Ashcroft, Frances M.
Frances Ashcroft British geneticist and physiologist
Ashcroft, Frances
Ashcroft, Frances 1952-
Ashcroft, Frances (Frances M.)
Ashcroft, Frances M, 1952-
אשקרופט, פרנסס
VIAF ID: 54220244 (Personal)
Permalink: http://viaf.org/viaf/54220244
Preferred Forms
- 200 _ | ‡a Ashcroft ‡b Frances M.
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- 100 1 _ ‡a Ashcroft, Frances M, ‡d 1952-
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- 100 1 _ ‡a Ashcroft, Frances M.
- 100 1 _ ‡a Ashcroft, Frances M.
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- 100 1 _ ‡a Ashcroft, Frances M.
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- 100 1 _ ‡a Ashcroft, Frances M.
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- 100 1 _ ‡a Ashcroft, Frances M.
- 100 1 _ ‡a Ashcroft, Frances ‡d 1952-
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- 100 0 _ ‡a Frances Ashcroft ‡c British geneticist and physiologist
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4xx's: Alternate Name Forms (19)
Works
Title | Sources |
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3-D structural and functional characterization of the purified KATP channel complex Kir6.2-SUR1. | |
An ABCC8 Nonsense Mutation Causing Neonatal Diabetes Through Altered Transcript Expression | |
Adult onset global loss of the fto gene alters body composition and metabolism in the mouse | |
Alexis Rockman : wonderful world. | |
Am Limit Leben und Überleben in Extremsituationen | |
Asymmetric switching in a homodimeric ABC transporter: a simulation study | |
ATP-dependent interaction of the cytosolic domains of the inwardly rectifying K+ channel Kir6.2 revealed by fluorescence resonance energy transfer | |
Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5 | |
Binding of sulphonylureas to plasma proteins - A KATP channel perspective. | |
Cardiac Dysfunction and Metabolic Inflexibility in a Mouse Model of Diabetes Without Dyslipidemia. | |
Changes in gene expression associated with FTO overexpression in mice | |
CLC-5 and KIF3B interact to facilitate CLC-5 plasma membrane expression, endocytosis, and microtubular transport: relevance to pathophysiology of Dent's disease | |
Crystal structure of the potassium channel KirBac1.1 in the closed state | |
Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies | |
Dissection-independent production of <i>Plasmodium</i> sporozoites from whole mosquitoes | |
Dysregulation of Glucagon Secretion by Hyperglycemia-Induced Sodium-Dependent Reduction of ATP Production | |
Enhanced PIP3 signaling in POMC neurons causes KATP channel activation and leads to diet-sensitive obesity | |
FTO demethylase activity is essential for normal bone growth and bone mineralization in mice | |
FTO influences adipogenesis by regulating mitotic clonal expansion | |
FTO is expressed in neurones throughout the brain and its expression is unaltered by fasting | |
Fumarate Hydratase Deletion in Pancreatic β Cells Leads to Progressive Diabetes | |
Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes. | |
Functional identification of islet cell types by electrophysiological fingerprinting | |
Gain-of-function mutations in the K(ATP) channel (KCNJ11) impair coordinated hand-eye tracking | |
A gating mutation at the internal mouth of the Kir6.2 pore is associated with DEND syndrome | |
A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes | |
A high-throughput assay for modulators of NNT activity in permeabilized yeast cells | |
How ATP inhibits the open K(ATP) channel | |
Hyperglycaemia induces metabolic dysfunction and glycogen accumulation in pancreatic β-cells | |
Increased NEFA levels reduce blood Mg2+ in hypertriacylglycerolaemic states via direct binding of NEFA to Mg2 | |
Influences: Find a friend | |
Insulin, c1992: | |
Insulin : molecular biology to pathology | |
Introduction. The blurred boundary between channels and transporters | |
Ion channels and disease : channelopathies | |
Is Type 2 Diabetes a Glycogen Storage Disease of Pancreatic β Cells? | |
The Kir6.2-F333I mutation differentially modulates KATP channels composed of SUR1 or SUR2 subunits | |
Life at the extremes : [the science of survival | |
The ligand-sensitive gate of a potassium channel lies close to the selectivity filter | |
Long-term exposure to glucose and lipids inhibits glucose-induced insulin secretion downstream of granule fusion with plasma membrane | |
Magnesium deficiency prevents high-fat-diet-induced obesity in mice | |
Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features | |
Monitoring real-time hormone release kinetics via high-content 3-D imaging of compensatory endocytosis | |
A mouse model for the metabolic effects of the human fat mass and obesity associated FTO gene | |
A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes | |
Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's disease | |
Mutations in the linker domain of NBD2 of SUR inhibit transduction but not nucleotide binding | |
Mutations of the same conserved glutamate residue in NBD2 of the sulfonylurea receptor 1 subunit of the KATP channel can result in either hyperinsulinism or neonatal diabetes | |
Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk | |
New insights into KATP channel gene mutations and neonatal diabetes mellitus | |
Ningen wa dokomade taerarerunoka | |
The Nucleotide-Binding Sites of SUR1: A Mechanistic Model | |
Nucleotide-dependent conformational changes in HisP: molecular dynamics simulations of an ABC transporter nucleotide-binding domain | |
Nucleotide inhibition of the pancreatic ATP-sensitive K+ channel explored with patch-clamp fluorometry | |
The obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylase | |
Overexpression of Fto leads to increased food intake and results in obesity | |
Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men. | |
Pancreatic β-Cells Express the Fetal Islet Hormone Gastrin in Rodent and Human Diabetes | |
Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects | |
Permanent neonatal diabetes: combining sulfonylureas with insulin may be an effective treatment | |
Potassium channel regulation | |
PPAR gamma 2 prevents lipotoxicity by controlling adipose tissue expandability and peripheral lipid metabolism | |
Reversible changes in pancreatic islet structure and function produced by elevated blood glucose | |
Role of the C-terminus of SUR in the differential regulation of β-cell and cardiac KATP channels by MgADP and metabolism. | |
Role of the transcription factor sox4 in insulin secretion and impaired glucose tolerance | |
Running out of time: the decline of channel activity and nucleotide activation in adenosine triphosphate-sensitive K-channels | |
Sensibilidad diferencial a la gliclazida de los canales de Katp en células beta y extrapancreáticas | |
The spark of life : electricity in the human body | |
Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes. | |
Sulfonylurea stimulation of insulin secretion | |
Systemic Administration of Glibenclamide Fails to Achieve Therapeutic Levels in the Brain and Cerebrospinal Fluid of Rodents | |
Tetrameric structure of SUR2B revealed by electron microscopy of oriented single particles | |
Type 2 diabetes mellitus: not quite exciting enough? | |
Uz izdzīvošanas robežas, 2002: | |
A vida no limite : a ciência da sobrevivência | |
Women in Metabolism: Part 3. | |
Życie w warunkach ekstremalnych / Frances Ashcroft. - Warszawa, 2002 | |
β-Cell dysfunction in diabetes: a crisis of identity? | |
생존의 한계 | |
人間はどこまで耐えられるのか | |
生命の閃光 : 体は電気で動いている |