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1. Full Text Humoral Reactivity of Renal Transplant-Waitlisted Patients to Cells From GGTA1/CMAH/B4GalNT2, and SLA Class I Knockout Pigs
by Martens, Gregory R and Reyes, Luz M and Butler, James R and Ladowski, Joseph M and Estrada, Jose L and Sidner, Richard A and Eckhoff, Devin E and Tector, Matt and Tector, A Joseph
Transplantation, ISSN 0041-1337, 04/2017, Volume 101, Issue 4, pp. e86 - e92
BACKGROUNDAntipig antibodies are a barrier to clinical xenotransplantation. We evaluated antibody binding of waitlisted renal transplant patients to 3 glycan... 
SURVIVAL | SURGERY | XENOTRANSPLANTATION | HLA-SPECIFIC ANTIBODIES | SWINE LEUKOCYTE ANTIGENS | NATURAL ANTIBODIES | IMMUNOLOGY | TRANSPLANTATION | POSITIVE CROSS-MATCH | SENSITIZED PATIENTS | KIDNEY-TRANSPLANTATION | REJECTION | EPITOPES | Mixed Function Oxygenases - deficiency | Immunoglobulin G - blood | Humans | Antigens, Heterophile - immunology | Transplantation, Heterologous | Galactosyltransferases - genetics | Galactosyltransferases - immunology | Antibodies, Heterophile - blood | Flow Cytometry | Immunity, Humoral | Swine | N-Acetylgalactosaminyltransferases - genetics | Waiting Lists | Galactosyltransferases - deficiency | N-Acetylgalactosaminyltransferases - deficiency | Animals, Genetically Modified | HLA Antigens - immunology | Genotype | Kidney Transplantation | Gene Knockout Techniques | Antigens, Heterophile - genetics | Mixed Function Oxygenases - immunology | Cross Reactions | Phenotype | Animals | Histocompatibility Antigens Class II - immunology | N-Acetylgalactosaminyltransferases - immunology | Protein Binding | Histocompatibility Antigens Class II - genetics | Mixed Function Oxygenases - genetics | Histocompatibility | Histocompatibility Testing - methods
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2. Full Text A fungal monooxygenase-derived jasmonate attenuates host innate immunity
by Patkar, Rajesh N and Benke, Peter I and Qu, Ziwei and Chen, Yuan Yi Constance and Yang, Fan and Swarup, Sanjay and Naqvi, Naweed I
Nature Chemical Biology, ISSN 1552-4450, 09/2015, Volume 11, Issue 9, pp. 733 - 740
Distinct modifications fine-tune the activity of jasmonic acid (JA) in regulating plant growth and immunity. Hydroxylated JA (12OH-JA) promotes flower and... 
12-OXO-PHYTODIENOIC ACID | DEFENSE | SALICYLIC-ACID | MAGNAPORTHE-ORYZAE | BIOCHEMISTRY & MOLECULAR BIOLOGY | FUSARIUM-OXYSPORUM | LEAVES | GENES | BLAST FUNGUS | PLANTS | RICE | Fungal Proteins - chemistry | Plant Immunity | Oxylipins - immunology | Plant Diseases - immunology | Cyclopentanes - chemistry | Plant Diseases - microbiology | Mixed Function Oxygenases - chemistry | Magnaporthe - immunology | Host-Pathogen Interactions - immunology | Plant Growth Regulators - chemistry | Cyclopentanes - immunology | Fungal Proteins - immunology | Oryza - microbiology | Magnaporthe - pathogenicity | Plant Growth Regulators - immunology | Magnaporthe - genetics | Oryza - immunology | Gene Expression Regulation, Fungal | Hydroxylation | Signal Transduction | Models, Molecular | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Fungal Proteins - genetics | Mixed Function Oxygenases - immunology | Plant Leaves - immunology | Oxylipins - metabolism | Recombinant Proteins - immunology | Cyclopentanes - metabolism | Methylation | Mixed Function Oxygenases - genetics | Plant Growth Regulators - metabolism | Oxylipins - chemistry | Plant Leaves - microbiology | Plant biology | Enzymes | Biosynthesis | Metabolites
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3. Full Text Silencing porcine CMAH and GGTA1 genes significantly reduces xenogeneic consumption of human platelets by porcine livers
by Butler, James Russell and Paris, Leela L and Blankenship, Ross L and Sidner, Richard A and Martens, Gregory R and Ladowski, Joseph M and Li, Ping and Estrada, Jose L and Tector, Matthew and Joseph Tector, A
Transplantation, ISSN 0041-1337, 2016, Volume 100, Issue 3, pp. 571 - 576
Background. A profound thrombocytopenia limits hepatic xenotransplantation in the pig-to-primate model. Porcine livers also have shown the ability to... 
