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Nature Genetics, ISSN 1061-4036, 12/2012, Volume 44, Issue 12, pp. 1355 - 1359
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 8, pp. e12381 - e12381
Background: KIR2DS5 gene encodes an activating natural killer cell receptor whose ligand is not known. It was recently reported to affect the outcome of... 
NATURAL-KILLER-CELLS | PCR-SSP | KIR | SUSCEPTIBILITY | BIOLOGY | RECEPTOR | POPULATIONS | ANKYLOSING-SPONDYLITIS | STEM-CELL TRANSPLANTATION | HLA-B27 | ENDOMETRIOSIS | Disease - genetics | Endometriosis - genetics | Receptors, KIR - genetics | Spondylitis, Ankylosing - genetics | Gene Frequency | Humans | Middle Aged | Male | Young Adult | Receptors, KIR - metabolism | Aged, 80 and over | Adult | Female | Aged | Graft Rejection - genetics | Medical research | Leukemia | Genes | HLA histocompatibility antigens | Arthritis | Transplantation | Lung cancer, Non-small cell | Hematopoietic stem cells | Rheumatoid factor | Killer cells | Histocompatibility antigens | Medicine, Experimental | Comparative analysis | Reproductive health | Multiplexing | Nephrology | Transplants & implants | Syngeneic grafts | Lung | Lung cancer | Stem cell transplantation | Grafting | Abortion | Confidence intervals | KIR2DS5 gene | Immunology | Classification | Bone marrow | Natural killer cells | Ankylosing spondylitis | Immunoglobulins | Typing | Psoriasis | Spontaneous abortion | Potassium channels (inwardly-rectifying) | Gynecology | Rheumatology | Non-small cell lung carcinoma | Endometriosis | Lung carcinoma | Obstetrics | Hemopoiesis | Graft rejection | Medicine | Rejection | Polymerase chain reaction | Spondylitis | Hospitals | Womens health | Rheumatoid arthritis | Stem cells | Ligands | Histocompatibility antigen HLA | Tissue typing | Kidney transplantation | Tumors | Index Medicus
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 09/2017, Volume 377, Issue 12, pp. 1156 - 1167
Journal Article
by Phelan, Catherine M and Kuchenbaecker, Karoline B and Tyrer, Jonathan P and Kar, Siddhartha P and Lawrenson, Kate and Winham, Stacey J and Dennis, Joe and Pirie, Ailith and Riggan, Marjorie J and Chornokur, Ganna and Earp, Madalene A and Lyra, Paulo C and Lee, Janet M and Coetzee, Simon and Beesley, Jonathan and McGuffog, Lesley and Soucy, Penny and Dicks, Ed and Lee, Anew and Barrowdale, Daniel and Lecarpentier, Julie and Leslie, Goska and Aalfs, Cora M and Aben, Katja K. H and Adams, Marcia and Adlard, Julian and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia and Aravantinos, Gerasimos and Arnold, Norbert and Arun, Banu K and Arver, Brita and Azzollini, Jacopo and Balmaña, Judith and Banerjee, Susana N and Barjhoux, Laure and Barkardottir, Rosa B and Bean, Yukie and Beckmann, Matthias W and Beeghly-Fadiel, Alicia and Benitez, Javier and Bermisheva, Marina and Bernardini, Marcus Q and Birrer, Michael J and Bjorge, Line and Black, Amanda and Blankstein, Kenneth and Blok, Marinus J and Bodelon, Clara and Bogdanova, Natalia and Bojesen, Anders and Bonanni, Bernardo and Borg, Åke and Bradbury, Angela R and Brenton, James D and Brewer, Carole and Brinton, Louise and Broberg, Per and Brooks-Wilson, Angela and Bruinsma, Fiona and Brunet, Joan and Buecher, Bruno and Butzow, Ralf and Buys, Sauna S and Caldes, Trinidad