X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (75233) 75233
Newspaper Article (540) 540
Newsletter (331) 331
Book Chapter (119) 119
Dissertation (39) 39
Conference Proceeding (33) 33
Publication (26) 26
Magazine Article (22) 22
Book / eBook (14) 14
Government Document (12) 12
Web Resource (7) 7
Trade Publication Article (5) 5
Book Review (3) 3
Reference (2) 2
Transcript (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (49986) 49986
animals (36548) 36548
fibroblasts (26305) 26305
male (21588) 21588
female (20023) 20023
mice (19020) 19020
cells, cultured (15433) 15433
fibroblasts - metabolism (15070) 15070
expression (12982) 12982
cell biology (12460) 12460
fibroblasts - pathology (11760) 11760
oncology (9505) 9505
adult (9402) 9402
middle aged (9089) 9089
rats (8988) 8988
gene expression (8060) 8060
cancer (7817) 7817
fibroblasts - drug effects (7810) 7810
proteins (7629) 7629
biochemistry & molecular biology (7429) 7429
pathology (7085) 7085
cells (7003) 7003
apoptosis (6877) 6877
fibroblasts - cytology (6550) 6550
immunohistochemistry (6471) 6471
research (6466) 6466
aged (6288) 6288
collagen (6179) 6179
fibrosis (6169) 6169
analysis (6060) 6060
cell line (6046) 6046
research article (6012) 6012
signal transduction (5988) 5988
inflammation (5752) 5752
multidisciplinary sciences (5342) 5342
cell proliferation (5302) 5302
medicine (5204) 5204
disease models, animal (5090) 5090
stem cells (4820) 4820
cell line, tumor (4768) 4768
activation (4760) 4760
medicine, research & experimental (4754) 4754
mutation (4538) 4538
angiogenesis (4408) 4408
tumors (4391) 4391
growth factors (4290) 4290
physiological aspects (4130) 4130
gene-expression (4111) 4111
mice, inbred c57bl (4068) 4068
in-vitro (4029) 4029
differentiation (3974) 3974
proliferation (3916) 3916
cytokines (3852) 3852
biology (3832) 3832
rodents (3815) 3815
science (3732) 3732
genetic aspects (3713) 3713
time factors (3711) 3711
immunology (3690) 3690
growth (3645) 3645
fibroblast growth factors (3629) 3629
surgery (3624) 3624
phenotype (3574) 3574
health aspects (3535) 3535
wound healing (3526) 3526
disease (3520) 3520
kinases (3375) 3375
cell differentiation (3371) 3371
skin - pathology (3370) 3370
skin (3369) 3369
genetics & heredity (3343) 3343
phosphorylation (3340) 3340
metastasis (3229) 3229
extracellular matrix (3203) 3203
rna, messenger - metabolism (3099) 3099
mice, knockout (3056) 3056
tumor cells, cultured (3027) 3027
fibroblasts - physiology (3016) 3016
blotting, western (2914) 2914
oxidative stress (2856) 2856
rats, sprague-dawley (2852) 2852
neurosciences (2847) 2847
care and treatment (2836) 2836
cell proliferation - drug effects (2785) 2785
physiology (2776) 2776
genes (2739) 2739
adolescent (2726) 2726
pathogenesis (2717) 2717
inhibition (2680) 2680
in-vivo (2650) 2650
gene (2638) 2638
protein (2600) 2600
rna, messenger - genetics (2574) 2574
cell division (2549) 2549
fibroblast-growth-factor (2538) 2538
gene expression regulation (2531) 2531
studies (2507) 2507
development and progression (2502) 2502
reverse transcriptase polymerase chain reaction (2475) 2475
transfection (2427) 2427
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (74731) 74731
Chinese (629) 629
Japanese (525) 525
Russian (398) 398
French (389) 389
German (379) 379
Spanish (66) 66
Polish (50) 50
Italian (46) 46
Portuguese (20) 20
Hungarian (16) 16
Ukrainian (8) 8
Arabic (4) 4
Korean (4) 4
Romanian (3) 3
Czech (2) 2
Dutch (2) 2
Finnish (2) 2
Hebrew (2) 2
Turkish (2) 2
Croatian (1) 1
Danish (1) 1
Norwegian (1) 1
Serbian (1) 1
Slovak (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The American Journal of Human Genetics, ISSN 0002-9297, 10/2017, Volume 101, Issue 4, pp. 552 - 563
The Sonic Hedgehog (SHH) pathway is a key signaling pathway orchestrating embryonic development, mainly of the CNS and limbs. In vertebrates, SHH signaling is... 
