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Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Adding a second method to PROTACs could improve cancer treatment.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Odontogenic keratocysts are caused by abnormal Hedgehog signaling and can lead to tooth and bone issues.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

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

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

The review suggests that while many AKR1C3 inhibitors show promise for treating certain cancers, more research is needed to confirm their effectiveness in humans.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

Fibroblast Growth Factors (FGFs) are important for tissue repair and regeneration, influencing cell behavior and other factors involved in healing, and are crucial in processes like wound healing, bone repair, and hair growth.

A specific enzyme is crucial for the bean plant's relationship with certain beneficial soil bacteria and fungi.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

The HR protein's role as a repressor is essential for controlling hair growth.

Rac1 is essential for proper hair structure and color.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

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

RXRα is crucial for proper immune response and links diet to immune function.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Zebrafish helped find new ways to prevent drug-induced hair cell death and potential treatments for hearing loss.

Laminin-511 is crucial for early hair growth and maintaining important hair development signals.

Phosphorylation of certain parts of the PIN3 protein is crucial for its role in plant root growth and response to gravity.

ACBP is crucial for healthy skin in mice.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

Hair growth and development are controlled by specific signaling pathways.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

FLCN helps control iron levels in cells.

OsUEV1B protein is essential for controlling phosphate levels in rice.