X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (265) 265
Book / eBook (18) 18
Publication (18) 18
Book Chapter (3) 3
Book Review (3) 3
Conference Proceeding (3) 3
Dissertation (1) 1
Magazine Article (1) 1
Newsletter (1) 1
Newspaper Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (209) 209
metal metabolism, inborn errors - genetics (121) 121
male (99) 99
animals (97) 97
index medicus (92) 92
female (91) 91
copper - metabolism (76) 76
metal metabolism, inborn errors - metabolism (57) 57
mutation (55) 55
copper (37) 37
metal metabolism, inborn errors - diagnosis (37) 37
iron - metabolism (36) 36
metabolism (36) 36
pediatrics (36) 36
infant, newborn (35) 35
mice (34) 34
biochemistry & molecular biology (33) 33
metals (33) 33
infant (32) 32
child (28) 28
genetics & heredity (28) 28
iron (28) 28
child, preschool (27) 27
metal metabolism, inborn errors - pathology (27) 27
liver - metabolism (26) 26
adult (25) 25
analysis (24) 24
clinical neurology (24) 24
dogs (24) 24
toxicology (24) 24
metal metabolism, inborn errors - veterinary (23) 23
molybdenum (23) 23
mutations (23) 23
toxicity (22) 22
endocrinology & metabolism (21) 21
homeostasis (21) 21
biochemistry, general (20) 20
metal metabolism, inborn errors - complications (20) 20
phenotype (20) 20
zinc - metabolism (20) 20
cation transport proteins - genetics (19) 19
gene (19) 19
life sciences (19) 19
zinc (19) 19
disease models, animal (18) 18
metal metabolism, inborn errors - physiopathology (18) 18
physiological aspects (18) 18
syndrome (18) 18
dog diseases - genetics (17) 17
pedigree (17) 17
adolescent (16) 16
genetic aspects (16) 16
liver (16) 16
research (16) 16
copper - toxicity (15) 15
disease (15) 15
expression (15) 15
hemochromatosis (15) 15
hepatolenticular degeneration - genetics (15) 15
middle aged (15) 15
neurosciences (15) 15
oxidative stress (15) 15
proteins (15) 15
cell biology (14) 14
enzymes (14) 14
hereditary hemochromatosis (14) 14
magnetic resonance imaging (14) 14
medicine, research & experimental (14) 14
metal metabolism, inborn errors - drug therapy (14) 14
ceruloplasmin - genetics (13) 13
genetics (13) 13
hemochromatosis - genetics (13) 13
medicine & public health (13) 13
metabolic diseases (13) 13
metal metabolism, inborn errors (13) 13
metal metabolism, inborn errors - enzymology (13) 13
metal metabolism, inborn errors - therapy (13) 13
molecular sequence data (13) 13
biological transport (12) 12
ceruloplasmin - deficiency (12) 12
copper - blood (12) 12
hematology (12) 12
internal medicine (12) 12
menkes disease (12) 12
metal metabolism, inborn errors - blood (12) 12
brain - pathology (11) 11
cation transport proteins - metabolism (11) 11
ceruloplasmin - metabolism (11) 11
deficiency (11) 11
diagnosis, differential (11) 11
gene expression (11) 11
genes (11) 11
health aspects (11) 11
heavy metals (11) 11
liver - pathology (11) 11
molybdenum cofactor deficiency (11) 11
zinc - deficiency (11) 11
adenosine triphosphatases - genetics (10) 10
brain - metabolism (10) 10
brain diseases - genetics (10) 10
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (279) 279
French (3) 3
German (3) 3
Japanese (2) 2
Polish (2) 2
Danish (1) 1
Spanish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Annual Review of Biochemistry, ISSN 0066-4154, 6/2016, Volume 85, pp. 485 - 514
Radical S -adenosylmethionine (SAM) enzymes catalyze an astonishing array of complex and chemically challenging reactions across all domains of life. Of... 
