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<h2 class="element-invisible">You are here</h2><div class="breadcrumb"><a href="/">Home</a> » <a href="/news-events">News & Events</a> » <a href="/news-events/nih-research-matters">NIH Research Matters</a></div> <div class="l-region l-region--section-header">
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<p class="publishdate"><span property="dc:date" datatype="xsd:dateTime" content="2007-12-31T00:00:00-05:00" class="date-display-single">December 31, 2007</span></p><div class='syndicate'><h1>2007 Research Highlights — Insights from the Lab</h1><div class="callout callout-with-border"><h3>Noteworthy Advances in Basic Research</h3>
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<p>NIH has nearly 6,000 NIH staff scientists and supports more than 325,000 researchers with competitive grants to all 50 states, the territories and more than 90 countries around the world. Here's just a small sampling of the accomplishments made by NIH-supported scientists in 2007.</p>
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<div class="teaser">
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<div class="teaser-thumbnail"><div class="media media-element-container media-thumbnail"><div id="file-13486" class="file file-image file-image-jpeg">
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<h2 class="element-invisible"><a href="/2007/20071203-stemcell.jpg">20071203-stemcell.jpg</a></h2>
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<img height="150" width="150" alt="Cell culture flasks used to propagate stem cells" title="Cell culture flasks used to propagate stem cells" class="media-element file-thumbnail" typeof="foaf:Image" src="https://www.nih.gov/sites/default/files/styles/thumbnail/public/news-events/research-matters/2007/20071203-stemcell.jpg?itok=-LurWkmN" /> </div>
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</div>
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</div></div>
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<h4 class="teaser-title"><a href="/news-events/nih-research-matters/versatile-human-stem-cells-created-without-embryos">Versatile Human Stem Cells Created Without Embryos</a></h4>
|
||
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||
<p class="teaser-description">By modifying only 4 genes in human skin cells, NIH-supported researchers found that they could "reprogram" the cells to give them the characteristics of embryonic stem cells. This major advance could open doors to innovative therapies in the future, where people's own cells might be reprogrammed and used to repair their damaged tissues and organs. The breakthrough might also eventually put to rest the ethical controversy surrounding stem cells. <a href="http://www.ncbi.nlm.nih.gov/pubmed/18029452?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum" title="PubMed Abstract: Induced pluripotent stem cell lines derived from human somatic cells.">PubMed Abstract »</a></p>
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<div class="teaser">
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<div class="teaser-thumbnail"><div class="media media-element-container media-thumbnail"><div id="file-13491" class="file file-image file-image-jpeg">
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<h2 class="element-invisible"><a href="/2007/20071203-macaque.jpg">20071203-macaque.jpg</a></h2>
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<div class="content">
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<img height="150" width="150" alt="a photo of a rhesus macaque searching for pests on a mate" title="a photo of a rhesus macaque searching for pests on a mate" class="media-element file-thumbnail" typeof="foaf:Image" src="https://www.nih.gov/sites/default/files/styles/thumbnail/public/news-events/research-matters/2007/20071203-macaque.jpg?itok=5sVsz1bh" /> </div>
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</div></div>
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<h4 class="teaser-title"><a href="/news-events/nih-research-matters/embryonic-stem-cell-milestone-achieved-primates">Embryonic Stem Cell Milestone Achieved in Primates</a></h4>
|
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|
||
<p class="teaser-description">Researchers achieved a major milestone in embryonic stem cell research, isolating embryonic stem cells for the first time from a cloned primate embryo. The scientists, funded by NIH, showed that the stem cells could turn into heart or nerve cells in the laboratory and had other characteristics of established embryonic stem cell lines. The technique, if developed in humans, could potentially be used to make personalized stem cells to treat diseases without worry of rejection by the patient's immune system. <a href="http://www.ncbi.nlm.nih.gov/pubmed/18004281?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum" title="PubMed Abstract: Producing primate embryonic stem cells by somatic cell nuclear transfer.">PubMed Abstract »</a></p>
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<div class="teaser-thumbnail"><div class="media media-element-container media-thumbnail"><div id="file-13426" class="file file-image file-image-jpeg">
