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Topical squaric acid dibutylester worsened discoid lupus erythematosus in a patient.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

A new carrier improves skin delivery of tofacitinib for treating inflammatory skin diseases.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

3-Deoxysappanchalcone helps human hair cells grow and stimulates hair growth in mice by affecting certain cell signaling pathways.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

The new polymer improves dyed hair's color, moisture, shine, and smoothness.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Protein-losing enteropathy worsened with lupus symptoms but improved with prednisolone.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

The new composite material is safe and has anticoagulant properties.

New biological pathways and potential treatment targets for male pattern baldness were identified.

A special hydrogel helps stem cells heal wounds better by boosting growth factors.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

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

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

A woman with skin and joint issues progressed from one type of lupus to another, highlighting the need to recognize complex conditions.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.