X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3675) 3675
Publication (488) 488
Book Review (486) 486
Patent (191) 191
Book / eBook (41) 41
Newsletter (35) 35
Book Chapter (28) 28
Conference Proceeding (9) 9
Transcript (9) 9
Dissertation (5) 5
Newspaper Article (5) 5
Magazine Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (3155) 3155
humans (1986) 1986
animals (1387) 1387
mutation (1182) 1182
male (1131) 1131
female (1111) 1111
genetic aspects (747) 747
mice (744) 744
proteins (642) 642
genes (583) 583
research (561) 561
biochemistry (486) 486
analysis (478) 478
genetics & heredity (462) 462
adult (460) 460
genetics (457) 457
multidisciplinary sciences (451) 451
research article (442) 442
phenotype (424) 424
biochemistry & molecular biology (422) 422
chemistry (421) 421
cell biology (418) 418
organic compounds (416) 416
physiological aspects (400) 400
mutations (396) 396
medicine (384) 384
gene expression (381) 381
enzymes (378) 378
gene (340) 340
article (339) 339
heterozygote (331) 331
dna (327) 327
middle aged (327) 327
expression (323) 323
science (321) 321
neurosciences (316) 316
gene mutations (308) 308
molecular sequence data (307) 307
microbiology (299) 299
metabolism (287) 287
genotype (286) 286
organic chemistry (285) 285
base sequence (282) 282
chemical compounds (280) 280
alleles (276) 276
cancer (272) 272
pedigree (265) 265
rodents (255) 255
endocrinology & metabolism (253) 253
genetic research (248) 248
oncology (248) 248
biology (238) 238
mice, knockout (237) 237
health aspects (231) 231
biology and life sciences (228) 228
child (227) 227
amino acid sequence (226) 226
mice, inbred c57bl (225) 225
polymerase chain reaction (224) 224
compound heterozygosity (223) 223
enzymology (220) 220
amino acids (218) 218
aged (212) 212
adolescent (209) 209
genomics (209) 209
wine (204) 204
molecular biology (201) 201
disease models, animal (200) 200
beer (197) 197
toxicology (197) 197
oxidative stress (195) 195
physiology (195) 195
pharmacology & pharmacy (194) 194
basic biological sciences (191) 191
identification (191) 191
metallurgy (191) 191
mutation or genetic engineering (190) 190
physical sciences (190) 190
spirits (190) 190
vinegar (190) 190
genomes (184) 184
heterocyclic compounds (183) 183
hematology (180) 180
nucleic acids (180) 180
compound heterozygous mutations (178) 178
care and treatment (176) 176
disease (175) 175
medicine and health sciences (170) 170
research and analysis methods (169) 169
child, preschool (168) 168
life sciences (168) 168
mutation - genetics (163) 163
signal transduction (163) 163
deoxyribonucleic acid--dna (159) 159
patients (159) 159
dna mutational analysis (158) 158
infant (158) 158
risk factors (158) 158
diseases (157) 157
cells (155) 155
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3960) 3960
French (69) 69
German (25) 25
Chinese (13) 13
Japanese (4) 4
Spanish (3) 3
Latvian (2) 2
Portuguese (2) 2
Arabic (1) 1
Czech (1) 1
Danish (1) 1
Greek (1) 1
Norwegian (1) 1
Polish (1) 1
Russian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Atherosclerosis and Thrombosis, ISSN 1340-3478, 2019, Volume 26, Issue 2, pp. 136 - 144
Aim: Dyslipidemia is the most common lipid metabolism disorder in humans, and its etiology remains elusive. Hypertriglyceridemia (HTG) is a type of... 
HTG | Compound mutation | Hypertriglyceridemia | LMF1 | TRIGLYCERIDE | ENZYME | GENE | PERIPHERAL VASCULAR DISEASE | ENDOPLASMIC-RETICULUM | LETHAL | LIPOPROTEIN-LIPASE | DEFICIENCY | Hypertriglyceridemia - genetics | Prognosis | Membrane Proteins - genetics | Humans | Middle Aged | Biomarkers - analysis | Hypertriglyceridemia - pathology | Male | Young Adult | Pedigree | Adult | Female | Heterozygote | Aged | Mutation | Original
Journal Article
Journal Article
Journal of Atherosclerosis and Thrombosis, ISSN 1340-3478, 2018
Aim: Dyslipidemia is the most common lipid metabolism disorder in humans, and its etiology remains elusive. Hypertriglyceridemia (HTG) is a type of... 
Hypertriglyceridemia | HTG | Compound mutation | LMF1
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, pp. e64045 - 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 | Index Medicus
Journal Article
Journal Article
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 2015, Volume 79, Issue 4, pp. 553 - 556
Journal Article
Journal of Clinical Laboratory Analysis, ISSN 0887-8013, 09/2018, Volume 32, Issue 7, pp. e22444 - n/a
ObjectiveTo investigate whether a novel compound heterozygous mutations c.257C>G (p.T86R)/c.176del16 (p.G59A fs*18) in GJB2 result in hearing loss.... 
SNHL | GJB2 | sequence analysis | compound heterozygous mutation | molecular dynamics simulation | CONNEXIN-26 | GENES | DEAFNESS PATIENTS | MEDICAL LABORATORY TECHNOLOGY | Spiral ganglion | GJB2 protein | Hearing | Molecular dynamics | Children | Mutation | Localization | Hearing impairment | Hearing loss | Index Medicus
Journal Article
Journal Article