polymicrogyria | developmental defects | hypomorphic variants | congenital ataxia | ciliopathies | SUFU | Joubert syndrome | Sonic Hedgehog | molar tooth sign | GLI3 | Congenital ataxia | Hypomorphic variants | Developmental defects | Ciliopathies | Polymicrogyria | Molar tooth sign | SHH | SIGNALING PATHWAY | GENETICS & HEREDITY | PLANAR CELL POLARITY | CEREBELLAR DEVELOPMENT | GLI PROTEINS | MUTATIONS | KIF7 | MEDULLOBLASTOMA | PHENOTYPIC SPECTRUM | PRIMARY CILIA | Abnormalities, Multiple - pathology | Skin - metabolism | Humans | Zinc Finger Protein Gli3 | Hedgehog Proteins - metabolism | Male | Bone Diseases, Developmental - genetics | Mutation, Missense | Cerebellum - abnormalities | Bone Diseases, Developmental - pathology | Gene Expression Regulation, Developmental | Kruppel-Like Transcription Factors - metabolism | Kidney Diseases, Cystic - genetics | Craniofacial Abnormalities - pathology | Female | Child | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Repressor Proteins - metabolism | Skin - pathology | Fibroblasts - metabolism | Repressor Proteins - chemistry | Signal Transduction | Cells, Cultured | Repressor Proteins - genetics | Eye Abnormalities - genetics | Fibroblasts - pathology | Genes, Recessive | Sequence Analysis, DNA | Cerebellum - pathology | Kidney Diseases, Cystic - pathology | Nerve Tissue Proteins - metabolism | Eye Abnormalities - pathology | Retina - abnormalities | Retina - pathology | Cohort Studies | Embryonic development | Usage | Gene mutations | Analysis | Nucleotide sequencing | Research | Diagnosis | Children | Health aspects | DNA sequencing
Journal Article
Neuron, ISSN 0896-6273, 04/2013, Volume 78, Issue 1, pp. 57 - 64
Valosin-containing protein (VCP) is a highly expressed member of the type II AAA+ ATPase family. VCP mutations are the cause of inclusion body myopathy,... 
LIPID-PEROXIDATION | SPINAL-CORD PATHOLOGY | MOUSE MODEL | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | DYSFUNCTION | BONE | NEUROSCIENCES | PAGET-DISEASE | TRANSGENIC MICE | REVEALS | RNA, Small Interfering - genetics | Humans | Middle Aged | Male | Frontotemporal Dementia - metabolism | Neurons - ultrastructure | Muscular Dystrophies, Limb-Girdle - genetics | Adenosine Triphosphate - metabolism | Membrane Potential, Mitochondrial - genetics | Muscular Dystrophies, Limb-Girdle - pathology | NAD - metabolism | Fibroblasts - metabolism | Animals, Newborn | Frontotemporal Dementia - genetics | Magnesium - metabolism | Mitochondria - pathology | Fibroblasts - pathology | Mutation - genetics | Myositis, Inclusion Body - genetics | Osteitis Deformans - pathology | Muscular Dystrophies, Limb-Girdle - metabolism | Analysis of Variance | Luminescent Proteins - genetics | Adenosine Triphosphatases - genetics | Mice | Lipid Peroxidation - genetics | RNA, Small Interfering - metabolism | Valosin Containing Protein | Osteitis Deformans - metabolism | Family Health | Cerebral Cortex - cytology | Case-Control Studies | Osteitis Deformans - genetics | Transfection | Mitochondria - genetics | Cell Cycle Proteins - genetics | Myositis, Inclusion Body - pathology | Adult | Female | Neuroblastoma - pathology | Frontotemporal Dementia - pathology | Adenosine Triphosphatases - deficiency | Mice, Inbred C57BL | Cells, Cultured | Cell Cycle Proteins - deficiency | Mitochondria - metabolism | Animals | Oxygen Consumption - genetics | Myositis, Inclusion Body - metabolism | Aged | Nervous system diseases | Neurosciences | Genes | Amyotrophic lateral sclerosis | Genetic aspects | Adenosine triphosphatase | Dementia | Proteins | Medical research | Phosphorylation | Biomedical research | Disease | Rodents | Respiration | Experiments | Patients | Report
Journal Article
Human Pathology, ISSN 0046-8177, 2015, Volume 49, pp. 27 - 32
Summary Complex I deficiency causes Leigh syndrome, fatal infant lactic acidosis, and neonatal cardiomyopathy. Mutations in more than 100 nuclear DNA and... 