UNITED-STATES | SURVIVAL | SURGERY | XENOTRANSPLANTATION | ACTIVATION | ACID | BABOONS | PHAGOCYTOSIS IN-VITRO | SEPSIS | IMMUNOLOGY | TRANSPLANTATION | DEFICIENT | COAGULATION | Mixed Function Oxygenases - deficiency | Platelet Adhesiveness | Asialoglycoprotein Receptor - deficiency | Blood Platelets - immunology | Humans | Antigens, Heterophile - immunology | Antigens, Heterophile - metabolism | Galactosyltransferases - genetics | Galactosyltransferases - immunology | Liver - immunology | Heterografts | Time Factors | Swine | Galactosyltransferases - deficiency | Asialoglycoprotein Receptor - genetics | Animals, Genetically Modified | Graft Rejection - prevention & control | Liver - metabolism | Thrombocytopenia - immunology | Cells, Cultured | Antibodies, Heterophile - metabolism | Graft Survival | Antibodies, Heterophile - immunology | Mixed Function Oxygenases - immunology | Thrombocytopenia - blood | Thrombocytopenia - metabolism | Animals | Blood Platelets - metabolism | Thrombocytopenia - prevention & control | Graft Rejection - immunology | Asialoglycoprotein Receptor - immunology | Mixed Function Oxygenases - genetics | Phagocytosis
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4. Full Text Immune Responses of HLA Highly Sensitized and Nonsensitized Patients to Genetically Engineered Pig Cells
by Zhang, Zhongqiang and Hara, Hidetaka and Long, Cassandra and Iwase, Hayato and Qi, Haizhi and Macedo, Camila and Mangiola, Massimo and Zeevi, Adriana and Ezzelarab, Mohamed and Ayares, David and Cooper, David K C and Wijkstrom, Martin
Transplantation, ISSN 0041-1337, 05/2018, Volume 102, Issue 5, pp. e195 - e204
BACKGROUNDWe investigated in vitro whether HLA highly sensitized patients with end-stage renal disease will be disadvantaged immunologically after a... 
SURGERY | SWINE LEUKOCYTE ANTIGENS | N-GLYCOLYLNEURAMINIC ACID | IMMUNOLOGY | TRANSPLANTATION | XENOGRAFT SURVIVAL | POSITIVE CROSS-MATCH | CLASS-I ANTIBODIES | HEART-TRANSPLANTATION | KIDNEY-TRANSPLANTATION | REGULATORY T-CELLS | HEMODIALYSIS-PATIENTS | STAGE RENAL-DISEASE | Membrane Cofactor Protein - deficiency | Mixed Function Oxygenases - deficiency | Humans | Galactosyltransferases - genetics | Kidney Transplantation - methods | Case-Control Studies | Galactosyltransferases - immunology | Isoantibodies - blood | Heterografts | Galactosyltransferases - deficiency | Kidney Failure, Chronic - immunology | Kidney Failure, Chronic - diagnosis | Kidney Failure, Chronic - surgery | Animals, Genetically Modified | Lymphocyte Activation | Graft Rejection - prevention & control | Cells, Cultured | HLA Antigens - immunology | Mixed Function Oxygenases - immunology | HLA Antigens - blood | Animals | B-Lymphocytes - immunology | Kidney Failure, Chronic - blood | Isoantibodies - immunology | Immunologic Memory | Membrane Cofactor Protein - genetics | T-Lymphocytes - immunology | Graft Rejection - immunology | Graft Rejection - genetics | Mixed Function Oxygenases - genetics | Sus scrofa | Membrane Cofactor Protein - immunology | Kidney Transplantation - adverse effects
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5. Full Text Immunogenicity of renal microvascular endothelial cells from genetically modified pigs
by Wang, Zheng-Yu and Li, Ping and Butler, James R and Blankenship, Ross L and Downey, Susan M and Montgomery, Jessica B and Nagai, Shunji and Estrada, Jose L and Tector, Matthew F and Joseph Tector, A
Transplantation, ISSN 0041-1337, 2016, Volume 100, Issue 3, pp. 533 - 537
Background. Disrupting the porcine GGTA1 and CMAH genes [double knockout (DKO)] that produce the gal-a(1,3)-gal and N-glycolylneuraminic acid xenoantigens... 
