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1

Schenkel-Brunner, Helmut. Human blood groups: Chemical and biochemical basis of antigen specificity. Wien: Springer-Verlag, 1995.

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2

Schenkel-Brunner, Helmut. Human blood groups: Chemical and biochemical basis of antigen specificity. 2nd ed. Wien: Springer, 2000.

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3

Human blood groups: Chemical and biochemical basis of antigen specificity. 2nd ed. Wien: Springer, 2000.

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4

Human blood groups: Chemical and biochemical basis of antigen specificity. Wien: Springer-Verlag, 1995.

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5

K, Pfeffer, ed. Function and specificity of [alpha/delta] T cells: International Workshop, Schloss Elmau, Bavaria, FRG, October 14-16, 1990. Berlin: Springer, 1991.

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6

Workshop on Mechanisms and Specificity of HIV Entry into Host Cells (1989 San Francisco, Calif.). Mechanisms and specificity of HIV entry into host cells. New York: Plenum Press, 1991.

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7

Special Programme for Research and Training in Tropical Diseases, Foundation for Innovative New Diagnostics, and Centers for Disease Control and Prevention (U.S.), eds. Malaria rapid diagnostic test performance: Results of WHO product testing of malaria RDTs : round 2 (2009). Geneva: World Health Organization on behalf of the Special Programme for Research and Training in Tropical Diseases, 2010.

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8

service), ScienceDirect (Online, ed. Tissue-specific vascular endothelial signals and vector targeting. Amsterdam: Elsevier, 2009.

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9

Landsteiner, Karl. The Specificity of Serological Reactions. Dover Publications, 1990.

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10

Ivanyi, Juraj, and Tom H. M. Ottenhoff, eds. Significance of antigen and epitope specificity in tuberculosis. Frontiers SA Media, 2015. http://dx.doi.org/10.3389/978-2-88919-451-3.

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11

Schenkel-Brunner, Helmut. Human Blood Groups: Chemical and Biochemical Basis of Antigen Specificity. 2nd ed. Springer, 2000.

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12

Human Blood Groups: Chemical and Biochemical Basis of Antigen Specificity. Springer, 2011.

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13

Schenkel-Brunner, Helmut. Human Blood Groups: Chemical and Biochemical Basis of Antigen Specificity. Springer Wien, 2012.

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14

Schenkel-Brunner, Helmut. Human Blood Groups: Chemical and Biochemical Basis of Antigen Specificity. Springer, 2013.

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15

Schenkel-Brunner, Helmut. Human Blood Groups: Chemical and Biochemical Basis of Antigen Specificity. Springer London, Limited, 2012.

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16

Lilja, Hans. Prostate-specific antigen and biomarkers for prostate cancer. Edited by James W. F. Catto. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0061.

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Prostate-specific antigen (PSA) is a kallikrein serine protease secreted by the prostate to liquefy the ejaculatory coagulum. Changes in the blood/prostate barrier allows PSA to enter the circulation in men with prostate cancer and other inflammatory prostatic diseases. The commonest method for detection of men at risk of prostate cancer is PSA testing, which is typically used in an opportunistic screening setting. The widespread use of PSA testing leads to overdiagnosis and overtreatment of many men with low-risk prostate cancer, but can allow the identification of those with significant disease requiring radical treatment. This lack of specificity for high-risk prostate cancer has led to the need for more accurate biomarkers or methods to improve the use of PSA testing.
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17

Pfeffer, Klaus. Function And Specificity Of Gama/delta T Cells (Current Topics in Microbiology & Immunology). Edited by Klaus Pfeffer. Springer, 1991.

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18

Marincola, Francesco M., and Dirk Nagorsen. Analyzing T Cell Responses: How to Analyze Cellular Immune Responses Against Tumor Associated Antigens. Springer, 2010.

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19

(Editor), Dirk Nagorsen, and F. M. Marincola (Editor), eds. Analyzing T Cell Responses: How to analyze cellular immune responses against tumor associated antigens. Springer, 2005.

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20

Marincola, Francesco M., and Dirk Nagorsen. Analyzing T Cell Responses: How to Analyze Cellular Immune Responses Against Tumor Associated Antigens. Springer London, Limited, 2006.

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21

Shulman, S. Tissue Specificity and Autoimmunity. Springer, 2011.

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22

Bjartell, Anders, and David Ulmert. Clinical features, assessment, and imaging of prostate cancer. Edited by James W. F. Catto. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0063.

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In contemporary practice, most patients with prostate cancer are diagnosed following a prostate-specific antigen (PSA) test and are asymptomatic at the time of diagnosis. Although serum PSA has a low specificity for prostate cancer, it can be used to single out patients with advanced disease. While most men do not have a palpable tumour at digital rectal examination (DRE), those with palpable or an elevated PSA test require transrectal ultrasonography-guided prostate biopsy in order to make a diagnosis of cancer. Tumours are staged clinically as localized, locally advanced, or metastatic. The urologist and the patient need the correct staging information for decision-making. A combination of several parameters (PSA value, Gleason grade and tumour extent on biopsy, and DRE findings) can be used in a variety of tools to predict the extent of the disease and treatment outcomes.
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23

Cazenave, Pierre-André, Jacques Urbain, and Heinz Köhler. Idiotypy in Biology and Medicine. Elsevier Science & Technology Books, 2013.

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24

Düzgünes, Nejat. Mechanisms and Specificity of HIV Entry into Host Cells. Springer London, Limited, 2012.

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25

Mechanisms and Specificity of HIV Entry into Host Cells. Springer, 1991.

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26

Düzgünes, Nejat. Mechanisms and Specificity of HIV Entry into Host Cells. Springer, 2012.

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27

Tissue-Specific Vascular Endothelial Signals and Vector Targeting. Elsevier Science & Technology Books, 2010.

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