Thursday, November 22, 2012

A*STAR scientists identify potential drug target for inflammatory diseases including cancers

A*STAR scientists identify potential drug target for inflammatory diseases including cancers [ Back to EurekAlert! ] Public release date: 21-Nov-2012
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Contact: Vithya Selvam
vithya_selvam@a-star.edu.sg
656-826-6291
Agency for Science, Technology and Research (A*STAR), Singapore

This discovery holds the potential to reduce healthcare costs for many common inflammatory diseases such as cancer and diabetes

1. A*STAR scientists have identified the enzyme, telomerase, as a cause of chronic inflammation in human cancers. Chronic inflammation is now recognized as a key underlying cause for the development of many human cancers, autoimmune disorders, neurodegenerative diseases, and metabolic diseases such as diabetes. This enzyme, which is known to be responsible for providing cancer cells the endless ability to divide, is now found to also jumpstart and maintain chronic inflammation in cancers.

2. In identifying this enzyme, inflammation can be prevented or reduced, and the common ailments can be alleviated. This discovery has considerable impact on healthcare because developing drugs to target telomerase can greatly reduce healthcare costs.

3. Currently, the annual costs and expenses associated with cancer and metabolic diseases such as diabetes amount to about $132 billion in the US alone . Although many safe and effective anti-inflammatory drugs such as aspirin are currently available on the market, these drugs sometimes have side effects because blocking inflammation is typically detrimental to normal physiology. Hence there exists a need for the development of cost-effective drugs that are targeted, so as to minimize side effects.

4. This collaborative research was conducted by scientists at A*STAR's Institute of Molecular and Cell Biology (IMCB) led by Assoc Prof Vinay Tergaonkar, A*STAR's Genome Institute of Singapore (GIS) and National University of Singapore. Other clinical collaborators include Cancer Science Institute of Singapore and Duke-NUS Graduate Medical School. The research findings were published on Nov. 18, 2012, in the prestigious scientific journal, Nature Cell Biology.

5. The team identified that telomerase directly regulates the production of inflammatory molecules that are expressed by NF-kB, a known master regulator of chronic inflammation. These molecules are critical for inflammation and cancer progression. By inhibiting telomerase activity in primary cancer cells obtained from patient samples, the scientists found that levels of IL-6, an inflammatory molecule known to be a key driver of human cancers, was reduced in expression as well. This is an important breakthrough that shows how targeting telomerase with drugs could potentially reduce inflammation, and hence get rid of cancer cells.

6. Dr Tergaonkar said, "These findings provide a unifying explanation for a decade worth of observations from leading laboratories in the field which show that chronic inflammation and telomerase hyperactivity co-exist in over 90 percent of human cancers. What we show that these two activities are actually interdependent. They also may lead to potentially novel drugs that will target a range of human ailments with inflammation as an underlying cause, which range from arthritis to cancer."

7. Prof Hong Wan Jin, Executive Director of IMCB, said, "The discovery speaks for the exceptional power of identifying novel mechanisms that have translational potential, through close collaborations among scientists in different A*STAR institutes, as well as to bring together both basic and clinical research scientists in Singapore. I am confident that we can expect more discoveries like this from Dr Tergaonkar's team."

###

Notes for Editor:

The research findings described in this media release can be found in the 18 November online issue of Nature Cell Biology, under the title, "Telomerase directly regulates NF-kB-dependent transcription" by Arkasubhra Ghosh1, Gaye Saginc2, Shi Chi Leow1, Ekta Khattar1, Eun Myong Shin1, Ting Dong Yan3, Marc Wong1, Zhizhuo Zhang4, Guoliang Li5, Wing-Kin Sung4,5, Jianbiao Zhou6, Wee Joo Chng6, Shang Li3, Edison Liu2 and Vinay Tergaonkar1,7

1 Laboratory of NF-kB Signaling, IMCB, Proteos, 138673, Singapore

2 Cancer Biology and Pharmacology, Genome Institute of Singapore, 138672, Singapore

3 Program in Cancer and Stem Cell Biology, Duke-NUS Graduate Medical School, 169857, Singapore

4 School of Computing, National University of Singapore, 119077, Singapore

5 Computational and Systems Biology, Genome Institute of Singapore, 138672, Singapore

6 Cancer Science Institute of Singapore, 119074, Singapore

7 Correspondence should be addressed to: Vinay Tergaonkar (vinayt@imcb.a-star.edu.sg)

AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (A*STAR)