SURVIVAL | SURGERY | XENOTRANSPLANTATION | HLA-SPECIFIC ANTIBODIES | BARRIER | N-GLYCOLYLNEURAMINIC ACID | ANTIGENS | IMMUNOLOGY | TRANSPLANTATION | IN-VITRO | REJECTION | EXPRESSION | BINDING | Mixed Function Oxygenases - deficiency | Kidney - blood supply | Humans | Antigens, Heterophile - immunology | Microvessels - metabolism | Antigens, Heterophile - metabolism | Galactosyltransferases - genetics | Immunoglobulin M - immunology | Microvessels - immunology | Galactosyltransferases - immunology | Immunoglobulin M - metabolism | Transfection | Immunoglobulin G - immunology | Swine | N-Acetylgalactosaminyltransferases - genetics | Galactosyltransferases - deficiency | Microvessels - cytology | N-Acetylgalactosaminyltransferases - deficiency | Animals, Genetically Modified | Endothelial Cells - metabolism | Cells, Cultured | Graft Survival | Gene Knockout Techniques | Mixed Function Oxygenases - immunology | Endothelial Cells - immunology | Phenotype | Animals | N-Acetylgalactosaminyltransferases - immunology | Mixed Function Oxygenases - genetics | Immunoglobulin G - metabolism
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6. Full Text Biochemical, Cellular, Physiological, and Pathological Consequences of Human Loss of N‐Glycolylneuraminic Acid
by Okerblom, Jonathan and Varki, Ajit
ChemBioChem, ISSN 1439-4227, 07/2017, Volume 18, Issue 13, pp. 1155 - 1171
About 2–3 million years ago, Alu‐mediated deletion of a critical exon in the CMAH gene became fixed in the hominin lineage ancestral to humans, possibly... 
diseases | Homo sapiens | sialic acids | evolution | CMAH | CHEMISTRY, MEDICINAL | DEAMINATED NEURAMINIC ACID | BIOCHEMISTRY & MOLECULAR BIOLOGY | HUMAN XENO-AUTOANTIBODIES | NONHUMAN SIALIC-ACID | 1ST 2 STEPS | BIFUNCTIONAL ENZYME CATALYZES | HANGANUTZIU-DEICHER ANTIGEN | VERTEBRATE AMINO-SUGARS | ACYL SIDE-CHAIN | ERYTHROCYTE BINDING ANTIGEN | DUCHENNE MUSCULAR-DYSTROPHY | Mixed Function Oxygenases - deficiency | Neoplasms - metabolism | Humans | Hearing Loss - immunology | Autoantibodies - biosynthesis | Muscular Dystrophies - genetics | Hearing Loss - metabolism | Neoplasms - genetics | Muscular Dystrophies - immunology | Neuraminic Acids - immunology | Gene Expression | Disease Susceptibility | Muscular Dystrophies - metabolism | Insulin Resistance | Neuraminic Acids - chemistry | Pan troglodytes | Hearing Loss - pathology | Muscular Dystrophies - pathology | Mixed Function Oxygenases - immunology | Biological Evolution | Hearing Loss - genetics | Animals | Neoplasms - immunology | Neuraminic Acids - metabolism | Mice | Mutation | Genome | Mixed Function Oxygenases - genetics | Neoplasms - pathology | Human evolution | Physiological aspects | Analysis | Chimpanzees | Antibodies | Gene deletion | Inactivation | Muscular dystrophy | Meat | Ethics | Clonal deletion | Primates | Deletion | Immune system | Pathogens | Hunting | Wound healing | Deactivation | Reproductive isolation | Inflammation | Sialic acids | Insulin | Hearing loss | Acids | Healing | Dystrophy | Cancer
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7. Full Text An in silico functional annotation and screening of potential drug targets derived from Leishmania spp. hypothetical proteins identified by immunoproteomics
by Chávez-Fumagalli, Miguel A and Schneider, Mônica S and Lage, Daniela P and Machado-de-Ávila, Ricardo A and Coelho, Eduardo A.F
Experimental Parasitology, ISSN 0014-4894, 05/2017, Volume 176, pp. 66 - 74
Leishmaniasis is a parasitic disease caused by the protozoan of the genus. While no human vaccine is available, drugs such as pentavalent antimonials,... 
