Articles

UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (153) 153
life sciences & biomedicine (146) 146
humans (133) 133
male (75) 75
female (74) 74
mutation (71) 71
animals (58) 58
genetics & heredity (57) 57
biological and medical sciences (56) 56
medical sciences (48) 48
genetic aspects (47) 47
child (44) 44
adolescent (41) 41
mice (38) 38
research (37) 37
adult (35) 35
cilia (35) 35
primary ciliary dyskinesia (35) 35
kartagener syndrome - genetics (34) 34
phenotype (34) 34
proteins (33) 33
respiratory system (33) 33
gene mutations (32) 32
genetics (31) 31
pedigree (31) 31
cell biology (27) 27
child, preschool (27) 27
movement disorders (27) 27
cilia - metabolism (25) 25
cilia - ultrastructure (25) 25
pediatrics (25) 25
dyneins - genetics (24) 24
fundamental and applied biological sciences. psychology (24) 24
otorhinolaryngologic diseases (24) 24
cilia - genetics (22) 22
cilia - pathology (22) 22
ciliary motility disorders - genetics (21) 21
dynein (21) 21
medical genetics (21) 21
physiological aspects (21) 21
young adult (21) 21
genes (20) 20
genetic disorders (19) 19
health aspects (19) 19
molecular sequence data (19) 19
biochemistry & molecular biology (18) 18
dna mutational analysis (18) 18
proteins - genetics (18) 18
risk factors (18) 18
genetics of eukaryotes. biological and molecular evolution (17) 17
mutation - genetics (17) 17
analysis (16) 16
cilia - physiology (15) 15
cilia and ciliary motion (15) 15
zebrafish (15) 15
diagnosis (14) 14
infant (14) 14
complex syndromes (13) 13
kidney diseases, cystic - genetics (13) 13
amino acid sequence (12) 12
cells (12) 12
homozygote (12) 12
middle aged (12) 12
molecular and cellular biology (12) 12
abridged index medicus (11) 11
base sequence (11) 11
gene expression (11) 11
genotype & phenotype (11) 11
infant, newborn (11) 11
kartagener syndrome - diagnosis (11) 11
nephrology. urinary tract diseases (11) 11
nephronophthisis (11) 11
syndrome (11) 11
ciliary motility disorders - pathology (10) 10
clinical neurology (10) 10
dyskinesia (10) 10
genotype (10) 10
kartagener syndrome - metabolism (10) 10
neurosciences & neurology (10) 10
proteins - metabolism (10) 10
respiratory tract diseases (10) 10
care and treatment (9) 9
cells, cultured (9) 9
defects (9) 9
general & internal medicine (9) 9
genes, recessive (9) 9
genetic research (9) 9
kartagener syndrome - pathology (9) 9
medicine (9) 9
microscopy (9) 9
neurology (9) 9
situs inversus - genetics (9) 9
urology & nephrology (9) 9
zebrafish - genetics (9) 9
axonemal dyneins (8) 8
axonemal dyneins - genetics (8) 8
axoneme - genetics (8) 8
dyneins - metabolism (8) 8
exons (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text NPHP proteins: gatekeepers of the ciliary compartment
by Heymut Omran
The Journal of cell biology, ISSN 0021-9525, 9/2010, Volume 190, Issue 5, pp. 715 - 717
Comment | Microtubules | Photoreceptors | Eye diseases | Gene expression regulation | Genetic mutation | Transition zones | Cytoplasm | Cilia | Cystic kidney diseases | Nephrons | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Chlamydomonas reinhardtii - ultrastructure | Cilia - pathology | Axoneme - metabolism | Retinal Degeneration - metabolism | Axoneme - pathology | Cilia - metabolism | Microscopy, Immunoelectron | Kidney Diseases, Cystic - pathology | Proteins - genetics | Kidney Diseases, Cystic - metabolism | Animals | Proteins - metabolism | Chlamydomonas reinhardtii - genetics | Axoneme - ultrastructure | Cilia - ultrastructure | Kidney Diseases, Cystic - genetics | Chlamydomonas reinhardtii - metabolism | Mutation | Retinal Degeneration - pathology | Proteins | Research | Cilia and ciliary motion | Cells | Index Medicus | Reviews
