Temat: "Case-Control Studies" - OpacWWW

Skocz do pozycji: 1.

Tytuł:: Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest China.
Autorzy:: Jin Y; Yunnan Fuwai Cardiovascular Hospital, 528 Shahe Road, 650032, Kunming, Yunnan, China.
Zhao M; Yunnan Fuwai Cardiovascular Hospital, 528 Shahe Road, 650032, Kunming, Yunnan, China.
Guo Q; Yunnan Fuwai Cardiovascular Hospital, 528 Shahe Road, 650032, Kunming, Yunnan, China.
Zhao W; Yunnan Fuwai Cardiovascular Hospital, 528 Shahe Road, 650032, Kunming, Yunnan, China.
Lei M; Yunnan Fuwai Cardiovascular Hospital, 528 Shahe Road, 650032, Kunming, Yunnan, China.
Zhang Y; Yunnan Fuwai Cardiovascular Hospital, 528 Shahe Road, 650032, Kunming, Yunnan, China.
Zhang Y; Yunnan Fuwai Cardiovascular Hospital, 528 Shahe Road, 650032, Kunming, Yunnan, China.
Shen Y; Yunnan Fuwai Cardiovascular Hospital, 528 Shahe Road, 650032, Kunming, Yunnan, China.
Lin K; The Department of Medical Genetics, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 935 Jiao ling Road, 650118, Kunming, Yunnan, China.
Yang Z; The Department of Medical Genetics, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 935 Jiao ling Road, 650118, Kunming, Yunnan, China.
Chu J; The Department of Medical Genetics, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 935 Jiao ling Road, 650118, Kunming, Yunnan, China.
Sun H; The Department of Medical Genetics, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 935 Jiao ling Road, 650118, Kunming, Yunnan, China. .
Luo Z; Yunnan Fuwai Cardiovascular Hospital, 528 Shahe Road, 650032, Kunming, Yunnan, China. .; Pokaż więcej
Źródło:: Italian journal of pediatrics [Ital J Pediatr] 2024 Apr 05; Vol. 50 (1), pp. 62. Date of Electronic Publication: 2024 Apr 05.
Typ publikacji:: Journal Article
MeSH Terms:: Heart Septal Defects, Atrial*/genetics
Polymorphism, Single Nucleotide*
Humans ; Alleles ; Case-Control Studies ; China/epidemiology ; Genetic Predisposition to Disease ; Genotype ; Vascular Endothelial Growth Factor Receptor-3/genetics

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 2.

Tytuł:: MTHFR A1298C polymorphism: a predictor of reduced risk of preeclampsia in Punjab, Pakistan.
Autorzy:: Mahmood S; Department of Biochemistry, Kinnaird College for Women, Lahore, Pakistan.
Younus A; Department of Biochemistry, Kinnaird College for Women, Lahore, Pakistan.
Nathaniel S; Department of Biochemistry, Kinnaird College for Women, Lahore, Pakistan.
Younas H; Department of Biochemistry, Kinnaird College for Women, Lahore, Pakistan.; Pokaż więcej
Źródło:: Hypertension in pregnancy [Hypertens Pregnancy] 2023 Dec; Vol. 42 (1), pp. 2187621.
Typ publikacji:: Journal Article
MeSH Terms:: Methylenetetrahydrofolate Reductase (NADPH2)*/genetics
Polymorphism, Single Nucleotide*
Pre-Eclampsia*/genetics
Female ; Humans ; Pregnancy ; Case-Control Studies ; Genetic Predisposition to Disease ; Genotype ; Pakistan

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 3.

Tytuł:: Homozygous C677T Methylenetetrahydrofolate Reductase (MTHFR) Polymorphism as a Risk Factor for Endometriosis: A Retrospective Case-Control Study.
Autorzy:: Delli Carpini G; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.
Giannella L; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.
Di Giuseppe J; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.
Montik N; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.
Montanari M; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.
Fichera M; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.
Crescenzi D; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.
Marzocchini C; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.
Meccariello ML; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.
Di Biase D; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.
Vignini A; Section of Biochemistry, Biology and Physics, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60126 Ancona, Italy.
Ciavattini A; Gynecologic Section, Department of Odontostomatologic and Specialized Clinical Sciences, Università Politecnica delle Marche, 60213 Ancona, Italy.; Pokaż więcej
Źródło:: International journal of molecular sciences [Int J Mol Sci] 2023 Oct 20; Vol. 24 (20). Date of Electronic Publication: 2023 Oct 20.
Typ publikacji:: Journal Article
MeSH Terms:: Polymorphism, Single Nucleotide*
Endometriosis*/genetics
Female ; Pregnancy ; Humans ; Case-Control Studies ; Retrospective Studies ; Methylenetetrahydrofolate Reductase (NADPH2)/genetics ; Genetic Predisposition to Disease ; Risk Factors ; Genotype

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 4.

