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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

New CRISPR/Cas9 variants and nanotechnology-based delivery methods are improving cancer treatment, but choosing the best variant and overcoming certain limitations remain challenges.

The research found specific genes and pathways that control fur development and color in young American minks.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Osteoma cutis is a rare, benign skin condition where bone forms in the skin.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

Editing the FGF5 gene in sheep increases fine wool growth.

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

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

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

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Six genetic conditions are often linked to complete scalp hair loss in children.

Cactus extract from Notocactus ottonis may help promote hair growth.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

Traumatic alopecia causes hair loss from pulling or rubbing, leading to broken hairs and changes in the scalp.

Brain-Derived Neurotrophic Factor (BDNF) slows down hair growth and promotes hair follicle regression.

Trichoscopy is a useful tool for diagnosing different hair and scalp diseases without surgery.

Trichoscopy helps tell apart alopecia areata and trichotillomania in Asians by looking at specific hair and scalp features.

Chemotherapy caused hair loss with specific patterns, but most patients had hair regrowth after treatment, while some had lasting hair loss.

Hair follicles are complex, dynamic mini-organs that help us understand cell growth, death, migration, and differentiation, as well as tissue regeneration and tumor biology.

Dermoscopy is a useful tool for identifying features of skin conditions, but more research is needed to define its role in dermatology.

Understanding hair follicle anatomy helps diagnose hair disorders.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.