Screening | Hypothetical proteins | Drug targets | Bioinformatics tools | Immunoproteomics | Leishmania spp | PROTECTION | DONOVANI | SUBCELLULAR-LOCALIZATION | CLASSIFICATION | PREDICTION | TRYPAREDOXIN PEROXIDASE | SERODIAGNOSIS | VISCERAL LEISHMANIASIS | PARASITOLOGY | PROTEOMICS | CHAGASI | Amino Acid Sequence | Computational Biology - methods | Models, Structural | Leishmania infantum - chemistry | Humans | Molecular Conformation | Mixed Function Oxygenases - chemistry | Protozoan Proteins - drug effects | Calpain - drug effects | Calpain - chemistry | Mixed Function Oxygenases - immunology | Drug Delivery Systems | Leishmaniasis, Visceral - drug therapy | Animals | Leishmania infantum - drug effects | Leishmania infantum - immunology | Calpain - immunology | Protozoan Proteins - chemistry | ROC Curve | Proteomics - methods | Mixed Function Oxygenases - drug effects | Protozoan Proteins - immunology | Viral antibodies | Amphotericin B | Analysis | Antibodies | Antiparasitic agents | Calpain | Leishmaniasis | Membrane proteins | Drugs | Index Medicus
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8. Full Text RELATIVE CONTRIBUTIONS OF THE FIVE MAJOR HUMAN CYTOCHROMES P450, 1A2, 2C9, 2C19, 2D6, AND 3A4, TO THE HEPATIC METABOLISM OF THE PROTEASOME INHIBITOR BORTEZOMIB
by Vinita Uttamsingh and Chuang Lu and Gerald Miwa and Liang-Shang Gan
Drug Metabolism and Disposition, ISSN 0090-9556, 11/2005, Volume 33, Issue 11, pp. 1723 - 1728
VELCADE (bortezomib, PS-341), reversibly inhibits the 20S proteasome and exhibits cytotoxic and antitumor activities. Pretreatment of cancer cells with... 
BORONIC ACIDS | CLEARANCE | IN-VITRO | AMITRIPTYLINE | VELCADE(TM) | POPULATIONS | PHARMACOLOGY & PHARMACY | HUMAN LIVER-MICROSOMES | POLYMORPHISM | MONOCLONAL-ANTIBODIES | IDENTIFICATION | Cytochrome P-450 CYP2C9 | Cytochrome P-450 CYP2D6 Inhibitors | Boronic Acids - metabolism | Cytochrome P-450 Enzyme Inhibitors | Cytochrome P-450 CYP3A | Humans | Microsomes, Liver - metabolism | Cytochrome P-450 Enzyme System - metabolism | Mixed Function Oxygenases - metabolism | Pyrazines - metabolism | Cytochrome P-450 Enzyme System - immunology | Cytochrome P-450 CYP1A2 Inhibitors | Recombinant Proteins - metabolism | Aryl Hydrocarbon Hydroxylases - antagonists & inhibitors | Aryl Hydrocarbon Hydroxylases - immunology | Cytochrome P-450 CYP1A2 - immunology | Bortezomib | Antibodies, Monoclonal - pharmacology | Enzyme Inhibitors - pharmacology | Protease Inhibitors - metabolism | Mixed Function Oxygenases - antagonists & inhibitors | Cytochrome P-450 CYP2D6 - immunology | Cytochrome P-450 CYP1A2 - metabolism | Mixed Function Oxygenases - immunology | Aryl Hydrocarbon Hydroxylases - metabolism | Cytochrome P-450 CYP2C19 | Cytochrome P-450 CYP2D6 - metabolism | Kinetics
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9. Full Text Modifying the sugar icing on the transplantation cake
by Cooper, David K. C
Glycobiology, ISSN 0959-6658, 06/2016, Volume 26, Issue 6, pp. 571 - 581
As a transplant surgeon, my interest in glycobiology began through my research into ABO-incompatible allotransplantation, and grew when my goal became... 
