X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (508) 508
Publication (20) 20
Book / eBook (13) 13
Patent (13) 13
Magazine Article (5) 5
Book Chapter (3) 3
Conference Proceeding (1) 1
Dissertation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (244) 244
female (153) 153
male (128) 128
adult (98) 98
middle aged (72) 72
index medicus (66) 66
aged (53) 53
dentistry, oral surgery & medicine (48) 48
adolescent (39) 39
surveys and questionnaires (37) 37
animals (35) 35
child (34) 34
netherlands (34) 34
dentistry (27) 27
time factors (27) 27
oncology (25) 25
public, environmental & occupational health (23) 23
reproducibility of results (22) 22
neoplasms - drug therapy (21) 21
research (21) 21
drug evaluation (20) 20
analysis (19) 19
child, preschool (19) 19
cell biology (17) 17
immunology (17) 17
rheumatoid arthritis (17) 17
age factors (16) 16
drug administration schedule (16) 16
drug therapy, combination (16) 16
mice (16) 16
bone marrow - drug effects (15) 15
children (15) 15
dose-response relationship, drug (15) 15
fear (15) 15
sex factors (15) 15
anxiety (14) 14
attitude to health (14) 14
biochemistry & molecular biology (14) 14
dna repair (14) 14
rheumatology (14) 14
cells, cultured (13) 13
clinical trials as topic (13) 13
methotrexate (13) 13
nickel (13) 13
prognosis (13) 13
risk factors (13) 13
breast neoplasms - drug therapy (12) 12
dentist-patient relations (12) 12
international (12) 12
kinetics (12) 12
methotrexate - therapeutic use (12) 12
patients (12) 12
pharmacology & pharmacy (12) 12
remission, spontaneous (12) 12
allergy (11) 11
dental care - psychology (11) 11
dermatology (11) 11
dna damage (11) 11
leukopenia - chemically induced (11) 11
medicine & public health (11) 11
neurosciences (11) 11
oral health (11) 11
prevalence (11) 11
psychometrics (11) 11
regression analysis (11) 11
antineoplastic agents - adverse effects (10) 10
attitude of health personnel (10) 10
biophysics (10) 10
cells (10) 10
chi-square distribution (10) 10
clinical neurology (10) 10
dental anxiety - psychology (10) 10
dentists - psychology (10) 10
medicine, research & experimental (10) 10
mutation (10) 10
proteins (10) 10
thrombocytopenia - chemically induced (10) 10
cancer (9) 9
care and treatment (9) 9
dentists (9) 9
disease (9) 9
doxorubicin - therapeutic use (9) 9
follow-up studies (9) 9
health aspects (9) 9
infant (9) 9
molecular biology (9) 9
nickel - immunology (9) 9
social dentistry (9) 9
surgery (9) 9
therapy (9) 9
treatment outcome (9) 9
ultraviolet rays (9) 9
validity (9) 9
aged, 80 and over (8) 8
analysis of variance (8) 8
antineoplastic agents - therapeutic use (8) 8
article (8) 8
burnout (8) 8
cell line (8) 8
disease models, animal (8) 8
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (4) 4
Gerstein Science - Stacks (3) 3
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
UTL at Downsview - May be requested (2) 2
Music - Storage2 (1) 1
Online Resources - Online (1) 1
Victoria University CRRS - Library use only (1) 1
Victoria University E.J. Pratt - Canadiana (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (528) 528
German (9) 9
Dutch (7) 7
French (5) 5
Chinese (2) 2
Korean (1) 1
Latin (1) 1
Spanish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Molecular Therapy, ISSN 1525-0016, 04/2001, Volume 3, Issue 4, pp. 565 - 573
X-linked severe combined immunodeficiency (XSCID) is caused by mutations in the IL-2 receptor γ chain (IL2RG) gene, resulting in absent T lymphocytes and... 