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<img height="150" width="150" alt="illustration of the brain" title="illustration of the brain " class="media-element file-thumbnail" typeof="foaf:Image" src="https://www.nih.gov/sites/default/files/styles/thumbnail/public/news-events/research-matters/2007/20071119-brain.jpg?itok=WM1i4nGg" /> </div>
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<h4 class="teaser-title"><a href="/news-events/nih-research-matters/tracking-neural-progenitor-cells-human-brain">Tracking Neural Progenitor Cells in the Human Brain</a></h4>
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<p class="teaser-description">Scientists developed the first noninvasive technique for detecting neural progenitor cells in the living human brain. Neural progenitor cells give birth to neurons and other types of brain cells. This new imaging method may eventually point to improved treatments and diagnostics for a host of brain-related disorders, including depression, Parkinson's disease and brain tumors. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17991865?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum" title="PubMed Abstract: Magnetic resonance spectroscopy identifies neural progenitor cells in the live human brain.">PubMed Abstract »</a></p>
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<h2 class="element-invisible"><a href="/2007/20071105-gpcr.jpg">20071105-GPCR.jpg</a></h2>
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<img height="150" width="150" alt="Three-dimensional model of protein" title="Three-dimensional model of protein" class="media-element file-thumbnail" typeof="foaf:Image" src="https://www.nih.gov/sites/default/files/styles/thumbnail/public/news-events/research-matters/2007/20071105-GPCR.jpg?itok=DkuEOuGb" /> </div>
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<h4 class="teaser-title"><a href="/news-events/nih-research-matters/scientists-unveil-structure-common-drug-target">Structure of Common Drug Target Unveiled</a></h4>
|
||
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<p class="teaser-description">More than 40 years after beta blockers were first used clinically, NIH-funded scientists finally got a close-up, 3-dimensional look at the drugs' molecular target: the β2-adrenergic receptor. The receptor is one of a family of proteins called G protein-coupled receptors (GPCRs), which carry signals across the cell membrane. GPCRs control critical bodily functions, several of our senses and the action of about half of today's pharmaceuticals. Better understanding of the receptor's molecular shape promises to help speed the discovery of new drugs and illuminate many aspects of human health and disease.<br />
|
||
<a href="http://www.ncbi.nlm.nih.gov/pubmed/17962519?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum">PubMed Abstract: GPCR engineering yields high-resolution structural insights into beta2-adrenergic receptor function »</a><br />
|
||
<a href="http://www.ncbi.nlm.nih.gov/pubmed/17962520?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum">PubMed Abstract: High-resolution crystal structure of an engineered human beta2-adrenergic G protein-coupled receptor »</a></p>
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<div class="teaser">
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<div class="teaser-thumbnail"><div class="media media-element-container media-thumbnail"><div id="file-13446" class="file file-image file-image-jpeg">
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<h2 class="element-invisible"><a href="/2007/20071105-brainbow.jpg">20071105-brainbow.jpg</a></h2>
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<img height="150" width="150" alt="A cluster of multicolored teardrop-shaped cells" title="A cluster of multicolored teardrop-shaped cells" class="media-element file-thumbnail" typeof="foaf:Image" src="https://www.nih.gov/sites/default/files/styles/thumbnail/public/news-events/research-matters/2007/20071105-brainbow.jpg?itok=9DpAY4uo" /> </div>
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<h4 class="teaser-title"><a href="/news-events/nih-research-matters/brain-many-colors">Brain Connections Revealed</a></h4>
|
||
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<p class="teaser-description">Using a clever genetic trick to generate dozens of different colors, NIH-supported researchers visualized hundreds of cells and their connections to each other in the brain. The scientists developed DNA constructs, which they call “Brainbows,” that randomly rearrange themselves to activate genes for different-colored fluorescent proteins. When the researchers created transgenic mice with Brainbows, individual neurons in the brain had distinctive colors, allowing them to accurately trace specific cells and their interactions with each other. This new tool will help scientists better understand how the brain and nervous system work. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17972876?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum" title="PubMed Abstract: Transgenic strategies for combinatorial expression of fluorescent proteins in the nervous system.">PubMed Abstract »</a></p>
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</div>
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<div class="teaser">