Tytuł:: Relationship between cancer stem cell-related SNPs and survival outcomes in patients with primary lung cancer.
Autorzy:: Xu X; Department of Epidemiology and Health Statistics, School of Public Health, Fujian Medical University, Fuzhou, China.
Liu Y; Department of Epidemiology and Health Statistics, School of Public Health, Fujian Medical University, Fuzhou, China.
Hu H; Department of Labor Health, School of Public Health, China Medical University, Shenyang, China.
Wang J; Department of Venereal Disease Prevention, Dermatology Hospital, Southern Medical University, Guangzhou, China.
Cai Y; Department of Health Toxicology, School of Public Health, Xiamen University, Xiamen, China.
Xie J; Sanming Dermatology Hospital, Sanming, China.
Kang M; Department of Thoracic Surgery, Fujian Medical University Union Hospital, Fuzhou, China. .
He F; Department of Epidemiology and Health Statistics, School of Public Health, Fujian Medical University, Fuzhou, China. .; Pokaż więcej
Źródło:: World journal of surgical oncology [World J Surg Oncol] 2023 Aug 11; Vol. 21 (1), pp. 243. Date of Electronic Publication: 2023 Aug 11.
Typ publikacji:: Journal Article
MeSH Terms:: Polymorphism, Single Nucleotide*
Lung Neoplasms*/genetics
Humans ; Quality of Life ; Genotype ; Prognosis ; Genetic Predisposition to Disease ; Case-Control Studies

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 5.

Tytuł:: Correlation investigation between a single nucleotide polymorphism in ADAMTS14 (rs4747096) and osteoarthritis: a meta-analysis.
Autorzy:: Li B; Department of Orthopedics, The People's Hospital of Weifang, 151 Guangwen Street, Kuiwen District, Weifang, 261000, Shandong, China.
Li X; Department of Orthopedics, The People's Hospital of Weifang, 151 Guangwen Street, Kuiwen District, Weifang, 261000, Shandong, China.
Zhang L; Department of Orthopedics, The People's Hospital of Weifang, 151 Guangwen Street, Kuiwen District, Weifang, 261000, Shandong, China.
Mou L; Department of Orthopedics, The People's Hospital of Weifang, 151 Guangwen Street, Kuiwen District, Weifang, 261000, Shandong, China. .; Pokaż więcej
Źródło:: Journal of orthopaedic surgery and research [J Orthop Surg Res] 2023 Aug 07; Vol. 18 (1), pp. 575. Date of Electronic Publication: 2023 Aug 07.
Typ publikacji:: Meta-Analysis; Journal Article
MeSH Terms:: ADAMTS Proteins*/genetics
Osteoarthritis*/genetics
Polymorphism, Single Nucleotide*
Humans ; Alleles ; Case-Control Studies ; Genetic Predisposition to Disease ; Odds Ratio ; Risk Factors

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 6.

Tytuł:: Screening properties of trend tests in genetic association studies.
Autorzy:: Jiang Z; Academy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing, 100190, People's Republic of China.; University of Chinese Academy of Sciences, Beijing, 100049, People's Republic of China.
Guo H; School of Mathematics and Statistics, Hubei Normal University, Huangshi, 435002, People's Republic of China.
Wang J; School of Mathematics and Statistics, Beijing Institute of Technology, Beijing, 100081, People's Republic of China. .; Pokaż więcej
Źródło:: Scientific reports [Sci Rep] 2023 Jun 05; Vol. 13 (1), pp. 9139. Date of Electronic Publication: 2023 Jun 05.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Genome-Wide Association Study*/methods
Polymorphism, Single Nucleotide*
Humans ; Case-Control Studies ; Genetic Association Studies ; Algorithms ; Models, Genetic ; Genetic Predisposition to Disease

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 7.

