Search Results - "Gardella, R"

Provisioning Inka feasts at Tiwanaku, Bolivia: the geographic origins of camelids in the Pumapunku complex by Knudson, Kelly J., Gardella, Kristin R., Yaeger, Jason

“…While political integration can be achieved by many means, here we focus on the use of feasting and statecraft in the Inka Empire of the Andean Late Horizon…”
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Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization by Drera, B, Castiglia, D, Zoppi, N, Gardella, R, Tadini, G, Floriddia, G, De Luca, N, Pedicelli, C, Barlati, S, Zambruno, G, Colombi, M

“…Dystrophic epidermolysis bullosa (DEB) pruriginosa (DEB‐Pr) is a rare variant of DEB due to COL7A1 dominant and recessive mutations, which is characterized by…”
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A Potent Novel Anti-HIV Protein from the Cultured Cyanobacterium Scytonema varium by Bokesch, Heidi R, O'Keefe, Barry R, McKee, Tawnya C, Pannell, Lewis K, Patterson, Gregory M. L, Gardella, Roberta S, Sowder, Raymond C, Turpin, Jim, Watson, Karen, Buckheit, Robert W, Boyd, Michael R

“…A new anti-HIV protein, scytovirin, was isolated from aqueous extracts of the cultured cyanobacterium Scytonema varium. The protein displayed potent…”
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Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13 by Coucke, P J, Wessels, M W, Van Acker, P, Gardella, R, Barlati, S, Willems, P J, Colombi, M, De Paepe, A

“…Background: Arterial tortuosity syndrome (ATS) is an uncommon connective tissue disorder of unknown aetiology. The most prominent feature is tortuosity of the…”
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Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in the type VII collagen gene by Gardella, R., Zoppi, N., Zambruno, G., Barlati, S., Colombi, M.

“…Summary Background Dystrophic epidermolysis bullosa (DEB) is a bullous skin disease caused by mutations in the type VII collagen gene (COL7A1). Objectives To…”
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Environmental toxins associated with recurrent pregnancy loss by Gardella, J R, Hill, 3rd, J A

“…Couples experiencing recurrent pregnancy loss are often concerned that toxins within the environment have contributed to their reproductive difficulty…”
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Identification of two splicing mutations in the collagen type VII gene (COL7A1) of a patient affected by the Localisata variant of recessive dystrophic epidermolysis bullosa by GARDELLA, R, BELLETTI, L, ZOPPI, N, MARINI, D, BARLATI, S, COLOMBI, M

“…Collagen type VII gene (COL7A1) has been demonstrated to be altered in several variants of dystrophic epidermolysis bullosa (DEB), with either recessive or…”
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Antibody‐mediated inhibition of EGFR reduces phosphate excretion and induces hyperphosphatemia and mild hypomagnesemia in mice by Ortega, Bernardo, Dey, Jason M., Gardella, Allison R., Proano, Jacob, Vaneerde, Deanna

“…Monoclonal antibody therapies targeting the EGF receptor (EGFR) frequently result in hypomagnesemia in human patients. In contrast, EGFR tyrosine kinase…”
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Tea Processing in China, circa 1885—A Photographic Essay by Gardella, Robert

“…At the time these photographs originated in an unspecified location in late-nineteenth-century China, the Chinese had been cultivating tea (Camellia sinensis)…”
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A -96C→T mutation in the promoter of the collagen type VII gene (COL7A1) abolishing transcription in a patient affected by recessive dystrophic epidermolysis bullosa by Gardella, Rita, Barlati, Sergio, Zoppi, Nicoletta, Tadini, Gianluca, Colombi, Marina

“…Hereditary dystrophic epidermolysis bullosa (DEB) refers to a group of clinically heterogeneous skin blistering diseases due to mutations in the collagen type…”
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Growth of Mycoplasma hyorhinis cultivar alpha on semisynthetic medium by GARDELLA, R. S, DEL GIUDICE, R. A

“…Services AEM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon…”
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Isolation and Characterization of Griffithsin, a Novel HIV-inactivating Protein, from the Red Alga Griffithsia sp. by Mori, Toshiyuki, O'Keefe, Barry R., Sowder, Raymond C., Bringans, Scott, Gardella, Roberta, Berg, Shannon, Cochran, Pamela, Turpin, Jim A., Buckheit, Robert W., McMahon, James B., Boyd, Michael R.

