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The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

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

Transglutaminase activity is important for skin and is found in both mammals and birds.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.

More research is needed to understand how testosterone is maintained in adult males.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Zinc can both inhibit and stimulate mouse hair growth, and might help recover hair after chemotherapy.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A specific gene mutation causes Olmsted syndrome.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.