Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation. - Wikidata - wikimedia - TriplyDB

Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

http://www.wikidata.org/entity/Q33882917

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Conservation and divergence of regulatory strategies at Hox Loci and the origin of tetrapod digits Transcriptional regulatory cascades in Runx2-dependent bone development Cartilage to bone transitions in health and disease Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutations The pisiform growth plate is lost in humans and supports a role for Hox in growth plate formation Association analysis between HOXD9 genes and the development of developmental dysplasia of the hip in Chinese female Han population.Genetic interactions between Shox2 and Hox genes during the regional growth and development of the mouse limb.Direct transcriptional targets of sex steroid hormones in bone.Reshuffling genomic landscapes to study the regulatory evolution of Hox gene clusters.Key pathways regulated by HoxA9,10,11/HoxD9,10,11 during limb development.Heads, Shoulders, Elbows, Knees, and Toes: Modular Gdf5 Enhancers Control Different Joints in the Vertebrate Skeleton Hox gene expression in the specialized limbs of the Iberian mole (Talpa occidentalis).A role for HOX13 proteins in the regulatory switch between TADs at the HoxD locus A unique stylopod patterning mechanism by Shox2-controlled osteogenesis.An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5'Hoxd-Gli3 antagonism.Understanding developmental mechanisms in the context of osteoarthritis.The chondrocytic journey in endochondral bone growth and skeletal dysplasia.How the pterosaur got its wings.Structure, function and evolution of topologically associating domains (TADs) at HOX loci.IL15RA is required for osteoblast function and bone mineralization.Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient.Use of RUNX2 expression to identify osteogenic progenitor cells derived from human embryonic stem cells.Ancient selection for derived alleles at a GDF5 enhancer influencing human growth and osteoarthritis risk.The origins, scaling and loss of tetrapod digits.Why location matters - site-specific factors in rheumatic diseases.The posterior HOXD locus: Its contribution to phenotype and malignancy of Ewing sarcoma.FGFR3 is a target of the homeobox transcription factor SHOX in limb development.A switch between topological domains underlies HoxD genes collinearity in mouse limbs.The Role of Hox in Pisiform and Calcaneus Growth Plate Formation and the Nature of the Zeugopod/Autopod Boundary.The HoxD cluster is a dynamic and resilient TAD boundary controlling the segregation of antagonistic regulatory landscapes.HOXA13 regulates Aldh1a2 expression in the autopod to facilitate interdigital programmed cell death.Chondrocyte cultures from human proximal interphalangeal finger joints.Association of a single nucleotide polymorphism in HOXB9 with developmental dysplasia of the hip: a case-control study.A function for all posterior Hoxd genes during digit development?A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation Homeotic transformations reflect departure from the mammalian 'rule of seven' cervical vertebrae in sloths: inferences on the Hox code and morphological modularity of the mammalian neck.An evolutionary and developmental perspective on the loss of regionalization in the limbs of derived ichthyosaurs Das 2q37-Deletionssyndrom Heterogeneous combinatorial expression of Hoxd genes in single cells during limb development

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P2860

Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

http://www.wikidata.org/entity/Q33882917

description

2010 nî lūn-bûn

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2010 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2010 թվականի մայիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

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Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

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Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

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Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

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Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

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Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

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Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

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Jochen Hecht

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Julia Friedrich

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Julia Haupt

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Muhammed Farooq

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Pablo Villavicencio-Lorini

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Pia Kuss

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Seval Türkmen

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Stefan Mundlos

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Regulation of number and size of digits by posterior Hox genes: A dose-dependent mechanism with potential evolutionary implications

Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract

Mutation of HOXA13 in hand-foot-genital syndrome

Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

Hox10 and Hox11 genes are required to globally pattern the mammalian skeleton

Regulation of the activity of the transcription factor Runx2 by two homeobox proteins, Msx2 and Dlx5

A mutational analysis of the 5' HoxD genes: dissection of genetic interactions during limb development in the mouse

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2877951

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