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The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

Neurotoxins can affect neurotransmitter release and have potential in treating muscle, pain, and cancer conditions, but more research is needed on how they work.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Eyelid cells share signaling components but differ in pathway activity.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Combining narrow-band ultraviolet B light and stem cell transplantation helps repigmentation in vitiligo by maintaining calcium balance in mice.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

The research identifies genes linked to wool quality in sheep and provides insights to improve wool production.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Dutasteride, usually used for prostate issues and hair loss, could potentially treat Amyotrophic Lateral Sclerosis (ALS) due to its neuroprotective, antioxidant, and anti-inflammatory properties, but more testing is needed.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

Coffee bean residue extract helps hair growth by activating cell processes.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

Melatonin improves tomato root growth and plant health at certain levels by affecting genes and hormones but can damage roots at high levels.

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

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Multiphoton microscopy is a promising tool for detailed skin imaging and could improve patient care if its challenges are addressed.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

Vitamin D receptor is crucial for skin wound healing.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

Too much Smad7 can cause serious changes in skin tissues, including problems with hair growth, thymus shrinkage, and eye development issues.

FLRG and follistatin have different roles in wound healing.

New research on prostamide F2α has led to treatments for glaucoma and eyelash growth and may have more medical uses.

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