X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
chromosome-1 (614) 614
humans (486) 486
genetics & heredity (321) 321
animals (305) 305
male (245) 245
female (230) 230
mice (175) 175
biochemistry & molecular biology (143) 143
gene (139) 139
chromosome mapping (134) 134
molecular sequence data (126) 126
expression (123) 123
oncology (122) 122
index medicus (111) 111
base sequence (108) 108
chromosomes, human, pair 1 (106) 106
adult (93) 93
cell biology (92) 92
mutation (92) 92
genes (85) 85
genetic aspects (84) 84
in situ hybridization, fluorescence (82) 82
dna (80) 80
middle aged (76) 76
phenotype (76) 76
locus (74) 74
karyotyping (71) 71
linkage (71) 71
identification (70) 70
chromosomes, human, pair 1 - genetics (67) 67
genetics (67) 67
amino acid sequence (66) 66
immunology (63) 63
aged (61) 61
research (61) 61
missense mutations (60) 60
genetic linkage (59) 59
mouse chromosome-1 (58) 58
genotype (57) 57
analysis (56) 56
human chromosome-1 (56) 56
biotechnology & applied microbiology (55) 55
rats (52) 52
membrane proteins - genetics (51) 51
polymerase chain reaction (51) 51
alleles (50) 50
gene expression (50) 50
chromosome 1 (48) 48
protein (47) 47
sequence (47) 47
genetic markers (46) 46
child (45) 45
child, preschool (45) 45
chromosome deletion (45) 45
cloning (45) 45
alzheimer disease - genetics (44) 44
infant (44) 44
neurosciences (43) 43
pedigree (43) 43
chromosomes (42) 42
presenilin-1 (42) 42
proteins (42) 42
region (42) 42
tumor cells, cultured (42) 42
multidisciplinary sciences (41) 41
cell line (40) 40
chromosome banding (40) 40
mice, inbred c57bl (40) 40
susceptibility (40) 40
alzheimer's disease (39) 39
genomics (39) 39
neuroblastoma (39) 39
clinical neurology (38) 38
cloning, molecular (38) 38
transfection (38) 38
tumors (38) 38
adolescent (37) 37
deletion (37) 37
localization (37) 37
mutations (37) 37
research article (37) 37
mouse (36) 36
short arm (36) 36
association (35) 35
cancer (35) 35
cells (35) 35
genetic research (35) 35
evolution (34) 34
prognosis (34) 34
chromosome aberrations (33) 33
familial alzheimers-disease (33) 33
in-situ hybridization (33) 33
long arm (33) 33
crosses, genetic (32) 32
heterozygosity (32) 32
genetic predisposition to disease (31) 31
genome (31) 31
neuroblastoma - genetics (31) 31
translocation, genetic (31) 31
family (30) 30
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Asian Pacific Journal of Cancer Prevention, ISSN 1513-7368, 2013, Volume 14, Issue 2, pp. 1077 - 1082
Background: Renal cell carcinoma (RCC) is a malignancy with a poor prognosis. We aimed to explore whether the expression of Long Non-Coding RNA (LncRNA) growth... 
Renal cell carcinoma | GAS5 | Long non-coding RNAs | TARGETED THERAPY | EXPRESSING DIPHTHERIA-TOXIN | PLASMID | CHROMOSOME-1 | REGULATORY SEQUENCES | BREAST-CANCER | H19 | GENE | ONCOLOGY | RISING INCIDENCE | GROWTH-ARREST
Journal Article
NEUROLOGY, ISSN 0028-3878, 03/2013, Volume 80, Issue 11, pp. 1003 - 1008
Objective: To understand the molecular basis and differential penetrance of febrile seizures and absence seizures in patients with the gamma 2(R43Q) GABA(A)... 
CHILDHOOD ABSENCE EPILEPSY | A RECEPTORS | ACID | CORTICAL INHIBITION | MOUSE MODEL | RECEPTOR GAMMA-2-SUBUNIT | MICE | FEBRILE SEIZURES | TONIC INHIBITION | DISTAL CHROMOSOME-1 | CLINICAL NEUROLOGY
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 4170 - 12
Recently, the Mucin-1 (MUC1) gene has been identified as a causal gene of autosomal dominant tubulointerstitial kidney disease (ADTKD). Most causative... 
