4/5 stars in the AppStore.It just didn't gain enough traction to be a commercial success. Finally, we took the decision to cut the spending and have begun to pull the game. We believe this is in the interest of the business and its shareholders, we make tough decisions here, but ultimately we believe they are the best decisions."
Blincoe continued, "It's a difficult decision to close down a part of the business which isn't performing, but with the new impetus behind the social mobile execution of our business plan, we believe that DNA Dynamics, operating through DNA Games, has a fantastic future. We are very much alive, kicking and looking forward to a successful future."
About DNA Dynamics, Inc. Headquartered in Leamington Spa in the United Kingdom, DNA Dynamics is a worldwide developer and publisher of graphically rich, interactive entertainment currently delivered on iOS, Android, Apple Mac and PC.Through its operating subsidiaries, the Company has created, acquired or licensed a portfolio of highly recognizable or emerging brands that broadly appeal to its consumer demographics, ranging from children to adults and casual gamers to serious enthusiasts.For more information, please go to http://www.dnadynamics.net. You can also follow the Company on Facebook and Twitter.
Forward-Looking Statements This press release may contain forward-looking statements, including information about management's view of DNA Dynamics, Inc.'s future expectations, plans and prospects. In particular, when used in the preceding discussion, the words "believes," "expects," "intends," "plans," "anticipates," or "may," and similar conditional expressions are intended to identify forward-looking statements. Any statements made in this news release other than those of historical fact, about an action, event or development, are forward-looking statements. These statements involve known and unknown risks, uncertainties and other factors, which may cause the results of DNA Dynamics, its subsidiaries and concepts to be materially different than those expressed or implied in such statements. Unknown or unpredictable factors also could have material adverse effects on DNA Dynamics' future results. The forward-looking statements included in this press release are made only as of the date hereof. DNA Dynamics cannot guarantee future results, levels of activity, performance or achievements. Accordingly, you should not place undue reliance on these forward-looking statements. Finally, DNA Dynamics undertakes no obligation to update these statements after the date of this release, except as required by law, and also takes no obligation to update or correct information prepared by third parties that are not paid for by DNA Dynamics.
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DNA Dynamics Update on Sports Title
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Knome Introduces the knoSYS™100; First Plug-and-Play Human Genome Interpretation System
Posted: at 6:14 pm
CAMBRIDGE, Mass.--(BUSINESS WIRE)--
Knome Inc. announced today that it is taking orders for the knoSYS100, the first plug-and-play, fully integrated hardware and software system designed to help researchers in medical and academic institutions interpret human whole genomes. The knoSYS100 was developed to help geneticists discover relevant genetic variation, investigate diseases of unknown cause, and create next generation in silico gene tests. Units will begin shipping in Q4, 2012.
Starting at $125,000, the knoSYS100 is based on Knomes big data informatics technology. The system will accept next generation sequence data from leading sequencers, including those sold by Illumina (ILMN), Life Technologies (LIFE), and Complete Genomics (GNOM).
Breaking the genome interpretation bottleneck
The difficulty and cost associated with human genome sequencing has largely been addressed, with the cost of sequencing a whole genome expected to decline to under $1,000 in 2013. But it still takes a team of researchers weeks to months to annotate, compare, and interpret genome data. This slow pace and the lack of robust tools have significantly limited the ability of researchers to scale the process of interpreting human genomes.
With an average throughput of one genome per day, the knoSYS100 eliminates the current informatics bottleneck in whole genome interpretationmatching the speed of todays fastest sequencers.
In the first half of this year, we saw the demand for genome interpretation surge as researchers in many of the worlds leading medical institutions started preparing for the broad utilization of whole genome interpretation for patient care, said Martin Tolar, MD, PhD, Chief Executive Officer of Knome. All of these institutions face the same issuehow to industrialize genome interpretation so that it is not only accurate, but fast.
More than a dozen of the worlds top medical institutions have joined an early access program to pilot Knomes genome interpretation technology, including: ARUP Laboratories, Cedars-Sinai Medical Center, Cincinnati Childrens Hospital, The Hospital for Sick Children (SickKids) in Toronto, Hyundai Cancer Institute at CHOC Childrens, University of Liverpool, and University of Verona.
An in silico genetic testing lab in a box
In addition to providing geneticists with query and visualization applications for conducting in-depth research into sets of whole genomes, the knoSYS100 ships with tools and libraries that allow developers to create in silico gene tests that can be run at the push of a button.
