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Allelic variation at the C-reactive protein gene associates to both hand osteoarthritis severity and serum high sensitive C-reactive protein levels in the GARP study

Annals of the rheumatic diseases, 2008-06, Vol.67 (6), p.877-879

2008

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Frequent somatic mutations and homozygous deletions of the p16 ( MTS1 ) gene in pancreatic adenocarcinoma

Nature genetics, 1994-09, Vol.8 (1), p.27-32

1994

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p53 mutations in pancreatic carcinoma and evidence of common involvement of homocopolymer tracts in DNA microdeletions

Cancer research (Chicago, Ill.), 1994-06, Vol.54 (11), p.3025-3033

1994

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Allelotype of pancreatic adenocarcinoma using xenograft enrichment

Cancer research (Chicago, Ill.), 1995-10, Vol.55 (20), p.4670-4675

1995

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Homozygous deletion map at 18q21.1 in pancreatic cancer

Cancer research (Chicago, Ill.), 1996-02, Vol.56 (3), p.490-494

1996

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Allelotype of pancreatic adenocarcinoma

Cancer research (Chicago, Ill.), 1994-05, Vol.54 (10), p.2761-2764

1994

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Molecular genetic profiles of colitis-associated neoplasms

Gastroenterology (New York, N.Y. 1943), 1994-08, Vol.107 (2), p.420-428

1994

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Abnormal Expression and Subcellular Distribution of Subunit Proteins of the AP-3 Adaptor Complex Lead to Platelet Storage Pool Deficiency in the Pearl Mouse

Blood, 1999-07, Vol.94 (1), p.146-155

1999

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Association of matrilin-3 polymorphisms with spinal disc degeneration and osteoarthritis of the first carpometacarpal joint of the hand

Annals of the rheumatic diseases, 2006-08, Vol.65 (8), p.1060-1066

2006

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Association of the frizzled‐related protein gene with symptomatic osteoarthritis at multiple sites

Arthritis and rheumatism, 2005-04, Vol.52 (4), p.1077-1080

2005

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Linkage Analysis of X-linked Cone-Rod Dystrophy: Localization to Xp11.4 and Definition of a Locus Distinct from RP2 and RP3

American journal of human genetics, 1998-01, Vol.62 (1), p.122-129

1998

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Frontostriatal measurement in treatment-naive children with obsessive-compulsive disorder

Archives of general psychiatry, 1997-09, Vol.54 (9), p.824

1997

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The β3A Subunit Gene (Ap3B1) of the Ap-3 Adaptor Complex Is Altered in the Mouse Hypopigmentation Mutant Pearl, a Model for Hermansky-Pudlak Syndrome and Night Blindness

Human molecular genetics, 1999-02, Vol.8 (2), p.323-330

1999

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Dental caries management at a rural district hospital in northern Rwanda: a neglected disease

Public health action, 2015-09, Vol.5 (3), p.158-161

2015

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Oculomotor response inhibition abnormalities in pediatric obsessive-compulsive disorder

Archives of general psychiatry, 1997-09, Vol.54 (9), p.831

1997

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The serotonin transporter polymorphism, 5HTTLPR, is associated with a faster response time to sertraline in an elderly population with major depressive disorder

Psychopharmacology, 2004-08, Vol.174 (4), p.525-529

2004

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Delayed treatment with monoclonal antibody IN-1 1 week after stroke results in recovery of function and corticorubral plasticity in adult rats

Journal of cerebral blood flow and metabolism, 2005-10, Vol.25 (10), p.1366-1375

2005

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Association between single-nucleotide polymorphisms in the endothelial lipase (LIPG) gene and high-density lipoprotein cholesterol levels

Biochimica et biophysica acta, 2004-02, Vol.1636 (1), p.40-46

2004

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The Practice of Continuous Deep Sedation Until Death in Flanders (Belgium), The Netherlands, and the U.K.: A Comparative Study

Journal of pain and symptom management, 2012-07, Vol.44 (1), p.33-43

2012

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“At the Foot of a Very Long Ladder”: Discussing the End of Life with Older People and Informal Caregivers

Journal of pain and symptom management, 2010-12, Vol.40 (6), p.857-869

2010

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An integrated genetic map of the pearl locus of mouse chromosome 13

Genome research, 1996-06, Vol.6 (6), p.538-544

1996

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The beta 3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness

Human molecular genetics, 1999-02, Vol.8 (2), p.323-330

1999

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A Guide to Jewish References in the Mexican Colonial Era, 1521-1821

2015

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The molecular biology and biochemistry of fruit ripening

1, 2013

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Genetics, Evolution and Radiation: Crossing Borders, the Interdisciplinary Legacy of Nikolay W. Timofeeff-Ressovsky

1, 2017

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Allelic variation at the C-reactive protein gene associates to both hand osteoarthritis severity and serum high sensitive C-reactive protein levels in the GARP study

Frequent somatic mutations and homozygous deletions of the p16 ( MTS1 ) gene in pancreatic adenocarcinoma

p53 mutations in pancreatic carcinoma and evidence of common involvement of homocopolymer tracts in DNA microdeletions

Allelotype of pancreatic adenocarcinoma using xenograft enrichment

Homozygous deletion map at 18q21.1 in pancreatic cancer

Allelotype of pancreatic adenocarcinoma

Molecular genetic profiles of colitis-associated neoplasms

Abnormal Expression and Subcellular Distribution of Subunit Proteins of the AP-3 Adaptor Complex Lead to Platelet Storage Pool Deficiency in the Pearl Mouse

Association of matrilin-3 polymorphisms with spinal disc degeneration and osteoarthritis of the first carpometacarpal joint of the hand

Association of the frizzled‐related protein gene with symptomatic osteoarthritis at multiple sites

Linkage Analysis of X-linked Cone-Rod Dystrophy: Localization to Xp11.4 and Definition of a Locus Distinct from RP2 and RP3

Frontostriatal measurement in treatment-naive children with obsessive-compulsive disorder

The β3A Subunit Gene (Ap3B1) of the Ap-3 Adaptor Complex Is Altered in the Mouse Hypopigmentation Mutant Pearl, a Model for Hermansky-Pudlak Syndrome and Night Blindness

Dental caries management at a rural district hospital in northern Rwanda: a neglected disease

Oculomotor response inhibition abnormalities in pediatric obsessive-compulsive disorder

The serotonin transporter polymorphism, 5HTTLPR, is associated with a faster response time to sertraline in an elderly population with major depressive disorder

Delayed treatment with monoclonal antibody IN-1 1 week after stroke results in recovery of function and corticorubral plasticity in adult rats

Association between single-nucleotide polymorphisms in the endothelial lipase (LIPG) gene and high-density lipoprotein cholesterol levels

The Practice of Continuous Deep Sedation Until Death in Flanders (Belgium), The Netherlands, and the U.K.: A Comparative Study

“At the Foot of a Very Long Ladder”: Discussing the End of Life with Older People and Informal Caregivers

An integrated genetic map of the pearl locus of mouse chromosome 13

The beta 3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness

A Guide to Jewish References in the Mexican Colonial Era, 1521-1821

The molecular biology and biochemistry of fruit ripening

Genetics, Evolution and Radiation: Crossing Borders, the Interdisciplinary Legacy of Nikolay W. Timofeeff-Ressovsky

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