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Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

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

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Hair samples can be used to create stem cells easily and non-invasively.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

Minoxidil affects collagen-related genes, potentially helping treat fibrosis.

Gene differences found in hair follicles linked to male baldness.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

Mouse models help understand alopecia areata and find treatments.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

Vitamin D is important for bones, hair, blood pressure, and breast development.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

Female pattern hair loss is common and should be treated early to prevent worsening, with Minoxidil being the main approved treatment.

More research is needed to find effective treatments for Female Pattern Hair Loss.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Men with Kennedy disease have less chance of hair loss.

K6hf is a unique protein found only in a specific layer of hair follicles.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.