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text When cilia go bad: cilia defects and ciliopathies
by Fliegauf, Manfred and Omran, Heymut and Benzing, Thomas
Nature reviews. Molecular cell biology, ISSN 1471-0072, 11/2007, Volume 8, Issue 11, pp. 880 - 893
Reproduction | Animals | Cilia - pathology | Ciliary Motility Disorders - pathology | Humans | Body Patterning | Organ Specificity | Cysts - pathology | Cilia - metabolism | Physiological aspects | Research | Cilia and ciliary motion | Abnormalities | Membrane proteins | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Genetic defects in ciliary structure and function
by Zariwala, Maimoona A and Knowles, Michael R and Omran, Heymut
Annual review of physiology, ISSN 0066-4278, 2007, Volume 69, Issue 1, pp. 423 - 450
Situs inversus | Kartagener syndrome | Primary ciliary dyskinesia (pcd) | Dynein | Cilia - physiology | Flagella - physiology | Ciliary Motility Disorders - physiopathology | Flagella - ultrastructure | Humans | Cilia - genetics | DNA - genetics | Dyneins - chemistry | Animals | Cilia - ultrastructure | Ciliary Motility Disorders - diagnosis | Dyneins - ultrastructure | Dyneins - genetics | Ciliary Motility Disorders - therapy | Ciliary Motility Disorders - genetics | Cilia and ciliary motion | Infertility, Male | Physiological aspects | Causes of | Genetic aspects | Research | Risk factors | Proteins | Genetics | Membranes | Genetic disorders | Respiratory system | Cells | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Transition von Patienten mit primärer ziliärer Dyskinesie
by Schmalstieg, Christian and Omran, Heymut
Pneumologe, ISSN 1613-5636, 03/2021, Volume 18, Issue 2, pp. 86 - 96
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia
by Lucas, Jane S and Barbato, Angelo and Collins, Samuel A and Goutaki, Myrofora and Behan, Laura and Caudri, Daan and Dell, Sharon and Eber, Ernst and Escudier, Estelle and Hirst, Robert A and Hogg, Claire and Jorissen, Mark and Latzin, Philipp and Legendre, Marie and Leigh, Margaret W and Midulla, Fabio and Nielsen, Kim G and Omran, Heymut and Papon, Jean-Francois and Pohunek, Petr and Redfern, Beatrice and Rigau, David and Rindlisbacher, Bernhard and Santamaria, Francesca and Shoemark, Amelia and Snijders, Deborah and Tonia, Thomy and Titieni, Andrea and Walker, Woolf T and Werner, Claudius and Bush, Andrew and Kuehni, Claudia E
The European respiratory journal, ISSN 0903-1936, 01/2017, Volume 49, Issue 1, pp. 1601090 - 1601090
Life Sciences & Biomedicine | Respiratory System | Science & Technology | Kartagener Syndrome - diagnosis | Microscopy, Electron, Transmission | Diagnosis, Differential | Cilia - pathology | Genetic Testing | Europe | Humans | Microscopy, Video | Kartagener Syndrome - genetics | Nitric Oxide - analysis | Delphi Technique | Societies, Medical | Review Literature as Topic | Fluorescent Antibody Technique | Cilia - ultrastructure | Literature reviews | Transmission electron microscopy | Genotyping | Primary ciliary dyskinesia | Microscopy | Nitric oxide | Diagnostic tests | Clinical trials | Diagnosis | Immunofluorescence | Dyskinesia
Journal Article
Details down arrow
6. Full Text Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis
by Burkhalter, Martin D and Sridhar, Arthi and Sampaio, Pedro and Jacinto, Raquel and Burczyk, Martina S and Donow, Cornelia and Angenendt, Max and Investigators, Competence Network For Congenital Heart Defects and Hempel, Maja and Walther, Paul and Pennekamp, Petra and Omran, Heymut and Lopes, Susana S and Ware, Stephanie M and Philipp, Melanie and Competence Network Congenital
