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Ovarian SAHA syndrome makes women with PCOS more resistant to insulin and increases their risk of blood sugar problems.

Plant root hair growth is mainly controlled by hormones like auxin and ethylene, which promote growth, while others like brassinosteroid inhibit it.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Human head hair proteins can be typed into eight distinct patterns, useful for genetic and forensic investigations.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Certain drugs change freshwater snail shells to a "banana" shape.

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

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

Adipose-derived stem cells show potential for skin rejuvenation and wound healing but require more research to overcome challenges and ensure safety.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Isotretinoin may cause hair loss, especially in women and young adults.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Peps help Arabidopsis plants grow more root hairs by affecting specific genes and calcium signaling.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Diagnosing PCOS in teenagers is challenging and should use strict criteria to avoid misdiagnosis and unnecessary worry.

D'orenone stops root hair growth by disrupting auxin transport, but adding auxin can reverse this.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The composite sponge helps heal diabetic wounds by reducing inflammation and promoting new blood vessel growth.

Male hormones and their interactions are crucial for male sexual development and characteristics.

Altering SSAT affects fat metabolism and body fat in mice.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Metabolic signals and cell shape influence how cells develop and change.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

SOX9 is essential for the development of various organs and hair follicles.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

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

Foxn1 is important for fat development, metabolism, and wound healing in skin.