For media queries and clarifications, please contact:

Vithya Selvam (Ms)
Senior Officer, Corporate Communications
Agency for Science, Technology and Research
Tel: (+65) 6826 6291
Email: vithya_selvam@a-star.edu.sg

About the Agency for Science, Technology and Research (A*STAR)

The Agency for Science, Technology and Research (A*STAR) is the lead agency for fostering world-class scientific research and talent for a vibrant knowledge-based and innovation-driven Singapore. A*STAR oversees 14 biomedical sciences and physical sciences and engineering research institutes, and six consortia & centres, located in Biopolis and Fusionopolis as well as their immediate vicinity.

A*STAR supports Singapore's key economic clusters by providing intellectual, human and industrial capital to its partners in industry. It also supports extramural research in the universities, and with other local and international partners.

For more information about A*STAR, please visit www.a-star.edu.sg.



[ Back to EurekAlert! ] [ | E-mail | Share Share ]

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AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.


A*STAR scientists identify potential drug target for inflammatory diseases including cancers [ Back to EurekAlert! ] Public release date: 21-Nov-2012
[ | E-mail | Share Share ]

Contact: Vithya Selvam
vithya_selvam@a-star.edu.sg
656-826-6291
Agency for Science, Technology and Research (A*STAR), Singapore

This discovery holds the potential to reduce healthcare costs for many common inflammatory diseases such as cancer and diabetes

1. A*STAR scientists have identified the enzyme, telomerase, as a cause of chronic inflammation in human cancers. Chronic inflammation is now recognized as a key underlying cause for the development of many human cancers, autoimmune disorders, neurodegenerative diseases, and metabolic diseases such as diabetes. This enzyme, which is known to be responsible for providing cancer cells the endless ability to divide, is now found to also jumpstart and maintain chronic inflammation in cancers.

2. In identifying this enzyme, inflammation can be prevented or reduced, and the common ailments can be alleviated. This discovery has considerable impact on healthcare because developing drugs to target telomerase can greatly reduce healthcare costs.

3. Currently, the annual costs and expenses associated with cancer and metabolic diseases such as diabetes amount to about $132 billion in the US alone . Although many safe and effective anti-inflammatory drugs such as aspirin are currently available on the market, these drugs sometimes have side effects because blocking inflammation is typically detrimental to normal physiology. Hence there exists a need for the development of cost-effective drugs that are targeted, so as to minimize side effects.

4. This collaborative research was conducted by scientists at A*STAR's Institute of Molecular and Cell Biology (IMCB) led by Assoc Prof Vinay Tergaonkar, A*STAR's Genome Institute of Singapore (GIS) and National University of Singapore. Other clinical collaborators include Cancer Science Institute of Singapore and Duke-NUS Graduate Medical School. The research findings were published on Nov. 18, 2012, in the prestigious scientific journal, Nature Cell Biology.

5. The team identified that telomerase directly regulates the production of inflammatory molecules that are expressed by NF-kB, a known master regulator of chronic inflammation. These molecules are critical for inflammation and cancer progression. By inhibiting telomerase activity in primary cancer cells obtained from patient samples, the scientists found that levels of IL-6, an inflammatory molecule known to be a key driver of human cancers, was reduced in expression as well. This is an important breakthrough that shows how targeting telomerase with drugs could potentially reduce inflammation, and hence get rid of cancer cells.

6. Dr Tergaonkar said, "These findings provide a unifying explanation for a decade worth of observations from leading laboratories in the field which show that chronic inflammation and telomerase hyperactivity co-exist in over 90 percent of human cancers. What we show that these two activities are actually interdependent. They also may lead to potentially novel drugs that will target a range of human ailments with inflammation as an underlying cause, which range from arthritis to cancer."

7. Prof Hong Wan Jin, Executive Director of IMCB, said, "The discovery speaks for the exceptional power of identifying novel mechanisms that have translational potential, through close collaborations among scientists in different A*STAR institutes, as well as to bring together both basic and clinical research scientists in Singapore. I am confident that we can expect more discoveries like this from Dr Tergaonkar's team."

