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IMMP2L
Cisplatin and Phenanthriplatin Modulate Long-Noncoding
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Abstracts from the 50Th European Society of Human Genetics Conference: Electronic Posters
REVIEW ARTICLE the Genetics of Autism
Characterizing Genomic Duplication in Autism Spectrum Disorder by Edward James Higginbotham a Thesis Submitted in Conformity
Mechanisms of Common Fragile Site Instability and Cancer
Visualizing Locus-Speciic Sister Chromatid Exchange Reveals Differential Patterns of Replication Stress-Induced Fragile Site Breakage
Genome-Wide Mapping in a House Mouse Hybrid Zone Reveals Hybrid Sterility Loci and Dobzhansky-Muller Interactions Leslie M Turner1,2, Bettina Harr1*
Downloaded from Bioscientifica.Com at 09/28/2021 09:08:00AM Via Free Access
Insight Into the Possible Formation Mechanism of the Intersex Phenotype of Lanzhou Fat-Tailed Sheep Using Whole-Genome Resequencing
Cytogenetics and Gene Discovery in Psychiatric Disorders
Genetic, Epigenetic and Transcriptome Studies of Tourette Syndrome and Tic Disorders
Impaired Replication Timing Promotes Tissue-Specific Expression
FANCD2 Binding Identifies Conserved Fragile Sites at Large Transcribed
Translocation Breakpoint at 7Q31 Associated with Tics: Further Evidence for IMMP2L As a Candidate Gene for Tourette Syndrome
Monoallelic Expression of the Human FOXP2 Speech Gene
Intragenic Deletions Affecting Two Alternative Transcripts of the IMMP2L Gene in Patients with Tourette Syndrome
Gene Expression Imputation Across Multiple Brain Regions Provides Insights Into Schizophrenia Risk
Top View
Large Transcription Units Unify Copy Number Variants and Common Fragile Sites Arising Under Replication Stress
Further Evidence for IMMP2L As a Candidate Gene for Tourette
Switching Off IMMP2L Signaling Drives Senescence Via Simultaneous Metabolic Alteration and Blockage of Cell Death
Genome-Wide Association Study of Comorbid Depressive Syndrome and Alcohol Dependence Alexis C
Mitochondria and Disease: Mutation and Expression Landscape of Mitochondri-Associated Genes in Different Disease Types
Common Chromosomal Fragile Sites—Conserved Failure Stories
Detection of Copy Number Variants in African Goats Using Whole Genome Sequence Data Wilson Nandolo1,2, Gábor Mészáros1, Maria Wurzinger1, Liveness J
Penn Medicine
Supplementary Table 8. Genes Expressed in HNSCC and That Map to Regions Exhibiting Recurrent Genomic Amplification in Head and Neck Carcinomas
Rare Structural Variation of Synapse and Neurotransmission Genes In
Discovery of the Human Genome Sequence in the Public and Private Databases
Supporting Information Materials and Methods
Comparing Therapeutically-Relevant Copy Number Profiles in African Americans and European Americans with Renal Cell Carcinoma
Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7Q31 Associated with Tourette Syndrome Erwin Petek,1,2 Christian Windpassinger,1 John B
Identifying Genetic Variation Contributing to Keratoconus
Materials and Methods All Python and R Code Used in These Analyses Is Available At
Genome-Wide Crispri Screening Identifies OCIAD1 As a Prohibitin
Rabbit Genome Analysis Reveals a Polygenic Basis for Phenotypic Change During Domestication
Interactome Mapping of the Mitochondrial Intermembrane Space Proteases Identifies a Novel Function of HTRA2