Citation Impact
Citing Papers
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TAZ Interacts with TTF-1 and Regulates Expression of Surfactant Protein-C
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Suppression of lung adenocarcinoma progression by Nkx2-1
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Regulation of the NPC2 protein‐mediated cholesterol trafficking by membrane lipids
2011
Prosaposin deficiency: further characterization of the sphingolipid activator protein-deficient sibs
1993
Molecular genetics of metachromatic leukodystrophy
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Obesity and thyroid function
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Emerging Biological Principles of Metastasis
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Poly(ADP-ribose): novel functions for an old molecule
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Membrane lipids: where they are and how they behave
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Body Fat Mass and Macronutrient Intake in Relation to Circulating Soluble Leptin Receptor, Free Leptin Index, Adiponectin, and Resistin Concentrations in Healthy Humans
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Negative regulation of Shh levels by Kras and Fgfr2 during hair follicle development
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Hyperactive Ras in developmental disorders and cancer
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Calmodulin Is Involved in the Ca2+-dependent Activation of Ceramide Kinase as a Calcium Sensor
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The emerging role of the fibroblast growth factor-23–klotho axis in renal regulation of phosphate homeostasis
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Reactive oxygen species have a causal role in multiple forms of insulin resistance
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Principles of lysosomal membrane degradation
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Influence of Cortisol Status on Leptin Secretion
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FGF-23 and secondary hyperparathyroidism in chronic kidney disease
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Metastatic colonization by circulating tumour cells
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Acute exogenous TSH administration stimulates leptin secretion in vivo
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Homozygous Deletion in the Coding Sequence of the c-mer Gene in RCS Rats Unravels General Mechanisms of Physiological Cell Adhesion and Apoptosis
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Chronic Kidney Disease
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A Resource of Cre Driver Lines for Genetic Targeting of GABAergic Neurons in Cerebral Cortex
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Type 2 alveolar cells are stem cells in adult lung
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Functions and metabolism of sphingolipids in Saccharomyces cerevisiae
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Activator proteins and topology of lysosomal sphingolipid catabolism
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Lysosomal storage diseases
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Fibroblast Growth Factor 23 and Risks of Mortality and End-Stage Renal Disease in Patients With Chronic Kidney Disease
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Biochemical Modulation of Cisplatin Mechanisms of Action: Enhancement of Antitumor Activity and Circumvention of Drug Resistance
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Molecular Basis of Combined Pituitary Hormone Deficiencies
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Aggregation-Induced Emission: Together We Shine, United We Soar!
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TheCaenorhabditis elegans spalt-like genesem-4restricts touch cell fate by repressing the selector Hox geneegl-5and the effector genemec-3
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State-of-the-science of endocrine disrupting chemicals, 2012
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The Caenorhabditis elegans mucolipin-like gene cup-5 is essential for viability and regulates lysosomes in multiple cell types
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Genetic Causes of Human Reproductive Disease
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Glycobiology: Toward Understanding the Function of Sugars
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Ganglioside metabolism. Enzymology, Topology, and regulation.
1993
Thyroid Hormone Regulation of Metabolism
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The Dendritic Cell Receptor for Endocytosis, Dec-205, Can Recycle and Enhance Antigen Presentation via Major Histocompatibility Complex Class II–Positive Lysosomal Compartments
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Antiinflammatory Action of Glucocorticoids — New Mechanisms for Old Drugs
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mTOR: a pharmacologic target for autophagy regulation
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FGF-23: More than a regulator of renal phosphate handling?
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Works of Dirk Schnabel being referenced
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity
2012
Free and protein bound leptin are distinct and independently controlled factors in energy regulation
2000
Implications of the Phenotype of POMC Deficiency for the Role of POMC‐Derived Peptides in Skin Physiology
1999
A mutation in the gene of a glycolipid‐binding protein (GM2 activator) that causes GM2‐gangliosidosis variant AB
1991
The organization of the gene for the human cerebroside sulfate activator protein
1991
Novel Activating Mutations of the Calcium-Sensing Receptor: The Calcilytic NPS-2143 Mitigates Excessive Signal Transduction of Mutant Receptors
2010
Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency
2002
Characterization of full‐length cDNAs and the gene coding for the human GM2 activator protein
1991
Molecular Cloning and Characterization of a Full-length Complementary DNA Encoding Human Acid Ceramidase
1996
Obesity Due to Proopiomelanocortin Deficiency: Three New Cases and Treatment Trials with Thyroid Hormone and ACTH4–10
2003
Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations
2006
Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3
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Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets
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Mutation in the sphingolipid activator protein 2 in a patient with a variant of Gaucher disease
1991
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency
2000
Molecular genetics of GM2-gangliosidosis AB variant: a novel mutation and expression in BHK cells
1993
Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency
2002
Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency
2002
Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common gene.
1992
Urinary excretion of galactosyl-hydroxylysine is a marker of growth in children.
1995