###

Notes for Editor:

The research findings described in this media release can be found in the 18 November online issue of Nature Cell Biology, under the title, "Telomerase directly regulates NF-kB-dependent transcription" by Arkasubhra Ghosh1, Gaye Saginc2, Shi Chi Leow1, Ekta Khattar1, Eun Myong Shin1, Ting Dong Yan3, Marc Wong1, Zhizhuo Zhang4, Guoliang Li5, Wing-Kin Sung4,5, Jianbiao Zhou6, Wee Joo Chng6, Shang Li3, Edison Liu2 and Vinay Tergaonkar1,7

1 Laboratory of NF-kB Signaling, IMCB, Proteos, 138673, Singapore

2 Cancer Biology and Pharmacology, Genome Institute of Singapore, 138672, Singapore

3 Program in Cancer and Stem Cell Biology, Duke-NUS Graduate Medical School, 169857, Singapore

4 School of Computing, National University of Singapore, 119077, Singapore

5 Computational and Systems Biology, Genome Institute of Singapore, 138672, Singapore

6 Cancer Science Institute of Singapore, 119074, Singapore

7 Correspondence should be addressed to: Vinay Tergaonkar (vinayt@imcb.a-star.edu.sg)

AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (A*STAR)

For media queries and clarifications, please contact:

Vithya Selvam (Ms)
Senior Officer, Corporate Communications
Agency for Science, Technology and Research
Tel: (+65) 6826 6291
Email: vithya_selvam@a-star.edu.sg

About the Agency for Science, Technology and Research (A*STAR)

The Agency for Science, Technology and Research (A*STAR) is the lead agency for fostering world-class scientific research and talent for a vibrant knowledge-based and innovation-driven Singapore. A*STAR oversees 14 biomedical sciences and physical sciences and engineering research institutes, and six consortia & centres, located in Biopolis and Fusionopolis as well as their immediate vicinity.

A*STAR supports Singapore's key economic clusters by providing intellectual, human and industrial capital to its partners in industry. It also supports extramural research in the universities, and with other local and international partners.

For more information about A*STAR, please visit www.a-star.edu.sg.



[ Back to EurekAlert! ] [ | E-mail | Share Share ]

?


AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.


Source: http://www.eurekalert.org/pub_releases/2012-11/afst-asi112012.php

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NHL labor talks to resume Wednesday morning

NEW YORK (AP) ? NHL owners and union officials are negotiating again at league headquarters Wednesday, the 67th day of the lockout.

The two sides are trying to work out impasses on core issues such as splitting revenue and player contracts. On Tuesday, union leaders met for internal discussions.

About a dozen players arrived at the league's headquarters Wednesday morning, along with lawyers and union executives.

If a deal is not struck soon, more games will have to be canceled in an already shortened season. The lockout has wiped out 327 games so far. The next games still scheduled are in December.

Source: http://news.yahoo.com/nhl-labor-talks-resume-wednesday-morning-214657712--nhl.html

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NB3 Foundation Releases Research On Childhood Obesity ...

From Indian Country?..

The Notah Begay III Foundation (NB3) and its partners recently published a report on childhood obesity and type 2 diabetes among Native children in New Mexico, made possible by the Robert Wood Johnson Foundation, PNM Resources Inc. and several other philanthropic funders.

In its executive summary, the NB3 Foundation warns ?this may be the first generation of Native American children that does not outlive their parents.? Though the study is specific to New Mexico, where dramatic health and educational disparities exist and American Indians make up 10.5 percent of the population, it is indicative of a public health crisis.

Study materials were culled from review of secondary literature, primary research and conversations with 255 stakeholders in Indian country, the nonprofit and government sectors, and the health arena including national foundations and research institutions. In four separate convenings, representatives discussed risk factors of obesity and type 2 diabetes; trends in at-risk behaviors; impact of policy at the federal, state, and tribal levels; existing collaborations and opportunities for collaborations; pertinent academic research; community-specific innovations/promising practices; and actionable recommendations. Participants? testimonies and input were documented at length.

The objective of the study was to understand the root causes of the growing rates of obesity and type 2 diabetes among American Indian youth and also shed light on ?barriers, challenges, unmet needs, and opportunities for action,? the executive report states.

