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1. Evolution in health and disease
by Stearns, S. C. 1946- (Stephen C.) and Koella, Jacob C
2008, 2nd ed., Oxford biology, ISBN 9780199207459, xxi, 374
Disease | Health | Medical genetics | Human evolution | Causes and theories of causation | Diseases | Evolution, Molecular | Genetics and Genomics | Evolutionary Biology | Disease Ecology and Epidemiology | Reproduction | Vaccination risks | Spontaneous abortion | Human genetic variation | Virulence | Antibiotic resistance | Autoimmune disease | Human history | Evolutionary conflicts | Cancer
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2. Evolution in health and disease
by Stearns, S. C. 1946- (Stephen C.) and Koella, Jacob C
2008, 2nd ed., Oxford biology, ISBN 9780199207459, xxi, 374
Disease | Health | Medical genetics | Human evolution | Causes and theories of causation | Diseases | Evolution, Molecular | Genetics and Genomics | Evolutionary Biology | Disease Ecology and Epidemiology | Reproduction | Vaccination risks | Spontaneous abortion | Human genetic variation | Virulence | Antibiotic resistance | Autoimmune disease | Human history | Evolutionary conflicts | Cancer
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3. Full Text Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion
by Pereza, Nina, M.D., Ph.D and Ostojić, Saša, M.D., Ph.D and Kapović, Miljenko, M.D., Ph.D and Peterlin, Borut, M.D., Ph.D
Fertility and sterility, ISSN 0015-0282, 2016, Volume 107, Issue 1, pp. 150 - 159.e2
Internal Medicine | Obstetrics and Gynecology | meta-analysis | Candidate gene | miscarriage | genetic polymorphism | evidence-based medicine | Life Sciences & Biomedicine | Obstetrics & Gynecology | Reproductive Biology | Science & Technology | Pregnancy | Genetic Predisposition to Disease | Phenotype | Genetic Association Studies | Risk Assessment | Abortion, Habitual - diagnosis | Humans | Risk Factors | Abortion, Habitual - genetics | Female | Case-Control Studies | Genetic research | Miscarriage | Abortion | Analysis | Medical genetics | Genes | Physiological aspects | Genetic polymorphisms | Index Medicus
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4. Full Text The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion
by Pereza, Nina and Ostojić, Saša and Smirčić, Anamarija and Hodžić, Alenka and Kapović, Miljenko and Peterlin, Borut
Journal of assisted reproduction and genetics, ISSN 1058-0468, 12/2015, Volume 32, Issue 12, pp. 1789 - 1794
Human Genetics | Pregnancy | Medicine & Public Health | Vascular endothelial growth factor A | Gynecology | Genetic polymorphism | Recurrent spontaneous abortion | Reproductive Medicine | Genetics & Heredity | Life Sciences & Biomedicine | Obstetrics & Gynecology | Reproductive Biology | Science & Technology | Genetic Association Studies | Humans | Abortion, Habitual - genetics | Female | Genotype | Male | Slovenia | Vascular Endothelial Growth Factor A - genetics | Case-Control Studies | INDEL Mutation | Polymorphism, Genetic | Endothelial growth factors | Genes | Medical genetics | Genetic research | Genetic aspects | Miscarriage | Gene expression | Abortion | Genetic polymorphisms | Index Medicus | Genetics
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5. Full Text MicroRNA-16 inhibits feto-maternal angiogenesis and causes recurrent spontaneous abortion by targeting vascular endothelial growth factor
by Zhu, Yongsheng and Lu, Hong and Huo, Zhenghao and Ma, Zhanbin and Dang, Jie and Dang, Wei and Pan, Lin and Chen, Jing and Zhong, Huijun
Scientific reports, ISSN 2045-2322, 10/2016, Volume 6, Issue 1, pp. 35536 - 35536
