Schedl, Andreas, 19..-....
Andreas Schedl
VIAF ID: 173597285 (Personal)
Permalink: http://viaf.org/viaf/173597285
Preferred Forms
- 100 0 _ ‡a Andreas Schedl
- 100 1 _ ‡a Schedl, Andreas, ‡d 19..-....
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
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Activation of beta-catenin signaling by Rspo1 controls differentiation of the mammalian ovary. | |
The adrenal capsule is a signaling center controlling cell renewal and zonation through Rspo3. | |
The adrenal cortex exhibits sexually dimorphic tissue renewal and disease development. | |
The Adult Adrenal Cortex Undergoes Rapid Tissue Renewal in a Sex-Specific Manner | |
Alternatively spliced isoforms of WT1 control podocyte-specific gene expression | |
Amplification of R-spondin1 signaling induces granulosa cell fate defects and cancers in mouse adult ovary. | |
The Angiocrine Factor Rspondin3 Is a Key Determinant of Liver Zonation | |
Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6. | |
Awakening the Bowman: inhibition of CXCL12 signaling activates parietal epithelial cells | |
Bone Marrow Transplantation Can Attenuate the Progression of Mesangial Sclerosis | |
The cerebellin 4 precursor gene is a direct target of SRY and SOX9 in mice | |
Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease | |
Chromosome jumping from flanking markers defines the minimal region for alf/hsdr-1 within the albino-deletion complex | |
Comprendre comment la protéine PX régule les activités de la télomérase | |
Conditional Sox9 ablation reduces chondroitin sulfate proteoglycan levels and improves motor function following spinal cord injury | |
Coronary Artery Formation Is Driven by Localized Expression of R-spondin3. | |
Deficiency of an enzyme of tyrosine metabolism underlies altered gene expression in newborn liver of lethal albino mice. | |
Deletion of long-range regulatory elements upstream of SOX9 causes campomelic dysplasia | |
Développement et homéostasie adrenogonadique : rôle des gènes WT1 et RSPO1 | |
Développement vasculaire rénal in vivo et ex vivo : vers la bio-ingénierie rénale | |
Duplex kidney formation: developmental mechanisms and genetic predisposition | |
Essential role of Sox9 in the pathway that controls formation of cardiac valves and septa | |
Étude fonctionnelle du gène WTX, un nouveau régulateur négatif de la voie de signalisation WNT/β-caténine, au cours du développement embryonnaire chez la souris | |
Les fonctions vitales de WT1 au cours de la vie des cellules progénitrices du rein embryonnaire | |
Gene interactions in gonadal development. | |
Genetic and molecular insights into genotype-phenotype relationships in osteopathia striata with cranial sclerosis (OSCS) through the analysis of novel mouse Wtx mutant alleles. | |
GREB1L (growth regulation by estrogen in breast cancer 1-like) régule le métabolisme cellulaire des acides gras et la pluripotence pendant la maturation des progéniteurs axiaux | |
The <i>−KTS</i> splice variant of WT1 is essential for ovarian determination in mice | |
Identification de nouvelles cibles de WT1 au cours de la néphrogenèse précoce et analyses fonctionnelles chez la souris | |
Identification of genes regulated by WT1 during kidney development and functional studies in the mouse. | |
In vivo and ex vivo analysis of vascular development in kidneys : towards renal bio-engineering. | |
An Inducible Mouse Model for PAX2-Dependent Glomerular Disease: Insights into a Complex Pathogenesis | |
Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalities. | |
Insights From The Small-Spotted Catshark : Kidney Development And The Persistence Of Renal Progenitor Cells In A Chondrichthyes Model | |
Local retinoic acid signaling directs emergence of the extraocular muscle functional unit | |
The major podocyte protein nephrin is transcriptionally activated by the Wilms' tumor suppressor WT1. | |
Modeling nephrotic syndrome using iPSC-derived kidney organoids | |
Molecular mapping of albino deletions associated with early embryonic lethality in the mouse. | |
