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Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Finasteride affects male rat genitalia development, causing abnormalities during specific pregnancy days.

A certain smell receptor in hair follicles can affect hair growth when activated by a synthetic sandalwood scent.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Tiny needles with valproic acid can effectively regrow hair.

An imbalance between certain immune cells is linked to a chronic skin condition and may be influenced by obesity, smoking, and autoimmune issues.

Hair follicle stem cells are a promising source for tissue repair and treating skin or hair diseases.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

FOXN1 gene variants cause low T cells and immune issues from birth.

K16 can partially replace K14 but causes hair loss and skin issues.

Mothers and newborns with dental fillings had higher mercury in their hair, but getting fillings during pregnancy didn't raise mercury levels further.

A mother's western diet can make her milk toxic, causing inflammation and hair loss in babies.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Eating glucoraphanin can help prevent psychosis in offspring whose mothers had immune system activation.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

Activating Notch in adult skin causes T cells and neural crest cells to gather, leading to skin issues.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Loss of Fz6 disrupts hair follicle and associated structures' orientation.

Wounds heal without scarring in early development but later result in scars, and studying Wnt signaling could help control scarring.