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DCHS2
Identification of the Binding Partners for Hspb2 and Cryab Reveals
Supplementary Table 1: Adhesion Genes Data Set
Genome Sequences of Tropheus Moorii and Petrochromis Trewavasae, Two Eco‑Morphologically Divergent Cichlid Fshes Endemic to Lake Tanganyika C
Biallelic Alteration and Dysregulation of the Hippo Pathway in Mucinous Tubular and Spindle Cell Carcinoma of the Kidney
Insights Into the Genetic Architecture of the Human Face
Transcriptomic and Epigenomic Characterization of the Developing Bat Wing
Nº Ref Uniprot Proteína Péptidos Identificados Por MS/MS 1 P01024
Genes Associated with the Progression of Neurofibrillary Tangles in Alzheimer’S Disease
The Landscape of Human STR Variation
Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family
From Syndromes to Normal Variation: a Candidate Gene Study of Interorbital Distances
Differentially Expressed Genes in Aneurysm Tissue Compared With
Detection of H3k4me3 Identifies Neurohiv Signatures, Genomic
The Landscape of Human STR Variation
A Novel Fanconi Anaemia Subtype Associated with a Dominant-Negative Mutation in RAD51
(12) United States Patent (10) Patent No.: US 9,163,284 B2 Liu Et Al
Name Aliases Binding Partner Physiology / Oncology References
Genome-Wide Association Study and Pathway Analysis for Female Fertility Traits in Iranian Holstein Cattle
Top View
High-Throughput Profiling of Off- Target DNA Cleavage Reveals RNA- Programmed Cas9 Nuclease Specificity
GABRA1 and STXBP1: Novel Genetic Causes of Dravet Syndrome Gemma L
Knocking-Out the Human Face Genes TBX15 and PAX1 in Mice Alters Facial and Other Physical Morphology
Uncovering the Variability, Regulatory Roles and Mutation Rates of Short Tandem Repeats by Thomas F
Network-Based Identification of Genetic Factors in Ageing, Lifestyle
Analysis of Protein-Coding Mutations in Hipscs and Their Possible Role During Somatic Cell Reprogramming
Genome-Wide Association Study in Japanese Females Identifies Fifteen
Genome‑Wide DNA Methylation Analysis in Permanent Atrial Fibrillation
Flexible Model-Based Joint Probabilistic Clustering of Binary and Continuous Inputs and Its Application to Genetic Regulation and Cancer
Changes in Nucleus Accumbens Gene
Genome-Wide Association Analysis of Age-At-Onset In
A Genome-Wide Association Scan Implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in Human Facial Variation
Identification of Core Genes and Prediction of Mirnas Associated with Osteoporosis Using a Bioinformatics Approach
A Catalog of Single Nucleotide Changes Distinguishing Modern
Identificação De Mutações Germinativas Em Pacientes Com Câncer Papilífero Familiar De Tireoide Através De Análise De Exoma