Search

everythinglearnresearchcommunity

for

Search:↓

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

The meeting presented new findings on hair stem cells, pigmentation, genetics, and modern hair treatment techniques.

A mother and her two daughters got a skin infection from their cat.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

The patient with total hair loss did not regrow hair despite treatment, indicating a poor outlook for this type of hair loss.

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

The study suggests that analyzing DNA can help treat hair loss, but more research is needed.

New understanding and treatments for hair loss are improving, but more research is needed.

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

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

AIRE deficiency causes hair loss similar to alopecia areata in mice.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A specific gene mutation causes Olmsted syndrome.

Dutasteride is more efficient than finasteride, but individual results vary.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

AGA causes hair loss by shrinking hair follicles due to DHT binding, and can be treated with finasteride and minoxidil.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Male pattern baldness involves hormones and cell signals affecting hair growth.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

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.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

The article concludes that while we understand a lot about how melanocytes age and how this can prevent cancer, there are still unanswered questions about certain pathways and genes involved.