X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (8344) 8344
Publication (1543) 1543
Book Review (49) 49
Book Chapter (27) 27
Conference Proceeding (14) 14
Dissertation (5) 5
Book / eBook (3) 3
Data Set (2) 2
Magazine Article (2) 2
Government Document (1) 1
Newsletter (1) 1
Newspaper Article (1) 1
Patent (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (5301) 5301
humans (3740) 3740
animals (3724) 3724
proteins (2338) 2338
cell biology (2317) 2317
gene expression (2309) 2309
mice (2242) 2242
biochemistry & molecular biology (1963) 1963
expression (1841) 1841
research (1812) 1812
genetic aspects (1651) 1651
transcription factors (1528) 1528
multidisciplinary sciences (1488) 1488
genes (1387) 1387
molecular sequence data (1380) 1380
research article (1376) 1376
female (1355) 1355
male (1196) 1196
signal transduction (1182) 1182
physiological aspects (1181) 1181
oncology (1165) 1165
transcription factors - metabolism (1105) 1105
mutation (1071) 1071
article (1029) 1029
base sequence (1029) 1029
plant sciences (1000) 1000
analysis (996) 996
transcription factors - genetics (996) 996
cell line, tumor (994) 994
apoptosis (986) 986
genetics & heredity (957) 957
cancer (943) 943
biology (929) 929
medicine (913) 913
protein binding (905) 905
gene-expression (878) 878
amino acid sequence (859) 859
science (849) 849
kinases (811) 811
phosphorylation (800) 800
rna (771) 771
promoter regions, genetic (769) 769
genetics (763) 763
life sciences (752) 752
gene expression regulation (741) 741
cell line (735) 735
transcription (729) 729
health aspects (727) 727
cell cycle (717) 717
activation (714) 714
dna-binding proteins - metabolism (713) 713
developmental biology (668) 668
dna (667) 667
binding sites (661) 661
cell proliferation (661) 661
transcription, genetic (655) 655
protein (641) 641
gene (636) 636
dna-binding proteins - genetics (618) 618
cells (615) 615
biochemistry (608) 608
forkhead transcription factors - metabolism (598) 598
cells, cultured (596) 596
rodents (588) 588
differentiation (576) 576
molecular biology (572) 572
gene expression regulation, plant (561) 561
gene expression regulation, developmental (559) 559
transcription factor (550) 550
homeodomain proteins - genetics (549) 549
plants (545) 545
rna, messenger - metabolism (531) 531
dead-box rna helicases - metabolism (526) 526
deoxyribonucleic acid--dna (518) 518
metastasis (518) 518
phenotype (503) 503
genomes (501) 501
stem cells (486) 486
genetic transcription (481) 481
identification (481) 481
dead-box rna helicases - genetics (480) 480
gene expression regulation, neoplastic (479) 479
arabidopsis - genetics (473) 473
mice, inbred c57bl (472) 472
immunology (470) 470
rna, messenger - genetics (466) 466
forkhead transcription factors - genetics (464) 464
studies (463) 463
development and progression (451) 451
cell growth (442) 442
homeodomain proteins - metabolism (441) 441
transfection (440) 440
arabidopsis (439) 439
tumors (436) 436
reverse transcriptase polymerase chain reaction (431) 431
growth (427) 427
genomics (425) 425
t-box domain proteins - genetics (424) 424
rna interference (421) 421
mice, knockout (419) 419
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Free Radical Biology and Medicine, ISSN 0891-5849, 05/2011, Volume 50, Issue 9, pp. 1196 - 1209
The sodium-dependent vitamin C transporter (SVCT) 2 is crucial for ascorbate uptake in metabolically active and specialized tissues. This study focused on the... 
Sp element | EGR | Ascorbic acid | Sodium-dependent vitamin C transporter 2 | Free radicals | Yin Yang-1 | MMA | YY1 | mithramycin A | sodium-dependent vitamin C transporter 2 | electrophoretic mobility-shift assay | TSS | EMSA | SVCT2 | ChIP | transcription start site | chromatin immunoprecipitation | RNA-POLYMERASE-II | VITAMIN-C | SUBNUCLEAR LOCALIZATION | INITIATOR ELEMENTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING-PROTEIN | PIG CORONARY-ARTERY | N-METHYLTRANSFERASE GENE | ENDOTHELIAL-CELLS | ENDOCRINOLOGY & METABOLISM | SMOOTH-MUSCLE-CELLS | TFII-I | Exons | Humans | Molecular Sequence Data | Sp1 Transcription Factor - metabolism | YY1 Transcription Factor - metabolism | GC Rich Sequence | Ascorbic Acid - metabolism | Organic Anion Transporters, Sodium-Dependent - genetics | Transfection | Chromatin Immunoprecipitation | Base Sequence | Early Growth Response Transcription Factors - genetics | Transcription, Genetic | Tumor Cells, Cultured | Sp3 Transcription Factor - metabolism | Promoter Regions, Genetic | Sodium-Coupled Vitamin C Transporters | Zinc Fingers | Sp3 Transcription Factor - genetics | Gene Expression Regulation | Binding Sites - genetics | YY1 Transcription Factor - genetics | Reverse Transcriptase Polymerase Chain Reaction | Symporters - metabolism | Animals | Early Growth Response Transcription Factors - metabolism | Sp1 Transcription Factor - genetics | Symporters - genetics | Protein Binding | Drosophila melanogaster | Organic Anion Transporters, Sodium-Dependent - metabolism | Genetic aspects | Promoters (Genetics) | DNA binding proteins | Genes | Protein binding | Transcription factors | EGR-1 protein | Gene regulation | YY1 protein | Guanylate cyclase | Sp1 protein | Tata box | Promoters | EGR-2 protein | ascorbic acid
