X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (262) 262
Publication (47) 47
Book Chapter (12) 12
Book / eBook (8) 8
Book Review (7) 7
Dissertation (5) 5
Newspaper Article (4) 4
Conference Proceeding (2) 2
Patent (1) 1
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (89) 89
osteogenesis imperfecta (86) 86
index medicus (64) 64
collagen (55) 55
osteogenesis imperfecta - genetics (54) 54
male (52) 52
animals (51) 51
mutation (48) 48
female (44) 44
child (37) 37
mice (35) 35
article (32) 32
collagen type i - genetics (30) 30
genetics & heredity (27) 27
osteogenesis imperfecta - metabolism (26) 26
child, preschool (25) 25
i collagen (25) 25
osteogenesis imperfecta - pathology (25) 25
phenotype (24) 24
biochemistry & molecular biology (23) 23
endocrinology & metabolism (23) 23
bone (20) 20
disease models, animal (20) 20
adult (19) 19
collagen type i - metabolism (19) 19
adolescent (17) 17
mineralization (17) 17
mutations (17) 17
osteogenesis imperfecta - physiopathology (17) 17
collagen - genetics (16) 16
analysis (15) 15
bones (15) 15
medicine, general & internal (15) 15
osteogenesis imperfecta - drug therapy (15) 15
proteins (15) 15
children (14) 14
collagen - metabolism (14) 14
genetic aspects (14) 14
hydroxylation (14) 14
abridged index medicus (13) 13
amino acid sequence (13) 13
bone density (13) 13
cells, cultured (13) 13
collagen type i - chemistry (13) 13
fractures (13) 13
genetics (13) 13
molecular sequence data (13) 13
osteoblasts - metabolism (13) 13
osteoporosis (13) 13
base sequence (12) 12
bisphosphonates (12) 12
pedigree (12) 12
radiography (12) 12
research (12) 12
bone and bones - pathology (11) 11
density (11) 11
physiological aspects (11) 11
aged (10) 10
fibroblasts (10) 10
genes, recessive (10) 10
infant (10) 10
middle aged (10) 10
mouse model (10) 10
bone and bones - metabolism (9) 9
disease (9) 9
endoplasmic-reticulum (9) 9
expression (9) 9
hydroxylases (9) 9
infant, newborn (9) 9
mice, mutant strains (9) 9
mutation - genetics (9) 9
osteogenesis imperfecta - diagnostic imaging (9) 9
prolyl 3-hydroxylation (9) 9
therapy (9) 9
bone diseases (8) 8
cell biology (8) 8
ehlers-danlos-syndrome (8) 8
enzymes (8) 8
femur - diagnostic imaging (8) 8
fibroblasts - metabolism (8) 8
genetic disorders (8) 8
genotype (8) 8
histomorphometry (8) 8
membrane glycoproteins - genetics (8) 8
mice, knockout (8) 8
osteogenesis (8) 8
osteogenesis imperfecta - therapy (8) 8
proteoglycans - genetics (8) 8
risk factors (8) 8
sclerostin antibody (8) 8
type i collagen (8) 8
alleles (7) 7
antibodies (7) 7
articles (7) 7
cartilage-associated protein (7) 7
collagen - chemistry (7) 7
crtap (7) 7
cyclophilins - genetics (7) 7
endoplasmic reticulum (7) 7
extracellular matrix - metabolism (7) 7
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (5) 5
Art - Library use only (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Robarts - May be requested in 6-10 wks (1) 1
Trinity College (John W Graham) - Reference (1) 1
UTL at Downsview - May be requested (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Genetics in Medicine, ISSN 1098-3600, 2018, Volume 21, Issue 5, pp. 1233 - 1239
Purpose: Growth deficiency is a cardinal feature of osteogenesis imperfecta (OI) types III and IV, caused by pathogenic variants in type I collagen.... 
type III OI | osteogenesis imperfecta | growth curves | type IV OI | HEIGHT VELOCITY | HORMONE | GENETICS & HEREDITY | MUTATIONS | WEIGHT | GIRLS | CHARTS | AXIS
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 11/2019, Volume 43, Issue 11, pp. 1554 - 1559
Melorheostosis is a rare sclerosing bone disease characterized by excessive cortical bone deposition that is frequently on the differential diagnosis for bone... 
Journal Article
Nature Reviews Endocrinology, ISSN 1759-5029, 05/2009, Volume 5, Issue 5, pp. 241 - 243
Journal Article
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, ISSN 0884-0431, 08/2019
Sclerostin antibody (Scl-Ab) is an anabolic bone agent that has been shown to increase bone mass in clinical trials of adult diseases of low bone mass, such as... 
Journal Article
Bone, ISSN 8756-3282, 08/2019, p. 115047
Bruck syndrome (BRKS) is the rare disorder that features congenital joint contractures often with pterygia and subsequent fractures, early on called... 
Journal Article
Bone, ISSN 8756-3282, 2016
Abstract Sclerostin antibody has demonstrated a bone-forming effect in pre-clinical models of osteogenesis imperfecta, where mutations in collagen or... 
Orthopedics
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 08/2013, Volume 98, Issue 8, pp. 3095 - 3103
Journal Article
Nature Reviews Endocrinology, ISSN 1759-5029, 05/2009, Volume 5, Issue 5, pp. 241 - 243
A clinical review of studies on bisphosphonate therapy for pediatric osteoporosis has revealed that they increase BMD, but whether they also improve fracture... 
INDUCED OSTEOPETROSIS | OSTEOGENESIS IMPERFECTA | PAMIDRONATE | THERAPY | ENDOCRINOLOGY & METABOLISM | Bone Density - drug effects | Humans | Diphosphonates - therapeutic use | Osteoporosis - drug therapy | Child | Diphosphonates - adverse effects | Diphosphonates - pharmacology
Journal Article
Bone, ISSN 8756-3282, 06/2016, Volume 87, p. 120
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1016/j.bone.2016.04.011 The... 
Collagen | Analysis | Osteogenesis imperfecta
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 10/2015, Volume 97, Issue 4, p. 521
  The evolutionarily conserved transmembrane anterior posterior transformation 1 protein, encoded by TAPT1, is involved in murine axial skeletal patterning,... 
Proteins | Genetic disorders | Morphology | Mutation | Cells
Journal Article