X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
chondrodystrophy (189) 189
index medicus (76) 76
mutation (63) 63
humans (62) 62
animals (50) 50
female (48) 48
cartilage (41) 41
male (39) 39
genetics & heredity (37) 37
dwarfism (33) 33
chondrocytes (32) 32
dysplasia (32) 32
collagen (28) 28
mice (28) 28
man (27) 27
bone (26) 26
proteins (26) 26
genetics (23) 23
growth plate (23) 23
skeleton (23) 23
mutations (22) 22
osteochondrodysplasias - genetics (22) 22
analysis (21) 21
biochemistry & molecular biology (20) 20
pregnancy (20) 20
gene (19) 19
phenotype (19) 19
adult (18) 18
genes (18) 18
chondrogenesis (17) 17
fetuses (17) 17
medicine (17) 17
bones (16) 16
bone dysplasia (15) 15
expression (15) 15
ossification (15) 15
research article (15) 15
rodents (15) 15
bone growth (14) 14
extracellular matrix (14) 14
phenotypes (14) 14
proteoglycans (14) 14
radiography (14) 14
adolescent (13) 13
animal models (13) 13
cell biology (13) 13
genomes (13) 13
hypoplasia (13) 13
infant, newborn (13) 13
mouse (13) 13
multidisciplinary sciences (13) 13
science (13) 13
cattle (12) 12
genetic aspects (12) 12
abnormalities (11) 11
case reports (11) 11
child (11) 11
deoxyribonucleic acid--dna (11) 11
fibroblasts (11) 11
genetic disorders (11) 11
research (11) 11
veterinary sciences (11) 11
biochemistry (10) 10
chondrodysplasia (10) 10
developmental biology (10) 10
disease (10) 10
enzymes (10) 10
growth (10) 10
life sciences (10) 10
pedigree (10) 10
apoptosis (9) 9
children (9) 9
chondrocytes - metabolism (9) 9
endoplasmic reticulum (9) 9
gene deletion (9) 9
gene expression (9) 9
pathology (9) 9
pediatrics (9) 9
prenatal diagnosis (9) 9
protein (9) 9
signal transduction (9) 9
skeletal dysplasia (9) 9
spine (9) 9
vertebrae (9) 9
achondroplasia (8) 8
aggrecan (8) 8
article (8) 8
biology (8) 8
cell proliferation (8) 8
child, preschool (8) 8
clonal deletion (8) 8
genomics (8) 8
genotype & phenotype (8) 8
infant (8) 8
nanomelia (8) 8
osteoarthritis (8) 8
osteochondrodysplasias - pathology (8) 8
ultrasound (8) 8
x chromosome (8) 8
age (7) 7
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Australasian Journal of Dermatology, ISSN 0004-8380, 05/2019, Volume 60, Issue 2, pp. e160 - e162
Journal Article
Journal of Orthopaedic Research, ISSN 0736-0266, 12/2019, Volume 37, Issue 12, pp. 2550 - 2560
ABSTRACT Osteoarthritis (OA) is a degenerative joint disease associated with chronic pain and disability in humans and companion animals. The canine species... 
synovial inflammation | chondrodystrophy | FGF4 retrogene | Wnt pathway | osteoarthritis
Journal Article
The Journal of cell biology, ISSN 0021-9525, 06/2019, Volume 218, Issue 6, pp. 1853 - 1870
In childhood, skeletal growth is driven by transient expansion of cartilage in the growth plate. The common belief is that energy production in this hypoxic... 
Phenotypes | Deactivation | Growth rate | Fetuses | Chains | Inactivation | Metabolism | Diseases | Chondrodystrophy | Cartilage | Growth plate | Mitochondria | Cell death | Glycolysis | Hypoxia | Extracellular matrix | Mice | Children | Electron transport | Life Sciences
Journal Article
International Journal of Paleopathology, ISSN 1879-9817, 06/2015, Volume 9, pp. 1 - 7
Two articulating chicken bones from a feast deposit, dated to the 16th century, from Chester, exhibit lesions consistent with the skeletal disorder... 
Chicken | ‘Creeper’ mutation | Selective breeding | Chondrodystrophy | 'Creeper' mutation | HEREDITARY CHONDRODYSTROPHY | DEFORMITY | PALEONTOLOGY | INFECTION | BONE | PATHOLOGY | FOWL
Journal Article
Морфологія, ISSN 1997-9665, 01/2013, Volume 7, Issue 2, pp. 98 - 101
The results of the influence of high doses of aminobifosfonate "Pamired" on condition of metaepifisate plates of long bones. The aim of investigation is to... 
metaepifisate plate | pamired | chondrodystrophy
Journal Article
Clinical Genetics, ISSN 0009-9163, 01/2019, Volume 95, Issue 1, pp. 160 - 164
In many children with short stature, the etiology of the decreased linear growth remains unknown. We sought to identify the underlying genetic etiology in a... 
short stature | growth | chondrogenesis | GENETICS & HEREDITY | Medicine, Experimental | Medical research | Genetic aspects | Gene expression | Growth plate | Phenotypes | Nonsense mutation | Etiology | Chondrocytes | siRNA | Children | Mutation | Chondrogenesis | Chondrodystrophy
Journal Article
Archives of Disease in Childhood, ISSN 0003-9888, 10/2017, Volume 102, Issue Suppl 3, p. A30
BackgroundWe illustrate our early experience of whole body micro-CT in stillbirths and early gestation termination of pregnancies, with particular respect to... 
