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Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

A calf in Scotland likely had Schmallenberg virus from its mother.

The document suggests that targeting the hormone DHT could be a more effective treatment for prostate cancer than targeting testosterone.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Human skin xenografting could improve our understanding of skin development, renewal, and healing.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

The current understanding of frontal fibrosing alopecia involves immune, genetic, hormonal factors, and possibly environmental triggers, but more research is needed for effective treatments.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Topical 5-Fluorouracil can rarely cause nerve damage, especially in people with a certain genetic deficiency.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.