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Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

Intermediate filaments are crucial for cell differentiation and stem cell function.

Key proteins and pathways regulate wool fiber diameter in Alpine Merino sheep.

The testes produce important hormones like testosterone and others that play key roles in male body functions.

Some women with PCOS have rare genetic variants linked to the condition.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Blocking miR-27a increases sheep hair follicle stem cell growth and decreases cell death, which could help improve wool quality and treat hair loss.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

Accurate diagnosis and timely, tailored treatments improve outcomes in obstetrics and gynecology.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

The document explains how to identify different hair problems using a microscope.

Non-coding RNAs help control hair growth in cashmere goats.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Epimorphin, a protein, plays a key role in the development of hair follicles in human fetuses, but it doesn't help in maintaining the stem cell population of the follicular skin layer.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

A mutation in mice causes hair loss and immune problems.

Chromosomal differences affect how muscle cells respond to testosterone.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.