N-glycolylneuraminic acid | xenotransplantation | β(1,4)N-acetylgalactosaminyltransferase | ABO-incompatibility | galactose-α(1,3)-galactose | glycobiology | pig | PORCINE HEMATOPOIETIC-CELLS | ANTI-GAL ANTIBODIES | KIDNEY PK15 CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICALLY-ENGINEERED PIGS | NATURAL ANTIBODIES | GENE-KNOCKOUT PIGS | ALPHA-GALACTOSYL EPITOPES | beta(1,4)N-acetylgalactosaminyltransferase | galactose-alpha(1,3)-galactose | HEART-TRANSPLANTATION | DISSEMINATED INTRAVASCULAR COAGULATION | Galactosyltransferases - deficiency | Gene Expression | Animals, Genetically Modified | Graft Rejection - prevention & control | Humans | Graft Survival | Galactosyltransferases - genetics | Galactosyltransferases - immunology | Mixed Function Oxygenases - immunology | Transplantation, Homologous | Transplantation, Heterologous - methods | Papio | Animals | Immunoglobulin G - biosynthesis | Swine | Gene Deletion | Antigens - biosynthesis | Antigens - immunology | Organ Transplantation - methods | Mixed Function Oxygenases - genetics | Mixed Function Oxygenases - drug effects | Immunoglobulin M - biosynthesis | Special Issue - Translational Glycobiology
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10. Metabolic-epigenetic crosstalk in macrophage activation
by Baardman, Jeroen and Licht, Iris and De Winther, Menno P.J and Van Den Bossche, Jan
Epigenomics, ISSN 1750-1911, 10/2015, Volume 7, Issue 7, pp. 1155 - 1164
Epigenetic enzymes are emerging as crucial controllers of macrophages, innate immune cells that determine the outcome of many inflammatory diseases. Recent... 
macrophages | metabolism | histone acetylation and methylation | inflammation | chromatin-modifying enzymes | epigenetics | HISTONE DEACETYLASE 3 | METHYLATION | ACETYLATION | DEPENDENT GENE-EXPRESSION | DEMETHYLASES | INHIBITION | DNA | GENETICS & HEREDITY | POLARIZATION | REQUIREMENT | Chromatin - metabolism | Epigenesis, Genetic | Humans | Intracellular Signaling Peptides and Proteins - immunology | Mixed Function Oxygenases - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | Histone Deacetylases - immunology | Glycolysis - drug effects | Isoenzymes - immunology | Glycolysis - genetics | Oxidative Phosphorylation - drug effects | Interleukin-4 - pharmacology | Isoenzymes - metabolism | Proto-Oncogene Proteins - immunology | Protein-Arginine N-Methyltransferases - genetics | Acetylation | Ketoglutaric Acids - metabolism | Chromatin - drug effects | Intracellular Signaling Peptides and Proteins - genetics | Macrophages - immunology | NAD - metabolism | Repressor Proteins - metabolism | Chromatin - chemistry | Proto-Oncogene Proteins - metabolism | Protein-Arginine N-Methyltransferases - immunology | Histone Deacetylases - genetics | Isoenzymes - genetics | Repressor Proteins - genetics | Histone Deacetylases - metabolism | Proto-Oncogene Proteins - genetics | Immunity, Innate | Acetyl Coenzyme A - metabolism | Mixed Function Oxygenases - immunology | Polyamines - metabolism | Protein-Arginine N-Methyltransferases - metabolism | Macrophages - metabolism | Histones - genetics | Repressor Proteins - immunology | Lipopolysaccharides - pharmacology | Macrophages - drug effects | Histones - metabolism | Macrophage Activation - drug effects | Mixed Function Oxygenases - genetics | Interferon-gamma - pharmacology | S-Adenosylmethionine - metabolism
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11. Full Text Myeloid hypoxia-inducible factor 1α prevents airway allergy in mice through macrophage-mediated immunoregulation
by Toussaint, M and Fievez, L and Drion, P.-V and Cataldo, D and Bureau, F and Lekeux, P and Desmet, C.J
Mucosal Immunology, ISSN 1933-0219, 05/2013, Volume 6, Issue 3, pp. 485 - 497
Hypoxia-inducible factor (HIF) has important roles in promoting pro-inflammatory and bactericidal functions in myeloid cells. Conditional genetic ablation of... 