human IL2 receptor γ chain | MFG-S-hIL2RG | in vivo selection | retroviral vector | hematopoietic stem cell gene therapy | murine XSCID | human X severe combined immunodeficiency (XSCID) | ex vivo gene therapy | human IL2 receptor chain | Retroviral vector | Murine XSCID | In vivo selection | Hematopoietic stem cell gene therapy | Ex vivo gene therapy | Human IL2 receptor γ chain | Human X severe combined immunodeficiency (XSCID) | INTERLEUKIN-2 | MEDICINE, RESEARCH & EXPERIMENTAL | ADENOSINE-DEAMINASE | SINGLE-CENTER | human IL2 receptor gamma chain | MURINE MODEL | THERAPY | BONE-MARROW TRANSPLANTATION | LONG TERMINAL REPEAT | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | HEMATOPOIETIC STEM-CELLS | GENETICS & HEREDITY | MOLECULAR-BASIS | EXPRESSION | Blotting, Southern | Humans | Male | RNA, Messenger - metabolism | Receptors, Interleukin-2 - genetics | Flow Cytometry | Retroviridae - metabolism | Retroviridae - genetics | T-Lymphocytes - metabolism | Time Factors | Female | X Chromosome - genetics | B-Lymphocytes - metabolism | Disease Models, Animal | Genetic Linkage | Lymphocytes - metabolism | Promoter Regions, Genetic | Transduction, Genetic | Mice, Inbred C57BL | Severe Combined Immunodeficiency - therapy | Hematopoietic Stem Cells - metabolism | Mice, SCID | Blotting, Northern | Animals | Mice | Models, Genetic | Mutation | Genetic Vectors | DNA, Complementary - metabolism | 3T3 Cells | Genetic Therapy - methods
Journal Article
by Braun, Daniela A and Rao, Jia and Mollet, Geraldine and Schapiro, David and Daugeron, Marie-Claire and Tan, Weizhen and Gribouval, Olivier and Boyer, Olivia and Revy, Patrick and Jobst-Schwan, Tilman and Schmidt, Johanna Magdalena and Lawson, Jennifer A and Schanze, Denny and Ashraf, Shazia and Ullmann, Jeremy F P and Hoogstraten, Charlotte A and Boddaert, Nathalie and Collinet, Bruno and Martin, Gaëlle and Liger, Dominique and Lovric, Svjetlana and Furlano, Monica and Guerrera, I Chiara and Sanchez-Ferras, Oraly and Hu, Jennifer F and Boschat, Anne-Claire and Sanquer, Sylvia and Menten, Björn and Vergult, Sarah and De Rocker, Nina and Airik, Merlin and Hermle, Tobias and Shril, Shirlee and Widmeier, Eugen and Gee, Heon Yung and Choi, Won-Il and Sadowski, Carolin E and Pabst, Werner L and Warejko, Jillian K and Daga, Ankana and Basta, Tamara and Matejas, Verena and Scharmann, Karin and Kienast, Sana D and Behnam, Babak and Beeson, Brendan and Begtrup, Amber and Bruce, Malcolm and Ch'ng, Gaik-Siew and Lin, Shuan-Pei and Chang, Jui-Hsing and Chen, Chao-Huei and Cho, Megan T and Gaffney, Patrick M and Gipson, Patrick E and Hsu, Chyong-Hsin and Kari, Jameela A and Ke, Yu-Yuan and Kiraly-Borri, Cathy and Lai, Wai-Ming and Lemyre, Emmanuelle and Littlejohn, Rebecca Okashah and Masri, Amira and Moghtaderi, Mastaneh and Nakamura, Kazuyuki and Ozaltin, Fatih and Praet, Marleen and Prasad, Chitra and Prytula, Agnieszka and Roeder, Elizabeth R and Rump, Patrick and Schnur, Rhonda E and Shiihara, Takashi and Sinha, Manish D and Soliman, Neveen A and Soulami, Kenza and Sweetser, David A and Tsai, Wen-Hui and Tsai, Jeng-Daw and Topaloglu, Rezan and Vester, Udo and Viskochil, David H and Vatanavicharn, Nithiwat and Waxler, Jessica L and Wierenga, Klaas J and Wolf, Matthias T F and Wong, Sik-Nin and Leidel, Sebastian A and Truglio, Gessica and Dedon, Peter C and Poduri, Annapurna and Mane, Shrikant and Lifton, Richard P and Bouchard, Maxime and Kannu, Peter and Chitayat, David and Magen, Daniella and Callewaert, Bert and van Tilbeurgh, Herman and Zenker, Martin and ...
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 10, pp. 1529 - 1529
Galloway-Mowat syndrome (GAMOS) is an autosomal-recessive disease characterized by the combination of early-onset nephrotic syndrome (SRNS) and microcephaly... 
YEAST | UNFOLDED PROTEIN RESPONSE | TRANSFER-RNA MODIFICATION | DNA | KINASE | SECKEL-SYNDROME | GENOME MAINTENANCE | WDR73 | GALLOWAY-MOWAT SYNDROME | MASS-SPECTROMETRY | GENETICS & HEREDITY | Metalloendopeptidases - genetics | Protein-Serine-Threonine Kinases - deficiency | Microcephaly - genetics | Humans | Metalloendopeptidases - deficiency | Apoptosis - genetics | Multiprotein Complexes - genetics | Nephrotic Syndrome - genetics | DNA Repair - genetics | Telomere Homeostasis - genetics | Endoplasmic Reticulum Stress - genetics | Intracellular Signaling Peptides and Proteins - deficiency | Hernia, Hiatal - genetics | Intracellular Signaling Peptides and Proteins - genetics | Podocytes - metabolism | RNA, Transfer - metabolism | Protein-Serine-Threonine Kinases - genetics | Models, Molecular | Nephrotic Syndrome - pathology | Zebrafish | Cytoskeleton - ultrastructure | Nephrosis - genetics | Gene Knockout Techniques | Carrier Proteins - genetics | Podocytes - ultrastructure | Zebrafish Proteins - deficiency | Animals | RNA Processing, Post-Transcriptional - genetics | CRISPR-Cas Systems | Protein Conformation | Mice | Mutation | Zebrafish Proteins - genetics | Cell Movement | Genetic disorders | Gene mutations | Development and progression | Nephrotic syndrome | Genetic aspects | Microcephaly | Health aspects | Cell proliferation | Brain | CRISPR | Genes | DNA damage | Genomes | Lethality | Kinases | Proteins | Genotype & phenotype | Microencephaly | Actin | Biopsy | Cytoskeleton | Scientific imaging | Endoplasmic reticulum | Mass spectrometry | Deoxyribonucleic acid--DNA | Apoptosis | Life Sciences
Journal Article
Journal Article
Journal Article
Journal Article