Tytuł:: A Multigene-Panel Study Identifies Single Nucleotide Polymorphisms Associated with Prostate Cancer Risk.
Autorzy:: Manca MA; Dipartimento di Scienze Biomediche, University of Sassari, 07100 Sassari, Italy.
Scarpa F; Dipartimento di Scienze Biomediche, University of Sassari, 07100 Sassari, Italy.
Cossu D; Dipartimento di Scienze Biomediche, University of Sassari, 07100 Sassari, Italy.
Simula ER; Dipartimento di Scienze Biomediche, University of Sassari, 07100 Sassari, Italy.
Sanna D; Dipartimento di Scienze Biomediche, University of Sassari, 07100 Sassari, Italy.
Ruberto S; Dipartimento di Scienze Biomediche, University of Sassari, 07100 Sassari, Italy.
Noli M; Dipartimento di Scienze Biomediche, University of Sassari, 07100 Sassari, Italy.
Ashraf H; Dipartimento di Scienze Biomediche, University of Sassari, 07100 Sassari, Italy.
Solinas T; Dipartimento di Scienze Mediche, Chirurgiche e Sperimentali, Università di Sassari, 07100 Sassari, Italy.; Struttura Complessa di Urologia, Azienda Ospedaliera Universitaria, 07100 Sassari, Italy.
Madonia M; Dipartimento di Scienze Mediche, Chirurgiche e Sperimentali, Università di Sassari, 07100 Sassari, Italy.; Struttura Complessa di Urologia, Azienda Ospedaliera Universitaria, 07100 Sassari, Italy.
Cusano R; CRS4, 09010 Pula, Italy.
Sechi LA; Dipartimento di Scienze Biomediche, University of Sassari, 07100 Sassari, Italy.; Struttura Complessa di Microbiologia e Virologia, Azienda Ospedaliera Universitaria, 07100 Sassari, Italy.; Pokaż więcej
Źródło:: International journal of molecular sciences [Int J Mol Sci] 2023 Apr 20; Vol. 24 (8). Date of Electronic Publication: 2023 Apr 20.
Typ publikacji:: Journal Article
MeSH Terms:: Polymorphism, Single Nucleotide*
Prostatic Neoplasms*/genetics
Male ; Humans ; Genotype ; Inflammation/genetics ; Prostate ; Genetic Predisposition to Disease ; Case-Control Studies

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 8.

Tytuł:: SNP in PTPN22 , PADI4, and STAT4 but Not TRAF1 and CD40 Increase the Risk of Rheumatoid Arthritis in Polish Population.
Autorzy:: Budlewski T; Department of Rheumatology, Medical University of Lodz, 92-115 Lodz, Poland.
Sarnik J; Department of Rheumatology, Medical University of Lodz, 92-115 Lodz, Poland.
Galita G; Department of Clinical Chemistry and Biochemistry, Medical University of Lodz, 92-215 Lodz, Poland.; Doctoral Study in Molecular Genetics, Cytogenetics and Medical Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, 90-236 Lodz, Poland.
Dragan G; Department of Clinical Chemistry and Biochemistry, Medical University of Lodz, 92-215 Lodz, Poland.
Brzezińska O; Department of Rheumatology, Medical University of Lodz, 92-115 Lodz, Poland.
Popławska M; Biobank, Department of Immunology and Allergy, Medical University of Lodz, 92-213 Lodz, Poland.
Popławski T; Department of Pharmaceutical Microbiology and Biochemistry, Medical University of Lodz, 92-215 Lodz, Poland.
Makowska J; Department of Rheumatology, Medical University of Lodz, 92-115 Lodz, Poland.; Pokaż więcej
Źródło:: International journal of molecular sciences [Int J Mol Sci] 2023 Apr 20; Vol. 24 (8). Date of Electronic Publication: 2023 Apr 20.
Typ publikacji:: Journal Article
MeSH Terms:: Polymorphism, Single Nucleotide*
Arthritis, Rheumatoid*/epidemiology
Arthritis, Rheumatoid*/genetics
Humans ; TNF Receptor-Associated Factor 1/genetics ; Poland/epidemiology ; Genetic Predisposition to Disease ; Genotype ; Alleles ; Case-Control Studies ; Gene Frequency ; Protein Tyrosine Phosphatase, Non-Receptor Type 22/genetics ; STAT4 Transcription Factor/genetics

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 9.

