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Complementary Functions of the Flippase ATP8B1 and the Floppase ABCB4 in Maintaining Canalicular Membrane Integrity

Gastroenterology (New York, N.Y. 1943), 2011-11, Vol.141 (5), p.1927-1937.e4

2011

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The Human Scavenger Receptor CD36

The Journal of biological chemistry, 2009-06, Vol.284 (24), p.16277-16288

2009

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KDM2A integrates DNA and histone modification signals through a CXXC/PHD module and direct interaction with HP1

Nucleic acids research, 2017-02, Vol.45 (3), p.1114

2017

Volltextzugriff (PDF)

The Human Scavenger Receptor CD36: glycosylation status and its role in trafficking and function

The Journal of biological chemistry, 2009-06, Vol.284 (24), p.16277-16288

2009

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Membrane phosphatidylserine distribution as a non-apoptotic signalling mechanism in lymphocytes

Nature cell biology, 2005-08, Vol.7 (8), p.808-816

2005

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Repacking of the transmembrane domains of P-glycoprotein during the transport ATPase cycle

The EMBO journal, 2001-10, Vol.20 (20), p.5615-5625

2001

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Renal Chloride Channel, CLCN5, Mutations in Dent's Disease

Journal of bone and mineral research, 1999-09, Vol.14 (9), p.1536-1542

1999

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Cd36, a class B scavenger receptor, functions as a monomer to bind acetylated and oxidized low‐density lipoproteins

Protein science, 2007-11, Vol.16 (11), p.2531-2541

2007

Volltextzugriff (PDF)

Mutational analysis of PHEX gene in X-linked hypophosphatemia

The journal of clinical endocrinology and metabolism, 1998-10, Vol.83 (10), p.3615-3623

1998

Volltextzugriff (PDF)

Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11

The New England journal of medicine, 1989-07, Vol.321 (4), p.218

1989

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Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22

Human molecular genetics, 1993-12, Vol.2 (12), p.2129-2134

1993

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Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies

The Journal of clinical investigation, 1993-06, Vol.91 (6), p.2351-2357

1993

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Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH

Human genetics, 1995-08, Vol.96 (2), p.183-187

1995

Volltextzugriff (PDF)

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene

Human genetics, 1996-06, Vol.97 (6), p.732-741

1996

Volltextzugriff (PDF)

Linkage Studies of a Missouri Kindred with Autosomal Dominant Spondyloepimetaphyseal Dysplasia (SEMD) Indicate Genetic Heterogeneity

Journal of bone and mineral research, 1997-08, Vol.12 (8), p.1204-1209

1997

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Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1

Human genetics, 1996, Vol.97 (1), p.60-68

1996

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Mutational Analysis of PHEX Gene in X-Linked Hypophosphatemia1

The journal of clinical endocrinology and metabolism, 1998-10, Vol.83 (10), p.3615-3623

1998

Volltextzugriff (PDF)

TAXATION

Loyola University of Chicago law journal, 1990-01, Vol.21 (2), p.633

1990

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Mothers' Speech to Young Children: Variation in Context

Developmental medicine and child neurology, 1977-10, Vol.19 (5), p.629-638

1977

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6 versus 12 months of adjuvant trastuzumab for HER2-positive early breast cancer (PERSEPHONE): 4-year disease-free survival results of a randomised phase 3 non-inferiority trial

The Lancet (British edition), 2019-06, Vol.393 (10191), p.2599-2612

2019

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Teaching health and safety: Problems and possibilities for learner-centered training

American journal of industrial medicine, 1992, Vol.22 (5), p.665-676

1992

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Complementary Functions of the Flippase ATP8B1 and the Floppase ABCB4 in Maintaining Canalicular Membrane Integrity

The Human Scavenger Receptor CD36

KDM2A integrates DNA and histone modification signals through a CXXC/PHD module and direct interaction with HP1

The Human Scavenger Receptor CD36: glycosylation status and its role in trafficking and function

Membrane phosphatidylserine distribution as a non-apoptotic signalling mechanism in lymphocytes

Repacking of the transmembrane domains of P-glycoprotein during the transport ATPase cycle

Renal Chloride Channel, CLCN5, Mutations in Dent's Disease

Cd36, a class B scavenger receptor, functions as a monomer to bind acetylated and oxidized low‐density lipoproteins

Mutational analysis of PHEX gene in X-linked hypophosphatemia

Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies

Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of μ-calpain as the multiple endocrine neoplasia type 1 gene

Linkage Studies of a Missouri Kindred with Autosomal Dominant Spondyloepimetaphyseal Dysplasia (SEMD) Indicate Genetic Heterogeneity

Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1

Mutational Analysis of PHEX Gene in X-Linked Hypophosphatemia1

TAXATION

Mothers' Speech to Young Children: Variation in Context

6 versus 12 months of adjuvant trastuzumab for HER2-positive early breast cancer (PERSEPHONE): 4-year disease-free survival results of a randomised phase 3 non-inferiority trial

Teaching health and safety: Problems and possibilities for learner-centered training

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