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Publications by Yanan Xiong
Disruption of WNT Production in SHH Lineage Causes Bone Malformation in Mice, Mimicking Human Malik-Percin Type Syndactyly
FEBS Letters
Genetics
Cell Biology
Molecular Biology
Biochemistry
Structural Biology
Biophysics
Related publications
Lineage-Specific WNT Reporter Elucidates Mesenchymal WNT Signaling During Bone Repair
American Journal of Pathology
Forensic Medicine
Pathology
Disruption of Sorting Nexin 5 Causes Respiratory Failure Associated With Undifferentiated Alveolar Epithelial Type I Cells in Mice
PLoS ONE
Multidisciplinary
Mutations in HOXD13 Underlie Syndactyly Type v and a Novel Brachydactyly-Syndactyly Syndrome
American Journal of Human Genetics
Genetics
Shared Effects of DISC1 Disruption and Elevated WNT Signaling in Human Cerebral Organoids
Translational Psychiatry
Psychiatry
Molecular Neuroscience
Biological Psychiatry
Mental Health
Cellular
Genetic Causes of Congenital Malformation in India
International Journal of Human Genetics
Genetics
WNT Signaling in Bone
Clinical Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Histamine Synthesis by Cells of the Macrophage Lineage in Bone Marrow of Mice
Bioscience, Biotechnology and Biochemistry
Organic Chemistry
Applied Microbiology
Molecular Biology
Biochemistry
Analytical Chemistry
Medicine
Biotechnology
Disruption of the Adenosine Deaminase Gene Causes Hepatocellular Impairment and Perinatal Lethality in Mice.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Disruption of Intraflagellar Protein Transport in Photoreceptor Cilia Causes Leber Congenital Amaurosis in Humans and Mice
Cilia
Cell Biology
