The present archbishop was not a bad man, in his way.

Was archbishop for a long time, into his old age.

Four years later the Archbishop asked her to return as she was needed at the hospital and with the children.

Since 1678, the city is the seat of an archbishop.

He served as archbishop until his death at the age of 60.

At the beginning, only the archbishop lived here and church building did not take place.

He would serve as Archbishop for the next 26 years.

The archbishop called the world a good place, even wonderful.

It is not known when a new archbishop will be named.

"All this has come together over the last few days," the Archbishop said.

"The archbishop has been doing this for the better part of seven and a half months now," he said.

Throughout the evening, the Archbishop said little; the women did the talking.

The Archbishop looked down at the floor and shook his head.

On August 1, 1977 the former archbishop died of age.

I did not know the archbishop would involve anyone else.

"I think the good archbishop is going to support our cause, Paul."

Only 12 percent of those interviewed were able to name him as the new archbishop.

Five months later, where the Archbishop will live has still not been settled.

"You have made your decision then," the archbishop said, his blue eyes hard and cold.

The right side is the personal seal of the Archbishop.

He resigned in 1877 and was then made an Archbishop.

The church is led by one archbishop and four bishops.

The 68-year-old archbishop was not injured and continued the service.

The king and the archbishop, indeed, had agreed upon this between themselves.

He wondered whether the Archbishop would have learned about the fire.

Follicle stimulating hormone stimulates both the production of androgen binding protein by Sertoli cells, and the formation of the blood-testis barrier.

Androgen binding protein is essential to concentrating testosterone in levels high enough to initiate and maintain spermatogenesis, which can be 20-50 times higher than the concentration found in blood.

Testosterone is required in large local concentrations to maintain the process, which is achieved via the binding of testosterone by androgen binding protein present in the seminiferous tubules.

This is a list of actin-binding proteins in alphabetical order.

Alpha-actinin is an actin-binding protein with multiple roles in different cell types.

The prolin-rich domain interacts with cortactin and actin-binding protein 1.

Profilin as a ubiquitous actin-binding protein is associated with most actin monomers in cells.

Profilin is an actin-binding protein involved in the dynamic turnover and restructuring of the actin cytoskeleton.

Sla2p is an actin-binding protein involved in endocytosis, thus indicating HIP1 in this role.

A class of actin-binding proteins, called cross-linking proteins, dictate the formation of these structures.

Filamin is an actin-binding protein involved in cytokinesis and ring canal formation [ 38, 39].

ADF/cofilin is a family of actin-binding proteins which disassembles actin filaments.

Villin is a 92.5 kDa tissue-specific actin-binding protein associated with the actin core bundle of the brush border.

Gelsolin is an actin-binding protein that is a key regulator of actin filament assembly and disassembly.

Nebulin is an actin-binding protein which is localized to the thin filament of the sarcomeres in skeletal muscle.

Actin-binding proteins (also known as ABP) are proteins that bind to actin.

Subsequently, ADP-actin dissociates slowly from the pointed end, a process significantly accelerated by the actin-binding protein, cofilin.

Three-helix bundles often occur in actin-binding proteins and in DNA-binding proteins.

They contain actin filaments cross-linked into bundles by actin-binding proteins, e.g. fascin and fimbrin.

ADF/cofilins are small actin-binding proteins composed of a single ADF-H domain.

Actin-binding protein anillin is a protein that in humans is encoded by the ANLN gene.

This triterpene can inhibit the phosphorylation of the cofilin protein, a family of actin-binding proteins that disassembles actin filaments.

The product of this gene belongs to the actin-binding proteins ADF (Actin-Depolymerizing Factor)/cofilin family.

Many actin-binding proteins, including α-actinin, β-spectrin, dystrophin, utrophin and fimbrin, do this through the actin-binding calponin homology domain.

Members of the coronin family, such as CORO1B, are WD repeat-containing actin-binding proteins that regulate cell motility.

Adenylate Cyclase Associated Protein is an actin-binding protein that was originally identified as a binding partner for adenylate cyclase.

These structures are regulated by many other classes of actin-binding proteins, including motor proteins, branching proteins, severing proteins, polymerization promoters, and capping proteins.

Because Shroom3 is an actin-binding protein and accumulates on the apical side, the most likely mechanism is that Shroom3 aggregates the actin meshwork, generating a squeezing force.