tRNA modifications | radicals | Elongator | iron-sulfur cluster | adenosylmethionine | viperin | lipoic acid | molybdenum cofactor | Lipoic acid | Molybdenum cofactor | Viperin | TRNA modifications | Iron-sulfur cluster | S-adenosylmethionine | Radicals | IRON-SULFUR PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | MITOCHONDRIAL TRANSFER-RNAS | ANTIVIRAL PROTEIN VIPERIN | AMYOTROPHIC-LATERAL-SCLEROSIS | ADENOSYL-L-METHIONINE | LIPOIC ACID BIOSYNTHESIS | HEPATITIS-C VIRUS | PHENYLALANINE TRANSFER-RNA | MOLYBDENUM COFACTOR DEFICIENCY | GENOME-WIDE ASSOCIATION | Diabetes Mellitus, Type 2 - genetics | Humans | Histone Acetyltransferases - genetics | Iron-Sulfur Proteins - genetics | Intracellular Signaling Peptides and Proteins - metabolism | Thioctic Acid - metabolism | Heart Defects, Congenital - genetics | tRNA Methyltransferases - genetics | Heart Defects, Congenital - enzymology | Histone Acetyltransferases - metabolism | Nuclear Proteins - genetics | Intracellular Signaling Peptides and Proteins - genetics | tRNA Methyltransferases - metabolism | Gene Expression | Metal Metabolism, Inborn Errors - genetics | Neurodegenerative Diseases - pathology | Oxidoreductases - metabolism | Oxidoreductases - genetics | Diabetes Mellitus, Type 2 - enzymology | Heart Defects, Congenital - pathology | Metal Metabolism, Inborn Errors - pathology | Neurodegenerative Diseases - genetics | Nuclear Proteins - metabolism | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Proteins - genetics | Proteins - metabolism | Metal Metabolism, Inborn Errors - enzymology | Iron-Sulfur Proteins - metabolism | Diabetes Mellitus, Type 2 - pathology | Mutation | S-Adenosylmethionine - metabolism | Neurodegenerative Diseases - enzymology | Health aspects | Methionine
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 3/2018, Volume 41, Issue 2, pp. 187 - 196
Molybdenum cofactor deficiency is an autosomal recessive inborn error of metabolism, which results from mutations in genes involved in Moco biosynthesis. Moco... 
Human Genetics | Biochemistry, general | Pediatrics | S -sulfocysteine | Metabolic Diseases | Internal Medicine | Kozak-sequence | Urothione | Molybdenum cofactor | Medicine & Public Health | Moco deficiency | Sulfite oxidase | MOCS1 | cPMP | S-sulfocysteine | MEDICINE, RESEARCH & EXPERIMENTAL | MECHANISM | SULFITE OXIDASE DEFICIENCY | READING FRAMES | IDENTIFICATION | INBORN-ERRORS | GENE | METABOLISM | BIOSYNTHESIS | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | MUTATIONS | Metal Metabolism, Inborn Errors - metabolism | Genetic Predisposition to Disease | Peptide Fragments - metabolism | Frameshift Mutation | Metal Metabolism, Inborn Errors - genetics | Humans | Child, Preschool | Male | Nuclear Proteins - metabolism | Pteridines - metabolism | Metal Metabolism, Inborn Errors - diet therapy | Diet, Protein-Restricted | Coenzymes - metabolism | Magnetic Resonance Imaging | Metalloproteins - metabolism | Phenotype | Metal Metabolism, Inborn Errors - diagnosis | Age of Onset | HEK293 Cells | Nuclear Proteins - genetics | Child | Peptide Fragments - genetics | Proteins | Physiological aspects | Sulfites | Molybdenum | Analysis | Urine | Phenotypes | Translation | Inborn errors of metabolism | Transcription | Translation initiation | Frameshift mutation | Protein deficiency | Sulfite | Neurodegeneration | Genetic analysis | Translation termination | Children | Mutation | Seizures
Journal Article
Journal Article
Brain, ISSN 0006-8950, 2013, Volume 136, Issue 3, pp. 872 - 881
Journal Article
Current Opinion in Clinical Nutrition and Metabolic Care, ISSN 1363-1950, 06/2016, Volume 19, Issue 4, pp. 276 - 281
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, p. e64045
Zinc concentrations in breast milk are considerably higher than those of the maternal serum, to meet the infant's requirements for normal growth and... 
ALKALINE-PHOSPHATASES | SYNAPTIC VESICLES | EPITHELIAL-CELLS | PREMATURE-INFANTS | MULTIDISCIPLINARY SCIENCES | TRANSPORT COMPLEXES | VERTEBRATE CELLS | ACRODERMATITIS-ENTEROPATHICA | CONFERS RESISTANCE | SECRETORY PATHWAY | MAMMARY-GLAND | Metal Metabolism, Inborn Errors - metabolism | Lactation | Exons | Zinc - metabolism | Humans | Breast Feeding | Molecular Sequence Data | Infant | Milk, Human - chemistry | Base Sequence | Cation Transport Proteins - genetics | Female | Ion Transport | B-Lymphocytes - metabolism | Milk, Human - metabolism | Amino Acid Sequence | Cell Line | B-Lymphocytes - cytology | Metal Metabolism, Inborn Errors - genetics | Metal Metabolism, Inborn Errors - pathology | Asian Continental Ancestry Group | Animals | Cations, Divalent | Chickens | Heterozygote | Mutation | Growth Disorders | Zinc in the body | Tryptophan | Genetic aspects | Breast feeding | Neonates | Pediatrics | Breastfeeding & lactation | Epithelial cells | Serine | Infants | Genomes | Food science | Family medical history | Leucine | Dermatitis | Substitutes | Reduction | Missense mutation | Newborn babies | Arginine | Rodents | Life sciences | Mammary gland | Milk | Nutrient deficiency | Congenital diseases | Baldness | Review boards | Secretion | Zinc | Medicine | Babies | Zinc compounds | Womens health | Breast | Diabetes | Alzheimers disease | Breast milk
Journal Article