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Rh-related antigen CD47 is the signal-transducer integrin-associated protein

The Journal of biological chemistry, 1994-01, Vol.269 (3), p.1567-1570

1994

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Neural-Specific Expression, Genomic Structure, and Chromosomal Localization of the Gene Encoding the Zinc-Finger Transcription Factor NGFI-C

Proceedings of the National Academy of Sciences - PNAS, 1992-05, Vol.89 (10), p.4739-4743

1992

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Mapping Human Telomere Regions with YAC and P1 Clones: Chromosome-Specific Markers for 27 Telomeres Including 149 STSs and 24 Polymorphisms for 14 Proterminal Regions

Genomics (San Diego, Calif.), 1996-09, Vol.36 (3), p.492-506

1996

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Cloning, Heterologous Expression, and Chromosomal Localization of Human Inositol Polyphosphate 1-Phosphatase

Proceedings of the National Academy of Sciences - PNAS, 1993-06, Vol.90 (12), p.5833-5837

1993

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Index, Comprehensive Microsatellite, and Unified Linkage Maps of Human Chromosome 14 with Cytogenetic Tie Points and a Telomere Microsatellite Marker

Genomics (San Diego, Calif.), 1995-10, Vol.29 (3), p.653-664

1995

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Subregional Localization of 21 Chromosome 7-Specific Expressed Sequence Tags (ESTs) by FISH Using Newly Identified YACs and P1s

Genomics (San Diego, Calif.), 1997-12, Vol.46 (3), p.491-494

1997

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cDNA Sequence and Chromosomal Localization of Human Enterokinase, the Proteolytic Activator of Trypsinogen

Biochemistry (Easton), 1995-04, Vol.34 (14), p.4562-4568

1995

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Neural-specific expression, genomic structure, and chromosomal localization of the gene encoding the zinc-finger transcription factor NGFI-C

Proceedings of the National Academy of Sciences - PNAS, 1992-07, Vol.89 (14), p.6663-6663

1992

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Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

Human molecular genetics, 2002-04, Vol.11 (8), p.961-969

2002

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Urbanization, migration, and indigenous health in Peru

American journal of human biology, 2023-08, Vol.35 (8), p.e23904-n/a

2023

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Birth mode and infectious morbidity risks in Qom children of Argentina

American journal of human biology, 2019-03, Vol.31 (2), p.e23200-n/a

2019

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Introduction: The evolutionary and biocultural causes and consequences of rising cesarean birth rates

American journal of human biology, 2019-03, Vol.31 (2), p.n/a

2019

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Effects of whole blood leukoreduction on platelet function and hemostatic parameters

Transfusion medicine (Oxford, England), 2019-10, Vol.29 (5), p.351-357

2019

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Direct genomic selection

Nature methods, 2005-01, Vol.2 (1), p.63-69

2005

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Evaluation of a Novel Fibrin Sealant Patch in Hemorrhage Control After Vascular or Hepatic Injury

Military medicine, 2019-03, Vol.184 (3-4), p.e290-e296

2019

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Retrofittable plug-flow reactor for in situ high-temperature vibrating sample magnetometry with well-controlled gas atmospheres

Review of scientific instruments, 2023-06, Vol.94 (6)

2023

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Breastfeeding: New Anthropological Approaches

1, 2018

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An RNA interference-based screen of transcription factor genes identifies pathways necessary for sensory regeneration in the avian inner ear

The Journal of neuroscience, 2011-03, Vol.31 (12), p.4535-4543

2011

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Mutational and Haplotype Analyses of Families with Familial Partial Lipodystrophy (Dunnigan Variety) Reveal Recurrent Missense Mutations in the Globular C-Terminal Domain of Lamin A/C

American journal of human genetics, 2000-04, Vol.66 (4), p.1192-1198

2000

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Genomic organization of human surfactant protein D (SP-D). SP-D is encoded on chromosome 10q22.2-23.1

The Journal of biological chemistry, 1993-02, Vol.268 (4), p.2976-2983

1993

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SNTG1, the gene encoding gamma 1-syntrophin: a candidate gene for idiopathic scoliosis

