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After chemotherapy for a gestational trophoblastic tumor, normal pregnancy rates are possible, but there's a slightly higher risk of the tumor reoccurring in future pregnancies.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Extracts from three Polynesian plants were found to promote hair growth by affecting cell growth and gene expression related to hair.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

ICL is a condition with low CD4+ T cells like AIDS but not caused by HIV, and normal CD4+ T cell counts may vary between men and women.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Adding a specific gene to skin cells can help treat skin disorders like psoriasis.

New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Swiss Holstein cattle with curly, short hair carry genes from the Simmental breed.

Different amounts of daylight affect cashmere growth in goats by changing the activity of certain genes and molecules.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Manipulating the catagen and telogen phases of hair growth could lead to treatments for hair disorders.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.