The NB3 Foundation stresses that turning the tide against childhood obesity and type 2 diabetes requires a collective effort?among tribes, non-profits, entities in the public and private sectors, policy makers, institutionalized philanthropy, parents, families, schools, and the youth themselves.

Overall, a strong call for action was issued for the following:

? Clear and responsible leadership and advocacy that is led by Native Americans in partnership with appropriate non-Native American partners;

? A strong respect and understanding for the importance of culture in the development of any future strategies or a comprehensive framework that will foster transformation on this issue;

? Time and resources for collaboration and national/statewide/local education;

? Peer mentoring, network building, technical assistance, and education about issues and the latest trends in the field of obesity and type 2 diabetes prevention and mechanisms to share data and best practices that can enlighten the development of model programs;

? Investment in more community-based data collection, evaluation, and research into root causes and potential community solutions to health issues having positive outcomes for Native American children;

To read the full story?..Click here

Source: http://www.lensaunders.com/wp/?p=7172

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Wednesday, November 21, 2012

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There is an essential legitimate difference from the present along with a bank loan. A very generous family member or even good friend could give you $5000 with regard to auto repairs, as an example. If there's no expectation associated with payment, the amount of money can be viewed a gift. The actual giver couldn't file suit regarding payment later inside a civil suit. When the borrowed funds provider designates the amount of money just like a loan as well as the customer will pay back again a buck, the bucks can be viewed a real bank loan as well as the loan provider may demand repayment anytime. Little statements legal courts invest much of period determining regardless of whether the deal which include money will be a present or even bank loan. For this reason documents is very important when creating personal financial loans in order to close friends or loved ones.

The requirements to get a loan are pretty straight forward. If you are employed, having a monthly earnings of $800 or higher, and also have a bank account, you satisfy the basic qualifications. A number of loan providers within our network may have additional requirements.

Money lending products are unprotected financial products removed on your next salary. Because they're short-term lending products, they can be little; varying from $100 to $1500 and also repayment arrives in your next pay day. They could be very helpful regarding conquering a brief monetary urgent situation, however really should not be regarded as the long-term monetary option.

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The majority of loan programs are addressed by finance institutions or another professional lenders. They might use a variety of conditions to determine if your possible client is actually qualified for a financial loan. Earlier credit score is virtually always considered, along with current revenue and also assets. The objective of the borrowed funds can be a good issue-a set up expense possibility might have a lot more appeal as compared to an misguided concept for any new cafe. 1 essential consideration could be the revenue in order to credit card debt percentage in the client. May the client have the ability to pay for the bank loan back again interest? Skilled loan providers generally 'sell' cash, consequently borrowers should be aware simply how much financing actually 'costs' when it comes to real money.

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Source: http://vikcheroky.livejournal.com/345075.html

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Get Samsung's HDTV Black Friday deals today

Featured

2 days

Panasonic TC-P50UT50

Sizes go up, prices fall.?These are the two hallmark rules of the TV land. Just a few years ago, $800 couldn?t buy you a screen much larger ... Read more

16 hrs.

If you're interested in Samsung HDTVs,?Black Friday?comes early for you. As predicted by HD Guru, Samsung has lowered its prices on these 19 LED and plasma TVs for its dealers' Black Friday specials, with savings up to 53 percent.

But why don't you have to wait until Friday? Samsung controls the minimum price on most of its HDTVs through a relatively new Unilateral Pricing Program. On Sunday,?in anticipation of Black Friday deals, Samsung lowered its minimum pricing.?Amazon changed prices accordingly, though its brick-and-mortar competitors?haven't yet.?These are the prices most?will charge?when they open their doors Thursday night or Friday morning?for their Black Friday sales, and who knows? Maybe some will drop their prices sooner, in response to Amazon's early move.