Tytuł:: Assessment of the Potential Role of Selected Single Nucleotide Polymorphisms (SNPs) of Genes Related to the Functioning of Regulatory T Cells in the Pathogenesis of Psoriasis.
Autorzy:: Purzycka-Bohdan D; Department of Dermatology, Venereology and Allergology, Medical University of Gdansk, 80-210 Gdansk, Poland.
Nedoszytko B; Department of Dermatology, Venereology and Allergology, Medical University of Gdansk, 80-210 Gdansk, Poland.; Molecular Laboratory, Invicta Fertility and Reproductive Centre, 81-740 Sopot, Poland.
Sobalska-Kwapis M; Biobank Laboratory, Department of Oncobiology and Epigenetics, Faculty of Biology and Environmental Protection, University of Lodz, 90-237 Lodz, Poland.
Zabłotna M; Department of Dermatology, Venereology and Allergology, Medical University of Gdansk, 80-210 Gdansk, Poland.
Żmijewski MA; Department of Histology, Medical University of Gdansk, 80-211 Gdansk, Poland.
Wierzbicka J; Department of Histology, Medical University of Gdansk, 80-211 Gdansk, Poland.
Gleń J; Department of Dermatology, Venereology and Allergology, Medical University of Gdansk, 80-210 Gdansk, Poland.
Strapagiel D; Biobank Laboratory, Department of Oncobiology and Epigenetics, Faculty of Biology and Environmental Protection, University of Lodz, 90-237 Lodz, Poland.
Szczerkowska-Dobosz A; Department of Dermatology, Venereology and Allergology, Medical University of Gdansk, 80-210 Gdansk, Poland.
Nowicki RJ; Department of Dermatology, Venereology and Allergology, Medical University of Gdansk, 80-210 Gdansk, Poland.; Pokaż więcej
Źródło:: International journal of molecular sciences [Int J Mol Sci] 2023 Mar 23; Vol. 24 (7). Date of Electronic Publication: 2023 Mar 23.
Typ publikacji:: Journal Article
MeSH Terms:: Polymorphism, Single Nucleotide*
Psoriasis*/genetics
Psoriasis*/metabolism
Humans ; T-Lymphocytes, Regulatory/metabolism ; Genetic Predisposition to Disease ; RNA, Messenger ; Case-Control Studies

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 10.

Tytuł:: Association of the rs2111234, rs3135499, rs8057341 polymorphisms in the NOD2 gene with leprosy: A case-control study in the Norte de Santander, Colombia population.
Autorzy:: Bustos MA; Grupo de Investigación en Enfermedades Parasitarias, Tropicales e Infecciosas (GIEPATI), Universidad de Pamplona, Pamplona, Norte de Santander, Colombia.
Castañeda-Castañeda LD; Grupo de Dermatología General, Hospital Universitario- Centro Dermatológico Federico Lleras Acosta, Bogotá, Colombia.; Research Institute, Group of Basic Sciences in Health (CBS)-FUCS, Fundación Universitaria de Ciencias de la Salud-FUCS, Bogotá, Colombia.
Acosta CR; Grupo de Dermatología Tropical, Hospital Universitario- Centro Dermatológico Federico Lleras Acosta, Bogotá, Colombia.
García D; Grupo de Dermatología General, Hospital Universitario- Centro Dermatológico Federico Lleras Acosta, Bogotá, Colombia.; Grupo de Dermatología Tropical, Hospital Universitario- Centro Dermatológico Federico Lleras Acosta, Bogotá, Colombia.
Bohada DP; Grupo de Investigación en Enfermedades Parasitarias, Tropicales e Infecciosas (GIEPATI), Universidad de Pamplona, Pamplona, Norte de Santander, Colombia.
Rodríguez R; Grupo de Investigación en Enfermedades Parasitarias, Tropicales e Infecciosas (GIEPATI), Universidad de Pamplona, Pamplona, Norte de Santander, Colombia.
Guerrero MI; Grupo de Dermatología Tropical, Hospital Universitario- Centro Dermatológico Federico Lleras Acosta, Bogotá, Colombia.; Pokaż więcej
Źródło:: PloS one [PLoS One] 2023 Mar 06; Vol. 18 (3), pp. e0281553. Date of Electronic Publication: 2023 Mar 06 (Print Publication: 2023).
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Polymorphism, Single Nucleotide*
Leprosy*/genetics
Humans ; Female ; Case-Control Studies ; Colombia/epidemiology ; Mycobacterium leprae ; Nod2 Signaling Adaptor Protein/genetics

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 11.

