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Different enzymes are active in different parts of developing mouse organs.

Different body areas in mice produce different hair types due to interactions between skin layers.

Children with autism have lower levels of essential and toxic trace elements in their hair.

FGF13 gene changes cause excessive hair growth in a rare condition.

Edar signaling is crucial for controlling hair growth and regression.

People with ectodermal dysplasias often have reduced saliva production and should get saliva tests.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

There is not enough evidence to support health claims about soy isoflavones.

The hair of two ancient Chilean mummies is well-preserved and contains high levels of heavy metals.

The document concludes that understanding and treatments for alopecia areata have significantly advanced, now recognizing it as an autoimmune disorder.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

A 4-year-old boy with a rare type of rickets and hair loss improved in bone health but not hair growth after vitamin D and calcium treatment.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Dental pulp stem cells are better for tissue repair, while fat tissue stem cells may be more suited for wound healing and hair growth.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Scientists have developed a new method using stem cells to grow and transplant hair follicles, which could be useful for hair regeneration treatments.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

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

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

A 6-year-old boy developed excessive hair growth after taking diazoxide for low blood sugar.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Laser treatment and synovial fluid can change hair follicle cells to resemble joint cells, with the changes being more significant when both treatments are used together.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.