As always, remember that this pricing is subject to change, and can be very volatile around Black Friday.?Here's the current?list of sale-price Samsung?TVs:

Samsung UN26EH4000 26-Inch 720p 60Hz LED?
Retail $300 -?Now $227.99

Samsung UN32EH4003 32-Inch 720p 60Hz LED
Retail $420 - Now $247.99

Samsung UN32EH5000 32-Inch 1080p 60Hz LED
Retail?$450 -?Now 327.99

Samsung UN39EH5003 39-Inch 1080p 60Hz LED
Retail $550 -?Now $397.99

Samsung UN40EH6030 40-Inch 1080p 120Hz LED 3-D
Retail $930 -?Now $497.99

Samsung UN46EH5000 46-Inch 1080p 60Hz LED
Retail $980 -?Now $577.99

Samsung UN46EH5300 46-Inch 1080p 60Hz LED
Retail $1,020 -?Now $597.99

Samsung UN50EH5000 50-Inch 1080p 60Hz LED
Retail $1,500 -?Now $697.99

Samsung UN55ES6003 55-Inch 1080p 120Hz LED
Retail $2,000 -?Now $997.99

Samsung PN60E530 60-Inch 1080p 600Hz plasma
Retail $1,650 -?Now $847.99

Samsung UN60ES6003 60-Inch 1080p 120Hz LED
Retail $2,570 -?Now $1,297.99

Samsung UN60ES6100 60-Inch 1080p 240 Clear Motion Rate Slim LED
Retail $2,670 -?Now $1,397.99

Samsung UN46ES7500 46-Inch 1080p 240Hz 3-D Slim LED
Retail $2,280 -?Now $1,497.99

Samsung UN55ES7500 55-Inch 1080p 240Hz 3-D Slim LED
Retail $3,050 - Now $1,997.99

Samsung UN60ES7500 60-Inch 1080p 240Hz 3-D Slim LED
Retail $3,680 -?Now $2,497.99

Samsung PN51E8000 51-Inch 1080p 600Hz Ultra Slim Plasma 3-D
Retail $2,200 -?Now $1,197.99

Samsung UN60ES8000 60-Inch 1080p 240Hz 3-D Slim LED
Retail $4,070 -?Now $2,697.99

Samsung PN51E8000 51-Inch 1080p 600Hz Ultra Slim Plasma 3-D
Retail $2,200 -?Now $1,197.99

Samsung UN60ES8000 60-Inch 1080p 240Hz 3-D Slim LED
Retail $4,070 -?Now $2,697.99

More from HD Guru:

Source: http://www.nbcnews.com/technology/technolog/how-get-samsungs-hdtv-black-friday-deals-today-1C7154883

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Tuesday, November 20, 2012

Bransa Cana confident about the Grade A1 480 metres flat race at ...

Bransa Cana confident about the Grade A1 480 metres flat race at Sheffield

Perry Barr will become the hosting venue for the Grade A1 480 metres flat race on Tuesday, 20th November. Heading on for claiming their share from the total prize money of ?97 are, Bransa Cana, Cyclers Race, Catcherintherye, Maeves Prince, Overdale Fantasy and Barracuda Sky.

With the advantage of the red box is, Bransa Cana, while breaking out of the very opposite gate will be, Barracuda Sky.

Bidding for a hat-trick tonight through the race is the four-year-old black dog, Bransa Cana. He has now been racing since the three seasons and has got quite remarkable experience right up his sleeve.

His very first and the only Grade A1 attempt was in a 480 metres flat race on 1st May at Perry Barr. It turned fruitless as the blue trap, Bransa Cana, ended fifth after taking 29.63 seconds to complete the track distance.

The race was won by the favourite entry, Movealong Tevez, who made the transit to the other end in 29.33 seconds, leading by two lengths.

Boherduff Light?s son has been unbeaten in the last two attempts of the season and both of them were Grade A2 events.

The red trap won the Grade A2 480 metres flat race on 30th October, 2012 at Perry Barr. The favourite entry was quick to set the pace, ran by the rail, led from the very first spot, and held in there until the wire. It took him 29.30 seconds to make it to the other end of the wire.

Missing success by the mark of short head?s was, Catcherinthereye.

The I. Walker trained struck a back-to-back by winning the Grade A2 480 metres flat race on 11th November, 2012 at Perry Barr.

This time the four-year-old out of, Uncanny, was swift to get into a high gear. Breaking from the second slot, he stayed by the rail and reeled in for the wire from the very first spot. He declared dominance over the rest of the line-up in 29.00, leading by a length.

He is backed by 5 to 1 chances for the race tonight while the most favoured candidate for the race is the 9 to 4 shot, Cyclers Ace.