and Caligo, Maria A and Campbell, Ian and Cannioto, Rikki and Carney, Michael E and Cescon, Terence and Chan, Salina B and Chang-Claude, Jenny and Chanock, Stephen and Chen, Xiao Qing and Chiew, Yoke-Eng and Chiquette, Jocelyne and Chung, Wendy K and Claes, Kathleen B. M and Conner, Thomas and Cook, Linda S and Cook, Jackie and Cramer, Daniel W and Cunningham, Julie M and D'Aloisio, Aimee A and Daly, Mary B and Damiola, Francesca and Damirovna, Sakaeva Dina and Dansonka-Mieszkowska, Agnieszka and Dao, Fanny and Davidson, Rosemarie and Defazio, Anna and Delnatte, Capucine and Doheny, Kimberly F and Diez, Orland and Ding, Yuan Chun and Doherty, Jennifer Anne and Domchek, Susan M and Dorfling, Cecilia M and Dörk, Thilo and ... and KConFab Investigators and EMEMBRACE Study and GEMO Study Collaborators and OPAL Study Grp and AOCS Study Grp and HEBON Study and AOCS study group and EMBRACE Study and OPAL study group and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 5, pp. 680 - 691
Journal Article
PLoS Genetics, ISSN 1553-7390, 2014, Volume 10, Issue 6, pp. e1004451 - e1004451
Journal Article
by Santen, Gijs W. E and Aten, Emmelien and Vulto-van Silfhout, Anneke T and Pottinger, Caroline and van Bon, Bregje W. M and van Minderhout, Ivonne J. H. M and Snowdowne, Ronelle and van der Lans, Christian A. C and Boogaard, Merel and Linssen, Margot M. L and Vijfhuizen, Linda and van der Wielen, Michiel J. R and Vollebregt, M. J. Ellen and Breuning, Martijn H and Kriek, Marjolein and van Haeringen, Arie and den Dunnen, Johan T and Hoischen, Alexander and Clayton-Smith, Jill and de Vries, Bert B. A and Hennekam, Raoul C. M and van Belzen, Martine J and Almureikhi, Mariam and Baban, Anwar and Barbosa, Mafalda and Ben-Omran, Tawfeg and Berry, Katherine and Bigoni, Stefania and Boute, Odile and Brueton, Louise and van der Burgt, Ineke and Canham, Natalie and Chandler, Kate E and Chrzanowska, Krystyna and Collins, Amanda L and de Toni, Teresa and Dean, John and den Hollander, Nicolette S and Flore, Leigh Anne and Fryer, Alan and Gardham, Alice and Graham, John M and Harrison, Victoria and Horn, Denise and Jongmans, Marjolijn C and Josifova, gana and Kant, Sarina G and Kapoor, Seema and Kingston, Helen and Kini, Usha and Kleefstra, Tjitske and Krajewska-Walasek, Małgorzata and Kramer, Nancy and Maas, Saskia M and Maciel, Patricia and Mancini, Grazia M. S and Maystadt, Isabelle and McKee, Shane and Milunsky, Jeff M and Nampoothiri, Sheela and Newbury-Ecob, Ruth and Nikkel, Sarah M and Parker, Michael J and Pérez-Jurado, Luis A and Robertson, Stephen P and Rooryck, Caroline and Shears, Debbie and Silengo, Margherita and Singh, Ankur and Smigiel, Robert and Soares, Gabriela and Splitt, Miranda and Stewart, Helen and Sweeney, Elizabeth and Tassabehji, May and Tuysuz, Beyhan and van Eerde, Albertien M and Vincent-Delorme, Catherine and Wilson, Louise C and Yesil, Gozde and Coffin-Siris Consortium and Coffin-Siris consortium and the Coffin-Siris consortium
Human mutation, ISSN 1059-7794, 2013, Volume 34, Issue 11, pp. 1519 - 1528
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2012, Volume 7, Issue 7, pp. e40668 - e40668
Background: Endometriosis is a chronic gynecological benign disease that shares several features similar to malignancy. Mitochondrial DNA (mtDNA) mutations... 
WOMEN | OXIDATIVE STRESS | REGION POLYMORPHISM | INSTABILITY | INCREASED RISK | MULTIDISCIPLINARY SCIENCES | NITRIC-OXIDE | LARGE DELETIONS | CANCER | ASSOCIATION | DNA MUTATIONS | Microsatellite Instability | Endometriosis - genetics | Humans | Genome, Mitochondrial - genetics | Molecular Sequence Data | Mitochondrial Proteins - genetics | Mutation, Missense | Germ-Line Mutation - genetics | Case-Control Studies | Genetic Variation | Haplotypes - genetics | DNA, Mitochondrial - genetics | Mitochondria - genetics | DNA Mutational Analysis | Electron Transport Complex I - genetics | Base Sequence | Gene Deletion | Female | Amino Acid Sequence | Genetic Predisposition to Disease | Computational Biology | Endometriosis - pathology | Mitochondria - metabolism | India | Electron Transport Complex I - chemistry | Mitochondrial Proteins - chemistry | Neoplasm Staging | Codon | Gene mutations | Analysis | Genes | Genomics | Endometriosis | Development and progression | Genetic aspects | Genomes | Mitochondrial DNA | Glycine | Tumors | Index Medicus | Oxidative stress | Disease | Pathogenesis | Serine | Homology | Population studies | Biochemistry | Thyroid gland | Malignancy | Tissue analysis | Microsatellite instability | Leukocytes | Tissues | Ovarian cancer | Mitochondria | Missense mutation | Deoxyribonucleic acid | Aging | Genetics | Bioindicators | Endometrium | Stability | Microsatellites | Health risks | Metabolism | Patients | Superposition (mathematics) | White blood cells | ND5 gene | Mutagenesis | Womens health | Heteroplasmy | DNA | Infertility | Biomarkers | Mutation | Variation
Journal Article
Science, ISSN 0036-8075, 10/2010, Volume 330, Issue 6001, pp. 228 - 231
Journal Article
PloS one, ISSN 1932-6203, 2012, Volume 7, Issue 11, pp. e47374 - e47374
Endometriosis is determined by genetic factors, and the prevalence of genetic polymorphisms varies greatly depending on the ethnic group studied. The objective... 
17-BETA-HYDROXYSTEROID-DEHYDROGENASE 3 | ANDROGEN RECEPTOR | PROTEIN | OVARIAN RESPONSE | MULTIDISCIPLINARY SCIENCES | FOLLICLE-STIMULATING-HORMONE | RISK | AMNIOTIC-FLUID | ASSOCIATION | SINGLE-NUCLEOTIDE POLYMORPHISMS | PHOSPHORYLATION SITES | Estradiol - blood | Gene Frequency - genetics | Phosphorylation | Demography | Endometriosis - genetics | Receptors, FSH - chemistry | Receptors, FSH - genetics | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Molecular Sequence Data | Young Adult | Haplotypes - genetics | Aromatase - genetics | China | Estrogens - genetics | Adult | Female | Amino Acid Sequence | Genetic Predisposition to Disease | Estrogens - biosynthesis | Gene Regulatory Networks - genetics | Endometriosis - surgery | Endometriosis - blood | Risk Factors | Glycosylation | Mutation - genetics | Homozygote | Estradiol Dehydrogenases - genetics | Endometriosis - metabolism | Polymorphism, Single Nucleotide - genetics | Estrogen | Cytochrome P-450 | Endometriosis | Development and progression | Amino acids | Ionization | Analysis | Physiological aspects | Phenols | Genetic aspects | Single nucleotide polymorphisms | Chromosomes | Mass spectrometry | Protein kinases | Cytochrome | Drugs | Dehydrogenases | Laboratories | Estrogens | Genes | AKT protein | Biosynthesis | Single-nucleotide polymorphism | Drug development | Kinases | Proteins | Genotype & phenotype | Aromatase | Genetic factors | Bioinformatics | Enzymes | Gynecology | Health risks | Amino acid sequence | Mass spectroscopy | Ribosomal protein S6 | Metabolism | Obstetrics | Minority & ethnic groups | Mutants | Medicine | Ribosomal protein S6 kinase | Androgens | Hospitals | Acids | Infertility | Endocrinology | Polymorphism | Index Medicus
Journal Article