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<div class="teaser-thumbnail"><div class="media media-element-container media-thumbnail"><div id="file-13061" class="file file-image file-image-jpeg">
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<h2 class="element-invisible"><a href="/2007/20070423-monkey.jpg">20070423-monkey.jpg</a></h2>
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<div class="content">
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<img height="150" width="150" alt="Silhouette of rhesus macaque on a background of the letters A, C, T, and G, which represent the chemical components of the genome" title="Silhouette of rhesus macaque on a background of the letters A, C, T, and G, which represent the chemical components of the genome" class="media-element file-thumbnail" typeof="foaf:Image" src="https://www.nih.gov/sites/default/files/styles/thumbnail/public/news-events/research-matters/2007/20070423-monkey.jpg?itok=NVke8nCm" /> </div>
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</div></div>
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<h4 class="teaser-title"><a href="/news-events/nih-research-matters/monkey-genome-gives-new-insight-into-what-makes-us-human">Monkey Genome Gives Insight into Humans</a></h4>
|
||
|
||
<p class="teaser-description">An international team of more than 170 scientists sequenced the genome of the rhesus macaque monkey and compared it to both the chimpanzee and human genomes. Their analysis revealed that the 3 primate species share about 93% of their DNA. The team also identified nearly 200 genes that appear to play key roles in differences between the species. These include genes involved in hair formation, the immune response and cell communication. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17431167?ordinalpos=13&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum" title="PubMed Abstract: Evolutionary and biomedical insights from the rhesus macaque genome.">PubMed Abstract »</a></p>
|
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</div>
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<div class="teaser">
|
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<div class="teaser-thumbnail"><div class="media media-element-container media-thumbnail"><div id="file-13346" class="file file-image file-image-jpeg">
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<h2 class="element-invisible"><a href="/2007/20070910-hearing.jpg">20070910-hearing.jpg</a></h2>
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<img height="150" width="150" alt="Tubular stereocilia on hair cell surface arranged in three rows of increasing heigh" title="Tubular stereocilia on hair cell surface arranged in three rows of increasing heigh" class="media-element file-thumbnail" typeof="foaf:Image" src="https://www.nih.gov/sites/default/files/styles/thumbnail/public/news-events/research-matters/2007/20070910-hearing.jpg?itok=2AoWWORG" /> </div>
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<h4 class="teaser-title"><a href="/news-events/nih-research-matters/proteins-pair-form-crucial-hearing-structure">Proteins Pair to Form Crucial Hearing Structure</a></h4>
|
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<p class="teaser-description">NIH scientists and their collaborators identified 2 proteins that appear to pair up at the precise location in the ear where sound vibrations are turned into electrical signals. The investigators also showed that a known deafness-causing mutation seemed to disrupt interactions between the 2 proteins, called cadherin 23 and protocadherin 15. The findings may eventually help scientists develop more precise treatments for hearing loss, a condition that affects more than 32 million people in the United States alone. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17805295?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum" title="PubMed Abstract: Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells.">PubMed Abstract »</a></p>
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<h4 class="teaser-title"><a href="/news-events/nih-research-matters/genetically-altered-mice-see-more-colorful-world">Genetically Altered Mice See a More Colorful World</a></h4>
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<p class="teaser-description">By giving mice the gene that allows people to see red hues, scientists created rodents that can see a wider range of colors. Mouse eyes normally have only 2 types of light-detecting photoreceptors, sensitive to blue and green light. NIH-funded scientists created genetically engineered mice that also had photoreceptors for red light, which are found in most primates. Tests showed that the altered mice could perceive different colors better than normal mice. The study suggests that the brains of mammals can quickly adapt to new sensory information. It also provides clues to the evolution of color vision. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17379811?ordinalpos=14&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum" title="PubMed Abstract: Emergence of novel color vision in mice engineered to express a human cone photopigment.">PubMed Abstract »</a></p>
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