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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Elevated CO2 can lessen the negative impact of water shortage on soybean roots and affects specific genes.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

The monkey's hair loss was due to an autoimmune disease, not genetics.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Vitamin D and calcium are important for quick and effective skin wound healing.

ACBP is essential for healthy skin and fur by maintaining the skin's barrier function.

Hairless gene not strongly linked to baldness.

Gene therapy shows promise for enhancing physical traits but faces ethical, safety, and regulatory challenges.

Prolactin affects when mice shed and grow hair.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

Wound covers with α-13'-COOH from vitamin E can improve and speed up wound healing.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Natural herbal compounds might treat certain medical conditions by reducing DHT levels, but more research is needed to confirm their effectiveness and safety.

New treatments for prostate cancer and BPH show promise, including novel compounds that target hormone synthesis and response.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Ptprq has multiple forms that change during inner ear development.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.