Molecular map of Chromosome 19 including three genes affecting bleeding time: ep, ru, and bm

Molecular Cloning: A Laboratory Manual

2001 • 133,517 citations

Molecular cloning: A laboratory manual

1990 • 85,659 citations

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1975 • 33,059 citations

Genomic sequencing.

1984 • 8,343 citations

The Metabolic Basis of Inherited Disease.

1988 • 7,933 citations

The Metabolic Basis of Inherited Disease

1990 • 4,327 citations

A genetic map of the mouse suitable for typing intraspecific crosses.

1992 • 1,114 citations

Cloning of the cDNA for the human beta 1-adrenergic receptor.

1987 • 577 citations

A Macintosh program for storage and analysis of experimental genetic mapping data

1993 • 507 citations

Heterogeneity in storage pool deficiency: studies on granule-bound substances in 18 patients including variants deficient in alpha- granules, platelet factor 4, beta-thromboglobulin, and platelet-derived growth factor

1979 • 239 citations

LyF-1, a transcriptional regulator that interacts with a novel class of promoters for lymphocyte-specific genes.

1991 • 203 citations

Patients with a prolonged bleeding time and normal aggregation tests may have storage pool deficiency: studies on one hundred six patients

1987 • 177 citations

Platelet storage pool deficiency in mouse pigment mutations associated with seven distinct genetic loci

1984 • 141 citations

Platelet responses and metabolism

1986 • 133 citations

Insertional mutation of ‘classical’ and novel genes in transgenic mice

1992 • 128 citations

Hereditary Defect in Platelet Function in Rats

1972 • 118 citations

Chediak-Higashi Syndrome

1987 • 112 citations

Three Recessive Mutations Producing Disproportionate Dwarfing in Mice

1968 • 109 citations

The Hermansky–Pudlak Syndrome

1985 • 104 citations

Genetic analysis of genomic imprinting: An Imprintor-1 gene controls inactivation of the paternal copy of the mouse Tme locus

1992 • 102 citations

LYSOSOMAL DYSFUNCTIONS ASSOCIATED WITH MUTATIONS AT MOUSE PIGMENT GENES

1979 • 97 citations

Platelet storage pool deficiency: diagnosis in patients with prolonged bleeding times and normal platelet aggregation

1990 • 94 citations

The Chediak-Higashi syndrome of cats.

1977 • 93 citations

The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene

1992 • 93 citations

Defect in 3′-phosphoadenosine 5′-phosphosulfate synthesis in brachymorphic mice

1982 • 87 citations

Sandy: a new mouse model for platelet storage pool deficiency

1991 • 70 citations

Genomic organization of adrenergic and serotonin receptors in the mouse: Linkage mapping of sequence-related genes provides a method for examining mammalian chromosome evolution

1991 • 63 citations

Cocoa: a new mouse model for platelet storage pool deficiency

1988 • 63 citations

LyF-1, a Transcriptional Regulator That Interacts with a Novel Class of Promoters for Lymphocyte-Specific Genes

1991 • 61 citations

Inherited abnormalities in platelet organelles and platelet formation and associated altered expression of low molecular weight guanosine triphosphate-binding proteins in the mouse pigment mutant gunmetal

1993 • 59 citations

Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha

1991 • 59 citations

Defect in 3′-phosphoadenosine 5′-phosphosulfate synthesis in brachymorphic mice

1982 • 54 citations

GENETIC ANALYSIS OF A MOUSE t COMPLEX LOCUS THAT IS HOMOLOGOUS TO A KIDNEY cDNA CLONE

1986 • 53 citations

Beige rat: a new animal model of Chediak-Higashi syndrome

1989 • 48 citations

Effects of ammonia on processing and secretion of precursor and mature lysosomal enzyme from macrophages of normal and pale ear mice: evidence for two distinct pathways.

1985 • 48 citations

Isolation, characterization, and chromosomal mapping of mouse P450 17α-hydroxylase/C17–20 lyase

1991 • 42 citations

DNA sequence polymorphism in an androgen-regulated gene is associated with alteration in the encoded RNAs.

1983 • 39 citations

The mouse pale ear pigment mutant as a possible animal model for human platelet storage pool deficiency

1981 • 38 citations

His-1 and His-2: identification and chromosomal mapping of two commonly rearranged sites of viral integration in a myeloid leukemia.

1991 • 35 citations

Characterization of platelets from normal mink and mink with the Chediak‐Higashi syndrome

1979 • 30 citations

Storage pool deficiency in platelets from Chediak-Higashi cattle

1979 • 29 citations

The Murine Chediak-Higashi Mutation and Other Murine Pigmentation Mutations

1981 • 27 citations

Progenitor cell defect correctable by bone marrow transplantation in five independent mouse models of platelet storage pool deficiency.

1986 • 14 citations

Lysosomal mutations increase susceptibility to anaesthetics

1989 • 10 citations

Localization of the gene for plasma retinol binding protein to the distal half of mouse chromosome 19

1991 • 8 citations

Mouse chromosome 19

1993 • 7 citations

Progress in Hematology, Vol. 1, 1956

1957 • 6 citations

Corrected centromere orientation for mouse Chromosome 19 MIT markers

1993 • 5 citations

The Chediak-Higashi syndrome (CHS) in Mansfield Pearl foxes (Omberg Pearl, Vulpes vulpes) and in arctic blue foxes (Alopex lagopus) is caused by gene mutation in homologous loci

1990 • 1 citations