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Cell Proliferation - genetics | Human Umbilical Vein Endothelial Cells - metabolism | Neovascularization, Physiologic - genetics | Humans | Mice, Inbred C57BL | 3' Untranslated Regions - genetics | MicroRNAs - metabolism | Decidua - pathology | Vascular Endothelial Growth Factor A - metabolism | Vascular Endothelial Growth Factor A - genetics | Cell Movement - genetics | Down-Regulation - genetics | Decidua - metabolism | Pregnancy | Animals | Base Sequence | Abortion, Habitual - genetics | Adult | Female | MicroRNAs - genetics | Placentation - genetics | Cell proliferation | Leukocyte migration | Pathogenesis | Decidua | Abortion | Angiogenesis | Placenta | 3' Untranslated regions | miRNA | Microvasculature | Vascular endothelial growth factor | Umbilical vein | Cell migration | Index Medicus
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6. Full Text Defining the role of FMR1 gene in unexplained recurrent spontaneous abortion
by Dean, Deepika Delsa and Agarwal, Sarita and Muthuswamy, Srinivasan
Journal of assisted reproduction and genetics, ISSN 1058-0468, 11/2019, Volume 36, Issue 11, pp. 2245 - 2250
Human Genetics | Molecular diagnosis | Medicine & Public Health | Gynecology | CGG repeats | Fragile X syndrome | Unexplained recurrent miscarriages | Reproductive Medicine | Genetics & Heredity | Life Sciences & Biomedicine | Obstetrics & Gynecology | Reproductive Biology | Science & Technology | Fragile X Syndrome - genetics | Prospective Studies | Humans | Mutation - genetics | Trinucleotide Repeats - genetics | Case-Control Studies | Pregnancy | Abortion, Habitual - genetics | Alleles | Primary Ovarian Insufficiency - genetics | Trinucleotide Repeat Expansion - genetics | Adult | Female | Heterozygote | Fragile X Mental Retardation Protein - genetics | Miscarriage | Fragile X mental retardation protein | Index Medicus | Genetics
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7. Full Text Analysis of genes coding for CD46, CD55, and C4b‐binding protein in patients with idiopathic, recurrent, spontaneous pregnancy loss
by Mohlin, Frida C and Mercier, Eric and Fremeaux‐Bacchi, Veronique and Liszewski, M. Kathryn and Atkinson, John P and Gris, Jean‐Christophe and Blom, Anna M
European journal of immunology, ISSN 0014-2980, 06/2013, Volume 43, Issue 6, pp. 1617 - 1629
Reproductive immunology | Complement system | Mutation | Complement inhibitor | Life Sciences & Biomedicine | Immunology | Science & Technology | Humans | Abortion, Habitual - immunology | CD55 Antigens - genetics | Mutation - genetics | Polymorphism, Genetic | Pregnancy | DNA Mutational Analysis | Abortion, Habitual - genetics | Complement C4b-Binding Protein - genetics | Fibrinogen - metabolism | Adult | Female | Membrane Cofactor Protein - genetics | Relapse | Pregnant women | Analysis | Genes | Genetic research | Protein binding | Diseases | Proteins | Medical research | Miscarriage | Index Medicus | mutation | complement inhibitor | reproductive immunology | complement system | Basic Medicine | Immunologi inom det medicinska området | Medical and Health Sciences | Medicin och hälsovetenskap | Immunology in the medical area | Medicinska och farmaceutiska grundvetenskaper
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8. Full Text Methylation status of imprinted genes DLK1-GTL2 , MEST ( PEG1 ), ZAC ( PLAGL1 ), and  LINE-1 elements in spermatozoa of normozoospermic men, unlike H19 imprinting control regions, is not associated with idiopathic recurrent spontaneous miscarriages
by Ankolkar, Mandar, M.Sc and Salvi, Vinita, M.D and Warke, Himangi, M.D and Vundinti, Babu Rao, Ph.D and Balasinor, N.H., Ph.D
Fertility and sterility, ISSN 0015-0282, 2013, Volume 99, Issue 6, pp. 1668 - 1673.e2
Internal Medicine | Obstetrics and Gynecology | normozoospermic | imprinting | IG-DMR | Recurrent spontaneous miscarriage | PLAGL1 | DNA methylation | MEST | Life Sciences & Biomedicine | Obstetrics & Gynecology | Reproductive Biology | Science & Technology | Abortion, Habitual - epidemiology | Humans | Long Interspersed Nucleotide Elements - genetics | Male | Abortion, Habitual - metabolism | Case-Control Studies | Intercellular Signaling Peptides and Proteins - metabolism | Tumor Suppressor Proteins - genetics | Abortion, Habitual - genetics | Cell Cycle Proteins - genetics | Female | Membrane Proteins - metabolism | Tumor Suppressor Proteins - metabolism | Membrane Proteins - genetics | Cell Cycle Proteins - metabolism | Intercellular Signaling Peptides and Proteins - genetics | DNA Methylation - genetics | RNA, Long Noncoding - genetics | Transcription Factors - genetics | Genomic Imprinting - genetics | Pregnancy | Proteins - genetics | Transcription Factors - metabolism | Proteins - metabolism | Genetic Markers - genetics | Spermatozoa - physiology | RNA, Long Noncoding - metabolism | Index Medicus
