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Electron Beam Tomography (EBT) is a useful additional test to stress testing for detecting heart disease.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Two new gene mutations cause a rare hair disorder.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

The flexible fixed-sequence testing method allows for more effective evaluation of multiple goals in a clinical trial while controlling the risk of false positives.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

CAG repeat length in the AR gene is not linked to PCOS risk in Iranian women.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Clomiphene citrate is a cheap and simple treatment for low testosterone that works as well as human chorionic gonadotropin, alone or combined, especially for men who want to keep their fertility.

A rare skin cancer on a man's elbow was successfully treated with surgery, showing no recurrence after one year.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

The tool iCOUNT helps understand how stem cells divide and affect tissue development and repair.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

MCHR2 gene duplications may be linked to alopecia areata.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.