about
Dynamic control of head mesoderm patterningEvolutionarily conserved morphogenetic movements at the vertebrate head-trunk interface coordinate the transport and assembly of hypopharyngeal structuresHypaxial muscle: controversial classification and controversial data?Comparative genomics of Lbx loci reveals conservation of identical Lbx ohnologs in bony vertebratesFate mapping identifies the origin of SHF/AHF progenitors in the chick primitive streak.Hypaxial muscle development.Dact genes are chordate specific regulators at the intersection of Wnt and Tgf-β signaling pathwaysExtrinsic versus intrinsic cues in avian paraxial mesoderm patterning and differentiation.Engrailed controls epaxial-hypaxial muscle innervation and the establishment of vertebrate three-dimensional mobility.Nanoparticles of alkylglyceryl-dextran-graft-poly(lactic acid) for drug delivery to the brain: Preparation and in vitro investigation.Antagonists of Wnt and BMP signaling promote the formation of vertebrate head muscle.Structure, expression and chromosomal localization of Zfp-1, a murine zinc finger protein gene.Time course and side-by-side analysis of mesodermal, pre-myogenic, myogenic and differentiated cell markers in the chicken model for skeletal muscle formation.The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development.An evolutionarily conserved Myostatin proximal promoter/enhancer confers basal levels of transcription and spatial specificity in vivo.A crucial role for Pax3 in the development of the hypaxial musculature and the long-range migration of muscle precursors.Wnt6 marks sites of epithelial transformations in the chick embryo.The molecular setup of the avian head mesoderm and its implication for craniofacial myogenesis.Lbx1 marks a subset of interneurons in chick hindbrain and spinal cord.To roll the eyes and snap a bite - function, development and evolution of craniofacial muscles.Dact gene expression profiles suggest a role for this gene family in integrating Wnt and TGF-β signaling pathways during chicken limb development.RGMa and RGMb expression pattern during chicken development suggest unexpected roles for these repulsive guidance molecules in notochord formation, somitogenesis, and myogenesis.Chicken dapper genes are versatile markers for mesodermal tissues, embryonic muscle stem cells, neural crest cells, and neurogenic placodes.Conservation of gene linkage in dispersed vertebrate NK homeobox clusters.Neural tube derived signals and Fgf8 act antagonistically to specify eye versus mandibular arch muscles.Protein and genomic organisation of vertebrate MyoR and Capsulin genes and their expression during avian development.The epaxial-hypaxial subdivision of the avian somite.Intrinsic, Hox-dependent cues determine the fate of skeletal muscle precursors.Early mesodermal phenotypes in splotch suggest a role for Pax3 in the formation of epithelial somites.The role of the notochord for epaxial myotome formation in the mouse.Notochord grafts.Specification of the hypaxial musculature.Control of dorsoventral pattern in the chick paraxial mesoderm.undulated phenotypes suggest a role of Pax-1 for the development of vertebral and extravertebral structures.The role of SF/HGF and c-Met in the development of skeletal muscle.Microduplication 10q24.31 in a Spanish girl with scoliosis and myopathy: The critical role ofLBXMoratorium callEstablishment of the epaxial–hypaxial boundary in the avian myotomeExpression of Claudin-3 during chick developmentThe dissociation of the Fgf-feedback loop controls the limbless state of the neck
P50
Q28239918-9FB5CD5D-C41D-458E-AD86-9AE34A2C2BCCQ28657945-B767C5C0-0592-4386-8FDC-AF74A620E4E2Q30863973-2CDC7C31-37C3-4B37-8A7E-5F8770DBC944Q33341486-BF96C7DD-EF27-43A0-931C-DB7328709AB9Q34525856-C10356BC-3501-4E57-8FF0-41A2562427A2Q34753310-A938DB80-5217-44F6-B309-BBE43734A959Q35220413-97A60FD0-40BB-45D1-A827-909831A59E33Q36892599-0FEEE1F4-3DC6-47AC-B642-EA0ADA100D60Q38625126-6107C09D-A813-4254-B7CC-5ECF7DDA3368Q38873713-B2E54970-57F7-4CEE-8605-D4687BF5D10AQ40385549-427A4502-C094-4ED9-988C-9CCC70FF3F77Q40540163-AD950A75-0131-4E7B-8D0E-01B7EC98D3F9Q40637660-C7EE3144-988B-4D39-AC2B-E4357DCB8BCDQ40825206-6BCF4456-998B-49BC-B7FC-AA6DDDB41121Q42465386-391E94A7-0A10-4A41-8D22-D29D8856F55CQ46176856-A42D5C10-7086-48A9-A8E3-ED1313DF6367Q48288266-8D465F41-E4FB-4D2E-AF3F-07AA9F5F3018Q48452480-CD374A28-B142-432D-B0DA-7DAA4EA983A7Q48964477-CF7C961F-4497-4456-9364-C9F575605E8EQ50056291-3A4E98D1-1F76-459E-9626-2C3034550DE8Q50759129-3F733DAB-FCA0-4075-B080-A774DBAF1074Q50779770-C5C5D3AF-5D9C-4668-B888-093B26AD5506Q51733787-B0A07239-CFA2-492F-93BD-4519A7476FE1Q51916504-46598A70-1B6D-473F-BEE5-870BC99CF05EQ52014945-C1AA2C96-DAA2-4C1F-AEED-EB933166D331Q52028658-987172A5-E202-4FE6-9D3F-EF1861939452Q52087360-7C8BFF3F-278B-4522-9C36-8805F9A1E722Q52100463-A6E43259-E5CC-4A55-AFED-5892AF0EDD85Q52126462-C41D9670-27CA-4071-BE02-6333FFF22B0DQ52174121-0B1CE4EC-DC71-46FF-BCE9-1A1B2BFE2236Q52175182-635E6F44-7791-410C-BCCD-24088EC3E0B1Q52187892-6DB25B53-81FC-46CE-92D3-DD0AE26C7C6EQ52192112-6973F59B-85F9-46EC-A2BC-1E9BF0672CC8Q52210195-08C755FD-32C8-48C9-A09B-A87A9E616FE6Q52980024-D2C56B58-2124-4DA9-AF75-4F71BF222DE8Q57817257-BC65CB6D-42D6-41DA-8388-852624173808Q59045600-740DA5F2-0B7E-408C-AD71-8225524AA4F2Q62180300-9400A380-541D-4582-8DDF-1830756C068AQ63340578-351936D4-0935-49AE-AAB5-E74A93D917FDQ63340587-36079CB0-CFE6-4E20-9AA1-28737CD0714F
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Susanne Dietrich
@ast
Susanne Dietrich
@en
Susanne Dietrich
@es
Susanne Dietrich
@sl
type
label
Susanne Dietrich
@ast
Susanne Dietrich
@en
Susanne Dietrich
@es
Susanne Dietrich
@sl
prefLabel
Susanne Dietrich
@ast
Susanne Dietrich
@en
Susanne Dietrich
@es
Susanne Dietrich
@sl
P1053
M-6515-2015
P106
P1153
56654862300
P21
P31
P3829
P496
0000-0001-8688-8992