The Journal of clinical investigation, ISSN 0021-9738, 05/2019, Volume 130, Issue 7, pp. 2841 - 2855
Development | Mitochondria | Cardiology | Genetic variation | Organogenesis | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Medical research | Genetic disorders | Analysis | Genes | Medicine, Experimental | Congenital heart disease | Mitochondrial DNA | Heart diseases | TOR protein | Heart | Neonates | Phenotypes | Congenital diseases | Cardiovascular disease | Genomes | Biosynthesis | Ribonucleic acid--RNA | Coronary artery disease | Asymmetry | DNA methylation | Tomography | Fibroblasts | Photoreceptors | Mutation | Respiration | Pancreas | Deoxyribonucleic acid--DNA | Symmetry | Cilia | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma
by Schindler, G and Capper, D and Meyer, J and Janzarik, W and Omran, H and Herold-Mende, C and Schmieder, K and Wesseling, P and Mawrin, C and Hasselblatt, M and Louis, D.N and Korshunov, A and Pfister, S and Hartmann, C and Paulus, W and Reifenberger, G and Deimling, A. Von
Acta neuropathologica, ISSN 0001-6322, 2011, Volume 121, Issue 3, pp. 397 - 405
Brain tumor | Pathology | Neurosciences | Ganglioglioma | V600E mutation | Medicine & Public Health | BRAF | Pleomorphic xanthoastrocytoma | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Astrocytoma - genetics | Gene Frequency - genetics | World Health Organization | Signal Transduction | Humans | Brain Neoplasms - pathology | Brain Neoplasms - genetics | Child, Preschool | Exons - genetics | Mutation, Missense - genetics | Young Adult | Ganglioglioma - genetics | Astrocytoma - pathology | Proto-Oncogene Proteins B-raf - genetics | Ganglioglioma - pathology | Adolescent | Adult | Nervous System Neoplasms - genetics | Retrospective Studies | Child | Nervous System Neoplasms - pathology | Medical colleges | Molecular genetics | Sarcoma | Neurons | Brain tumors | Oncology, Experimental | Melanoma | Thyroid diseases | Research | Codon | Gene mutations | Gliomas | Analysis | Genetic research | Genetic aspects | Cancer | Index Medicus | meningioma | Pediatrics | Exons | Glioblastoma | Clinical trials | Insertion | Adenoma | Neuronal-glial interactions | Missense mutation | Sheaths | Colon | Astrocytoma | Oncogenes | Peripheral nervous system | Astrocytes | Base pairs | Central nervous system diseases | Glioma | Pituitary | Codons | papillary thyroid carcinoma | Tumors
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text SARS‐CoV‐2 targets neurons of 3D human brain organoids
by Ramani, Anand and Müller, Lisa and Ostermann, Philipp N and Gabriel, Elke and Abida‐Islam, Pranty and Müller‐Schiffmann, Andreas and Mariappan, Aruljothi and Goureau, Olivier and Gruell, Henning and Walker, Andreas and Andrée, Marcel and Hauka, Sandra and Houwaart, Torsten and Dilthey, Alexander and Wohlgemuth, Kai and Omran, Heymut and Klein, Florian and Wieczorek, Dagmar and Adams, Ortwin and Timm, Jörg and Korth, Carsten and Schaal, Heiner and Gopalakrishnan, Jay
The EMBO journal, ISSN 0261-4189, 10/2020, Volume 39, Issue 20, pp. e106230 - n/a