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Knome Introduces the knoSYS™100; First Plug-and-Play Human Genome Interpretation System
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UMass Med professors are sleuths of the genome
Posted: at 6:14 pm
WORCESTER Two professors at the University of Massachusetts Medical School are playing a role in a global effort to unlock the mysteries of the human genome, which is the complete set of genetic instructions for humans.
Medical school professors Job Dekker and Zhiping Weng participated in an international consortium of scientists from 32 institutions that made headlines this month with its findings. The scientists involved in the Encyclopedia of DNA Elements project, or ENCODE, announced that parts of the genome often dismissed in the past as junk DNA actually play an important role in regulating what genes do.
Through the projects research, scientists have gained an understanding of 80.4 percent of the human genome, the UMass Medical School professors said.
That is a tremendous improvement in our understanding of the genome, said Mr. Dekker, who holds a doctorate and is professor of biochemistry and molecular pharmacology and co-director of the schools Systems Biology program.
Researchers involved in the project used a range of experimental approaches to understand what pieces of DNA are regulating genes. The research labs of Mr. Dekker and Ms. Weng, who holds a doctorate and is the director of the medical schools program in bioinformatics and integrative biology, worked on separate projects that contributed to the effort.
The findings of the international project appeared in 30 papers published in the journals Nature, Genome Research and Genome Biology. Mr. Dekker was the lead author of one of the Nature papers. The results of Ms. Wengs efforts were published in Genome Research. The consortiums work received funding from the National Human Genome Research Institute, part of the National Institutes of Health.
The professors touted the data produced by ENCODE which built upon the Human Genome Project completed in 2003 as the basis for further study in the genetic causes of human disease and a potential boon for pharmaceutical and other medical research.
For the past decade, Mr. Dekker has helped develop methods to create three-dimensional models of folded chromosomes. Those models can be used to determine which parts of the genome touch each other, according to the medical school.
Scientists have believed for a number of years that a regulatory element could control a gene by physically interacting with that gene, Mr. Dekker said. His goal is to measure the three-dimensional structure to see which regulatory elements physically touch what genes, he said.
We have gone from this view of the genome where we have here and there a gene and then large sections of unknown of territory, Mr. Dekker said. We now have a much richer picture of the genome, where we can see genes, and we can set lots and lots of these regulatory elements.
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Need-to-know news and views for UB faculty and staff
Posted: at 6:13 pm
Book reveals health hazards from coal By ELLEN GOLDBAUM Published: September 27, 2012
Coal kills. Thats the message of The Silent Epidemic: Coal and the Hidden Threat to Health by Alan H. Lockwood, UB emeritus professor of neurology.
His book examines how human health is harmed by the burning of coal, which supplies nearly half of the energy in the United States and a far greater percentage in industrializing countries, such as China, India and Brazil.
While Lockwood says its widely accepted that lifestyle choices are key determinants of health and longevity, air pollution is underappreciated as a factor behind causes of death in the U.S.
There are these environmental factors that you dont have as much control over that are important contributors to mortality and morbidity, he explains. Coal is a major contributing factor to the top four causes of death in the U.S.cancer, heart disease, respiratory disease and strokebut I think people are completely unaware that pollution from coal is responsible for huge numbers of deaths.
The book examines how coal is a factor in each of these diseases. Additional chapters examine the science, politics and economics of coal burning and global warming.
Beyond the top four causes of death, Lockwood adds, new scientific studies are beginning to show that coal burning also may play a role in neurodegenerative diseases, such as Alzheimers disease and Parkinsons disease.
Lockwood, a board member with Physicians for Social Responsibility, became interested in how coal affects human health while writing a white paper on the subject for the organization. All profits from the book will be donated to Physicians for Social Responsibility.
Thats when it really began to strike home with me that coal was a major source of air pollution damaging the health of Americans, he says. The worst health effects of coal are felt by residents of states in the Northeastern U.S., east of the Mississippi, where most coal is burned and where the power plants are the oldest.
Coal burning causes disease through two main mechanisms, Lockwood explains: the inflammatory response that inhaled particulate matter triggers in the body and the penetration into the brain of inhaled particulate matter.
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Need-to-know news and views for UB faculty and staff
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Join GSA in San Diego for the Nation's Premier Aging Conference!
Posted: at 6:13 pm
Public release date: 20-Sep-2012 [ | E-mail | Share ]
Contact: Todd Kluss tkluss@geron.org 202-587-2839 The Gerontological Society of America
The Gerontological Society of America (GSA) invites all journalists to attend its 65th Annual Scientific Meeting the country's largest interdisciplinary conference in the field of aging from November 14 to 18 in San Diego. Media representatives may register free of charge.
An estimated 4,000 professionals are expected to attend the five-day gathering at the San Diego Convention Center. The theme for 2012 is "Charting New Frontiers in Aging" and the program schedule contains more than 500 scientific sessions featuring research presented for the first time. Noteworthy meeting highlights include:
The complimentary media registration allows access to all scientific sessions and the Exhibit Hall. Badges and printed program materials can be picked up in the Press Room, which will be located in Room 5A at the Convention Center.
Registration information is available at http://www.geron.org/press. GSA has locked in special conference rates at three nearby hotels, which will be available until October 19.
We look forward to seeing you in San Diego!
###
The Gerontological Society of America (GSA) is the nation's oldest and largest interdisciplinary organization devoted to research, education, and practice in the field of aging. The principal mission of the Society and its 5,400+ members is to advance the study of aging and disseminate information among scientists, decision makers, and the general public. GSA's structure also includes a policy institute, the National Academy on an Aging Society, and an educational branch, the Association for Gerontology in Higher Education.
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Join GSA in San Diego for the Nation's Premier Aging Conference!
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Joslin Scientists Identify Molecular Process in Fat Cells That Influences Stress and Longevity
Posted: at 6:13 pm
Newswise BOSTON September 16, 2012 As part of their ongoing research investigating the biology of aging, the greatest risk factor for type 2 diabetes and other serious diseases, scientists at Joslin Diabetes Center have identified a new factor microRNA processing in fat tissue which plays a major role in aging and stress resistance. This finding may lead to the development of treatments that increase stress resistance and longevity and improve metabolism. The findings appear in the September 5 online edition of Cell Metabolism.
Over the past several years, it has become clear that fat cells (adipocytes) are more than just repositories to store fat. Indeed, fat cells secrete a number of substances that actively influence metabolism and systemic inflammation. Previous studies have found that reducing fat mass by caloric restriction (CR) or surgical or genetic means can promote longevity and stress resistance in species from yeast to primates. However, little is known about how CR and fat reduction produce these beneficial effects. This study investigated one type of molecular mediator change in microRNAs (miRNAs) and the processing enzymes required to make them that is influenced by aging and reversed by caloric restriction. miRNAs are involved in the formation of mature RNA.
Based on studies conducted using human cells, mice and C. elegans (a microscopic worm used as a model organism for aging studies), the researchers demonstrated that levels of multiple miRNAs, decrease in fat tissue (adipose) with age in all three species. This is due to a decrease in the critical enzyme required from converted pre-miRNAs to mature miRNAs, Dicer. In the human study, which compared the miRNA levels in preadipocytes (fat cell precusors) of young, middle-aged and older people, people aged 70 and older had the lowest miRNA levels. The fact that this change occurs in humans, mice and worms points to its significance as a general and important process, says lead author C. Ronald Kahn, MD, Chief Academic Officer at Joslin Diabetes Center and the Mary K. Iacocca Professor of Medicine at Harvard Medical School.
Caloric restriction, which has been shown to prolong lifespan and improve stress resistance in both mice and worms, prevents this decline of Dicer, and in the case of the mice, restore miRNAs to levels observed in young mice. Conversely, exposure of adipocytes to major stressors associated with aging and metabolic diseases, including toxic agents, Dicer levels decreased. Mice and worms engineered to have decreased Dicer expression in fat showed increased sensitivity to stress, a sign of premature aging. By contrast, worms engineered to overexpress Dicer in the intestine (the adipose tissue equivalent in worms) had greater stress resistance and lived longer.
Overall, these studies showed that regulation of miRNA processing in adipose-related tissues plays an important role in longevity and an organisms ability to respond to age-related and environmental stress. This study points to a completely new mechanism by which fat might affect lifespan and is the first time that anyone has looked at fat and miRNAs as factors in longevity, according to co-author T. Keith Blackwell, MD, PhD, co-head of Joslin's Section on Islet Cell and Regenerative Biology and Professor of Pathology at Harvard Medical School.
Based on this study, Blackwell suggests that finding ways to improve miRNA processing to keep miRNA levels up during aging might have a role in protecting against the stresses of everyday life and the development of age- and stress-related disease.
Dr. Kahn and the study investigators are currently working on ways to genetically control Dicer levels in the fat tissues of mice, to create mouse models that are more or less resistant to stress. We would love to find drugs that would mimic this genetic manipulation to produce a beneficial effect, says Dr. Kahn. If we can better understand the biology of aging, we might also understand how age impacts diabetes, says Kahn.
Study co-authors include Marcelo A. Mori, Prashant Raghavan, Jeremie Boucher, Stacey Robida-Stubbs, Yazmin Macotela, Steven J. Russell, and T. Keith Blackwell of Joslin; and James L. Kirkland and Thomas Thomou of the Mayo Clinic.
About Joslin Diabetes Center
Joslin Diabetes Center, located in Boston, Massachusetts, is the world's largest diabetes research and clinical care organization. Joslin is dedicated to ensuring that people with diabetes live long, healthy lives and offers real hope and progress toward diabetes prevention and a cure. Joslin is an independent, nonprofit institution affiliated with Harvard Medical School.
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Joslin Scientists Identify Molecular Process in Fat Cells That Influences Stress and Longevity
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Molecular process in fat cells that influences stress and longevity identified
Posted: at 6:13 pm
ScienceDaily (Sep. 26, 2012) As part of their ongoing research investigating the biology of aging, the greatest risk factor for type 2 diabetes and other serious diseases, scientists at Joslin Diabetes Center have identified a new factor -- microRNA processing in fat tissue -- which plays a major role in aging and stress resistance. This finding may lead to the development of treatments that increase stress resistance and longevity and improve metabolism.
The findings appear in the Sept. 5 online edition of Cell Metabolism.
Over the past several years, it has become clear that fat cells (adipocytes) are more than just repositories to store fat. Indeed, fat cells secrete a number of substances that actively influence metabolism and systemic inflammation. Previous studies have found that reducing fat mass by caloric restriction (CR) or surgical or genetic means can promote longevity and stress resistance in species from yeast to primates. However, little is known about how CR and fat reduction produce these beneficial effects. This study investigated one type of molecular mediator -- change in microRNAs (miRNAs) and the processing enzymes required to make them- that is influenced by aging and reversed by caloric restriction. miRNAs are involved in the formation of mature RNA.
Based on studies conducted using human cells, mice and C. elegans (a microscopic worm used as a model organism for aging studies), the researchers demonstrated that levels of multiple miRNAs, decrease in fat tissue (adipose) with age in all three species. This is due to a decrease in the critical enzyme required from converted pre-miRNAs to mature miRNAs, Dicer. In the human study, which compared the miRNA levels in preadipocytes (fat cell precusors) of young, middle-aged and older people, people aged 70 and older had the lowest miRNA levels. "The fact that this change occurs in humans, mice and worms points to its significance as a general and important process," says lead author C. Ronald Kahn, MD, Chief Academic Officer at Joslin Diabetes Center and the Mary K. Iacocca Professor of Medicine at Harvard Medical School.
Caloric restriction, which has been shown to prolong lifespan and improve stress resistance in both mice and worms, prevents this decline of Dicer, and in the case of the mice, restore miRNAs to levels observed in young mice. Conversely, exposure of adipocytes to major stressors associated with aging and metabolic diseases, including toxic agents, Dicer levels decreased. Mice and worms engineered to have decreased Dicer expression in fat showed increased sensitivity to stress, a sign of premature aging. By contrast, worms engineered to "overexpress" Dicer in the intestine (the adipose tissue equivalent in worms) had greater stress resistance and lived longer.
Overall, these studies showed that regulation of miRNA processing in adipose-related tissues plays an important role in longevity and an organism's ability to respond to age-related and environmental stress. "This study points to a completely new mechanism by which fat might affect lifespan and is the first time that anyone has looked at fat and miRNAs as factors in longevity," according to co-author T. Keith Blackwell, MD, PhD, co-head of Joslin's Section on Islet Cell and Regenerative Biology and Professor of Pathology at Harvard Medical School.
Based on this study, Blackwell suggests that "finding ways to improve miRNA processing to keep miRNA levels up during aging might have a role in protecting against the stresses of everyday life and the development of age- and stress-related disease."
Dr. Kahn and the study investigators are currently working on ways to genetically control Dicer levels in the fat tissues of mice, to create mouse models that are more or less resistant to stress. "We would love to find drugs that would mimic this genetic manipulation to produce a beneficial effect," says Dr. Kahn. "If we can better understand the biology of aging, we might also understand how age impacts diabetes," says Kahn.
Study co-authors include Marcelo A. Mori, Prashant Raghavan, Jeremie Boucher, Stacey Robida-Stubbs, Yazmin Macotela, Steven J. Russell, and T. Keith Blackwell of Joslin; and James L. Kirkland and Thomas Thomou of the Mayo Clinic.
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Molecular process in fat cells that influences stress and longevity identified
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Losing pounds won’t gain you longevity
Posted: at 6:13 pm
Alow-calorie diet can improve your overall health, immunity and metabolism. It may even help you squeeze into an outfit youve wanted to wear for years.