Dysplasia | Medical imaging | Fetuses | Gestation | Chondrodystrophy | Magnetic resonance imaging | Computed tomography | Early experience | Osteogenesis imperfecta | Bone (long) | Bone imaging | Ultrasound | Osteogenesis
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2019, Volume 14, Issue 10, p. e0223671
Genome-wide association studies (GWAS) have commonly been used to identify candidate genes that control economically important traits in livestock. Our... 
Usage | Beef cattle | Genetic aspects | Nucleotide sequencing | Single nucleotide polymorphisms | Research | DNA sequencing | Genes | Genomics | Linkage disequilibrium | Muscles | Genomes | Single-nucleotide polymorphism | Nucleotides | Bone diseases | Chondrodystrophy | Gene sequencing | Next-generation sequencing | Cattle | Livestock | Beef | Mutation | Chromosomes
Journal Article
JOURNAL OF CELL BIOLOGY, ISSN 0021-9525, 09/2019, Volume 218, Issue 9, pp. 3134 - 3152
Journal Article
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN 0027-8424, 07/2019, Volume 116, Issue 31, pp. 15570 - 15579
The type I TGF beta receptor TGF beta RI (encoded by Tgfbr1) was ablated in cartilage. The resulting Tgfbr1(Col2) mice exhibited lethal chondrodysplasia.... 
ACTIVATION | PROTEIN | BMP | CHONDROCYTES | MULTIDISCIPLINARY SCIENCES | cartilage | COMPONENTS | ALK5 | ALK1 | GROWTH-FACTOR-BETA | ARTICULAR-CARTILAGE | KINASE 1 ALK1 | DIFFERENTIATION | TGF beta | EXPRESSION | CHONDROGENESIS | Cartilage | Signaling | Growth plate | Intracellular signalling | Mice | Bone morphogenetic protein 9 | Ablation | Chondrodystrophy | Biological Sciences | PNAS Plus | TGFβ
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2017, Volume 114, Issue 43, p. 11476
Chondrodystrophy in dogs is defined by dysplastic, shortened long bones and premature degeneration and calcification of intervertebral discs. Independent... 
Fibroblast growth factor | Dysplasia | Abnormalities | Genomes | Breeding of animals | Intervertebral discs | Fibroblast growth factor 4 | Gene sequencing | Chondrodystrophy | Signaling | Dogs | Calcification | Bone dysplasia | Genetics | Bones | Bone (long) | Degeneration | Skeleton
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 12/2019, Volume 179, Issue 12, pp. 2490 - 2493
Desbuquois dysplasia (DBQD1 [MIM 251450]) is an autosomal recessive chondrodysplasia with micromelia, severe joint laxity and dislocations, and a... 
SNP‐microarray | consanguinity | Desbuquois dysplasia | prenatal | skeletal dysplasia | Femur | Dysplasia | Fetuses | Single-nucleotide polymorphism | Bone (axial) | Ossification | Chondrodystrophy | Pregnancy | Ultrasonic imaging | Prenatal diagnosis | DNA microarrays | Mutation | Ultrasound | Deoxyribonucleic acid--DNA
Journal Article
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN 1422-0067, 03/2019, Volume 20, Issue 5, p. 1008
The gene encoding the proteoglycan aggrecan (Agc1) is abundantly expressed in cartilage during development and adulthood, and the loss or diminished deposition... 
articular cartilage | NANOMELIA | MATRIX | COLLAGEN | ABNORMALITIES | osteoarthritis | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHONDRODYSTROPHY | atomic force microscopy | MATURATION | CHEMISTRY, MULTIDISCIPLINARY | MICE LACKING | DEGENERATION | aggrecan | DWARFISM | EXPRESSION
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 05/2011, Volume 155, Issue 5, pp. C1 - C1
In his 1892 monograph “Studies on the so‐called fetal rickets” [1892] (Untersuchungen über die sogenannte foetale Rachitis, chondrodystrophia foetalis, Verlag... 
Neonates | Dysplasia | Femur | Rickets | Fetuses | Epiphysis | Chondrodystrophy
Journal Article