A novel approach to selectively target neuronal subpopulations reveals genetic pathways that regulate tangential migration in the vertebrate hindbrain | |
Nrg1 and Mmd2, two genes are implicated in the developing gonad of mice. | |
Pax6 controls progenitor cell identity and neuronal fate in response to graded Shh signaling | |
La petite roussette : développement rénal dans un animal néonéphrogénique et caractéristiques moléculaires des progéniteurs rénaux. | |
Physical mapping of the albino-deletion complex in the mouse to localize alf/hsdr-1, a locus required for neonatal survival | |
The podocyte protein nephrin is required for cardiac vessel formation | |
Renal abnormalities and their developmental origin | |
Repression of CMIP transcription by WT1 is relevant to podocyte health. | |
The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouse | |
Retinoic acid synthesis by ALDH1A proteins is dispensable for meiosis initiation in the mouse fetal ovary | |
Rôle de la voie Wnt/ßcaténine dans la physiopathologie de la cortico-surrénale | |
Rôle de Tshz3 dans le développement et le fonctionnement du rein. | |
The role of Brn4/Pou3f4 and Pax6 in forming the pancreatic glucagon cell identity | |
Les rôles de HNF1B comme un facteur marque-page en mitose. | |
Rôles des altérations des gènes CTNNB1 et de ZNRF3 dans les carsinomes de la corticosurrénale | |
Roles of HNF1B as a book marking factor | |
Rspondin signaling in adrenal gland development and homeostasis. | |
Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT). | |
Sox8 acts redundantly in place of Sox9 during pathophysiological testicular development in R-spondin1 (RSPO1) loss-of-function mice. | |
Sox8 compense la perte de Sox9 pendant le développement testiculaire physiopathologique chez la souris présentant une perte de fonction du gène R-spondin1 | |
Sox9 Activation Highlights a Cellular Pathway of Renal Repair in the Acutely Injured Mammalian Kidney | |
SOX9 controls epithelial branching by activating RET effector genes during kidney development | |
SOX9 expression increases with malignant potential in tumors from patients with neurofibromatosis 1 and is not correlated to desert hedgehog | |
SOX9 expression is a general marker of basal cell carcinoma and adnexal-related neoplasms | |
Sox9 in testis determination | |
Sox9 induces testis development in XX transgenic mice | |
Sox9 is essential for outer root sheath differentiation and the formation of the hair stem cell compartment | |
Sox9 is expressed in mouse multipotent retinal progenitor cells and functions in Müller glial cell development | |
Testicular differentiation occurs in absence of R-spondin1 and Sox9 in mouse sex reversals | |
THSD7A, the second autoantigen in membranous nephropathy : new diagnostic test and identification of the immunodominant epitopes. | |
Towards the generation of adrenocortical cells from pluripotent stem cells. | |
Transcriptional control of kidney development by the Sox genes family. | |
The transcriptional control of trunk neural crest induction, survival, and delamination | |
Two splice variants of the Wilms' tumor 1 gene have distinct functions during sex determination and nephron formation | |
The Wilms' tumor gene Wt1 is required for normal development of the retina | |
The Wilms' tumour suppressor WT1 is involved in endothelial cell proliferation and migration: expression in tumour vessels in vivo | |
WT1 controls antagonistic FGF and BMP-pSMAD pathways in early renal progenitors | |
WT1 is a key regulator of podocyte function: reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis | |
Wt1 is not essential for hematopoiesis in the mouse | |
WT1 maintains adrenal-gonadal primordium identity and marks a population of AGP-like progenitors within the adrenal gland | |
The WTX/AMER1 gene family: evolution, signature and function | |
YAC transgenic analysis reveals Wilms' tumour 1 gene activity in the proliferating coelomic epithelium, developing diaphragm and limb. | |
A yeast artificial chromosome covering the tyrosinase gene confers copy number-dependent expression in transgenic mice. |