Pathology | Metabolic disease | Lethal neonatal lactic acidosis | Whole-exome sequencing | Mitochondriopathy | Complex I deficiency | ACAD9 defect | Mitochondrial hyperplasia | Multiorgan failure | DIAGNOSIS | CARDIOMYOPATHY | PATHOLOGY | GENE | DNA | EXPRESSION | Immunohistochemistry | Fibroblasts - enzymology | Diaphragm - pathology | Mitochondria, Heart - pathology | Electron Transport Complex I - deficiency | Humans | Hyperplasia | Male | Cardiomyopathy, Hypertrophic - enzymology | Acyl-CoA Dehydrogenases - genetics | Leigh Disease - pathology | Muscle Weakness - genetics | Amino Acid Metabolism, Inborn Errors - genetics | Autopsy | DNA Mutational Analysis | Electron Transport Complex I - genetics | Fatal Outcome | Muscle Weakness - pathology | Acyl-CoA Dehydrogenases - deficiency | Amino Acid Metabolism, Inborn Errors - pathology | Kidney Tubules - pathology | Infant, Newborn | Multiple Organ Failure - pathology | Acyl-CoA Dehydrogenase - genetics | Cardiomyopathy, Hypertrophic - genetics | Genetic Predisposition to Disease | Mitochondria, Liver - pathology | Mitochondria, Heart - enzymology | Fibroblasts - pathology | Leigh Disease - genetics | Acidosis, Lactic - pathology | Cardiomyopathy, Hypertrophic - diagnosis | Mitochondrial Diseases - enzymology | Phenotype | Acyl-CoA Dehydrogenase - deficiency | Kidney Tubules - enzymology | Acidosis - diagnosis | Multiple Organ Failure - enzymology | Acidosis - genetics | Amino Acid Metabolism, Inborn Errors - enzymology | Mitochondrial Diseases - pathology | Muscle Weakness - diagnosis | Acidosis, Lactic - genetics | Cause of Death | Acidosis, Lactic - enzymology | Amino Acid Metabolism, Inborn Errors - diagnosis | DNA, Mitochondrial - genetics | Muscle Weakness - enzymology | Transfection | Mitochondrial Diseases - genetics | Mitochondria, Muscle - enzymology | Mitochondria, Muscle - pathology | Leigh Disease - enzymology | Cells, Cultured | Multiple Organ Failure - genetics | Codon, Nonsense | Mitochondria, Liver - enzymology | Multiple Organ Failure - diagnosis | Diaphragm - enzymology | Acidosis - pathology | Leigh Disease - diagnosis | Acidosis - enzymology | Mitochondrial Diseases - diagnosis | Acidosis, Lactic - diagnosis | Cardiomyopathy, Hypertrophic - pathology | Infants (Newborn) | Muscles | Genetic aspects | Mitochondrial DNA | Liver | Heart | Urine | Cytochrome | Antigens | Enzymes | Cytomegalovirus | Cardiomyopathy | Defects | Musculoskeletal system | Databases | Rodents | Fibroblasts | Oxidation | Mutation | Metabolic disorders | Deoxyribonucleic acid--DNA
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2011, Volume 108, Issue 4, pp. 1609 - 1614
Radiation therapy can result in bone injury with the development of fractures and often can lead to delayed and nonunion of bone. There is no prevention or... 
Femur | Free radicals | Stem cells | Irradiation | Bone marrow | Bones | Physical trauma | Bone marrow cells | Radiation damage | Mesenchymal stem cells | CFU-fibroblast | Self-renewal | Angiography | Repopulation | Differentiation | MIGRATION | CAPACITY | differentiation | ANGIOGENESIS | MULTIDISCIPLINARY SCIENCES | OSTEOGENESIS | self-renewal | angiography | CHEMOTHERAPY | TRANSPLANTATION | ORIGIN | ENGRAFTMENT | THERAPY | repopulation | Femur - pathology | Leukocyte Common Antigens - metabolism | Mesenchymal Stromal Cells - radiation effects | Blood Vessels - pathology | Bone Marrow - radiation effects | Blood Vessels - radiation effects | Radiation Injuries, Experimental - etiology | Free Radicals - metabolism | Antigens, Ly - metabolism | Colony-Forming Units Assay | Membrane Proteins - metabolism | Radiation Injuries, Experimental - metabolism | Osteoblasts - radiation effects | Femur - metabolism | Mice, Inbred C57BL | Bone Marrow Cells - pathology | Mesenchymal Stromal Cells - metabolism | Thiobarbituric Acid Reactive Substances - metabolism | Bone Marrow Cells - radiation effects | Radiation Injuries, Experimental - pathology | Fibroblasts - pathology | Femur - radiation effects | Integrin beta1 - metabolism | Osteoblasts - pathology | Animals | Fibroblasts - radiation effects | Bone Marrow - pathology | Mice | Mesenchymal Stromal Cells - pathology | Bone Marrow Cells - metabolism | Physiological aspects | Complications and side effects | Stem cell research | Care and treatment | Radiotherapy | Biological Sciences
Journal Article
Nature cell biology, ISSN 1476-4679, 2017, Volume 19, Issue 3, pp. 224 - 237
Journal Article
Forensic Science International, ISSN 0379-0738, 2010, Volume 203, Issue 1, pp. 93 - 98
Journal Article
Journal of Dentistry, ISSN 0300-5712, 2016, Volume 56, pp. 19 - 32
Journal Article