“…Griffithsin (GRFT), a novel anti-HIV protein, was isolated from an aqueous extract of the red alga Griffithsia sp. The 121-amino acid sequence of GRFT has been…”
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Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient by Gardella, R., Nuytinck, L., Barlati, S., Van Acker, P., Tadini, G., De Paepe, A., Colombi, M.

“…Dystrophic epidermolysis bullosa (DEB) is a rare genetic skin disorder. In this report we have investigated an Italian child affected with recessive DEB (RDEB)…”
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Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome by Coucke, Paul J, Willaert, Andy, Wessels, Marja W, Callewaert, Bert, Zoppi, Nicoletta, De Backer, Julie, Fox, Joyce E, Mancini, Grazia M S, Kambouris, Marios, Gardella, Rita, Facchetti, Fabio, Willems, Patrick J, Forsyth, Ramses, Dietz, Harry C, Barlati, Sergio, Colombi, Marina, Loeys, Bart, De Paepe, Anne

“…Arterial tortuosity syndrome (ATS) is an autosomal recessive disorder characterized by tortuosity, elongation, stenosis and aneurysm formation in the major…”
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Design and initial characterization of a circular permuted variant of the potent HIV-inactivating protein cyanovirin-N by Barrientos, Laura G., Louis, John M., Hung, Jason, Smith, Trent H., O'Keefe, Barry R., Gardella, Roberta S., Mori, Toshiyuki, Boyd, Michael R., Gronenborn, Angela M.

“…A circular permuted variant of the potent human immunodeficiency virus (HIV)‐inactivating protein cyanovirin‐N (CV‐N) was constructed. New N‐ and C‐termini…”
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Genetic studies on the Tharu population of Nepal: restriction endonuclease polymorphisms of mitochondrial DNA by BREGA, A, GARDELLA, R, SEMINO, O, MORPURGO, G, ASTALDI RICOTTI, G. B, WALLACE, D. C, SANTACHIARA BENERECETTI, A. S

“…The mitochondrial DNAs (mtDNAs) of 91 Tharus from Nepal were screened for restriction fragment length polymorphisms (RFLPs) using six highly informative…”
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A frequent HindIII RFLP of the human fibronectin gene (FN1) by COLOMBI, M, GARDELLA, R, BARLATI, S

“…Images…”
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Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: A pilot case-control association study in an Italian sample by Magri, Chiara, Gardella, Rita, Barlati, Stefano Davide, Podavini, Damiano, Iatropoulos, Paraskevas, Bonomi, Silvia, Valsecchi, Paolo, Sacchetti, Emilio, Barlati, Sergio

“…Glutamatergic dysfunction is one of the major hypotheses for the pathogenesis of schizophrenia. The GRIA1 gene encodes for one (GluR1) of the four (GluR1–4)…”
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Genotype–Phenotype Correlation in Italian Patients with Dystrophic Epidermolysis Bullosa by Gardella, Rita, Castiglia, Daniele, Posteraro, Patrizia, Bernardini, Silvia, Zoppi, Nicoletta, Paradisi, Mauro, Tadini, Gianluca, Barlati, Sergio, McGrath, John A., Zambruno, Giovanna, Colombi, Marina

“…Dystrophic epidermolysis bullosa (DEB) is a rare skin disorder that is clinically heterogeneous and is transmitted either in dominant (DDEB) or recessive…”
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The microbicide cyanovirin-N expressed on the surface of commensal bacterium Streptococcus gordonii captures HIV-1 by GIOMARELLI, Barbara, PROVVEDI, Roberta, MEACCI, Francesca, MAGGI, Tiziana, MEDAGLINI, Donata, POZZI, Gianni, MORI, Toshiyuki, MCMAHON, James B, GARDELLA, Roberta, BOYD, Michael R

“…To explore the feasibility of expressing the potent HIV-inactivating protein, cyanovirin-N (CV-N), in the human commensal bacterium Streptococcus gordonii, as…”
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