TLS Online TPP Program

#Id: 6679

#Unit 3. Fundamental Processes

SR proteins are involved in exon definition in which they interact with U1 and U2AF forming commitment E complex.

TLS Online TPP Program

#Id: 6974

#Unit 8. Inheritance Biology

DOWN SYNDROME Also known as trisomy 21, is the most common autosomal aneuploidy in humans About 75% of the nondisjunction events that cause Down syndrome are maternal in origin, most arising in meiosis I. 

TLS Online TPP Program

#Id: 5200

#Unit 7. System Physiology – Animal

Stabilization of fibrin is catalyzed by activated factor XIII and Ca2

TLS Online TPP Program

#Id: 3333

#Unit 3. Fundamental Processes

Humans can exhibit a genetic disorder called xeroderma pigmentosum (XP), an autosomal-recessive disease that renders afflicted individuals highly sensitive to sunlight and results in skin lesions, including skin cancer.

TLS Online TPP Program

#Id: 6862

#Unit 3. Fundamental Processes

Some of the regions in the eye lack color, whereas others are red. This is because the white gene (required to develop red pigment) was inactivated by adjacent heterochromatin in some cells, but remained active in others.