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TURP specimens should be checked for various tumors, not just common prostate issues.

Hydrogel scaffolds can help wounds heal better and grow hair.

Hormonal interactions, especially involving DHT and estrogen, play a key role in BPH development and treatment.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Long-term use of azole antifungals can cause hair loss, hormonal imbalances, and severe skin reactions.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

FGF5 gene mutations cause long hair in domestic cats.

Young dogs and cats in Western Turkey often have skin infections caused by fungi, especially Microsporum canis.

Dissolving microneedles show promise for delivering medication through the skin but face challenges like manufacturing complexity and regulatory hurdles.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Understanding how DHT works is important for diagnosing and treating hormone-related disorders.

Hair analysis for stress and reproductive hormones in wildlife needs more research for accuracy across species.

Nanotube-based hair treatments could improve hair health and growth, and offer long-lasting effects.

Laser therapy improved surgical scar healing in dogs.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

The best method for urethral reconstruction is using hypoxia-preconditioned stem cells with autologous cells on a vascularized synthetic scaffold.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

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.

Cattle skin has leptin which might control skin and hair growth.

The study concluded that similar pathways regulate hair growth in dogs and mice, and these pathways are disrupted in dogs with Alopecia X, affecting stem cells and hormone metabolism.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Oral feline interferon-omega improved symptoms in diabetic cats with gingivostomatitis.