Journal Article
by Ivanovski, Ivan and Djuric, Olivera and Caraffi, Stefano Giuseppe and Santodirocco, Daniela and Pollazzon, Marzia and Rosato, Simonetta and Cordelli, Duccio Maria and Abdalla, Ebtesam and Accorsi, Patrizia and Adam, Margaret P and Ajmone, Paola Francesca and Badura-Stronka, Magdalena and Baldo, Chiara and Baldi, Maddalena and Bayat, Allan and Bigoni, Stefania and Bonvicini, Federico and Breckpot, Jeroen and Callewaert, Bert and Cocchi, Guido and Cuturilo, Goran and De Brasi, Daniele and Devriendt, Koenraad and Dinulos, Mary Beth and Hjortshøj, Tina Duelund and Epifanio, Roberta and Faravelli, Francesca and Fiumara, Agata and Formisano, Debora and Giordano, Lucio and Grasso, Marina and Grønborg, Sabine and Iodice, Alessandro and Iughetti, Lorenzo and Kuburovic, Vladimir and Kutkowska-Kazmierczak, Anna and Lacombe, Didier and Lo Rizzo, Caterina and Luchetti, Anna and Malbora, Baris and Mammi, Isabella and Mari, Francesca and Montorsi, Giulia and Moutton, Sebastien and Møller, Rikke S and Muschke, Petra and Nielsen, Jens Erik Klint and Obersztyn, Ewa and Pantaleoni, Chiara and Pellicciari, Alessandro and Pisanti, Maria Antonietta and Prpic, Igor and Poch-Olive, Maria Luisa and Raviglione, Federico and Renieri, Alessandra and Ricci, Emilia and Rivieri, Francesca and Santen, Gijs W and Savasta, Salvatore and Scarano, Gioacchino and Schanze, Ina and Selicorni, Angelo and Silengo, Margherita and Smigiel, Robert and Spaccini, Luigina and Sorge, Giovanni and Szczaluba, Krzysztof and Tarani, Luigi and Tone, Luis Gonzaga and Toutain, Annick and Trimouille, Aurelien and Valera, Elvis Terci and Vergano, Samantha Schrier and Zanotta, Nicoletta and Zenker, Martin and Conidi, Andrea and Zollino, Marcella and Rauch, Anita and Zweier, Christiane and Garavelli, Livia
Genetics in Medicine, ISSN 1098-3600, 09/2018, Volume 20, Issue 9, pp. 965 - 975
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 10/2014, Volume 164, Issue 10, pp. 2557 - 2566
Mowat–Wilson syndrome (MWS) is characterized by moderate to severe intellectual disability and distinctive facial features in association with variable... 
CHARGE syndrome | minor malformations | Mowat–Wilson syndrome | craniosynostosis | intellectual disability | Mowat-Wilson syndrome | Intellectual disability | Minor malformations | Craniosynostosis | MENTAL RETARDATION SYNDROME | SMAD-INTERACTING PROTEIN-1 | CLINICAL-FEATURES | BOX 1B GENE | SYNDROME PHENOTYPE | GENETICS & HEREDITY | MISSENSE MUTATION | HIRSCHSPRUNG-DISEASE | PATIENT | CEREBELLAR HYPOPLASIA | ZFHX1B GENE | Microcephaly - genetics | Face - abnormalities | Humans | Hirschsprung Disease - genetics | Child, Preschool | Infant | Male | Zinc Finger E-box Binding Homeobox 2 | Intellectual Disability - genetics | Young Adult | Facies | Adult | Female | Child | Abnormalities, Multiple - genetics | Infant, Newborn | Craniosynostoses - genetics | Craniosynostoses - diagnosis | Genetic Association Studies - methods | Microcephaly - diagnosis | Repressor Proteins - genetics | CHARGE Syndrome - diagnosis | Mutation - genetics | Homeodomain Proteins - genetics | Hirschsprung Disease - diagnosis | Intellectual Disability - diagnosis | CHARGE Syndrome - genetics | Phenotypes | Congenital diseases | Congenital defects | Intellectual disabilities | Epilepsy | Pattern recognition | Coronary artery disease | Corpus callosum | Choanal atresia | Eye | Hirschsprung's disease | Missense mutation | Microencephaly | Children | Mutation | Heart diseases | Genotypes
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 03/2009, Volume 149A, Issue 3, pp. 417 - 426
Journal Article
Journal Article
Journal Article
European Journal of Medical Genetics, ISSN 1769-7212, 2005, Volume 48, Issue 2, pp. 97 - 111
Journal Article
PAEDIATRIA CROATICA, ISSN 1330-1403, 04/2010, Volume 54, Issue 2, pp. 105 - 109
We report on two children with phenotypic characteristics of Mowat-Wilson syndrome associated with complex cardiac malformotions. In molecular genetic analysis... 
MOLECULAR | MENTAL-RETARDATION | ANOMALIES | HIRSCHSPRUNG-DISEASE | PEDIATRICS | MUTATIONS | GENETIC | ZFHX1B | DELETIONS | BOX 1B GENE | CONGENITAL ABNORMALITIES
Journal Article