Search

everythinglearnresearchcommunity

for

Search:↓

The conclusion is that certain traits, including perceived facial aging and BMI, are linked to perceived youthfulness differently in men and women.

The conclusion is that certain traits, including perceived facial aging and BMI, are linked to how youthful people look, with some differences between males and females.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

Scientists successfully edited a goat's genes to grow more and longer cashmere hair.

The research found genes that change during cashmere goat hair growth and could help determine the best time to harvest cashmere.

A specific gene mutation causes long hair in Angora rabbits.

The complement system might be involved in the development of alopecia areata and could lead to new treatments.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

Diabetes causes lasting cell dysfunctions, leading to serious complications even after blood sugar is controlled.

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

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Female pattern hair loss has multiple causes and treatments, with new therapies showing promise.

Thyroid and reproductive hormones, BMI, and excess hair are linked in Iraqi women with PCOS.

Docetaxel often causes hair loss, with limited effective treatments and no cure for permanent hair loss.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Melatonin helps hair grow by activating the RORα receptor in goats.

New understanding and treatments for hair loss are improving, but more research is needed.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Androgenetic alopecia is linked to heart disease, metabolic issues, and mental health problems.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

The document concludes that stopping shaving or removing affected hair can alleviate Pseudofolliculitis barbae (PFB).