|
ID |
Name |
Source |
pValue |
FDR B&H |
FDR B&Y |
Bonferroni |
Genes from Input
|
Genes in Annotation
|
1
|
20542501
|
Immunolocalization of humanin in human sperm and testis.
|
Pubmed
|
5.706E-13
|
1.214E-9
|
1.106E-8
|
2.913E-9
|
4
|
9
|
2
|
19623253
|
Humanin: a novel central regulator of peripheral insulin action.
|
Pubmed
|
5.706E-13
|
1.214E-9
|
1.106E-8
|
2.913E-9
|
4
|
9
|
3
|
25630734
|
The human mitochondrial genome may code for more than 13 proteins.
|
Pubmed
|
9.508E-13
|
1.214E-9
|
1.106E-8
|
4.855E-9
|
4
|
10
|
4
|
23402768
|
Humanin: a harbinger of mitochondrial-derived peptides?
|
Pubmed
|
9.508E-13
|
1.214E-9
|
1.106E-8
|
4.855E-9
|
4
|
10
|
5
|
12732850
|
Humanin peptide suppresses apoptosis by interfering with Bax activation.
|
Pubmed
|
1.494E-12
|
1.525E-9
|
1.391E-8
|
7.627E-9
|
4
|
11
|
6
|
19477263
|
Evidence for potential functionality of nuclearly-encoded humanin isoforms.
|
Pubmed
|
3.235E-12
|
2.360E-9
|
2.151E-8
|
1.652E-8
|
4
|
13
|
7
|
12009529
|
Evidence for in vivo production of Humanin peptide, a neuroprotective factor against Alzheimer's disease-related insults.
|
Pubmed
|
3.235E-12
|
2.360E-9
|
2.151E-8
|
1.652E-8
|
4
|
13
|
8
|
11371646
|
A rescue factor abolishing neuronal cell death by a wide spectrum of familial Alzheimer's disease genes and Abeta.
|
Pubmed
|
4.529E-12
|
2.891E-9
|
2.635E-8
|
2.312E-8
|
4
|
14
|
9
|
21423176
|
Analysis of the myosin-II-responsive focal adhesion proteome reveals a role for Ã?-Pix in negative regulation of focal adhesion maturation.
|
Pubmed
|
1.179E-6
|
6.690E-4
|
6.098E-3
|
6.021E-3
|
4
|
286
|
10
|
25275127
|
HIV-1 Nef and Vpu are functionally redundant broad-spectrum modulators of cell surface receptors, including tetraspanins.
|
Pubmed
|
6.054E-5
|
7.258E-4
|
6.616E-3
|
3.091E-1
|
2
|
40
|
11
|
16289162
|
The identification of myocilin-associated proteins in the human trabecular meshwork.
|
Pubmed
|
6.680E-5
|
7.258E-4
|
6.616E-3
|
3.411E-1
|
2
|
42
|
12
|
16625196
|
DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.
|
Pubmed
|
2.028E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
2
|
73
|
13
|
19199708
|
Proteomic analysis of human parotid gland exosomes by multidimensional protein identification technology (MudPIT).
|
Pubmed
|
2.141E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
3
|
414
|
14
|
8722009
|
Structure and evolution of mammalian ribosomal proteins.
|
Pubmed
|
2.436E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
2
|
80
|
15
|
15189156
|
The molecular mechanics of eukaryotic translation.
|
Pubmed
|
2.881E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
2
|
87
|
16
|
12370371
|
Uniquely conformed peptide-containing beta 2-microglobulin-free heavy chains of HLA-B2705 on the cell surface.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
17
|
20873220:gr
|
[Analysis of clusterin gene (CLU/APOJ) polymorphism in Alzheimer's disease patients and in normal cohorts from Russian populations].
|
GeneRIF
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
18
|
17911426:gr
|
B27 disease is a new autoimmune disease that affects millions of people.