Tytuł:: Association between the HTR1A rs6295 gene polymorphism and suicidal behavior: an updated meta-analysis.
Autorzy:: Hernández-Díaz Y; División Académica Multidisciplinaria de Jalpa de Méndez, Universidad Juárez Autónoma de Tabasco, Carretera Estatal Libre Villahermosa-Comalcalco Km. 27+000 S/N Rancheria Ribera Alta, 86205, Jalpa de Méndez, Tabasco, Mexico.
Tovilla-Zárate CA; División Académica Multidisciplinaria de Comalcalco, Universidad Juárez Autónoma de Tabasco, Comalcalco, Tabasco, Mexico.
Castillo-Avila RG; División Académica de Ciencias de La Salud, Universidad Juárez Autónoma de Tabasco, Villahermosa, Tabasco, Mexico.
Juárez-Rojop IE; División Académica de Ciencias de La Salud, Universidad Juárez Autónoma de Tabasco, Villahermosa, Tabasco, Mexico.
Genis-Mendoza AD; Laboratorio de Genómica de Enfermedades Psiquiátricas Y Neurodegenerativas, Instituto Nacional de Medicina Genómica, Ciudad de México, Mexico.
López-Narváez ML; Hospital Chiapas Nos Une Dr. Gilberto Gómez Maza, Secretaría de Salud de Chiapas, Tuxtla Gutiérrez, Chiapas, Mexico.
Villar-Juárez GE; Escuela de Ciencias de La Salud, Universidad Anahuac Querétaro, Querétaro, Mexico.
González-Castro TB; División Académica Multidisciplinaria de Jalpa de Méndez, Universidad Juárez Autónoma de Tabasco, Carretera Estatal Libre Villahermosa-Comalcalco Km. 27+000 S/N Rancheria Ribera Alta, 86205, Jalpa de Méndez, Tabasco, Mexico. .; Pokaż więcej
Źródło:: European archives of psychiatry and clinical neuroscience [Eur Arch Psychiatry Clin Neurosci] 2023 Feb; Vol. 273 (1), pp. 5-14. Date of Electronic Publication: 2022 Oct 10.
Typ publikacji:: Review; Meta-Analysis; Journal Article
MeSH Terms:: Suicidal Ideation*
Polymorphism, Single Nucleotide*
Humans ; Case-Control Studies ; Odds Ratio ; Genetic Predisposition to Disease ; Receptor, Serotonin, 5-HT1A/genetics

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 12.

Tytuł:: Influence of Single-Nucleotide Polymorphisms on Vitamin D Receptor Expression in Periodontal Ligament Fibroblasts as a Response to Orthodontic Compression.
Autorzy:: Küchler EC; Department of Orthodontics, University of Regensburg, 93047 Regensburg, Germany.; Department of Biomaterials, University of Uberaba, Uberaba 38010-200, Brazil.
Schröder A; Department of Orthodontics, University of Regensburg, 93047 Regensburg, Germany.
Spanier G; Department of Maxillofacial Surgery, University of Regensburg, 93047 Regensburg, Germany.
Thedei G Jr; Department of Biomaterials, University of Uberaba, Uberaba 38010-200, Brazil.
Carvalho Ribeiro de Oliveira MB; Department of Biomaterials, University of Uberaba, Uberaba 38010-200, Brazil.
de Menezes-Oliveira MAH; Department of Biomaterials, University of Uberaba, Uberaba 38010-200, Brazil.
Proff P; Department of Orthodontics, University of Regensburg, 93047 Regensburg, Germany.
Kirschneck C; Department of Orthodontics, University of Regensburg, 93047 Regensburg, Germany.; Pokaż więcej
Źródło:: International journal of molecular sciences [Int J Mol Sci] 2022 Dec 15; Vol. 23 (24). Date of Electronic Publication: 2022 Dec 15.
Typ publikacji:: Journal Article
MeSH Terms:: Genetic Predisposition to Disease*
Polymorphism, Single Nucleotide*
Receptors, Calcitriol*/genetics
Tooth Movement Techniques*
Stress, Mechanical*
Humans ; Case-Control Studies ; Genotype ; Periodontal Ligament/cytology ; Fibroblasts

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 13.

