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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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Disclaimer: The Visible Embryo web site is provided for your general information only. The information contained on this site should not be treated as a substitute for medical, legal or other professional advice. Neither is The Visible Embryo responsible or liable for the contents of any websites of third parties which are listed on this site.
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Pregnancy Timeline by SemestersFetal 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 HemispheresFemale Reproductive SystemEnd of Embryonic PeriodEnd of Embryonic PeriodFirst Thin Layer of Skin AppearsThird TrimesterSecond TrimesterFirst TrimesterFertilizationDevelopmental Timeline
Click weeks 0 - 40 and follow fetal growth
Google Search artcles published since 2007
 
August 26, 2011--------News Archive


A Question of Gene Silencing
Researchers have found a new way to selectively turn off genes that don't code for proteins which will help identify each gene's function, and perhaps identify cancers.

Scented Products Emit Hazardous Chemicals
Chemical sleuthing has uncovered that fragrance in consumer laundry products contains hazardous chemicals. Some which are even carcinogens.

August 25, 2011--------News Archive

Human Stem Cells Made From Amnionic Fluid
Human epithelial cells transplanted from human amnionic fluid reduce pulmonary fibrosis, and even stimulate lung regeneration in mice.

Scale Models Rule
Body patterns stay in sync with size as an embryo grows into an adult. Observed in the wing of the fruit fly, these patterns most likely exist in all organisms.

Chronic Disease Caused by Fat Cells?
Fat cells in people with metabolic syndrome have biomarkers for insulin resistance and chronic inflammation, conditions in diabetes and cardiovascular disease.

August 24, 2011--------News Archive

In the Early Life of An Embryo, Chaos Lurks
A calcium wave sparks embryonic cell division, doubling as a synchronizer of all further cell division in order for chaos to be reined in and ordered growth to persist.

Smoking Affects Fetal Infant Brain Worse than Feared
Researchers pin-point smoking specifically and find a 40% increase in damage to the fetus.

August 23, 2011--------News Archive

Boys Reach Sexual Maturity Younger and Younger
The phase between being physically but not socially adult is getting longer.

When Cell Fishing Games Go Wrong
Trial-and-error "fishing" for DNA in the nucleus may be the most important cause of female infertility.

A Sticky Egg Captures The Sperm
A sugar molecule makes the outer coat of a human egg 'sticky', which is vital for enabling the sperm and egg to bind together.

At Last, Reason Why Stress Damages DNA
Adreneline produced by chronic stress, degrades the protein p53 which is considered a tumor suppressor protein and "guardian of the genome."

August 21, 2011--------News Archive

The Basis for Head and Sex Organ Deformities
Data reveals a possible therapy using vitamin B2 to reverse enzyme defects is specific areas of fetal development.

Mother’s BMI Linked to Fatter Babies
Babies of mothers with a higher pre-pregnancy body mass index (BMI) are fatter and have more fat in their liver, a study has found.

Celiac Disease May Explain Some Women's Infertility
A recent study found increased rates of celiac disease in women who present with unexplained infertility.

WHO Child Growth Charts

When an egg cell is being formed, the cellular machinery which separates chromosomes is extremely imprecise at fishing them out of the cell's interior, scientists at the European Molecular Biology Laboratory (EMBL) in Heidelberg, Germany, have discovered.

The unexpected degree of trial-and-error involved in this process could explain why errors in the number of chromosomes in the egg cell are the leading cause of miscarriages and severe congenital diseases such as trisomies like Down's syndrome, as well as an important cause of female infertility. The findings are published online today in Cell.

Our cells have two copies of each chromosome, one inherited from our mother and the other from our father. An oocyte, the cell that matures into an egg cell, has to discard half of its chromosomes, keeping only the maternal or paternal copy of each. To do so, fibres called microtubules act like fishing lines, attaching themselves to chromosomes and reeling them in to opposite sides of the cell. However, the EMBL scientists discovered that these microtubules are much worse fishermen than expected, often incorrectly hooking onto a chromosome and having to let it go again.

"We saw that they have to go through several tries before getting the connection right," says Jan Ellenberg, who led the work at EMBL: "overall, 90% of all chromosomes get connected in the wrong way, and therefore the pathway that corrects these errors is heavily used."

The difficulty in the oocyte is that two fishing lines cast from opposite sides of the cell have to attach themselves to the maternal and paternal copies of the same chromosome. Each of those chromosome copies has a protein structure called a kinetochore, which acts like the magnet in a toy fish, providing the spot for the microtubule 'fishing lines' to attach themselves. The EMBL scientists were the first to track the movement of all kinetochores throughout the whole 8 hours of the first round of cell division in mouse egg cells, which are very similar to human ones.

"We were able to get very high resolution images for extended periods of time," explains Tomoya Kitajima, who carried out the work, "because our lab developed a microscope that automatically searches for chromosomes, zooms in, and scans only the area they are in, doing very little damage to the cell".

Children playing magnetic fishing games often accuse others of cheating, using their fishing rod to move a fish into a position that makes it easier to catch. Ellenberg and Kitajima's time-lapse videos show that fishing microtubules also 'cheat' in this way. At earlier stages of cell division, before they start attaching themselves to kinetochores, microtubules interact with the arms of the chromosomes, nudging them into position in a 'belt' around the centre of the spindle.

But not even this chromosome belt, which had never been observed before, is enough to ensure that microtubules fish out the chromosomes correctly.

The EMBL scientists' results show that kinetochore attachment is much more error-prone in this type of cell division, called meiosis, than in mitosis, the simpler form of cell division through which other cells in our body split in two. This is probably because the egg cell precursor is an inordinately large cell, and because in meiosis microtubules emanate from around 80 different places in the cell, rather than stemming only from two poles as they do in mitosis.

"Our findings provide a very plausible explanation for the high rate of errors during egg formation. They form the basis to focus our future work on age-related female infertility, as it seems very likely that a component of the pathway that corrects these errors will be involved" Ellenberg concludes.

Original article: http://www.eurekalert.org/pub_releases/2011-08/embl-fgg081511.php