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Genetic complexity in Joubert syndrome and related disorders

Kidney international, 2007-12, Vol.72 (12), p.1421-1423

Harris, P.C.

2007

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Determinants of renal volume in autosomal-dominant polycystic kidney disease

Kidney international, 2008-01, Vol.73 (1), p.108-116

2008

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Semi-supervised labelling of the femur in a whole-body post-mortem CT database using deep learning

Computers in biology and medicine, 2020-07, Vol.122, p.103797-103797, Article 103797

2020

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Effect of density gradient material upon ex-vivo neutrophil extracellular trap (NET) formation

Free radical biology & medicine, 2012-09, Vol.53, p.S168-S168

2012

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Therapeutic mTOR Inhibition in Autosomal Dominant Polycystic Kidney Disease: What Is the Appropriate Serum Level?

American journal of transplantation, 2010-07, Vol.10 (7), p.1701-1706

2010

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A mouse model of autosomal recessive polycystic kidney disease with biliary duct and proximal tubule dilatation

Kidney international, 2007-08, Vol.72 (3), p.328-336

2007

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Hyperproliferation of PKD1 cystic cells is induced by insulin-like growth factor-1 activation of the Ras/Raf signalling system

Kidney international, 2007-07, Vol.72 (2), p.157-165

2007

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Ziliopathien

Medizinische Genetik, 2009-03, Vol.21 (1), p.14-20

2009

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Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite marker

The Lancet (British edition), 1991-12, Vol.338 (8781), p.1484-1487

1991

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Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)

American journal of human genetics, 1994-08, Vol.55 (2), p.365-371

1994

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The TSC2/PKD1 Contiguous Gene Syndrome

Contributions to nephrology, 1997-01, Vol.122, p.76-82

1997

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The comparative value of five calcium sources for laying hens

Poultry science, 1976-05, Vol.55 (3), p.1046-1051

1976

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The Mouse Homologue of the Polycystic Kidney Disease Gene (Pkd1) Is a Single-Copy Gene

Genomics (San Diego, Calif.), 1996-06, Vol.34 (2), p.233-235

1996

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Heterotopic ossification of the Achilles tendon following ankle fracture: a case report

Foot and ankle surgery, 2000, Vol.6 (4), p.275-279

2000

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Egg inclusions from brown and white shell eggs as observed with the scanning electron microscope [Meat spots]

Poultry science, 1974-01, Vol.53 (5), p.1768-1771

1974

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Construction of a Map of Chromosome 16 by Using Radiation Hybrids

Proceedings of the National Academy of Sciences - PNAS, 1992-01, Vol.89 (1), p.104-108

1992

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Characterization of three de novo derivative chromosomes 16 by reverse chromosome painting and molecular analysis

American journal of human genetics, 1993-05, Vol.52 (5), p.987-997

1993

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Evidence of linkage disequilibrium in the Spanish polycystic kidney disease 1 population

American journal of human genetics, 1994-05, Vol.54:5

1994

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A long-range restriction map between the α-globin complex and a marker closely linked to the polycystic kidney disease 1 (PKD1) locus

Genomics (San Diego, Calif.), 1990-06, Vol.7 (2), p.195-206

1990

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DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE

The Lancet (British edition), 1989-10, Vol.334 (8667), p.819-824

1989

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Observations of possible thiaminase activity in scallop viscera fed in broiler diets. Case report

Poultry science, 1975-07, Vol.54 (4), p.1299-1301

1975

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Evaluation of the fluorescence activated cell sorter (FACS) for human karyotype analysis and chromosome sorting

Harris, P.C

1984

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Molecular analysis of autosomal dominant polycystic kidney disease

Acta biologica Slovenica, 2000, Vol.43 (1-2)

Harris, P.C. (John Radcliffe Hospital, Headington (United Kingdom). Molecular Medicine Inst.)

2000

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De novo truncation of chromosome 16p and healing with (TTAGGG)[sub n] in the [alpha]-thalassemia/mental retardation syndrome (ATR-16)

American journal of human genetics, 1993-04, Vol.52:4

1993

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Molecular and Hematologic Characterization of Scottish-Irish Type (ϵγδβ)° Thalassemia

Blood, 1990-11, Vol.76 (10), p.2132-2138

1990

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Genetic complexity in Joubert syndrome and related disorders

Determinants of renal volume in autosomal-dominant polycystic kidney disease

Semi-supervised labelling of the femur in a whole-body post-mortem CT database using deep learning

Effect of density gradient material upon ex-vivo neutrophil extracellular trap (NET) formation

Therapeutic mTOR Inhibition in Autosomal Dominant Polycystic Kidney Disease: What Is the Appropriate Serum Level?

A mouse model of autosomal recessive polycystic kidney disease with biliary duct and proximal tubule dilatation

Hyperproliferation of PKD1 cystic cells is induced by insulin-like growth factor-1 activation of the Ras/Raf signalling system

Ziliopathien

Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite marker

Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)

The TSC2/PKD1 Contiguous Gene Syndrome

The comparative value of five calcium sources for laying hens

The Mouse Homologue of the Polycystic Kidney Disease Gene (Pkd1) Is a Single-Copy Gene

Heterotopic ossification of the Achilles tendon following ankle fracture: a case report

Egg inclusions from brown and white shell eggs as observed with the scanning electron microscope [Meat spots]

Construction of a Map of Chromosome 16 by Using Radiation Hybrids

Characterization of three de novo derivative chromosomes 16 by reverse chromosome painting and molecular analysis

Evidence of linkage disequilibrium in the Spanish polycystic kidney disease 1 population

A long-range restriction map between the α-globin complex and a marker closely linked to the polycystic kidney disease 1 (PKD1) locus

DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE

Observations of possible thiaminase activity in scallop viscera fed in broiler diets. Case report

Evaluation of the fluorescence activated cell sorter (FACS) for human karyotype analysis and chromosome sorting

Molecular analysis of autosomal dominant polycystic kidney disease

De novo truncation of chromosome 16p and healing with (TTAGGG)[sub n] in the [alpha]-thalassemia/mental retardation syndrome (ATR-16)

Molecular and Hematologic Characterization of Scottish-Irish Type (ϵγδβ)° Thalassemia

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