Tytuł:: In Silico Evaluation of Nonsynonymous SNPs in Human ADAM33: The Most Common Form of Genetic Association to Asthma Susceptibility.
Autorzy:: Mohkam M; Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Golkar N; Pharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.; Department of Pharmaceutics, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
Nabavizadeh SH; Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.; Department of Allergy and Clinical Immunology, Namazi Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.
Esmaeilzadeh H; Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.; Department of Allergy and Clinical Immunology, Namazi Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.
Berenjian A; School of Engineering, University of Waikato, Hamilton 3240, New Zealand.
Ghahramani Z; School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Golami A; Biotechnology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Alyasin S; Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.; Department of Allergy and Clinical Immunology, Namazi Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.; Pokaż więcej
Źródło:: Computational and mathematical methods in medicine [Comput Math Methods Med] 2022 Nov 12; Vol. 2022, pp. 1089722. Date of Electronic Publication: 2022 Nov 12 (Print Publication: 2022).
Typ publikacji:: Journal Article
MeSH Terms:: Polymorphism, Single Nucleotide*
Asthma*/genetics
Humans ; Genetic Predisposition to Disease ; ADAM Proteins/genetics ; Case-Control Studies

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 14.

Tytuł:: Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland.
Autorzy:: Clark JSC; Department of Clinical and Molecular Biochemistry, Pomeranian Medical University, Szczecin, Poland. .
van de Wetering T; Department of Clinical and Molecular Biochemistry, Pomeranian Medical University, Szczecin, Poland.
Marciniak B; Biobank Lab, Department of Molecular Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, 90-237, Lodz, Poland.
Żądzińska E; Department of Anthropology, Faculty of Biology and Environmental Protection, University of Lodz, 90-237, Lodz, Poland.; Biological Anthropology and Comparative Anatomy Research Unit, School of Medicine, University of Adelaide, Adelaide, SA, 5005, Australia.
Ciechanowicz A; Department of Clinical and Molecular Biochemistry, Pomeranian Medical University, Szczecin, Poland.
Kaczmarczyk M; Department of Clinical and Molecular Biochemistry, Pomeranian Medical University, Szczecin, Poland.
Boroń A; Department of Clinical and Molecular Biochemistry, Pomeranian Medical University, Szczecin, Poland.
Rydzewska K; Department of Clinical and Molecular Biochemistry, Pomeranian Medical University, Szczecin, Poland.
Posiadło K; Department of Clinical and Molecular Biochemistry, Pomeranian Medical University, Szczecin, Poland.
Strapagiel D; Biobank Lab, Department of Molecular Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, 90-237, Lodz, Poland.; Pokaż więcej
Źródło:: Scientific reports [Sci Rep] 2022 Nov 07; Vol. 12 (1), pp. 18923. Date of Electronic Publication: 2022 Nov 07.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Polymorphism, Single Nucleotide*
Genetic Predisposition to Disease*
Female ; Child ; Humans ; Male ; Poland ; Case-Control Studies ; Genotype ; Phenotype

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 15.

Tytuł:: Vitamin D-Related Single Nucleotide Polymorphisms as Risk Biomarker of Cardiovascular Disease.
Autorzy:: González Rojo P; Pharmacogenetics Unit, Pharmacy Service, University Hospital Virgen de las Nieves, 18014 Granada, Spain.
Pérez Ramírez C; Pharmacogenetics Unit, Pharmacy Service, University Hospital Virgen de las Nieves, 18014 Granada, Spain.; Department of Biochemistry and Molecular Biology II, Faculty of Pharmacy, Campus Universitario de Cartuja, University of Granada, 18071 Granada, Spain.
Gálvez Navas JM; Pharmacogenetics Unit, Pharmacy Service, University Hospital Virgen de las Nieves, 18014 Granada, Spain.; Department of Biochemistry and Molecular Biology II, Faculty of Pharmacy, Campus Universitario de Cartuja, University of Granada, 18071 Granada, Spain.
Pineda Lancheros LE; Pharmacogenetics Unit, Pharmacy Service, University Hospital Virgen de las Nieves, 18014 Granada, Spain.
Rojo Tolosa S; Pharmacogenetics Unit, Pharmacy Service, University Hospital Virgen de las Nieves, 18014 Granada, Spain.
Ramírez Tortosa MDC; Department of Biochemistry and Molecular Biology II, Faculty of Pharmacy, Campus Universitario de Cartuja, University of Granada, 18071 Granada, Spain.
Jiménez Morales A; Pharmacogenetics Unit, Pharmacy Service, University Hospital Virgen de las Nieves, 18014 Granada, Spain.; Pokaż więcej
Źródło:: International journal of molecular sciences [Int J Mol Sci] 2022 Aug 04; Vol. 23 (15). Date of Electronic Publication: 2022 Aug 04.
Typ publikacji:: Journal Article
MeSH Terms:: Cardiovascular Diseases*/genetics
Polymorphism, Single Nucleotide*
Biomarkers ; Case-Control Studies ; Genetic Predisposition to Disease ; Genotype ; Humans ; Receptors, Calcitriol/genetics ; Retrospective Studies ; Vitamin D ; Vitamins

Czasopismo naukowe

na półce

Pełny tekst Szczegóły

Skocz do pozycji: 16.

