Keyphrases
Rnf12
100%
E3 Ubiquitin Ligase
59%
Intellectual Disability
48%
Amplification Loop
30%
Germ Cell Specification
30%
USP26
30%
Stem Cells
30%
X Chromosome Inactivation
30%
Embryonic Stem Cell Differentiation
30%
Developmental Disorders
29%
Embryonic Stem Cells
26%
Rex1
26%
Phosphorylation
25%
Mouse Embryonic Stem Cells (mESCs)
23%
X-linked Intellectual Disability
22%
Protein Function
19%
Transcriptional Response
17%
Chromatin
17%
Phosphorylation Sites
17%
Ubiquitin
17%
E3 Ligase Activity
17%
Stem Cell Development
17%
Ubiquitin Ligase Activity
16%
Urogenital Diseases
15%
Rlim
15%
Dysregulated
15%
Signaling Network
15%
Embryonic Gene Expression
15%
Disease-causing mutations
15%
DYRK Kinase
15%
Activity-based Probes
15%
EphA2
15%
Coreceptor Switch
15%
Signaling Modules
15%
Protein Stability
15%
Receptor Protein Tyrosine Phosphatase
15%
Sensory Organs
15%
ERK5
15%
Severe Disease
15%
Functional Diversification
15%
MALDI-TOF Mass Spectrometry
15%
Early Embryo
15%
Neurodevelopmental
15%
Neural Differentiation
15%
Rejuvenation
15%
Phosphoproteomics
15%
Stem Cell Self-renewal
15%
Nanog
15%
Missense Variants
15%
Telomere
15%
Sample Preparation
15%
Protein Kinase
15%
Diaphragmatic Hernia
15%
Drosophilidae
15%
Kruppel-like Factor 2 (KLF2)
15%
Casein Kinase 2
15%
Neuroblast
15%
Organ Formation
15%
Cyclin-dependent Kinase 1 (CDK1)
15%
Ubiquitylation
14%
Gene Expression
12%
Protein Ubiquitylation
12%
Cell Fate Determination
11%
Xist
10%
Phosphomimetic
10%
FGF4
10%
Basic Regions
9%
Stem Cell Models
9%
Kinase Family
9%
Mammalian Cells
9%
Photocrosslinking
8%
Nave
8%
Hypogenitalism
7%
Molecular Spectra
7%
Likely Pathogenic Variant
7%
Phosphomutant
7%
Protein Phosphorylation
7%
Medical Research Council
7%
Non-coding RNA (ncRNA)
7%
Kindred
7%
Disease Severity
7%
Phenotypic Spectrum
7%
Sensory Organ Precursor
7%
Neuronal Function
7%
ERK2
7%
Asymmetric Cell Division
7%
Self-renewal
7%
Craniofacial Abnormalities
7%
Progenitor Cells
7%
Perinatal Lethality
7%
Disease Spectrum
7%
DNA Binding
7%
Clinical Features
7%
Molecular Mechanism
7%
X-linked
7%
Gene Dosage
6%
Germ Cell Development
6%
Pluripotency
6%
RING E3 Ligase
6%
Zscan4
6%
Cell Fate
6%
Epiblast
6%
Female Mice
6%
X Chromosome
6%
Gametogenesis
5%
Pluripotent Cells
5%
Developing World
5%
Therapeutic Potential
5%
Independent Self
5%
Transcriptional Network
5%
New Therapeutics
5%
Health Systems
5%
Patient's Will
5%
Urogenital Abnormalities
5%
Homeodomain
5%
Competing Interests
5%
Biochemistry, Genetics and Molecular Biology
Embryonic Stem Cell
80%
Ubiquitin-Conjugating Enzyme
65%
Stem Cell
52%
Intellectual Disability
49%
Ubiquitination
44%
Cellular Differentiation
38%
X-Inactivation
30%
Germ Cell
30%
Gene Expression
27%
Cell Maturation
22%
Protein Kinases
20%
Ubiquitin
19%
Gametogenesis
19%
Ubiquitin Ligase
18%
Drive
17%
KLF2
15%
FGF4
15%
Protein Stability
15%
Phosphoproteomics
15%
Missense
15%
Mass Spectrometry
15%
Neuroblast
15%
Receptor Tyrosine Phosphatase
15%
Rex1
15%
Protein Tyrosine Phosphatase
15%
Matrix-Assisted Laser Desorption-Ionization
15%
Stem Cell Self-Renewal
15%
Phosphomimetics
15%
Casein Kinase
15%
Telomere
15%
Kinase
14%
Phosphotransferase
14%
Cell Fate Determination
11%
DNA Binding
11%
Long Non-Coding RNA
10%
Quantitative Proteomics
10%
Transcription
10%
Transcription Factors
9%
Embryogenesis
8%
Gene Dosage
8%
Proteasome
7%
Derepression
7%
Transcriptional Repressor
7%
Human Genetic Disorder
7%
Protein Phosphorylation
7%
Cell Fate
7%
Homeodomain
7%
Cell Cycle
7%
Asymmetric Cell Division
7%
Precursor
7%
Progenitor Cell
7%
Serine
7%
Nerve Cell Differentiation
7%
Dynamics
6%
Signal Transduction
6%
X Chromosome
6%
Epiblast
6%
Enzymatic Activity
5%
Down Syndrome
5%
Biological Phenomena and Functions Concerning the Entire Organism
5%
Neural Plate
5%
Consensus Sequence
5%
Gene Promoter
5%
N-Terminus
5%
Sequence Motif
5%
Genetics
5%
Genomics
5%