TUBULOINTERSTITIAL KIDNEY-DISEASE | DIAGNOSIS | CELLS | MUC1 GENE | MANAGEMENT | MULTIDISCIPLINARY SCIENCES | CHROMOSOME-1 | DOMINANT | TYPE-1 | NEPHROPATHY | EXPRESSION | SMRT protein | Phenotypes | Kidneys | Mucin | Mutation | Kidney diseases
Journal Article
by Alasdair C. Ivens and Christopher S. Peacock and Elizabeth A. Worthey and Lee Murphy and Gautam Aggarwal and Matthew Berriman and Ellen Sisk and Marie-Adele Rajandream and Ellen Adlem and Rita Aert and Atashi Anupama and Zina Apostolou and Philip Attipoe and Nathalie Bason and Christopher Bauser and Alfred Beck and Stephen M. Beverley and Gabriella Bianchettin and Katja Borzym and Gordana Bothe and Carlo V. Bruschi and Matt Collins and Eithon Cadag and Laura Ciarloni and Christine Clayton and Richard M. R. Coulson and Ann Cronin and Angela K. Cruz and Robert M. Davies and Javier De Gaudenzi and Deborah E. Dobson and Andreas Duesterhoeft and Gholam Fazelina and Nigel Fosker and Alberto Carlos Frasch and Audrey Fraser and Monika Fuchs and Claudia Gabel and Arlette Goble and André Goffeau and David Harris and Christiane Hertz-Fowler and Helmut Hilbert and David Horn and Yiting Huang and Sven Klages and Andrew Knights and Michael Kube and Natasha Larke and Lyudmila Litvin and Angela Lord and Tin Louie and Marco Marra and David Masuy and Keith Matthews and Shulamit Michaeli and Jeremy C. Mottram and Silke Müller-Auer and Heather Munden and Siri Nelson and Halina Norbertczak and Karen Oliver and Susan O'Neil and Martin Pentony and Thomas M. Pohl and Claire Price and Bénédicte Purnelle and Michael A. Quail and Ester Rabbinowitsch and Richard Reinhardt and Michael Rieger and Joel Rinta and Johan Robben and Laura Robertson and Jeronimo C. Ruiz and Simon Rutter and David Saunders and Melanie Schäfer and Jacquie Schein and David C. Schwartz and Kathy Seeger and Amber Seyler and Sarah Sharp and Heesun Shin and Dhileep Sivam and Rob Squares and Steve Squares and Valentina Tosato and Christy Vogt and Guido Volckaert and Rolf Wambutt and Tim Warren and Holger Wedler and John Woodward and Shiguo Zhou and Wolfgang Zimmermann and Deborah F. Smith and Jenefer M. Blackwell and Kenneth D. Stuart and Bart Barrell and ...
Science, ISSN 0036-8075, 7/2005, Volume 309, Issue 5733, pp. 436 - 442
Journal Article
NEURON, ISSN 0896-6273, 11/1996, Volume 17, Issue 5, pp. 1005 - 1013
Mutations in the presenilin 1 (PS1) and presenilin 2 genes cosegregate with the majority of early-onset familial Alzheimer's disease (FAD) pedigrees. We now... 
A-BETA-42 | GENE | DOWN-SYNDROME | CHROMOSOME-1 | A-BETA | BETA-PROTEIN | AMYLOID PRECURSOR PROTEIN | NEUROSCIENCES | MISSENSE MUTATIONS | PEPTIDE | SENILE PLAQUES
Journal Article
Journal Article
Molecular Microbiology, ISSN 0950-382X, 10/2012, Volume 86, Issue 1, pp. 15 - 23
Journal Article
Kidney International, ISSN 0085-2538, 02/2012, Volume 81, Issue 3, pp. 280 - 292
Journal Article
Journal Article
Journal Article