But, according to a recent study, reducing your caloric intake will not increase your life expectancy.
Nature recently published the results of a 23-year-long study conducted at the National Institute of Aging in Maryland. Researchers at the NIA theorized that specific, calorie-restricted diets might prolong life in rhesus monkeys. However, to researchers surprise, dieting rhesus monkeys did not live any longer than non-dieting subjects.
WHATS A CR DIET?
The NIA study,according to the report in Nature,analyzed two primary groups of monkeys: the first control group followed a normal, yet nutritionally balanced, diet. The second followed a calorie-restricted diet, commonly known as a CR diet, in whichcaloric intake dropped by 10 to 40 percent.
I think whats really important to recognize with full calorie restriction is were studying aging and the processes of aging, NIA researcher Julie Mattison said in a phone interview.
Were studying why everything goes bad over time, and its possible that CR affects a lot of these organs.
For years, it has been believed that CR diets prolong life and improve overall health and immunity, according to the CR Society website. CR diets were also thought to stall the onset of age and weight-related diseases, such as cardiovascular disease, diabetes, arthritis and cancer.
Since the 1930s researchers have studied the benefits of CR diets in organisms such aslab rats, yeast, fruit flies and round worms. CR organisms in these studies, which often lived up to 30 to 50 percent longer than organisms with normal diets, prompted scientists to analyze the effects of CR diets in primates, including humans.
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Losing pounds won’t gain you longevity
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Celebrating longevity: the shape of the future
Posted: at 6:13 pm
Celebrating longevity: the shape of the future
The International Day of Older Persons next Monday (1 October) is a chance to consider the benefits our society gains from people living longer, says Senior Citizens Minister Jo Goodhew.
The day, which is dedicated to the celebration of older people throughout New Zealand and the rest of the world, will feature a wide range of events, including intergenerational activities and events focusing on positive ageing.
Nationally, the celebrations have already begun. There is a huge range of exciting things happening to recognise the valuable contribution older people make to our lives, our neighbourhoods, our workplaces and our communities said Mrs Goodhew.
This years international theme is Longevity: Shaping the Future. New Zealanders are living longer and healthier and it is important for individuals, employers, service providers and the Government to think about the implications and opportunities increased longevity brings. Planning is key take a minute or two to think about what you want your future to look like.
Our attitudes about ageing need to change because older New Zealanders are changing. Older Kiwis are a diverse group the majority are looking to keep active and enjoy life you only need to look at the number of older people still competing in sports events like New Zealands coast-to-coast. Older people keep volunteer organisations afloat and contribute to our communities in many ways.
By valuing and using the skills, knowledge and experience of older people, by caring for those who need it in a respectful manner, we will continue to build a great country to live in.
I encourage you to find out what is happening in your area and join me in celebrating older people. I will be attending events around the country from Christchurch to Whangarei during the week.
ends
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Itchy protease!
Posted: at 6:13 pm
How to put a stop to overactive protease, the culprit in eczema.
DERMATOLOGISTS agree that eczema is one of the most prevalent skin disorders, particularly in babies and children. The dry, itchy skin condition is so common that it affects approximately 10-15% of children at any one point in time.
Did you know that protease attacks play a vital role in the severity of your childs eczema?
Protease is an enzyme that is naturally present in the skin. The role of protease is to break down protein in the skin to allow for natural skin renewal. However, overactive protease breaks down the skin barrier, leaving it thin and weakened, allowing water loss, and irritants and allergens to inflame the skin.
Soap has been linked to the increase in protease activity in the skin, and an increase in skin pH, which leads to skin damage, and oftentimes becomes the trigger for flare-ups of eczema, especially in children.
Protease effectively breaks down protein in the skin to allow the natural desquamation process. In people with eczema, this skin barrier is disrupted, and as such, the skin barrier is more vulnerable to irritation by substances such as soaps and detergents.
Eczema occurs when the surface of the skin becomes weakened, allowing irritants and allergens to penetrate the skin barrier and cause inflammation. As such, parts of the body with naturally thin skin such as flexural areas and the face are prone to eczema.
So how can we monitor protease activity on our babys skin?
The answer is to be extra careful about the products we use on our babys skin. Instead of being distracted by nice smells and cute packaging, we should pay careful attention to the ingredients that make up the product and how they react with young, fragile skin.
It is important to use an extra gentle cleanser that helps prevent protease attacks, facilitates the repair of babys skin, and cleanses the skin, without disturbing the skins natural moisturising factors.
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Itchy protease!
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