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9. Full Text Association of kinase insert domain-containing receptor ( KDR ) gene polymorphisms with idiopathic recurrent spontaneous abortion in Korean women
by Rah, HyungChul, D.V.M., Ph.D and Jeon, Young Joo, M.S and Lee, Bo Eun, B.S and Choi, Dong Hee, M.D., Ph.D and Yoon, Tae Ki, M.D., Ph.D and Lee, Woo Sik, M.D., Ph.D and Kim, Nam Keun, Ph.D
Fertility and sterility, ISSN 0015-0282, 2013, Volume 99, Issue 3, pp. 753 - 760.e8
Internal Medicine | Obstetrics and Gynecology | KDR | RSA | kinase insert domain-containing receptor | polymorphism | Recurrent spontaneous abortion | Life Sciences & Biomedicine | Obstetrics & Gynecology | Reproductive Biology | Science & Technology | Haplotypes | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Risk Factors | Asian Continental Ancestry Group - genetics | Abortion, Habitual - ethnology | Protein Structure, Tertiary - genetics | Case-Control Studies | Polymorphism, Genetic | Vascular Endothelial Growth Factor Receptor-2 - genetics | Pregnancy | Young Adult | Vascular Endothelial Growth Factor Receptor-2 - chemistry | Abortion, Habitual - genetics | Adult | Female | Genetic Predisposition to Disease - ethnology | Asian Continental Ancestry Group - statistics & numerical data | Genetic research | Genetic aspects | Miscarriage | Abortion | Genes | Risk factors | Index Medicus
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10. Full Text C677T polymorphism increases the risk of early spontaneous abortion
by Liu, Yongjie and Zhang, Fan and Dai, Liang
Journal of assisted reproduction and genetics, ISSN 1058-0468, 8/2019, Volume 36, Issue 8, pp. 1737 - 1741
Human Genetics | Medicine & Public Health | Early spontaneous abortion | Gynecology | Male | MTHFR C677T polymorphism | Reproductive Medicine | Genetics & Heredity | Life Sciences & Biomedicine | Obstetrics & Gynecology | Reproductive Biology | Science & Technology | Abortion, Spontaneous - pathology | Genetic Predisposition to Disease | Humans | Risk Factors | Genotype | Case-Control Studies | Pregnancy | Young Adult | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Abortion, Spontaneous - etiology | Adult | Female | Polymorphism, Single Nucleotide | Genetic aspects | Miscarriage | Methylation | Abortion | Chromatography | Genetic polymorphisms | Nanoparticles | Phenotypes | Sperm | Semen | Alleles | DNA methylation | Methylenetetrahydrofolate reductase | Males | Gene polymorphism | Deoxyribonucleic acid--DNA | Polymorphism | Index Medicus | Genetics
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11. Full Text Comparative Genomic Hybridization–Array Analysis Enhances the Detection of Aneuploidies and Submicroscopic Imbalances in Spontaneous Miscarriages
by Schaeffer, Anthony J and Chung, June and Heretis, Konstantina and Wong, Andrew and Ledbetter, David H and Lese Martin, Christa
American journal of human genetics, ISSN 0002-9297, 2004, Volume 74, Issue 6, pp. 1168 - 1174
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Biological and medical sciences | Medical sciences | Chromosome aberrations | Medical genetics | Nucleic Acid Hybridization | Trisomy | Chromosome Banding | Abortion, Spontaneous - genetics | Oligonucleotide Array Sequence Analysis | Chromosomes, Human - genetics | Humans | Prenatal Diagnosis | Aneuploidy | In Situ Hybridization, Fluorescence | Gene Dosage | Pregnancy | Karyotyping | Chromosome Aberrations | Female | Retrospective Studies | Human genetics | Research | Index Medicus
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