Search Results - "Rogers, Geraldine R."

Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis by Russell, Laura J, DiGiovanna, John J, Rogers, Geraldine R, Steinert, Peter M, Hashem, Nemat, Compton, John G, Bale, Sherri J

“…We recently mapped the disease locus for severe autosomal recessive lamellar ichthyosis (LI) to chromosome 14q11 and showed complete linkage with TGM1, the…”
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Proteomic analysis of embryonic stem cell-derived neural cells exposed to the antidepressant paroxetine by McHugh, Patrick C., Rogers, Geraldine R., Loudon, Barbara, Glubb, Dylan M., Joyce, Peter R., Kennedy, Martin A.

“…Antidepressant drugs can have significant effects on the mood of a patient suffering from major depression or other disorders. The pharmacological actions of…”
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Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene by Hamrock, David J, Marekov, Lyuben N, Laurenzi, Vincenzo De, Rizzo, William B, Rogers, Geraldine R, Steinert, Peter M, Markova, Nelli, Compton, John G

“…Sjögren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder characterized by mental retardation, spasticity and ichthyosis. SLS patients have a…”
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Polymorphisms of DRD4 and DRD3 and risk of avoidant and obsessive personality traits and disorders by Joyce, Peter R., Rogers, Geraldine R., Miller, Allison L., Mulder, Roger T., Luty, Suzanne E., Kennedy, Martin A.

“…We investigated whether polymorphisms of the dopamine D4 receptor ( DRD4) and polymorphisms of the dopamine D3 receptor ( DRD3) were associated with…”
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Linkage mapping of wool keratin and keratin-associated protein genes in sheep by McLaren, R J, Rogers, G R, Davies, K P, Maddox, J F, Montgomery, G W

“…The keratins and keratin-associated proteins (KAPs) are a large heterogeneous group of proteins that make up about 90% of the wool fiber. Heteropolymers of the…”
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Genomic Organization and Expression of the Human Fatty Aldehyde Dehydrogenase Gene (FALDH) by Rogers, Geraldine R., Markova, Nedialka G., De Laurenzi, Vincenzo, Rizzo, William B., Compton, John G.

“…Mutations in the fatty aldehyde dehydrogenase (FALDH) gene cause Sjögren-Larsson syndrome (SLS)—a disease characterized by mental retardation, spasticity, and…”
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Patching together the genetics of Gorlin syndrome by Bale, S J, Falk, R T, Rogers, G R

“…Gorlin syndrome is an autosomal dominant disorder characterized by developmental defects and susceptibility to cancer, especially to basal cell carcinomas. The…”
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Age-dependent antidepressant pharmacogenomics: polymorphisms of the serotonin transporter and G protein β3 subunit as predictors of response to fluoxetine and nortriptyline by Joyce, Peter R., Mulder, Roger T., Luty, Suzanne E., McKenzie, Janice M., Miller, Allison L., Rogers, Geraldine R., Kennedy, Martin A.

“…In 169 depressed patients randomized to treatment with either fluoxetine or nortriptyline, we examined whether polymorphisms of the serotonin transporter and…”
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Age-dependent antidepressant pharmacogenomics: polymorphisms of the serotonin transporter and G protein [Beta]3 subunit as predictors of response to fluoxetine and nortriptyline by Joyce, Peter R, Mulder, Roger T, Luty, Suzanne E, McKenzie, Janice M, Miller, Allison L, Rogers, Geraldine R, Kennedy, Martin A

“…In 169 depressed patients randomized to treatment with either fluoxetine or nortriptyline, we examined whether polymorphisms of the serotonin transporter and…”
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Age-dependent antidepressant pharmacogenomics: polymorphisms of the serotonin transporter and G protein beta3 subunit as predictors of response to fluoxetine and nortriptyline by Joyce, Peter R, Mulder, Roger T, Luty, Suzanne E, McKenzie, Janice M, Miller, Allison L, Rogers, Geraldine R, Kennedy, Martin A

“…In 169 depressed patients randomized to treatment with either fluoxetine or nortriptyline, we examined whether polymorphisms of the serotonin transporter and…”
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The basal cell nevus syndrome (gorlin syndrome): Genotype-phenotype correlation by Bale, Sherri J., Falk, Roni T., Rogers, Geraldine R.

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Genetic homogeneity in Sjögren-Larsson syndrome : linkage to chromosome 17p in families of different non-Swedish ethnic origins by ROGERS, G. R, RIZZO, W. B, ZLOTOGORSKI, A, NEMAT HASHEM, MINJOO LEE, COMPTON, J. G, BALE, S. J

“…Sjögren-Larsson syndrome (SLS) is a rare, autosomal recessive disorder that is characterized by congenital ichthyosis, mental retardation, and spastic diplegia…”
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Sjögren-Larsson Syndrome Is Caused by a Common Mutation in Northern European and Swedish Patients by De Laurenzi, Vincenzo, Rogers, Geraldine R., Tarcsa, Edit, Carney, Gael, Marekov, Lyuben, Bale, Sherri J., Compton, John G., Markova, Nelli, Steinert, Peter M., Rizzo, William B.

“…Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by congenital ichthyosis, mental retardation, and spastic diplegia or…”
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