Tytuł:: Analysis of Nuclear Receptor Coactivator 5 (NCOA5) Messenger RNA Expression and rs2903908 Single Nucleotide Polymorphism of NCOA5 in an Egyptian Cohort with Behçet's Disease: A Single-Center Case-control Study.
Autorzy:: Koptan DMT; Faculty of Medicine, Kasr Al Ainy, Department of Clinical and Chemical Pathology, Cairo University, Egypt.
Rasheed Bahgat DM; Faculty of Medicine, Kasr Al Ainy, Department of Clinical and Chemical Pathology, Cairo University, Egypt.
Abdelrasool AA; Faculty of Medicine, Kasr Al Ainy, Department of Clinical and Chemical Pathology, Cairo University, Egypt.
Allam RSHM; Faculty of Medicine, Kasr Al Ainy, Department of Ophthalmology, Cairo University, Egypt.
Elgengehy FT; Faculty of Medicine, Kasr Al Ainy, Department of Rheumatology and Rehabilitation, Cairo University, Egypt.
Abdel Baki NM; Faculty of Medicine, Kasr Al Ainy, Department of Rheumatology and Rehabilitation, Cairo University, Egypt.
Medhat BM; Faculty of Medicine, Kasr Al Ainy, Department of Rheumatology and Rehabilitation, Cairo University, Egypt.; Pokaż więcej
Źródło:: Ocular immunology and inflammation [Ocul Immunol Inflamm] 2022 Aug; Vol. 30 (6), pp. 1436-1446. Date of Electronic Publication: 2021 Jul 13.
Typ publikacji:: Journal Article
MeSH Terms:: Behcet Syndrome*/diagnosis
Behcet Syndrome*/genetics
Nuclear Receptor Coactivators*/genetics
Nuclear Receptor Coactivators*/metabolism
Polymorphism, Single Nucleotide*
Female ; Humans ; Male ; Case-Control Studies ; Egypt/epidemiology ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; RNA, Messenger/genetics ; RNA, Messenger/metabolism

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 17.

Tytuł:: Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population.
Autorzy:: Sarwar S; Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan. .
Shabana; Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan. .
Tahir A; Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan.
Liaqat Z; Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan.
Naseer S; Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan.
Seme RS; Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan.
Mehmood S; Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan.
Shahid SU; Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan.
Hasnain S; Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan.; Pokaż więcej
Źródło:: Italian journal of pediatrics [Ital J Pediatr] 2022 Jul 23; Vol. 48 (1), pp. 124. Date of Electronic Publication: 2022 Jul 23.
Typ publikacji:: Journal Article
MeSH Terms:: Heart Septal Defects, Ventricular*/genetics
Polymorphism, Single Nucleotide*
Alleles ; Basic Helix-Loop-Helix Transcription Factors/genetics ; Case-Control Studies ; Child ; Genetic Predisposition to Disease ; Genotype ; Humans ; Infant, Newborn ; Pakistan/epidemiology ; Transcription Factors/genetics ; Vascular Endothelial Growth Factor A/genetics

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 18.

Tytuł:: The G allele of the IGF1 rs2162679 SNP is a potential protective factor for any myopia: Updated systematic review and meta-analysis.
Autorzy:: Meng B; Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Wang K; Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Huang Y; Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Wang Y; Beijing Friendship Hospital, Capital Medical University, Beijing, China.; Pokaż więcej
Źródło:: PloS one [PLoS One] 2022 Jul 21; Vol. 17 (7), pp. e0271809. Date of Electronic Publication: 2022 Jul 21 (Print Publication: 2022).
Typ publikacji:: Journal Article; Meta-Analysis; Systematic Review
MeSH Terms:: Insulin-Like Growth Factor I*/genetics
Myopia*/genetics
Polymorphism, Single Nucleotide*
Alleles ; Case-Control Studies ; Genetic Predisposition to Disease ; Humans ; Protective Factors

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 19.

