Search

everythinglearnresearchcommunity

for

Search:↓

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Finasteride effectively treats male hair loss, increasing length and thickness.

Mutation in hairless gene may increase hair loss risk.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

Hairless HRS/J mice resist Bacillus anthracis skin infections due to high numbers of immune cells, not because they lack hair follicles.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

Key genes linked to hair growth and cancer were identified in hairless mice.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Early hair loss common in Chinese males, linked to family history and smoking; early treatment advised.

Found 32 genes linked to male baldness, affecting hair growth and stress-related pathways.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Hair loss can be reversed or even cured using advanced hair restoration techniques, with rare complications like swelling and bleeding.

Acne is a common skin condition that can be influenced by diet, lifestyle, and hormones, and requires a treatment approach that includes psychological considerations.

Men who start balding at age 20 may have a higher chance of getting aggressive prostate cancer.

Secondary amenorrhea has many causes and requires thorough evaluation to treat and restore menstrual cycles.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Dihydrotestosterone (DHT) is crucial for conditions like male-pattern baldness and acne, and measuring a byproduct, androstanediol glucuronide, is a better way to assess DHT's effects than DHT blood levels.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.