t0m4

medicalstate:

The last line of a 17th century poem by John Donne prompted Louise Noble’s quest. “Women,” the line read, are not only “Sweetness and wit,” but “mummy, possessed.”

Sweetness and wit, sure. But mummy? In her search for an explanation, Noble, a lecturer of English at the University of New England in Australia, made a surprising discovery: That word recurs throughout the literature of early modern Europe, from Donne’s “Love’s Alchemy” to Shakespeare’s “Othello” and Edmund Spenser’s “The Faerie Queene,” because mummies and other preserved and fresh human remains were a common ingredient in the medicine of that time. In short: Not long ago, Europeans were cannibals.

The question was not “Should you eat human flesh?” says one historian, but, “What sort of flesh should you eat?”

Read more here.

okological:

aDiatomea by MRK
   aDiatomea are a series of diatom-like artificial life forms generated by code. MRK classifies each variant or permutation of these mathematical creatures in taxonomic studies, giving Victorian diatom art a 21st century redux. The full series of aDiatomea can be seen at MRK’s project website. Limited edition, archival quality prints are available at inPRNT.

okological:

aDiatomea by MRK

   aDiatomea are a series of diatom-like artificial life forms generated by code. MRK classifies each variant or permutation of these mathematical creatures in taxonomic studies, giving Victorian diatom art a 21st century redux. The full series of aDiatomea can be seen at MRK’s project website. Limited edition, archival quality prints are available at inPRNT.

cranquis:

iwannabetheverybest-medic:

Advice for American Med Schools (but includes piles of stuff that would be great for anyone about to plunge into the rather demanding world of Medicine).

Intro

1st Year 

2nd Year

3rd Year (Part A)

3rd Year (Part B)

3rd Year (Part C)

3rd Year (Part D)

4th Year

Special Features: 
1st Year Deleted Scene 
Qualities of an Ideal Doctor 
Prevention of Procrastination

Oh, and if you’re not already following this guy: why not?!

What a nice link-collection of some of my posts! Thank you for putting that together.

(My guilt-ridden soul admits that I need to get around to creating a “Best Of” and “FAQ” links-page on my Tumblr… someday, Cranquis, someday…)

EDIT: And here’s the Intern Year of Residency survival-tips post!

milesian:

You are made of Ever Morphing Four dimensional Fractals!
(Vertical progression through the human brain)

milesian:

You are made of Ever Morphing Four dimensional Fractals!

(Vertical progression through the human brain)

Layers of Your Scalp

medicalstate:

An acronym for the layers in your scalp is amusingly, SCALP:

  • Skin
  • Connective tissue (Dense)
  • Aponeurosis
  • Loose connective tissue
  • Periosteum

Well that is one less thing to worry about I guess. Next concept!

sciencenote:

Most scientists believe that cancer happens when several genes of a particular group of cells become mutated. Some people may have more inherited mutations than others, and even with the same amount of environmental exposure, some people are simply more likely to develop cancer.
The following types of genes contribute to cancer:
Tumor suppressor genes are protective genes. Normally, they suppress (limit) cell growth by monitoring the rate at which cells divide into new cells, repairing mismatched DNA (a cause of mutations), and controlling cell death. When a tumor suppressor gene is mutated (due to heredity or environmental factors), cells continue to grow and can eventually form a tumor. BRCA1, BRCA2, and p53 are examples of tumor suppressor genes. In fact, nearly 50% of all cancers involve a missing or damaged p53 gene.
Oncogenes turn a healthy cell into a cancerous one. HER2/neu and ras are two common oncogenes.
DNA repair genes fix any mistakes made when DNA is replicated (copied). Mistakes that aren’t fixed become mutations, which may eventually lead to cancer, especially if the mutation occurs in a tumor suppressor gene or oncogene.
DNA Repair GenesA third type of gene associated with cancer is the group involved in DNA repair and maintenance of chromosome structure. Environmental factors, such asionizing radiation, UV light, and chemicals, can damage DNA. Errors in DNA replication can also lead to mutations. Certain gene products repair damage to chromosomes, thereby minimizing mutations in the cell. When a DNA repair gene is mutated its product is no longer made, preventing DNA repair and allowing further mutations to accumulate in the cell. These mutations can increase the frequency of cancerous changes in a cell. A defect in a DNA repair gene called XP (Xeroderma pigmentosum) results in individuals who are very sensitive to UV light and have a thousand-fold increase in the incidence of all types of skin cancer. There are seven XP genes, whose products remove DNA damage caused by UV light and other carcinogens. Another example of a disease that is associated with loss of DNA repair is Bloom syndrome, an inherited disorder that leads to increased risk of cancer, lung disease, and diabetes. The mutated gene in Bloom syndrome, BLM, is required for maintaining the stable structure of chromosomes. Individuals with Bloom syndrome have a high frequency of chromosome breaks and interchanges, which can result in the activation of oncogenes. 

sciencenote:

Most scientists believe that cancer happens when several genes of a particular group of cells become mutated. Some people may have more inherited mutations than others, and even with the same amount of environmental exposure, some people are simply more likely to develop cancer.

The following types of genes contribute to cancer:

  • Tumor suppressor genes are protective genes. Normally, they suppress (limit) cell growth by monitoring the rate at which cells divide into new cells, repairing mismatched DNA (a cause of mutations), and controlling cell death. When a tumor suppressor gene is mutated (due to heredity or environmental factors), cells continue to grow and can eventually form a tumor. BRCA1BRCA2, and p53 are examples of tumor suppressor genes. In fact, nearly 50% of all cancers involve a missing or damaged p53 gene.

  • Oncogenes turn a healthy cell into a cancerous one. HER2/neu and ras are two common oncogenes.

  • DNA repair genes fix any mistakes made when DNA is replicated (copied). Mistakes that aren’t fixed become mutations, which may eventually lead to cancer, especially if the mutation occurs in a tumor suppressor gene or oncogene.

DNA Repair Genes
A third type of gene associated with cancer is the group involved in DNA repair and maintenance of chromosome structure. Environmental factors, such asionizing radiation, UV light, and chemicals, can damage DNA. Errors in DNA replication can also lead to mutations. Certain gene products repair damage to chromosomes, thereby minimizing mutations in the cell. When a DNA repair gene is mutated its product is no longer made, preventing DNA repair and allowing further mutations to accumulate in the cell. These mutations can increase the frequency of cancerous changes in a cell. A defect in a DNA repair gene called XP (Xeroderma pigmentosum) results in individuals who are very sensitive to UV light and have a thousand-fold increase in the incidence of all types of skin cancer. There are seven XP genes, whose products remove DNA damage caused by UV light and other carcinogens. Another example of a disease that is associated with loss of DNA repair is Bloom syndrome, an inherited disorder that leads to increased risk of cancer, lung disease, and diabetes. The mutated gene in Bloom syndrome, BLM, is required for maintaining the stable structure of chromosomes. Individuals with Bloom syndrome have a high frequency of chromosome breaks and interchanges, which can result in the activation of oncogenes.