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Welcome to The Visible Embryo, a comprehensive educational resource on human development from conception to birth.

The Visible Embryo provides visual references for changes in fetal development throughout pregnancy and can be navigated via fetal development or maternal changes.

The National Institutes of Child Health and Human Development awarded Phase I and Phase II Small Business Innovative Research Grants to develop The Visible Embryo. Initally designed to evaluate the internet as a teaching tool for first year medical students, The Visible Embryo is linked to over 600 educational institutions and is viewed by more than ' million visitors each month.


WHO International Clinical Trials Registry Platform
The World Health Organization (WHO) has created a new Web site to help researchers, doctors and patients obtain reliable information on high-quality clinical trials. Now you can go to one website and search all registers to identify clinical trial research underway around the world!



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Pregnancy Timeline by SemestersFemale Reproductive SystemFertilizationThe Appearance of SomitesFirst TrimesterSecond TrimesterThird TrimesterFetal liver is producing blood cellsHead may position into pelvisBrain convolutions beginFull TermWhite fat begins to be madeWhite fat begins to be madeHead may position into pelvisImmune system beginningImmune system beginningPeriod of rapid brain growthBrain convolutions beginLungs begin to produce surfactantSensory brain waves begin to activateSensory brain waves begin to activateInner Ear Bones HardenBone marrow starts making blood cellsBone marrow starts making blood cellsBrown fat surrounds lymphatic systemFetal sexual organs visibleFinger and toe prints appearFinger and toe prints appearHeartbeat can be detectedHeartbeat can be detectedBasic Brain Structure in PlaceThe Appearance of SomitesFirst Detectable Brain WavesA Four Chambered HeartBeginning Cerebral HemispheresEnd of Embryonic PeriodEnd of Embryonic PeriodFirst Thin Layer of Skin AppearsThird TrimesterDevelopmental Timeline
Click weeks 0 - 40 and follow fetal growth
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November 25, 2011--------News Archive

Women at Low Risk Can Safely Choose Birth Style
Women with low risk pregnancies should be able to choose where they give birth, concludes The Birthplace in England national prospective cohort study.

Finger (Mal)formation Function of Desert DNA
Explaining the diversity of leg shapes in the animal kingdom and hereditary defects in finger formation.

Key Molecular Switch for Telomere Extension Found
For the first time, a key target for DNA damage is found that must be chemically modified to enable an enzyme thought to play a key role in cancer and aging.

New Role for Gene in Maintaining Steady Weight
Findings may help combat obesity and diabetes.

November 24, 2011--------News Archive

New Facts About Stuttering
Some forms of persistent stuttering are caused by mutations in a gene governing the recycling of old cell parts - not speech.

Preventing Preemie Brain Injury
New advances could eventually help reduce the number of premature babies who develop cerebral palsy, epilepsy or behavioral disorders such as ADHD.

Short Stature May Be Due To a 'Shortage' of Genes
Research suggests that uncommon genetic deletions are associated with short stature.

November 23, 2011--------News Archive

Intestinal Disorder, Preemies and AB Blood Type
Preemies with the AB blood type who develop NEC are nearly three times as likely to die from it as preemies with other blood types.

Babies Fed Fish Before 9 Months Wheeze Less
But pre-natal pain and fever antibiotics taken by mom in pregnancy, or by the baby in the first-week of life, increase risk of "pre-school wheeze."

Physical Activity Improves Quality Of Sleep
People sleep significantly better and feel more alert during the day if they get at least 150 minutes of exercise a week, a new study concludes.

November 22, 2011--------News Archive

Critical Molecules For Hearing/Balance Discovered
Gene-therapy trial will attempt to restore hearing in deaf mice.

Tweaking One Gene Makes Muscles Twice As Strong
Salk scientists and their collaborators find new avenue for treating muscle degeneration in people who can't exercise.

Fruit Fly Intestine Holds Secret to Fountain of Youth
Long-lived fruit flies offer Salk scientists clues to slowing human aging and fighting disease.

November 21, 2011--------News Archive

Nerve Cells Key to making Sense of All of Our Senses
Scientists have unraveled how the brain manages to process complex, rapidly changing, and often conflicting sensory signals and make sense of our world.

Discovery of A New Muscle Repair Gene
Thanks to next-generation DNA sequencing, an international team of scientists have discovered more about the function of muscle stem cells.

Immune System Governs Stem Cell Regeneration
Controlling a stem cell transplant recipient’s immune response may be major key to successful bone regeneration.

WHO Child Growth Charts



New research sifts through the entire genome of thousands of human subjects to look for genetic variation associated with height.

The results of the study, published by Cell Press in the December issue of the American Journal of Human Genetics, suggest that uncommon genetic deletions are associated with short stature.

Height is a highly heritable trait that is associated with variation in many different genes. "Despite tremendous recent progress in finding common genetic variants associated with height, thus far these variants only explain about 10% of the variation in adult height," explains senior study author, Dr. Joel N Hirschhorn, from Children's Hospital Boston and the Broad Institute.

"It has been estimated that about half of height variation could eventually be accounted for by the sorts of variants we've been looking at, so it is possible that other types of genetic variants, such as copy number variants (CNVs), may also contribute to the genetic variation in stature."

A copy number variant or CNV, can be either an excess (or gain) in genetic material or an absence (deletion) of parts of the genome. Some CNVs are common and observed often in the human genome. Other CNVs are rare or occur with low frequency.

Dr. Hirschhorn, co-authors Dr. Yiping Shen and Dr. Andrew Dauber, and their colleagues were interested in looking for associations of human stature with CNVs, as this has not been done before.

"To investigate whether CNVs play a role in short or tall stature, we conducted a genome-wide association study of copy number in a cohort of children who had comparative genomic screening for clinical reasons and we observed an excess of rare deletions in children with short stature," says Dr. Shen. "We extended our findings to a large population-based cohort, and again observed an excess of low frequency deletions in shorter individuals."

The findings were not due to known gene deletion syndromes and no significant associations were observed between CNV and tall stature.

Taken together, these results demonstrate that there is a correlation between low frequency genetic deletions and decreasing height.

"Our findings strongly support the hypothesis that increasing burden of lower frequency deletions can lead to shorter stature, and suggest that this phenomenon extends to the general population," concludes Dr. Dauber.

Original article: http://www.eurekalert.org/pub_releases/2011-11/cp-iss111811.php