| |
|
|
|
|
|
|
|
|
1. |
Record Nr. |
UNINA9910458563803321 |
|
|
Titolo |
The leucocyte antigen factsbook [[electronic resource] /] / A. Neil Barclay ... [et al.] |
|
|
|
|
|
|
|
Pubbl/distr/stampa |
|
|
San Diego, : Academic Press, : Harcourt Brace & Co., c1997 |
|
|
|
|
|
|
|
ISBN |
|
1-281-07675-9 |
9786611076757 |
0-08-053543-7 |
|
|
|
|
|
|
|
|
Edizione |
[2nd ed.] |
|
|
|
|
|
Descrizione fisica |
|
1 online resource (625 p.) |
|
|
|
|
|
|
Collana |
|
|
|
|
|
|
Altri autori (Persone) |
|
|
|
|
|
|
Disciplina |
|
|
|
|
|
|
Soggetti |
|
CD antigens |
HLA histocompatibility antigens |
Leucocytes |
Electronic books. |
|
|
|
|
|
|
|
|
Lingua di pubblicazione |
|
|
|
|
|
|
Formato |
Materiale a stampa |
|
|
|
|
|
Livello bibliografico |
Monografia |
|
|
|
|
|
Note generali |
|
Accompanied by: 1 wall chart : col. |
|
|
|
|
|
|
Nota di bibliografia |
|
Includes bibliographical references and index. |
|
|
|
|
|
|
Nota di contenuto |
|
Front Cover; The Leucocyte Antigen: Factsbook; Copyright Page; Contents; Preface; Abbreviations; Dedication; Section I: THE INTRODUCTORY CHAPTERS; Chapter 1. Introduction; Chapter 2. The Discovery and Biochemical Analysis of Leucocyte Surface Antigens; Chapter 3. Protein Superfamilies and Cell Surface Molecules; Chapter 4. The Architecture and Interactions of Leucocyte Surface Molecules; Section II: THE LEUCOCYTE ANTIGENS; CD1; CD2; CD3/TCR; CD4; CD5; CD6; CD7; CD8; CD9; CD10; CD11a; CD11b; CD11c; Integrin aD subunit; CDw12; CD13; CD14; CD15; CD15s; CD16; CDw17; CD18; CD19; CD20; CD21; CD22 |
CD23CD24; CD26; CD27; CD28; CD29; CD30; CD31; CD32; CD33; CD34; CD35; CD36; CD37; CD38; CD39; CD40; CD41; CD42a,b; CD43; CD44; CD45; CD46; CD47; CD48; CD49a; CD49b; CD49c; CD49d; CD49e; CD49f; CD50; CD51; CD52; CD53; CD54; CD55; CD56; CD57; CD58; CD59; CD60; CD61; CD62E; CD62L; CD62P; CD63; CD64; CD65; CD66; CD68; CD69; CD70; CD71; CD72; CD73; CD74; CDw75; CDw76; CD77; CD79/BCR; CD80; CD81; CD82; CD83; CDw84; CD85; CD86; CD87; CD88; CD89; CD90; CD91; CDw92; CD93; CD94; CD95; CD96; |
|
|
|
|
|
|
|
|
|
|
|
CD97; CD98; CD99; CD100; CD101; CD102; CD103; CD104; CD105; CD106; CD107a, CD107b; CDw108; CD109; CD117 |
CD120a, CD120bCD134; CD135; CDw137; CD138; CD147; CD148; CDw150; CD151; CD152; CD153; CD154; CD161; CD162; CD163; CD166; 114/A10; 2B4; 4-1BBL; Aminopeptidase A; B-G; Chemokine receptors; c-kitL; CMRF35 antigen; DEC-205; DNAM-1; ESL-1; F4/80; FasL; FceRI; FLT3 ligand; FPR; Galectin 3; G-CSFR; GM-CSFR; GlyCAM-1; gp42; gp49; HTm4; IFN?R; IL-1R; IL-2R; IL-3R; IL-4R; IL-5R; IL-6R; IL-7R; IL-8R; IL-9R; IL-10R; IL-11R; IL-12R; IL-13R; IL-14R; IL-15R; IL-17R; Integrin ß7 subunit; KIR family; L1; LAG-3; LDLR; LPAP; ltk; Ly-6; Ly-9; Ly-49; Mac-2-BP; Macrophage lectin; MAdCAM-1; Mannose receptor; MARCO |
M-CSFRMDR1; MHC Class I; MHC Class II; MS2; NKG2 family; OX2; OX40L; PC-1; PD-1; RT6; Sca-2; Scavenger RI and II; Sialoadhesin; Thrombopoietin receptor; WC1; Index; CD antigen expression of haemopoietic cells |
|
|
|
|
|
|
Sommario/riassunto |
|
A volume in the popular FactsBook Series, the First Edition of The Leucocyte Antigen FactsBook was hugely successful. The new Second Edition has been completely revised, updated, and expanded by 65% to include new findings and up-to-date key references. The introductory chapters have also been updated, especially in terms of nomenclature, the role of the World Wide Web, and new structural data. The Leucocyte Antigen FactsBook, Second Edition contains more than 200 entries, with approximately 70 new entries, on all the molecules specifically expressed in the s |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