Human genetics, 2004-06, Vol.115 (1), p.81-89

2004

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Isolation, Characterization, and Chromosomal Mapping of the Human Nkx6.1 Gene (NKX6A), a New Pancreatic Islet Homeobox Gene

Genomics (San Diego, Calif.), 1997-03, Vol.40 (2), p.367-370

1997

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A 1.5-Megabase Yeast Artificial Chromosome Contig from Human Chromosome 10q11.2 Connecting Three Genetic Loci (RET, D10S94, and D10S102) Closely Linked to the MEN2A Locus

Proceedings of the National Academy of Sciences - PNAS, 1993-01, Vol.90 (2), p.492-496

1993

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Human Cholecystokinin Type A Receptor Gene: Cytogenetic Localization, Physical Mapping, and Identification of Two Missense Variants in Patients with Obesity and Non-Insulin-Dependent Diabetes Mellitus (NIDDM)

Genomics (San Diego, Calif.), 1997-06, Vol.42 (2), p.331-335

1997

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Improved predictive test for MEN2, using flanking dinucleotide repeats and RFLPs

American journal of human genetics, 1992-12, Vol.51 (6), p.1430-1442

1992

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Rh-related antigen CD47 is the signal-transducer integrin-associated protein

Neural-Specific Expression, Genomic Structure, and Chromosomal Localization of the Gene Encoding the Zinc-Finger Transcription Factor NGFI-C

Mapping Human Telomere Regions with YAC and P1 Clones: Chromosome-Specific Markers for 27 Telomeres Including 149 STSs and 24 Polymorphisms for 14 Proterminal Regions

Cloning, Heterologous Expression, and Chromosomal Localization of Human Inositol Polyphosphate 1-Phosphatase

Index, Comprehensive Microsatellite, and Unified Linkage Maps of Human Chromosome 14 with Cytogenetic Tie Points and a Telomere Microsatellite Marker

Subregional Localization of 21 Chromosome 7-Specific Expressed Sequence Tags (ESTs) by FISH Using Newly Identified YACs and P1s

cDNA Sequence and Chromosomal Localization of Human Enterokinase, the Proteolytic Activator of Trypsinogen

Neural-specific expression, genomic structure, and chromosomal localization of the gene encoding the zinc-finger transcription factor NGFI-C

Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

Urbanization, migration, and indigenous health in Peru

Birth mode and infectious morbidity risks in Qom children of Argentina

Introduction: The evolutionary and biocultural causes and consequences of rising cesarean birth rates

Effects of whole blood leukoreduction on platelet function and hemostatic parameters

Direct genomic selection

Evaluation of a Novel Fibrin Sealant Patch in Hemorrhage Control After Vascular or Hepatic Injury

Retrofittable plug-flow reactor for in situ high-temperature vibrating sample magnetometry with well-controlled gas atmospheres

Breastfeeding: New Anthropological Approaches

An RNA interference-based screen of transcription factor genes identifies pathways necessary for sensory regeneration in the avian inner ear

Mutational and Haplotype Analyses of Families with Familial Partial Lipodystrophy (Dunnigan Variety) Reveal Recurrent Missense Mutations in the Globular C-Terminal Domain of Lamin A/C

Genomic organization of human surfactant protein D (SP-D). SP-D is encoded on chromosome 10q22.2-23.1

SNTG1, the gene encoding gamma 1-syntrophin: a candidate gene for idiopathic scoliosis

Isolation, Characterization, and Chromosomal Mapping of the Human Nkx6.1 Gene (NKX6A), a New Pancreatic Islet Homeobox Gene

A 1.5-Megabase Yeast Artificial Chromosome Contig from Human Chromosome 10q11.2 Connecting Three Genetic Loci (RET, D10S94, and D10S102) Closely Linked to the MEN2A Locus

Human Cholecystokinin Type A Receptor Gene: Cytogenetic Localization, Physical Mapping, and Identification of Two Missense Variants in Patients with Obesity and Non-Insulin-Dependent Diabetes Mellitus (NIDDM)

Improved predictive test for MEN2, using flanking dinucleotide repeats and RFLPs

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