1.

Record Nr.

UNISA996396645103316

Autore

Hawkins John <17th cent.>

Titolo

The clerk's tutor for writing [[electronic resource] /] / Written and engraved by Edw. Cocker

Pubbl/distr/stampa

London, : Printed for Jo. Streater, Ja. Flesher, and Hen. Twyford. Sold in Vine Court Middle Temple, 1667

Descrizione fisica

[12], 360 p., [6] leaves of plates

Altri autori (Persone)

CockerEdward <1631-1675.>

Soggetti

Copybooks - England

Forms (Law) - England

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Note generali

Engraved t.p. containing a perpetual almanac; six leaves of writing specimens.

"This book is by Hawkins ... and the t.p. only claims the plates, not the letterpress for Cocker"--DNB (concerning The young clerk's tutor for writing, 1st ed., 1660?).

Reproduction of original in Newberry Library.

Imperfect: lacks p. 185-208.

This item is identified at reel 22:9 as Wing C4832A (number cancelled in Wing CD-ROM, 1996), and at reel 2265:8 as Wing (CD-ROM, 1996) H1174A.

Sommario/riassunto

eebo-0101



2.

Record Nr.

UNINA9910585941103321

Autore

Levtchenko Elena N

Titolo

Cellular and Molecular Mechanisms of Nephropathic Cystinosis

Pubbl/distr/stampa

Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022

Descrizione fisica

1 online resource (230 p.)

Soggetti

Medicine and Nursing

Pharmacology

Lingua di pubblicazione

Inglese

Formato

Materiale a stampa

Livello bibliografico

Monografia

Sommario/riassunto

Nephropathic cystinosis (MIM # 219800) is a rare autosomal recessive disorder caused by mutations in the lysosomal cystine transporter cystinosin, encoded by the CTNS gene (17p13.2). This devastating condition initially affects kidneys and subsequently many other organs including eyes, thyroid, pancreas, muscles, and brain. While lysosomal cystine storage is a key feature of the disease and the main target of current therapy, recent groundbreaking research has revealed that cystinosin has diverse functions in cells, being involved in vesicle trafficking, energy homeostasis, and cell death mechanisms. These discoveries deepen our insights into the mechanisms of cystinosis and of lysosomal biology in general. In this Special Issue dedicated to the pioneer of cystinosis research Dr. Jerry Schneider, we highlight the state-of-the-art understanding of cellular and molecular mechanisms of various disease features, opening new horizons for innovative treatment strategies for cystinosis and potentially other lysosomal storage diseases.