The views expressed in this article are the writer's own and in no way represent bettor.com?s official editorial policy.

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Source: http://blogs.bettor.com/Bransa-Cana-confident-about-the-Grade-A1-480-metres-flat-race-at-Sheffield-a202723

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Tuesday, November 13, 2012

Marketing And Selling Your Unfinished Product - Small Business ...

Customers buying into what you have before you have it is good for business. Alicia A. Cook, R & B singer andsongwriter, also known as Alicia Keys, is doing it. Why not small business owners?

marketing unfinished product

At the time of this writing, you can pre-order Alicia Keys latest album, Girl On Fire. Once the songs are available on Nov 27th, 2012, you?ll receive your copy of the music, via iTunes download. In the meantime, girls can get involved in the movement via social media by sharing their personal stories and videos of being inspired, surviving and overcoming challenges.

It?s Organic, It?s Passionate ? It?s Marketing

Of course, the artist and the machine behind Alicia Keys is using television, radio, internet and print to promote this campaign. The average small business owner doesn?t have that kind of budget.

Since you can make some serious waves with online marketing, what you really need is a marketing mindset that makes sense. Let?s look at a marketing trend first, and then your strategy.

In the 2012 November Trend Briefing: Presumers, TrendWatching?discusses:

?Why consumer involvement with products and services pre-launch is set to go mainstream.?

Prospects are becoming clients long before the product is actually available.

It?s Relationship Marketing At It?s Best

It?s the opportunity to build a loyal fan base that buys into what you have, literally, before you have it. They may even help you promote it.

This type of connection pulls your audience into the movement. It can make them a part of the product, particularly if you receive and implement their feedback. The pre-launch can also increase sales and brand loyalty and decrease anxiety because you already know that somebodies want what you have because they paid for it already.

Yes, pre-launches, pre-orders, pre-sales feel good. But if you go this route, then you need to keep a few things in mind.

Deliver The Product That You Promised

If something changes, communicate it. ?In all good conscious and integrity, you can?t take people?s money and then do whatever you want to do with it. If your people buy into your dream, then you need to create what you said you were going to create.

With crowd-funding platforms like IndieGogo or KickStarter, that book, film, innovative product can get the support that you have been looking for, but it has to come to life at some point. The people who buy during the pre-launch are a part of the dream. You?ll feel good every time a new purchase or donation comes in.

You?ll feel inspired, motivated, but also obligated. If you don?t want your dream to turn into a nightmare, be sure that you can finish what you start before you spend your supporters? money.

Delineate A Timeline That You Can Actually Live Up To?

Some people are awful with timing. They promise things on a Monday and 52 Mondays later it?s still not done. But when you?re receiving pre-orders, you need a timeline that you can meet.

If you think you can deliver the goods in December, then add a month to that or get some one who has done what you are doing to have a look at your timeline. Give yourself enough time to get this right. People will be pleasantly surprised if you deliver early (which is better than being irritated and vocal).

Don?t Leave Your People In The Dark?

Talk to your people. While they probably don?t want to know every little detail, they do want to be in the loop. Let them know how it?s coming. Let them know what stage you?re in. Say something:

  • ?The book just went to the first editor?
  • ?Documentary filming in Daytona today?
  • ?Just finished the prototype for my widget! Excited but still a long way to go. I?ll keep you posted.?

The right kind of communication goes a long way.

Crowd-Funding Is Not The Only Way To Get Support

In Selling $2000+ Worth Of My Unfinished Book freelance consultant, Brennan Dunn, explains how 57 people managed to purchase his first book before he finished it. Most of those sales came from having a great online sales page and letting his email list know what he was doing.

He also shared on Facebook and Twitter. So if people were interested, they could go to the sales page to get more information, to pre-order the book or to at the least subscribe to his blog.

Final Marketing Note

Movies are promoted months before they?re finished. Why should you wait to start marketing? If you are good with finishing what you started, then why wait to start selling?

But if you?re NOT so good with timelines and production management, then at least give people a chance to join your, ?I?m Interested? list. When your product is ready, you have someone who wants to hear about it.

Alicia Keys Photo via Shutterstock


Source: http://smallbiztrends.com/2012/11/marketing-selling-unfinished-product.html

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