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Finasteride side effects in young men may be linked to specific gene variations.

Certain gene variations are linked to better memory in healthy Chinese women.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

A new gene variant causes glucocorticoid resistance in a mother and son.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Vitamin D receptor helps control hair growth genes in skin cells.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

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

New genetic mutations linked to rare skin disorders were found in three newborns.

The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.