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Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

New treatments for Alopecia Areata, like JAK inhibitors, show promise for hair regrowth and are likely to change future treatment approaches.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Dupilumab is being tested for many new skin, respiratory, and gastrointestinal conditions.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Changing the amount of PLC5 in Arabidopsis affects root growth and drought resistance, with less PLC5 slowing root growth and more PLC5 improving drought tolerance but hindering root hair growth.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Traditional Chinese medicinal foods may help manage long-term post-COVID symptoms.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Hormones affect skin aging, and treatments targeting hormonal balance may improve skin health.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

The p53 protein has complex, sometimes contradictory functions, including tumor suppression and promoting cell survival.

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

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

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

The symposium concluded that understanding how different species repair tissue and how this changes with age can help advance regenerative medicine.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Understanding skin structure and development helps diagnose and treat skin disorders.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

Histone modification is key in treating chronic inflammatory skin diseases.

Early signs of PCOS in girls, like irregular periods and polycystic ovaries, suggest a need for early diagnosis and intervention to prevent further health issues.

Drugs targeting the JAK/STAT pathway can improve atopic dermatitis but vary in effectiveness for vitiligo and alopecia areata, with generally mild safety concerns.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.