Tau pathology | brain organoids | cell death | SARS‐CoV-2 | neurons | SARS-CoV-2 | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Neurons - virology | Animals | Chlorocebus aethiops | Organoids | Betacoronavirus - physiology | Humans | Cell Death | Brain - virology | tau Proteins - metabolism | Nervous System Diseases - virology | Vero Cells | Tropism | Neuroimaging | Brain | Phosphorylation | Pandemics | Neurons | Abnormalities | Severe acute respiratory syndrome | Central nervous system | Viral diseases | Nervous system | Exposure | Infections | Coronaviruses | Severe acute respiratory syndrome coronavirus 2 | COVID-19 | Axons | Neurotoxicity | Tau protein | Cell death | Public health | Index Medicus | Life Sciences | Neuroscience | Microbiology, Virology & Host Pathogen Interaction | Molecular Biology of Disease
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia
by Mitchison, Hannah M and Schmidts, Miriam and Loges, Niki T and Freshour, Judy and Dritsoula, Athina and Hirst, Rob A and O'Callaghan, Christopher and Blau, Hannah and Al Dabbagh, Maha and Olbrich, Heike and Beales, Philip L and Yagi, Toshiki and Mussaffi, Huda and Chung, Eddie M. K and Omran, Heymut and Mitchell, David R
Nature genetics, ISSN 1061-4036, 04/2012, Volume 44, Issue 4, pp. 381 - 389
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Complex syndromes | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Medical genetics | Microtubule-Associated Proteins - chemistry | Microtubule-Associated Proteins - genetics | Humans | Bacterial Proteins - chemistry | Molecular Sequence Data | Male | Kartagener Syndrome - genetics | Chlamydomonas reinhardtii - genetics | Base Sequence | Female | Situs Inversus - genetics | Cytoplasm - genetics | Amino Acid Sequence | Zebrafish Proteins - chemistry | Zebrafish Proteins - metabolism | Bacterial Proteins - genetics | Sequence Analysis, DNA | Zebrafish - genetics | Cilia - genetics | Phenotype | Sequence Alignment | Animals | Axonemal Dyneins - biosynthesis | Pedigree | Bacterial Proteins - metabolism | Polymorphism, Single Nucleotide | Mutation | Zebrafish Proteins - genetics | Physiological aspects | Genetic aspects | Research | Gene mutations | Movement disorders | Dynein | Proteins | Genotype & phenotype | Motility | Sperm | Genes | Ear diseases | Genetics | Cytoplasm | Molecular weight | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry
by Olbrich, Heike and Schmidts, Miriam and Werner, Claudius and Onoufriadis, Alexandros and Loges, Niki T and Raidt, Johanna and Banki, Nora Fanni and Shoemark, Amelia and Burgoyne, Tom and Al Turki, Saeed and Hurles, Matthew E and Köhler, Gabriele and Schroeder, Josef and Nürnberg, Gudrun and Nürnberg, Peter and Chung, Eddie M.K and Reinhardt, Richard and Marthin, June K and Nielsen, Kim G and Mitchison, Hannah M and Omran, Heymut and UK10K Consortium
American journal of human genetics, ISSN 0002-9297, 10/2012, Volume 91, Issue 4, pp. 672 - 684
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Complex syndromes | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Haplotypes | Genetic Predisposition to Disease | Humans | Genetic Loci - genetics | Molecular Sequence Data | Male | Kartagener Syndrome - genetics | DNA Mutational Analysis - methods | Genes, Recessive | Cilia - genetics | Homozygote | Chromosomes, Human, Pair 1 | Pedigree | Base Sequence | RNA Splicing - genetics | Chromosomes, Human, Pair 16 | Adult | Female | Situs Inversus - genetics | Mutation | Hydrocephalus - genetics | Microfilament Proteins - genetics | Siblings | Usage | Motility | Gene mutations | Cilia and ciliary motion | Exome sequencing | Physiological aspects | Causes of | Genetic aspects | Research | Movement disorders | Cells | Proteins | Chronic obstructive pulmonary disease | Genetic disorders | Rodents | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights