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1
المؤلفون: Maria Pia Foschini, Riccardo Masetti, Luca Morandi, Enrico Di Oto, Maria C. Cucchi, Giovanni Battista Biserni, Zsuzsanna Varga
المساهمون: Di Oto, Enrico, Biserni, Giovanni B., Varga, Zsuzsanna, Morandi, Luca, Cucchi, Maria C., Masetti, Riccardo, Foschini, Maria P., University of Zurich, Foschini, Maria P
مصطلحات موضوعية: 0301 basic medicine, Male, Settore MED/18 - CHIRURGIA GENERALE, Androgen, 1307 Cell Biology, X chromosome, 0302 clinical medicine, Genes, X-Linked, Ductal, Receptors, 80 and over, Breast, skin and connective tissue diseases, Sex Chromosome Aberrations, Aged, 80 and over, medicine.diagnostic_test, Carcinoma, Ductal, Breast, General Medicine, Middle Aged, Androgen receptor, Gynecomastia, Receptors, Androgen, 030220 oncology & carcinogenesis, Male breast cancer, Human, Adult, Sex Chromosome Aberration, Invasive ductal carcinoma, Breast Neoplasms, 610 Medicine & health, Biology, Chromosomes, Pathology and Forensic Medicine, Breast Neoplasms, Male, 03 medical and health sciences, FISH, 10049 Institute of Pathology and Molecular Pathology, 1312 Molecular Biology, medicine, Humans, Neoplastic transformation, Genetic marker, Molecular Biology, Aged, Polysomy, Chromosomes, Human, X, Carcinoma, Gene Amplification, Cancer, Cell Biology, X-Linked, medicine.disease, 2734 Pathology and Forensic Medicine, 030104 developmental biology, Genes, Cancer research, Fluorescence in situ hybridization
وصف الملف: STAMPA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7e9709423d6f8ef50672b815002144a
http://hdl.handle.net/11585/673441 -
2
المؤلفون: Rohan, Sharma, Valerie M, Harris, Joshua, Cavett, Biji T, Kurien, Ke, Liu, Kristi A, Koelsch, Anum, Fayaaz, Kaustubh S, Chaudhari, Lida, Radfar, David, Lewis, Donald U, Stone, C Erick, Kaufman, Shibo, Li, Barbara, Segal, Daniel J, Wallace, Michael H, Weisman, Swamy, Venuturupalli, Jennifer A, Kelly, Bernardo, Pons-Estel, Roland, Jonsson, Xianglan, Lu, Jacques-Eric, Gottenberg, Juan-Manuel, Anaya, Deborah S, Cunninghame-Graham, Andrew J W, Huang, Michael T, Brennan, Pamela, Hughes, Ilias, Alevizos, Corinne, Miceli-Richard, Edward C, Keystone, Vivian P, Bykerk, Gideon, Hirschfield, Gunnel, Nordmark, Sara Magnusson, Bucher, Per, Eriksson, Roald, Omdal, Nelson L, Rhodus, Maureen, Rischmueller, Michael, Rohrer, Marie, Wahren-Herlenius, Torsten, Witte, Marta, Alarcón-Riquelme, Xavier, Mariette, Christopher J, Lessard, John B, Harley, Wan-Fai, Ng, Astrid, Rasmussen, Kathy L, Sivils, R Hal, Scofield
المصدر: Arthritis Rheumatol
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosarioمصطلحات موضوعية: Gene dosage, Bayes theorem, Turner syndrome, Karyotype 46, Karyotype, Sex Chromosome Disorders of Sex Development, Gene Dosage, Turner Syndrome, Trisomy, Major clinical study, XX, Polymorphism, Single Nucleotide, Chromosome mosaicism, Chromosomes, Article, X chromosome, Systemic lupus erythematosus, Genetics, Lupus Erythematosus, Systemic, Humans, Polymorphism, Alleles, Sex Chromosome Aberrations, Priority journal, Allele, Chromosomes, Human, X, Epilepsy, Mosaicism, X chromosome aberration, Bayes Theorem, Single Nucleotide, Thyroid disease, Single nucleotide polymorphism, Oligomenorrhea, Sjogren's Syndrome, Statistics and numerical data, Karyotyping, Sex chromosome aberration, Female, Cohort analysis, Controlled study, Sjoegren syndrome, Human
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::08e215409e94379e8724aa01011e4474
https://europepmc.org/articles/PMC8262088/ -
3
المؤلفون: Monica Miozzo, Mauro Podda, Francesca Donato, Annarosa Floreani, Lisa Caliari, Roberta Lazzari, Sabine Oertelt-Prigione, Ana Lleo, Palma Finelli, Ilaria Bianchi, Pietro Invernizzi, Massimo Colombo, M. Eric Gershwin
المساهمون: Lleo, A, Oertelt Prigione, S, Bianchi, I, Caliari, L, Finelli, P, Miozzo, M, Lazzari, R, Floreani, A, Donato, F, Colombo, M, Gershwin, M, Podda, M, Invernizzi, P
المصدر: Journal of Autoimmunity. 41:87-91
مصطلحات موضوعية: Adult, Male, Sex Chromosome Aberration, Aging, Immunology, Population, Autoimmunity, Haploinsufficiency, Sex Factor, Biology, Y chromosome, medicine.disease_cause, Autoimmune Disease, Autoimmune Diseases, Sex Factors, Primary biliary cirrhosis, Primary biliary cirrosis, medicine, Humans, Immunology and Allergy, Age Factor, education, Sex Chromosome Aberrations, In Situ Hybridization, Fluorescence, X chromosome, Autoantibodies, Aged, Aged, 80 and over, Autoimmune disease, Chromosomes, Human, X, education.field_of_study, Chromosomes, Human, Y, Liver Cirrhosis, Biliary, Age Factors, Autoantibody, Middle Aged, medicine.disease, Autoantibodie, Primary biliary cirrosi, Female, Human
وصف الملف: STAMPA
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4
المؤلفون: Liu, Ke, Kurien, Biji T, Zimmerman, Sarah L, Kaufman, Kenneth M, Taft, Diana H, Kottyan, Leah C, Lazaro, Sara, Weaver, Carrie A, Ice, John A, Adler, Adam J, Chodosh, James, Radfar, Lida, Rasmussen, Astrid, Stone, Donald U, Lewis, David M, Li, Shibo, Koelsch, Kristi A, Igoe, Ann, Talsania, Mitali, Kumar, Jay, Maier-Moore, Jacen S, Harris, Valerie M, Gopalakrishnan, Rajaram, Jonsson, Roland, Lessard, James A, Lu, Xianglan, Gottenberg, Jacques-Eric, Anaya, Juan-Manuel, Cunninghame-Graham, Deborah S, Huang, Andrew J W, Brennan, Michael T, Hughes, Pamela, Illei, Gabor G, Miceli-Richard, Corinne, Keystone, Edward C, Bykerk, Vivian P, Hirschfield, Gideon, Xie, Gang, Ng, Wan-Fai, Nordmark, Gunnel, Eriksson, Per, Omdal, Roald, Rhodus, Nelson L, Rischmueller, Maureen, Rohrer, Michael, Segal, Barbara M, Vyse, Timothy J, Wahren-Herlenius, Marie, Witte, Torsten, Pons-Estel, Bernardo, Alarcon-Riquelme, Marta E, Guthridge, Joel M, James, Judith A, Lessard, Christopher J, Kelly, Jennifer A, Thompson, Susan D, Gaffney, Patrick M, Montgomery, Courtney G, Edberg, Jeffrey C, Kimberly, Robert P, Alarcón, Graciela S, Langefeld, Carl L, Gilkeson, Gary S, Kamen, Diane L, Tsao, Betty P, McCune, W Joseph, Salmon, Jane E, Merrill, Joan T, Weisman, Michael H, Wallace, Daniel J, Utset, Tammy O, Bottinger, Erwin P, Amos, Christopher I, Siminovitch, Katherine A, Mariette, Xavier, Sivils, Kathy L, Harley, John B, Scofield, R Hal
المصدر: Liu, K, Kurien, B T, Zimmerman, S L, Kaufman, K M, Taft, D H, Kottyan, L C, Lazaro, S, Weaver, C A, Ice, J A, Adler, A J, Chodosh, J, Radfar, L, Rasmussen, A, Stone, D U, Lewis, D M, Li, S, Koelsch, K A, Igoe, A, Talsania, M, Kumar, J, Maier-Moore, J S, Harris, V M, Gopalakrishnan, R, Jonsson, R, Lessard, J A, Lu, X, Gottenberg, J E, Anaya, J M, Cunninghame-Graham, D S, Huang, A J W, Brennan, M T, Hughes, P, Illei, G G, Miceli-Richard, C, Keystone, E C, Bykerk, V P, Hirschfield, G, Xie, G, Ng, W F, Nordmark, G, Eriksson, P, Omdal, R, Rhodus, N L, Rischmueller, M, Rohrer, M, Segal, B M, Vyse, T J, Wahren-Herlenius, M, Witte, T, Pons-Estel, B, Alarcón-Riquelme, M E, Guthridge, J M, James, J A, Lessard, C J, Kelly, J A, Thompson, S D, Gaffney, P M, Montgomery, C G, Edberg, J C, Kimberly, R P, Alarcón, G S, Langefeld, C L, Gilkeson, G S, Kamen, D L, Tsao, B P, Joseph McCune, W, Salmon, J E, Merrill, J T, Weisman, M H, Wallace, D J, Utset, T O, Bottinger, E P, Amos, C I, Siminovitch, K A, Mariette, X, Sivils, K L, Harley, J B & Hal Scofield, R 2016, ' X Chromosome Dose and Sex Bias in Autoimmune Diseases : Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome ', Arthritis and Rheumatology, vol. 68, no. 5, pp. 1290-1300 . https://doi.org/10.1002/art.39560
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosarioمصطلحات موضوعية: Gene dosage, Liver Cirrhosis, Sarcoidosis, Sex Chromosome Disorders of Sex Development, Case control study, Trisomy, Major clinical study, XXX, Article, Fluorescence, Chromosomes, Autoimmune Diseases, X chromosome, Systemic lupus erythematosus, Rheumatoid, Autoimmune disease, Prevalence, Live birth, Humans, Rheumatoid arthritis, Sex Distribution, Sex Chromosome Aberrations, In Situ Hybridization, Priority journal, Lupus Erythematosus, Fluorescence in situ hybridization, Arthritis, Systemic, Biliary, Quality control, Polymerase chain reaction, Single nucleotide polymorphism, Sjogren's Syndrome, Primary biliary cirrhosis, Sex chromosome aberration, Case-Control Studies, Female, Sex, Karyotype 47, Controlled study, Sex ratio, Human
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::91a8d14a779b1e48419c88bc9d60bd3d
https://kclpure.kcl.ac.uk/en/publications/4c555296-7e94-42ca-a2c8-33338c8b3dbe -
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المؤلفون: Aydemir, Hüseyin, Karkucak, Mutlu, Cimen, Hacı İbrahim, Halis, Fikret, Kumsar, Şükrü, Sonbahar, Adil E.
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi//Tıbbi Genetik Anabilim Dalı., Yakut, Tahsin
مصطلحات موضوعية: Adult, Male, Letter, Blood sampling, Clinical article, Multiplex polymerase chain reaction, Centromere, Karyotype, Research & experimental medicine, Medical ethics, Chromosome analysis, Sex chromosome aberrations, X chromosome, Case report, Genetics, Humans, Deletions, Sex chromosome disorders of sex development, Genetic variation, Medicine, research & experimental, Chromosomes, human, Y, Azoospermia, Male infertility, Chromosome deletion Y, Biotechnology & applied microbiology, Y chromosome, Mosaicism, 45,X/46,XY mosaicism, Disorder of sex development, Genetics & heredity, DNA isolation, Chromosome deletion, Doppler ultrasonography, Phenotype, Echocardiography, Sex chromosome aberration, Y chromosome microdeletion, Semen analysis, Human
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______9458::3fce55adef142a271f6c50ba16431c9f
http://hdl.handle.net/11452/32963 -
6
المؤلفون: Mauro Giacca, Luisa Mestroni
المساهمون: L., Mestroni, Giacca, Mauro
المصدر: eLS
Scopus-Elsevier
CIÊNCIAVITAE
Europe PubMed Centralمصطلحات موضوعية: Cardiomyopathy, Dilated, genetics, X Chromosome, Male, medicine.medical_specialty, genetics, Female, Gene, X Chromosome, Cardiomyopathy, Genetic Linkage, Chromosome Disorders, Disease, Biology, Bioinformatics, Right ventricular cardiomyopathy, Dystrophin, Pathogenesis, Molecular genetics, Dilated, medicine, genetics, Chromosome Aberration, Animals, Cardiomyopathy, genetics, Chromosome Aberrations, genetics, Chromosome Disorders, Chromosome Mapping, Dystrophin, genetics, Female, Genes, Dominant, genetics, Genetic Linkage, genetics, Humans, Male, Molecular Biology, Pedigree, Sex Chromosome Aberrations, Animals, Humans, genetics, Molecular Biology, Sex Chromosome Aberrations, Genes, Dominant, Chromosome Aberrations, Genetics, Genetic heterogeneity, Chromosome Mapping, Autosomal dominant trait, Dilated cardiomyopathy, medicine.disease, Pedigree, Genes, genetics, Humans, Male, Molecular Biology, Pedigree, Sex Chromosome Aberration, Female, Cardiology and Cardiovascular Medicine
وصف الملف: STAMPA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a2dfc5adc16cfa88c74582d2744b102
https://doi.org/10.1097/00001573-199705000-00012 -
7
المؤلفون: Caner, Vildan, Aybek, Hulya, Bagci, Huseyin, Cetin, Gokhan Ozan, Duzcan, Fusun, Aybek, Zafer, Tepeli, Emre
مصطلحات موضوعية: Adult, Male, infertility, male, aneuploidy, hybridization in situ, fluorescence, testis size, Aneuploidy, Chromosomes, Human, Y/*genetics, Humans, Infertility, Male/*genetics, Karyotyping, Oligospermia/genetics, Sex Chromosome Aberrations, male infertility, X chromosome, controlled study, human, sex chromosome aberration, fluorescence in situ hybridization, Infertility, Male, oligospermia, mitosis, clinical article, Chromosomes, Human, Y, Y chromosome, article, karyotyping, chromosome satellite association, priority journal, centromere, spermatozoon count, incidence, Hybridization in situ, fluorescence, somatic cell
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::731c35248c78bb85bad922c04fee785d
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/12042 -
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10دورية أكاديمية
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