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A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Children under 10 can experience hair thinning without hormone issues, and it may improve with treatment.

Minoxidil use can cause trichostasis spinulosa in long-term hair loss patients.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Plica neuropathica is a tangled hair condition that may be caused by hair damage or psychiatric issues and is treated by cutting the hair and addressing mental health.

Myotonic dystrophy may be classified as a segmental progeroid disorder.

Human prostate cells produce more WISP1/CCN4 when there's not enough oxygen.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

A child with a rare vitamin D-resistant condition improved with treatment.

A kidney transplant patient developed leprosy, likely due to immunosuppression and genetic factors, and improved with treatment.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

Wedelolactone may help treat chronic diseases by acting as an antioxidant and affecting important proteins.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

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.

Hair loss may be an early sign of serious illnesses like Hodgkin disease.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

A girl inherited excessive body hair from her mother and grandmother.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

Early balding linked to higher heart disease risk.

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.