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TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

pbn-STAC effectively finds strategies for cellular reprogramming using deep reinforcement learning.

Thallium is highly toxic, causing severe health issues, and Prussian blue is the best antidote.

Thymic stromal lymphopoietin (TSLP) promotes hair growth by stimulating specific skin cells.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

The document's conclusion cannot be provided because the document is not available or cannot be understood.

Two new gene mutations cause a rare hair disorder.

Hair loss and polyneuropathy improved, but severe vision impairment persisted.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

Thallium poisoning is serious, affecting nerves and organs, and is treated by reducing absorption and removing it from the body.

Better diagnosis and control of thallium poisoning are needed to prevent severe outcomes.

Thallium poisoning from contaminated tortillas caused severe symptoms and was mostly fatal or led to long-term health issues.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Different sPLA2 enzymes have unique roles in phospholipid metabolism and biological processes.

Netherton's disease causes multiple hair defects.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Researchers converted human embryonic stem cells into trophoblast stem cells using specific transcription factors.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.