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A protein complex called mTORC1 likely affects when hair growth starts in mice.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

A cosmetic procedure can lower the hairline by up to 10 cm, with high satisfaction but potential for temporary sensation loss and rare risks.

A blood test level of 3.2 ng/mL of Antimüllerian hormone is good for identifying polycystic ovarian morphology in European women aged 25–45.

A new method extracts red dyes from wool without damaging it, although it slightly weakens the wool.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

A new model can predict drug-disease links well, helping drug research.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

A new hyaluronan-based biomatrix successfully supports the growth of mouse ovarian follicles, producing healthy eggs.

A woman with scalp lymphoma and hair loss improved with radiotherapy, highlighting the need for biopsies in similar cases.

A holistic approach combining medical, surgical, and psychological therapies is essential for effectively managing diabetes.

A young woman had a rare skin reaction to a medication for her joint disease, and a combination therapy improved her condition.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

A new compound was created in 2010 that can control oil production when applied to the skin, and its effects are completely reversible after two weeks.

A woman's hair turned white after taking a cancer drug called dasatinib.

A bioink with 15% gelatin and 150 mM calcium chloride works best for 3D printing skin models.

A standardized drug development platform is essential for efficient and effective drug repurposing, especially during pandemics.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A woman with lupus and antiphospholipid syndrome had bone damage, showing the need for careful treatment.

A woman had hair loss, nail changes, and skin peeling after a COVID-19 infection, which got better on their own.

A young woman's symptoms suggested PCOS, but tests and surgery confirmed and treated a rare ovarian tumor, resolving her condition.

A protein called sFRP4 can slow down hair regrowth.

A special receptor in sensory nerve endings helps control how they respond to stretching.

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

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

A certain medication improved severe itching in a boy with liver and bowel disease by reducing histamine levels, suggesting a new treatment target.

A rare benign cheek tumor was successfully removed from a 15-year-old girl without complications or recurrence.