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Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Diabetes causes lasting cell dysfunctions, leading to serious complications even after blood sugar is controlled.

The conclusion is that women under 35 should start fertility checks after 12 months of trying to conceive, women over 35 after 6 months, and women over 40 should start immediately. The checks should include ovulation status, reproductive tract structure, and male partner's semen evaluation.

Eyelid cells share signaling components but differ in pathway activity.

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.

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Adult acne is often related to hormonal disorders, especially in women, and may need long-term treatment involving specialists.

Eating a high inositol diet significantly improves insulin resistance and hormone levels in women with PCOS.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Different hair care practices and conditions affect African American hair and scalp health, requiring specialized knowledge for treatment.

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

Hair shaft disorders are diagnosed through examination and history, with general care and some treatments offering improvement.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Five Weimaraners had a milder form of color dilution alopecia causing hair loss and skin issues.

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

The most common skin problems in Indian children are infections and eczemas.

Woolly hair is a rare genetic condition with no effective treatments.

The document concludes that non-scarring alopecias can be reversed, but scarring alopecias cause permanent hair loss.

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

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

Swiss Holstein cattle with curly, short hair carry genes from the Simmental breed.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Lipedematous scalp is mainly caused by an increase in fat tissue under the skin and is different from lipedematous alopecia.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Finasteride and minoxidil are effective FDA-approved treatments for androgenetic alopecia.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.