Tytuł:: Association of SNPs in the FK-506 binding protein (FKBP5) gene among Han Chinese women with polycystic ovary syndrome.
Autorzy:: Ma X; Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Shandong University, Jinan, 250012, Shandong, China.; Key Laboratory of Reproductive Endocrinology of Ministry of Education, Shandong University, Jinan, 250012, Shandong, China.; Shandong Provincial Clinical Medicine Research Center for Reproductive Health, Shandong University, Jinan, 250012, Shandong, China.
Wang Z; Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Shandong University, Jinan, 250012, Shandong, China.; Key Laboratory of Reproductive Endocrinology of Ministry of Education, Shandong University, Jinan, 250012, Shandong, China.; Shandong Provincial Clinical Medicine Research Center for Reproductive Health, Shandong University, Jinan, 250012, Shandong, China.
Zhang C; Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Shandong University, Jinan, 250012, Shandong, China.; Key Laboratory of Reproductive Endocrinology of Ministry of Education, Shandong University, Jinan, 250012, Shandong, China.; Shandong Provincial Clinical Medicine Research Center for Reproductive Health, Shandong University, Jinan, 250012, Shandong, China.
Bian Y; Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Shandong University, Jinan, 250012, Shandong, China.; Key Laboratory of Reproductive Endocrinology of Ministry of Education, Shandong University, Jinan, 250012, Shandong, China.; Shandong Provincial Clinical Medicine Research Center for Reproductive Health, Shandong University, Jinan, 250012, Shandong, China.
Zhang X; Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Shandong University, Jinan, 250012, Shandong, China.; Key Laboratory of Reproductive Endocrinology of Ministry of Education, Shandong University, Jinan, 250012, Shandong, China.; Shandong Provincial Clinical Medicine Research Center for Reproductive Health, Shandong University, Jinan, 250012, Shandong, China.
Liu X; Central Laboratory, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250021, Shandong, China.
Cao Y; Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China. yz_.; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Shandong University, Jinan, 250012, Shandong, China. yz_.; Key Laboratory of Reproductive Endocrinology of Ministry of Education, Shandong University, Jinan, 250012, Shandong, China. yz_.; Shandong Provincial Clinical Medicine Research Center for Reproductive Health, Shandong University, Jinan, 250012, Shandong, China. yz_.
Zhao Y; Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China. .; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Shandong University, Jinan, 250012, Shandong, China. .; Key Laboratory of Reproductive Endocrinology of Ministry of Education, Shandong University, Jinan, 250012, Shandong, China. .; Shandong Provincial Clinical Medicine Research Center for Reproductive Health, Shandong University, Jinan, 250012, Shandong, China. .; Central Laboratory, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250021, Shandong, China. .; Pokaż więcej
Źródło:: BMC medical genomics [BMC Med Genomics] 2022 Jul 04; Vol. 15 (1), pp. 149. Date of Electronic Publication: 2022 Jul 04.
Typ publikacji:: Journal Article
MeSH Terms:: Polycystic Ovary Syndrome*/genetics
Polymorphism, Single Nucleotide*
Tacrolimus Binding Proteins/*genetics
Androgens ; Case-Control Studies ; China ; Female ; Humans

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Skocz do pozycji: 20.

Tytuł:: Interleukin-17A gene single nucleotide polymorphism and its relation to fungal growth in psoriatic patients: A preliminary study.
Autorzy:: Sanad EMK; Faculty of Medicine, Department of Dermatology, Benha University, Benha, Egypt.
Nazmy NN; Faculty of Medicine, Department of Dermatology, Benha University, Benha, Egypt.
Abd-El Hamid El Sayed R; Faculty of Medicine, Medical Microbiology and Immunology Department, Benha University, Benha, Egypt.
Hamed AM; Faculty of Medicine, Department of Dermatology, Benha University, Benha, Egypt.; Pokaż więcej
Źródło:: Journal of cosmetic dermatology [J Cosmet Dermatol] 2022 Jul; Vol. 21 (7), pp. 3059-3067. Date of Electronic Publication: 2021 Nov 06.
Typ publikacji:: Journal Article
MeSH Terms:: Fungi*/classification
Interleukin-17*/genetics
Polymorphism, Single Nucleotide*
Psoriasis*/genetics
Skin*/microbiology
Case-Control Studies ; Genetic Predisposition to Disease ; Humans ; Microbiota ; Polymorphism, Restriction Fragment Length

Czasopismo naukowe

na półce

Pełny tekst Pełny tekst Szczegóły

Informacja

Wyszukujesz frazę ""Case-Control Studies"" wg kryterium: Temat

Źródło danych

Ogranicz do:

Ogranicz do bazy

Typ dokumentu

Temat

Wydawca

Publikacja

Język