DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» LMBR1
LMBR1
Disruption of a Long-Range Cis-Acting Regulator for Shh Causes Preaxial Polydactyly
A Novel ZRS Variant Causes Preaxial Polydactyly Type I by Increased Sonic Hedgehog Expression in the Developing Limb Bud
Fly LMBR1/LIMR-Type Protein Lilipod Promotes Germ-Line Stem Cell Self-Renewal by Enhancing BMP Signaling
HHS Public Access Author Manuscript
Selection Signatures Scan in Several Italian Sheep Breeds Identifies Genes Influencing Micronutrient Metabolism S
A Novel ZRS Mutation Leads to Preaxial Polydactyly Type 2 in a Heterozygous Form and Werner Mesomelic Syndrome in a Homozygous Form Julia E
Variation in Protein Coding Genes Identifies Information Flow
Physical Mapping of QTL for Tuber Yield
Supplementary Table 1 Double Treatment Vs Single Treatment
Genome Provides Insights Into Vertebrate Evolution
Whole Genome Resequencing Reveals an Association of ABCC4 Variants with Preaxial Polydactyly in Pigs Cheng Ma1,2,3, Saber Khederzadeh1,2,3, Adeniyi C
Primepcr™Assay Validation Report
Extensive Viral Mimicry of Human Proteins in AIDS, Multiple Sclerosis and Other Autoimmune Disorders, Late-Onset and Familial Al
The Identification of a Novel Transcript Variant of Chicken Lmbr1 and the Sequence Variation Analysis
Tear Lipocalin and Lipocalin-Interacting Membrane Receptor
Reciprocal Mouse and Human Limb Phenotypes Caused by Gain- and Loss-Of-Function Mutations Affecting Lmbr1
Molecular Characterization of a Rare Analphoid Supernumerary Marker
NIH Public Access Author Manuscript Clin Dysmorphol
Top View
Supplemental Material.Pdf
Prenatal Diagnosis of Hemivertebrae-A Likely Association
LMBR1 Antibody Cat
Mutations in HODX13 and ZRS/LMBR1 Genes and Chromosomal Abnormalities Cause Congenital Limb Defects
HBV DNA Integration and Clonal Hepatocyte Expansion in Chronic Hepatitis B Patients Considered Immune Tolerant
Strategies for Mapping and Cloning Quantitative Trait Genes in Rodents
The Chromatin Architecture of the Chromosomal Region 7Q36.3, Frequently Rearranged in Leukemic Cells, Is Evolutionary Conserved
1 Supplementary Material Figure S1. Volcano Plot of Differentially
Mutation Analysis of a Large Chinese Pedigree with Congenital Preaxial Polydactyly
Identity-By-Descent Refines Mapping of Candidate Regions for Preaxial Polydactyly II /III in a Large Chinese Pedigree
Genetic Determinants of Radiographic Knee Osteoarthritis in African Americans
Positional Cloning of the Gene Mutated in Hereditary Motor and Sensory Neuropathy- Russe (HMSNR)
Nosology and Classification of Genetic Skeletal Disorders: 2015 Revision
Elimination of a Long-Range Cis-Regulatory Module Causes
Lmbr1 Expression in Early Embryo Development Stages in White Leghorn and Chinese Silky*
Hedgehog: Functions and Mechanisms
Investigation De-Novo Variants in XIRP1 Associated with Polydactyly and Polysyndactyly in Holstein Cattle Marina Braun*, Maren H
Mouse Lmbr1 Conditional Knockout Project (CRISPR/Cas9)
Genome-Wide Linkage Analysis and Association Study Identifies Loci for Polydactyly In
Genome-Wide Linkage Analysis and Association Study Identifies Loci For
Bacillus Anthracis' Lethal Toxin Induces Broad Transcriptional Responses In
A Statistical Framework to Predict Functional Non-Coding Regions in the Human Genome Through Integrated Analysis of Annotation Data
Mouse Lmbr1 Knockout Project (CRISPR/Cas9)
A 300-Kb Microduplication of 7Q36.3 in a Patient with Triphalangeal Thumb