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Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Meis1 is crucial for skin health and tumor development.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

Certain essential oils can activate a human skin receptor, potentially helping with skin disorders.

Immune cells affect hair growth and could lead to new hair loss treatments.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Researchers found that certain RNA molecules might play a role in the growth of Cashmere goat hair.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

A specific protein in chicken embryos links early skin layers to feather development.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Whale genes show changes that help them live in water, like less hair and better flippers.

Scientists made safflower seeds produce a human growth factor that could help with hair growth and wound healing.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

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