|
GeneRIF
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
19
|
23916069
|
HLA-B27 and antigen presentation: at the crossroads between immune defense and autoimmunity.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
20
|
16493052
|
Lack of tyrosine 320 impairs spontaneous endocytosis and enhances release of HLA-B27 molecules.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
21
|
17274979:gr
|
Regulation of clusterin expression in mammary epithelial cells.
|
GeneRIF
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
22
|
11556975
|
Sequence, genetics and serology of a new HLA-B allele: B*4903.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
23
|
18945256
|
The prevalence, clinical features and association of HLA-B27 in sacroiliitis associated with established Crohn's disease.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
24
|
22701550
|
Plasma apolipoprotein levels are associated with cognitive status and decline in a community cohort of older individuals.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
25
|
22320938
|
HLA-B*07 is a high risk allele for familial cervical cancer.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
26
|
25339761
|
A view of the E2-CD81 interface at the binding site of a neutralizing antibody against hepatitis C virus.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
27
|
23956249
|
Evolution of radiographic damage in ankylosing spondylitis: a 12 year prospective follow-up of the OASIS study.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
28
|
18424159
|
Low frequency of HLA-B27 in ankylosing spondylitis patients from Turkey.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
29
|
24600035
|
Molecular basis of a dominant T cell response to an HIV reverse transcriptase 8-mer epitope presented by the protective allele HLA-B*51:01.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
30
|
15649646
|
Differential effects of clusterin/apolipoprotein J on cellular growth and survival.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
31
|
19013628
|
Cellular vimentin content regulates the protein level of hepatitis C virus core protein and the hepatitis C virus production in cultured cells.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
32
|
21705835
|
HLA-B27 association with uveitis in an Asian Indian population.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
33
|
22461701:gr
|
HLA-B7-restricted EBV-specific CD8+ T cells are dysregulated in multiple sclerosis.
|
GeneRIF
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
34
|
15891642
|
Sensorineural hearing impairment in patients with Pmp22 duplication, deletion, and frameshift mutations.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
35
|
21630085
|
Regulation of chemosensitivity and migration by clusterin in non-small cell lung cancer cells.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
36
|
21644226:gr
|
[Identification of a novel allele HLA-B*15:129 by polymerase chain reaction with allele group-specific primers].
|
GeneRIF
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
37
|
26248534
|
Prevalence of HLA-B27 in Moroccan healthy subjects and patients with ankylosing spondylitis and mapping construction of several factors influencing AS diagnosis by using multiple correspondence analysis.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
38
|
16641285:gr
|
Different domains of CD81 mediate distinct stages of hepatitis C virus pseudoparticle entry.
|
GeneRIF
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
39
|
18176708:gr
|
Immunohistochemical expression of vimentin, calponin and HHF-35 in salivary gland tumors.
|
GeneRIF
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
40
|
9190204
|
Topogenesis of a nucleolar protein: determination of molecular segments directing nucleolar association.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
41
|
18852831
|
Of race, ethnicity, and rash: the genetics of antiepileptic drug-induced skin reactions.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
42
|
16490286
|
Clusterin in cerebrospinal fluid: analysis of carbohydrates and quantification of native and glycosylated forms.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
43
|
7675244
|
Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 gene.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
44
|
21337347
|
Report of a novel mutation in the PMP22 gene causing an axonal neuropathy.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
45
|
17580542
|
[Hla-B27 gene: polymorphism, evolution, distribution, and association with spondyloartopathies].
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
46
|
17050693
|
Monitoring intermediate filament assembly by small-angle x-ray scattering reveals the molecular architecture of assembly intermediates.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
47
|
14581692:gr
|
Hypoglossal neuropathy in hereditary neuropathy with liability to pressure palsy.
|
GeneRIF
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
48
|
7626703
|
Expression of apolipoprotein J in the uterus is associated with tissue remodeling.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
49
|
7725306
|
HLA class I variation in Australian aborigines: characterization of allele B*1521.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|
50
|
26610302
|
The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis.
|
Pubmed
|
2.893E-4
|
7.258E-4
|
6.616E-3
|
1.000E0
|
1
|
1
|