2. |
Record Nr. |
UNINA9910300066103321 |
|
|
Titolo |
Inherited Chorioretinal Dystrophies : A Textbook and Atlas / / edited by Bernard Puech, Jean-Jacques De Laey, Graham E. Holder |
|
|
|
|
|
|
|
Pubbl/distr/stampa |
|
|
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 |
|
|
|
|
|
|
|
|
|
ISBN |
|
|
|
|
|
|
Edizione |
[1st ed. 2014.] |
|
|
|
|
|
Descrizione fisica |
|
1 online resource (477 p.) |
|
|
|
|
|
|
Disciplina |
|
599935 |
610 |
611.01816 |
616.07 |
|
|
|
|
|
|
|
|
Soggetti |
|
Ophthalmology |
Medical genetics |
Pathology |
Medical Genetics |
|
|
|
|
|
|
|
|
Lingua di pubblicazione |
|
|
|
|
|
|
Formato |
Materiale a stampa |
|
|
|
|
|
Livello bibliografico |
Monografia |
|
|
|
|
|
Note generali |
|
Description based upon print version of record. |
|
|
|
|
|
|
Nota di bibliografia |
|
Includes bibliographical references and index at the end of each chapters. |
|
|
|
|
|
|
|
|
Nota di contenuto |
|
Investigations -- Introduction to molecular genetics and genetic testing for retinal dystrophies- Electrophysiological testing -- Dark adaptation -- Fluorescein angiography -- ICG angiography -- Fundus autofluorescence in retinal dystrophies -- Spectral-domain optical coherence tomography in hereditary retinal dystrophies. Inherited Retinal Dystrophies -- Inherited stationary disorders of the retina -- Retinitis pigmentosa and allied disorders -- Leber congenital amaurosis -- Retinitis punctata albescens -- Usher Syndromes -- Cone and Cone-rod dystrophies -- Enhanced S-Cone syndrome -- Chorioretinopathies: Choroideremia and gyrate atrophy -- Late onset retinal degeneration -- Stargardt Disease -- Bestrophinopathies -- Retinal dystrophies associated with the PRPH2 gene -- Alström syndrome -- Bardet-Biedl syndrome -- Cohen syndrome -- Juvenile neuronal ceroid lipofuscinosis (JNCL) -- Adult Refsum disease -- Abetalipoproteinemia -- LCHAD deficiency -- Jalili syndrome -- |
|
|
|
|
|
|
|
|
|
|
|
Spinocerebellar ataxia -- Dominant cystoid macular dystrophy -- Autosomal dominant Stargardt-like macular dystrophy (ELOVL4). - Spastic paraplegia and retinal degeneration. Kjellin syndrome -- Autosomal dominant drusen -- Cuticular drusen -- Extensive macular atrophy with pseudodrusen-like appearance (EMAP) -- Congenital hypotrichosis with juvenile macular dystrophy -- Mitochondrial retinopathies -- Sorsby fundus dystrophy -- Bietti crystalline corneoretinal dystrophy -- Cystinosis -- Oxalosis -- Alport syndrome -- X-linked retinoschisis -- Paramacular choriocapillaris atrophy -- Exudative vitreoretinopathy -- Stickler syndrome -- Wagner syndrome -- Incontinentia pigmenti Type II (IP2) -- Ganglion cell disease -- Pseudoxanthoma elasticum -- Aicardi Syndrome -- Chorioretinal dysplasia-microcephaly-mental retardation syndrome (Azial-Dufier syndrome) -- Alagille syndrome -- Future therapies for retinitis pigmentosa. |
|
|
|
|
|
|
Sommario/riassunto |
|
This lavishly illustrated atlas provides indispensable information to clinicians, geneticists and visual scientists working with inherited retinal diseases. It is filled with high-quality images, up-to-date genetic information and comprehensive electrophysiology. The data for each individual disorder have been summarised in an accessible, reader-friendly format for easy reference. The illustrations include colour fundus photographs, fluorescein angiograms, OCT scans, electrophysiological studies and pedigrees. The editors and authors are well-known experts in the field and have drawn upon their extensive experience to produce this unique atlas. |
|
|
|
|
|
|
|
| |