348 results on '"Stricker, Sigmar"'
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2. Dynamic remodeling of septin structures fine-tunes myogenic differentiation
3. Author Correction: Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation
4. Odd skipped-related 1 controls the pro-regenerative response of fibro-adipogenic progenitors
5. Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation
6. A local subset of mesenchymal cells expressing the transcription factor Osr1 orchestrates lymph node initiation
7. Mesenchymal Osr1+ cells regulate embryonic lymphatic vessel formation.
8. Tissue cross talks governing limb muscle development and regeneration
9. Molecular Evolution of Mammalian Sex Differentiation
10. Lgr5 and Col22a1 Mark Progenitor Cells in the Lineage toward Juvenile Articular Chondrocytes
11. ADAM19 cleaves the PTH receptor and associates with brachydactyly type E
12. “Mesenchymal Osr1+ cells regulate embryonic lymphatic vessel formation”
13. Aging impairs muscle regeneration by desynchronizing matrix mechano-signaling and macrophage immunomodulation via fibro-adipogenic progenitors
14. Mutations in Bone Morphogenetic Protein Receptor 1B Cause Brachydactyly Type A2
15. Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures
16. Inhibitory SMAD6 interferes with BMP dependent generation of muscle progenitor cells and perturbs proximodistal pattern of murine limb muscles
17. Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis
18. skNAC and Smyd1 in transcriptional control
19. Regulation of cell polarity in the cartilage growth plate and perichondrium of metacarpal elements by HOXD13 and WNT5A
20. Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis
21. ROR-Family Receptor Tyrosine Kinases
22. Odd skipped-related 1 controls the pro-regenerative response of Fibro-Adipogenic Progenitors
23. Limb Development
24. Receptor tyrosine kinase-like orphan receptor 2 (ROR2) and Indian hedgehog regulate digit outgrowth mediated by the phalanx-forming region
25. Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development
26. Faulty Initiation of Proteoglycan Synthesis Causes Cardiac and Joint Defects
27. Prickle1 is necessary for the caudal migration of murine facial branchiomotor neurons
28. Mesenchymal Osr1 Cells Orchestrate Lymph Node Initiation
29. Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model
30. Neurofibromin 1 controls metabolic balance and Notch-dependent quiescence of juvenile myogenic progenitors
31. Fibroadipogenic Progenitors contribute to microvascular repair during skeletal muscle regeneration
32. A misplaced IncRNA causes brachydactyly in humans
33. Wnt-ligand-dependent interaction of TAK1 (TGF-β-activated kinase-1) with the receptor tyrosine kinase Ror2 modulates canonical Wnt-signalling
34. Acetylcholine Receptor Pathway Mutations Explain Various Fetal Akinesia Deformation Sequence Disorders
35. Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome
36. A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range
37. Prdm16-mediated H3K9 methylation controls fibro-adipogenic progenitors identity during skeletal muscle repair
38. Local retinoic acid signaling directs emergence of the extraocular muscle functional unit
39. Posterior Neural Plate-Derived Cells Establish Trunk and Tail Somites in the Axolotl (Ambystoma mexicanum)
40. Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunit
41. Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion
42. FGF and ROR2 Receptor Tyrosine Kinase Signaling in Human Skeletal Development
43. Expression of Type XXIII Collagen mRNA and Protein
44. Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit
45. Role of Runx genes in chondrocyte differentiation
46. Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia
47. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion
48. BMP Signaling Determines the Proximodistal Pattern of Limb Muscles by Spatiotemporal Control of Myogenic Progenitor Cells
49. Neurofibromin (Nf1) is required for skeletal muscle development
50. Cell autonomous requirement of neurofibromin (Nf1) for postnatal muscle hypertrophic growth and metabolic homeostasis
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