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Interrelated role of Klotho and calcium-sensing receptor in parathyroid hormone synthesis and parathyroid hyperplasia

Proceedings of the National Academy of Sciences - PNAS, 2018-04, Vol.115 (16), p.E3749-E3758

2018

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TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

Nature genetics, 2005-07, Vol.37 (7), p.739-744

2005

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Opinions of African American adults about the use of apolipoprotein L1 (ApoL1) genetic testing in living kidney donation and transplantation

American journal of transplantation, 2021-03, Vol.21 (3), p.1197-1205

2021

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Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor

Nature, 2006-02, Vol.439 (7076), p.599-603

2006

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Mutations in ACTN4 , encoding α-actinin-4, cause familial focal segmental glomerulosclerosis

Nature genetics, 2000-03, Vol.24 (3), p.251-256

2000

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Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint

Journal of the American Society of Nephrology, 2002-12, Vol.13 (12), p.3016-3023

POLLAK, Martin R

2002

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Mutational and biological analysis of α-actinin-4 in focal segmental glomerulosclerosis

Journal of the American Society of Nephrology, 2005-12, Vol.16 (12), p.3694-3701

2005

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Alpha-actinin-4-mediated FSGS: an inherited kidney disease caused by an aggregated and rapidly degraded cytoskeletal protein

PLoS biology, 2004-06, Vol.2 (6), p.e167-794

2004

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Mice deficient in alpha -actinin-4 have severe glomerular disease

The Journal of clinical investigation, 2003-06, Vol.111 (11), p.1683-1690

2003

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The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormone

The Journal of clinical investigation, 2003-04, Vol.111 (7), p.1021-1028

2003

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NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele

The Journal of clinical investigation, 2002-12, Vol.110 (11), p.1659-1666

2002

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A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Nature genetics, 1995-12, Vol.11 (4), p.389-394

1995

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The genetic basis of FSGS and steroid-resistant nephrosis

Seminars in nephrology, 2003-03, Vol.23 (2), p.141-146

Pollak, Martin R.

2003

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NPHS2 R229Q functional variant is associated with microalbuminuria in the general population

Kidney international, 2004-03, Vol.65 (3), p.1026-1030

2004

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Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Cell, 1993-12, Vol.75 (7), p.1297-1303

1993

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Extracellular calcium elicits a chemokinetic response from monocytes in vitro and in vivo

The Journal of clinical investigation, 2000-05, Vol.105 (9), p.1299-1305

2000

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Cultured podocytes establish a size-selective barrier regulated by specific signaling pathways and demonstrate synchronized barrier assembly in a calcium switch model of junction formation

Journal of the American Society of Nephrology, 2005-06, Vol.16 (6), p.1593-1602

2005

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Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation

Heart (British Cardiac Society), 2004-12, Vol.90 (12), p.1487-1488

2004

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Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism : effects of mutant gene dosage on phenotype

The Journal of clinical investigation, 1994-03, Vol.93 (3), p.1108-1112

1994

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A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13

Kidney international, 1998-02, Vol.53 (2), p.282-286

1998

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A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31

Journal of the American Society of Nephrology, 2000-09, Vol.11 (9), p.1674-1680

2000

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More on Clinical Renal Genetics

Clinical journal of the American Society of Nephrology, 2010-04, Vol.5 (4), p.563-567

2010

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Familial focal segmental glomerulosclerosis

Current opinion in nephrology and hypertension, 2001-03, Vol.10 (2), p.183-187

2001

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Evolution of the primate trypanolytic factor APOL1

日本小児腎臓病学会雑誌, 2014, Vol.27(2), pp.141-142

2014

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Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2

Nature genetics, 1993-10, Vol.5 (2), p.201-204

1993

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Interrelated role of Klotho and calcium-sensing receptor in parathyroid hormone synthesis and parathyroid hyperplasia

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

Opinions of African American adults about the use of apolipoprotein L1 (ApoL1) genetic testing in living kidney donation and transplantation

Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor

Mutations in ACTN4 , encoding α-actinin-4, cause familial focal segmental glomerulosclerosis

Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint

Mutational and biological analysis of α-actinin-4 in focal segmental glomerulosclerosis

Alpha-actinin-4-mediated FSGS: an inherited kidney disease caused by an aggregated and rapidly degraded cytoskeletal protein

Mice deficient in alpha -actinin-4 have severe glomerular disease

The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormone

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele

A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

The genetic basis of FSGS and steroid-resistant nephrosis

NPHS2 R229Q functional variant is associated with microalbuminuria in the general population

Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Extracellular calcium elicits a chemokinetic response from monocytes in vitro and in vivo

Cultured podocytes establish a size-selective barrier regulated by specific signaling pathways and demonstrate synchronized barrier assembly in a calcium switch model of junction formation

Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation

Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism : effects of mutant gene dosage on phenotype

A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13

A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31

More on Clinical Renal Genetics

Familial focal segmental glomerulosclerosis

Evolution of the primate trypanolytic factor APOL1

Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2

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