Search Results - "Kimak, M A"
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1
Hereditary Lymphedema: Evidence for Linkage and Genetic Heterogeneity
Published in Human molecular genetics (01-12-1998)“…Hereditary or primary lymphedema is a developmental disorder of the lymphatic system which leads to a disabling and disfiguring swelling of the extremities…”
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2
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema
Published in Nature genetics (01-06-2000)“…Primary lymphoedema is a rare, autosomal dominant disorder that leads to a disabling and disfiguring swelling of the extremities and, when untreated, tends to…”
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3
Truncating mutations in FOXC2 cause multiple lymphedema syndromes
Published in Human molecular genetics (15-05-2001)“…Hereditary lymphedemas are developmental disorders of the lymphatics resulting in edema of the extremities due to altered lymphatic flow. One such disorder,…”
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4
VEGFR3 gene structure, regulatory region, and sequence polymorphisms
Published in The FASEB journal (01-04-2001)“…Vascular endothelial growth factor receptor 3 (VEGFR-3) is required for cardiovascular development during embryogenesis. In adults, this receptor is expressed…”
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5
Energy requirements for diphtheria toxin translocation are coupled to the maintenance of a plasma membrane potential and a proton gradient
Published in The Journal of biological chemistry (05-04-1988)“…Translocation of diphtheria toxin (DT) or ricin to the cytosol is the rate-limiting step responsible for (pseudo) first-order decline in protein synthesis…”
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6
PI-10
Published in Clinical pharmacology and therapeutics (01-02-2006)“…AIM To develop a population pharmacokinetic (PK) model using sparse data sampling from a geriatric depressed population with five‐year paroxetine treatment and…”
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Paroxetine: population pharmacokinetic analysis in late‐life depression using sparse concentration sampling
Published in British journal of clinical pharmacology (01-05-2006)“…Aim To develop a population pharmacokinetic (PK) model using sparse sampling of long‐term treatment with paroxetine in elderly depressed subjects,…”
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Lymphedema-distichiasis syndrome and FOXC2 gene mutation
Published in American journal of ophthalmology (01-10-2002)“…PURPOSE: To describe the clinical characteristics of a family with autosomal dominant lymphedema-distichiasis syndrome and to report the results of analysis of…”
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