Search Results - "Jacobson, D R"
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Variant-Sequence Transthyretin (Isoleucine 122) in Late-Onset Cardiac Amyloidosis in Black Americans
Published in The New England journal of medicine (13-02-1997)“…Isolated cardiac amyloidosis appearing late in life (senile cardiac amyloidosis) was first described in the 19th and early 20th centuries. 1 , 2 Pathological…”
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2
Somatotopic mapping of the human primary motor cortex with functional magnetic resonance imaging
Published in Neurology (01-05-1995)“…We applied functional magnetic resonance imaging (FMRI) to map the somatotopic organization of the primary motor cortex using voluntary movements of the hand,…”
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3
A familial syndrome of unilateral polymicrogyria affecting the right hemisphere
Published in Neurology (10-01-2006)“…A number of familial syndromes of bilateral polymicrogyria (PMG) have been described, but reported unilateral PMG cases have generally been sporadic. The…”
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4
Detection of K-ras oncogene mutations in bronchoalveolar lavage fluid for lung cancer diagnosis
Published in JNCI : Journal of the National Cancer Institute (19-07-1995)“…Lung cancer is the leading cause of cancer deaths in the United States. A long-standing goal of cancer researchers has been to develop tests that would…”
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5
Oral phenylalanine loading in dopa-responsive dystonia : A possible diagnostic test
Published in Neurology (01-05-1997)“…To determine if there is abnormal phenylalanine and biopterin metabolism in patients with dopa-responsive dystonia (DRD), we measured plasma levels of…”
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6
Pax-6 Is First Expressed in a Region of Ectoderm Anterior to the Early Neural Plate: Implications for Stepwise Determination of the Lens
Published in Developmental biology (01-03-1994)“…The Pax-6 gene encodes a DNA-binding transcription factor essential to normal development of the mammalian eye. We have found that in the chick embryo, the…”
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7
Cognitive Mapping Without Sight: four preliminary studies of spatial learning
Published in Journal of environmental psychology (01-09-1998)“…This paper illustrates the application of cognitive mapping to people with visual impairments and blindness. It gives perspectives on past research, outlines…”
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8
Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutations
Published in Annals of neurology (01-07-1998)“…Mutations in the GTP-cyclohydrolase I (GCH) gene have been identified as a cause of two disorders: autosomal dominant hereditary progressive…”
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A protein associated with axon growth, GAP-43, is widely distributed and developmentally regulated in rat CNS
Published in The Journal of neuroscience (01-06-1986)“…Development or regeneration of axons in several systems is accompanied by 20-100-fold increases in the synthesis of an acidic, axonally transported membrane…”
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10
Increased prevalence of K-ras oncogene mutations in lung adenocarcinoma
Published in Cancer research (Chicago, Ill.) (01-04-1995)“…Reported estimates of ras mutation prevalence in lung adenocarcinoma of 15-24% may be underestimates because of the insensitivity of the assays used. We have…”
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11
Techniques to Collect and Analyze the Cognitive Map Knowledge of Persons with Visual Impairment Or Blindness: Issues of Validity
Published in Journal of visual impairment & blindness (01-07-1997)“…This article is an assessment of a variety of techniques used by researchers in the fields of geography, psychology, urban planning, and cognitive science to…”
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12
Transthyretin amyloidosis (serine 44) with headache, hearing loss, and peripheral neuropathy
Published in Neurology (01-11-1998)“…A 32-year-old man of Irish descent presented with severe progressive headache and sensorineural hearing loss. MRI/magnetic resonance angiography head scans…”
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13
Revised transthyretin ile 122 allele frequency in African-Americans
Published in Human genetics (01-08-1996)“…The transthyretin (TTR) Ile 122 variant is associated with cardiac amyloidosis in individuals of African descent. To determine the prevalence of the allele…”
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14
A highly sensitive assay for mutant ras genes and its application to the study of presentation and relapse genotypes in acute leukemia
Published in Oncogene (01-02-1994)“…Most studies of ras oncogene activation use assays for ras mutations based on the polymerase chain reaction (PCR) of DNA segments containing ras exons 1 and 2,…”
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15
Amyloid fibril composition and transthyretin gene structure in senile systemic amyloidosis
Published in Laboratory investigation (01-11-1995)“…In many different forms of amyloidosis, transthyretin (TTR) comprises the major amyloid fibril protein. In the familial forms, various TTR mutations are linked…”
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16
Transthyretin Pro55, a variant associated with early-onset, aggressive, diffuse amyloidosis with cardiac and neurologic involvement
Published in Human genetics (01-05-1992)“…Mutations in the protein transthyretin cause amyloidosis involving the heart, peripheral nerves, and other organs. A family from West Virginia developed an…”
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17
Primary structure and transcriptional regulation of GAP-43, a protein associated with nerve growth
Published in Cell (19-06-1987)“…Nerve regeneration and developmental outgrowth of axons are both correlated with increased synthesis of an axonal membrane protein designated GAP-43…”
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18
Molecular genetic tumor markers in the early diagnosis and screening of non-small-cell lung cancer
Published in Annals of oncology (1995)“…Little progress has been made in decreasing lung cancer mortality by applying conventional methods to early diagnosis and screening. Recent advances in…”
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19
A Protein Induced during Nerve Growth (GAP-43) Is a Major Component of Growth-Cone Membranes
Published in Science (American Association for the Advancement of Science) (15-08-1986)“…Growth cones are specialized structures that form the distal tips of growing axons. During both normal development of the nervous system and regeneration of…”
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20
Variable-mode helical CT: imaging protocols
Published in American journal of roentgenology (1976) (01-06-1995)“…Helical CT provides a rapidly acquired, accurately registered, two-dimensional data set during the phase of maximum vascular and parenchymal enhancement. The…”
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