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ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits

Journal of molecular medicine (Berlin, Germany), 2019-01, Vol.97 (1), p.1-17

Hearn, Tom

2019

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ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits

Journal of molecular medicine (Berlin, Germany), 2019-01, Vol.97 (1), p.1-17

Hearn, Tom

2019

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Elevated oxysterol levels in human and mouse livers reflect nonalcoholic steatohepatitis[S]

Journal of lipid research, 2019-07, Vol.60 (7), p.1270-1283

2019

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Subcellular Localization of ALMS1 Supports Involvement of Centrosome and Basal Body Dysfunction in the Pathogenesis of Obesity, Insulin Resistance, and Type 2 Diabetes

Diabetes (New York, N.Y.), 2005-05, Vol.54 (5), p.1581-1587

2005

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Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1

Gene, 2010-07, Vol.460 (1-2), p.20-29

2010

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In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets

Journal of endocrinology, 2010-11, Vol.207 (2), p.151-161

2010

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Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition

European journal of cell biology, 2012-09, Vol.91 (9), p.675-686

2012

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Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p

Genome research, 2003-02, Vol.13 (2), p.159-172

2003

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Evidence for centriolar satellite localization of CDK1 and cyclin B2

Cell cycle (Georgetown, Tex.), 2013-06, Vol.12 (11), p.1802-1803

2013

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Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alström syndrome

Human mutation, 2007-11, Vol.28 (11), p.1114-1123

2007

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Evidence for reciliation of RPE1 cells in late G1 phase, and ciliary localisation of cyclin B1

FEBS open bio, 2013-01, Vol.3 (1), p.334-340

2013

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Mutation of ALMS1 , a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome

Nature genetics, 2002-05, Vol.31 (1), p.79-83

2002

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Detection of southward intracontinental subduction of Tibetan lithosphere along the Bangong-Nujiang suture by P-to-S converted waves

Geology (Boulder), 2004-03, Vol.32 (3), p.209

2004

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Transcriptional regulation of the Alstroem syndrome gene ALMS1 by members of the RFX family and Sp1

Gene, 2010-07, Vol.460 (1-2), p.20-29

2010

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Narrowing the Critical Region within 11q24–qter for Hypoplastic Left Heart and Identification of a Candidate Gene, JAM3, Expressed during Cardiogenesis

Genomics (San Diego, Calif.), 2002-04, Vol.79 (4), p.475-478

2002

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Subcellular localization of alms 1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes

Diabetes (New York, N.Y.), 2005, Vol.54 (5), p.1581-1587

2005

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Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms

Genome research, 2002-01, Vol.12 (1), p.67-80

2002

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Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alstroem syndrome

Nature genetics, 2002-05, Vol.31 (1), p.79-83

2002

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Structure and Evolution of the Tibetan Plateau from INDEPTH Geophysical Surveys

Eos (Washington, D.C.), 2006-09, Vol.87

2006

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Daphnia magna egg piRNA cluster expression profiles change as mothers age

BMC genomics, 2022-06, Vol.23 (1), p.429-14, Article 429

2022

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DNA methylation differs extensively between strains of the same geographical origin and changes with age in Daphnia magna

Epigenetics & chromatin, 2021-01, Vol.14 (1), p.4-4, Article 4

2021

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Genome-wide methylation is modified by caloric restriction in Daphnia magna

BMC genomics, 2019-03, Vol.20 (1), p.197-197, Article 197

2019

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Daphnia magna modifies its gene expression extensively in response to caloric restriction revealing a novel effect on haemoglobin isoform preference

Molecular ecology, 2020-09, Vol.29 (17), p.3261-3276

2020

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Integrating Prostate-specific Antigen Kinetics into Contemporary Predictive Nomograms of Salvage Radiotherapy After Radical Prostatectomy

European urology oncology, 2022-06, Vol.5 (3), p.304-313

2022

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ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits

ALMS1 and Alström syndrome: a recessive form of metabolic, neurosensory and cardiac deficits

Elevated oxysterol levels in human and mouse livers reflect nonalcoholic steatohepatitis[S]

Subcellular Localization of ALMS1 Supports Involvement of Centrosome and Basal Body Dysfunction in the Pathogenesis of Obesity, Insulin Resistance, and Type 2 Diabetes

Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1

In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets

Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition

Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p

Evidence for centriolar satellite localization of CDK1 and cyclin B2

Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alström syndrome

Evidence for reciliation of RPE1 cells in late G1 phase, and ciliary localisation of cyclin B1

Mutation of ALMS1 , a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome

Detection of southward intracontinental subduction of Tibetan lithosphere along the Bangong-Nujiang suture by P-to-S converted waves

Transcriptional regulation of the Alstroem syndrome gene ALMS1 by members of the RFX family and Sp1

Narrowing the Critical Region within 11q24–qter for Hypoplastic Left Heart and Identification of a Candidate Gene, JAM3, Expressed during Cardiogenesis

Subcellular localization of alms 1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes

Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms

Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alstroem syndrome

Structure and Evolution of the Tibetan Plateau from INDEPTH Geophysical Surveys

Daphnia magna egg piRNA cluster expression profiles change as mothers age

DNA methylation differs extensively between strains of the same geographical origin and changes with age in Daphnia magna

Genome-wide methylation is modified by caloric restriction in Daphnia magna

Daphnia magna modifies its gene expression extensively in response to caloric restriction revealing a novel effect on haemoglobin isoform preference

Integrating Prostate-specific Antigen Kinetics into Contemporary Predictive Nomograms of Salvage Radiotherapy After Radical Prostatectomy

Monoacidic Inhibitors of the Kelch-like ECH-Associated Protein 1: Nuclear Factor Erythroid 2‑Related Factor 2 (KEAP1:NRF2) Protein–Protein Interaction with High Cell Potency Identified by Fragment-Based Discovery

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