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The conclusion is that women under 35 should start fertility checks after 12 months of trying to conceive, women over 35 after 6 months, and women over 40 should start immediately. The checks should include ovulation status, reproductive tract structure, and male partner's semen evaluation.

Edar signaling is crucial for controlling hair growth and regression.

Fatp4 is crucial for healthy skin development and function.

Aging slows wound healing due to weaker cells and immune response.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

EGFR helps control how hair grows and forms without needing p53 protein.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Special proteins are important for skin balance, healing, and aging, and affect skin stem cells.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Afro-textured hair needs personalized care due to its unique genetic traits.

Different types of hair loss require specific treatments, and new treatments are being developed.

Monilethrix causes fragile, patchy hair loss.

ACBP is crucial for healthy skin in mice.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Hair keratins evolved from ancient proteins, diversifying through gene changes, crucial for forming claws and later hair in mammals.

pCLCA2 protein may help maintain skin structure and function.

Obesity is linked to various skin conditions and issues, and losing weight can improve these conditions.

The study identified 12 potential biomarkers for hair loss and how they affect hair growth.

Knocking out certain genes in mice helps understand skin and hair growth problems.

Long COVID affects over half of COVID-19 survivors, causing a range of symptoms like fatigue and neurological issues, with no specific treatment yet.

Transglutaminase activity is important for skin and is found in both mammals and birds.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

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.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The Notch signaling pathway is important for hair follicle development and could help create treatments for hair disorders.

Advances in genetics may lead to targeted treatments for hair disorders.

Vitiligo causes white skin patches, often starts before age 20, and is linked to other health issues.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Natural products may help treat skin inflammation from abnormal adrenal hormones.