(Q28593346)

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Loss of Sox9 in the periotic mesenchyme affects mesenchymal expansion and differentiation, and epithelial morphogenesis during cochlea development in the mouse

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PubMed publication ID

31 January 2017

Loss of Sox9 in the periotic mesenchyme affects mesenchymal expansion and differentiation, and epithelial morphogenesis during cochlea development in the mouse (English)

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PubMed publication ID

31 January 2017

SRY (sex determining region Y)-box 9

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GOA release 2020-03-11

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object named as

Ralf Kist

6

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Mark-Oliver Trowe

1

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PubMed publication ID

31 January 2017

Sadrick Shah

2

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PubMed publication ID

31 January 2017

Marianne Petry

3

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PubMed publication ID

31 January 2017

Rannar Airik

4

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PubMed publication ID

31 January 2017

Karin Schuster-Gossler

5

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PubMed publication ID

31 January 2017

Andreas Kispert

7

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31 January 2017

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publication date

1 June 2010

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PubMed publication ID

31 January 2017

Developmental Biology

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PubMed publication ID

31 January 2017

342

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PubMed publication ID

31 January 2017

1

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PubMed publication ID

31 January 2017

51–62

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PubMed publication ID

31 January 2017

The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6

1 reference

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1 reference

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Type IX collagen is crucial for normal hearing

1 reference

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1 reference

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Visualization of cartilage formation: insight into cellular properties of skeletal progenitors and chondrodysplasia syndromes.

1 reference

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Sox9 is required for invagination of the otic placode in mice

1 reference

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1 reference

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SOX9 directly regulates the type-II collagen gene

1 reference

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7 January 2021

Fine structure of extracellular matrix and basal laminae in two types of abnormal collagen production: L-proline analog-treated otocyst cultures and disproportionate micromelia (Dmm/Dmm) mutants

1 reference

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7 January 2021

Sox9 is required for cartilage formation

1 reference

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7 January 2021

Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization

1 reference

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Patterning and morphogenesis of the vertebrate inner ear.

1 reference

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Cooperative function of Tbx1 and Brn4 in the periotic mesenchyme is necessary for cochlea formation

1 reference

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Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis

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The T-box transcription factor Tbx18 maintains the separation of anterior and posterior somite compartments

1 reference

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Fdp, a new fibrocyte-derived protein related to MIA/CD-RAP, has an in vitro effect on the early differentiation of the inner ear mesenchyme

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7 January 2021

Changes in the types of collagen synthesized during chondrogenesis of the mouse otic capsule

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7 January 2021

In vitro growth and differentiation of mammalian sensory hair cell progenitors: a requirement for EGF and periotic mesenchyme

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Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion

1 reference

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Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear

1 reference

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Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

1 reference

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7 January 2021

Role of FGF3 in otic capsule chondrogenesis in vitro: an antisense oligonucleotide approach

1 reference

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7 January 2021

Epithelial control of periotic mesenchyme chondrogenesis.

1 reference

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7 January 2021

A Col9a1 enhancer element activated by two interdependent SOX9 dimers.

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7 January 2021

Conservation of the hedgehog/patched signaling pathway from flies to mice: induction of a mouse patched gene by Hedgehog

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7 January 2021

All for one and one for all: condensations and the initiation of skeletal development

1 reference

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7 January 2021

Loss of Sox9 function results in defective chondrocyte differentiation of mouse embryonic stem cells in vitro

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2010.03.014

7 January 2021

Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B

1 reference

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7 January 2021

Fgf20 is required for sensory epithelial specification in the developing cochlea

1 reference

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7 January 2021

The collagen family members as cell adhesion proteins

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7 January 2021

A systematic screen for genes expressed in definitive endoderm by Serial Analysis of Gene Expression (SAGE).

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2010.03.014

7 January 2021

The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971.

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7 January 2021

Wnt/beta-catenin/Tcf signaling induces the transcription of Axin2, a negative regulator of the signaling pathway

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7 January 2021

Shaping the mammalian auditory sensory organ by the planar cell polarity pathway

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7 January 2021

Conditional inactivation of Sox9: a mouse model for campomelic dysplasia.

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Cloning and expression analysis of the mouse T-box gene Tbx18.

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Cell proliferation and cell death in the developing chick inner ear: spatial and temporal patterns

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Influences on the Coiling of the Cochlea

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Distinct contributions from the hindbrain and mesenchyme to inner ear morphogenesis.

1 reference

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7 January 2021

Bone morphogenetic protein 4 (BMP4): a regulator of capsule chondrogenesis in the developing mouse inner ear.

1 reference

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7 January 2021

Differential and overlapping expression pattern of SOX2 and SOX9 in inner ear development

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The phenotype of survivors of campomelic dysplasia

1 reference

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Planar and vertical signals control cellular differentiation and patterning in the mammalian cochlea.

1 reference

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Development of the mouse inner ear and origin of its sensory organs.

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Hindbrain signals in otic regionalization: walk on the wild side

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SRY-related HMG box 9 regulates the expression of Col4a2 through transactivating its enhancer element in mesangial cells

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SoxE factors function equivalently during neural crest and inner ear development and their activity is regulated by SUMOylation.

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TBX1 is required for inner ear morphogenesis

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Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

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Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential

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Large-scale screen for genes involved in gonad development.

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In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea

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Regulation of human COL9A1 gene expression. Activation of the proximal promoter region by SOX9

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Development of the Cochlea and its Coiling Mechanism

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7 January 2021

based on heuristic

inferred from DOI database lookup

The Campomelic Syndrome: Temporal Bone Histopathologic Features and Otolaryngologic Manifestations

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2010.03.014

7 January 2021

based on heuristic

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10.1016/J.YDBIO.2010.03.014

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release_rzmfvsochjelvfv4qzoulvmt6y

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https://api.fatcat.wiki/v0/release/rzmfvsochjelvfv4qzoulvmt6y

24 November 2022

based on heuristic

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

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