DUST MITE ALLERGEN | DEPENDENT INDUCTION | ACTIVATION | DENDRITIC CELLS | INFLAMMATION | LUNG INTERSTITIAL MACROPHAGES | ALVEOLAR MACROPHAGES | ASTHMA | HIF-1-ALPHA | IMMUNOLOGY | RECEPTOR 4 | Dendritic Cells - immunology | Mice, Inbred C57BL | Antigen Presentation - genetics | Mixed Function Oxygenases - metabolism | Signal Transduction - genetics | Respiratory Hypersensitivity - immunology | Mixed Function Oxygenases - immunology | Mice, Knockout | Antigens, Dermatophagoides - immunology | Organ Specificity - genetics | Immunosuppression | Animals | Myeloid Cells - immunology | T-Lymphocytes, Helper-Inducer - immunology | Interleukin-10 - metabolism | Female | Mice | Mixed Function Oxygenases - genetics | Interleukin-10 - immunology | Myeloid Differentiation Factor 88 - metabolism | Macrophages, Alveolar - immunology | Disease Models, Animal | Pyroglyphidae - immunology
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12. Full Text Modified glycan models of pig-to-human xenotransplantation do not enhance the human-anti-pig T cell response
by Butler, James R and Wang, Zheng-Yu and Martens, Gregory R and Ladowski, Joseph M and Li, Ping and Tector, Matthew and Tector, A. Joseph
Transplant Immunology, ISSN 0966-3274, 2016, Volume 35, pp. 47 - 51
Abstract Genetically modified porcine models of pig-to-human xenotransplantation offer the most immediate answer to a growing shortage of available solid... 
Allergy and Immunology | Sialic acid | Cellular responses | Xenotransplantation | T cell | Glycan | Animals, Genetically Modified | Coculture Techniques | Humans | Polysaccharides - genetics | Organ Transplantation | Galactosyltransferases - genetics | Polysaccharides - immunology | Galactosyltransferases - immunology | Mixed Function Oxygenases - immunology | Models, Immunological | Animals | Heterografts | Lymphocytes - immunology | Swine | CRISPR-Cas Systems | Mixed Function Oxygenases - genetics | Genetically modified animals | Analysis | Immunotherapy | Transplantation of organs, tissues, etc | Models | T cells
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13. Full Text The fate of human platelets exposed to porcine renal endothelium: a single-pass model of platelet uptake in domestic and genetically modified porcine organs
by Butler, James R., MD and Martens, Gregory R., MD and Li, Ping, PhD and Wang, Zheng-Yu, MD, PhD and Estrada, Jose L., PhD, DVM and Ladowski, Joseph M., MA and Tector, Matt, PhD and Tector, A. Joseph, MD, PhD
Journal of Surgical Research, ISSN 0022-4804, 2016, Volume 200, Issue 2, pp. 698 - 706
Abstract Background Thrombocytopenia may represent a significant challenge to the clinical application of solid-organ xenotransplantation. When studied in a... 
Surgery | Thrombocytopenia | Platelets | Xenotransplantation | Kidney | PIGS | SURGERY | CELLS | ACTIVATION | VON-WILLEBRAND-FACTOR | XENOGRAFT SURVIVAL | BABOON | COAGULATION | EXPRESSION | BINDING | Blood Platelets - immunology | Humans | Kidney - immunology | Postoperative Complications - prevention & control | Galactosyltransferases - genetics | Kidney Transplantation - methods | Galactosyltransferases - immunology | Sus scrofa - genetics | Kidney - metabolism | Liver - immunology | Swine | Thrombocytopenia - etiology | Animals, Genetically Modified | Endothelial Cells - metabolism | Liver - metabolism | Endothelium - immunology | Random Allocation | Gene Knockout Techniques | Mixed Function Oxygenases - immunology | Transplantation, Heterologous - methods | Endothelial Cells - immunology | Animals | Endothelium - metabolism | Blood Platelets - metabolism | Thrombocytopenia - prevention & control | Mixed Function Oxygenases - genetics | Sus scrofa - immunology | Genetic engineering | Analysis | Genetically modified organisms | Endothelium
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