Randomized clinical trial to evaluate the efficacy of a 5-day ceftiofur hydrochloride intramammary treatment on nonsevere gram-negative clinical mastitis
Schukken, Y.H., Bennett, G.J., Zurakowski, M.J., Sharkey, H.L., Rauch, B.J., Thomas, M.J., Ceglowski, B., Saltman, R.L., Belomestnykh, N., Zadoks, R.N.
Published in Journal of dairy science (01.12.2011)
Published in Journal of dairy science (01.12.2011)
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Journal Article
Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome
Williamson, Kathleen A., Hever, Ann M., Rainger, Joe, Rogers, R. Curtis, Magee, Alex, Fiedler, Zdenek, Keng, Wee Teik, Sharkey, Freddie H., McGill, Niolette, Hill, Clare J., Schneider, Adele, Messina, Mario, Turnpenny, Peter D., Fantes, Judy A., van Heyningen, Veronica, FitzPatrick, David R.
Published in Human molecular genetics (01.05.2006)
Published in Human molecular genetics (01.05.2006)
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Journal Article
Characterization of minority HIV-1 drug resistant variants in the United Kingdom following the verification of a deep sequencing-based HIV-1 genotyping and tropism assay
Silver, Nicholas, Paynter, Mary, McAllister, Georgina, Atchley, Maureen, Sayir, Christine, Short, John, Winner, Dane, Alouani, David J, Sharkey, Freddie H, Bergefall, Kicki, Templeton, Kate, Carrington, David, Quiñones-Mateu, Miguel E
Published in AIDS research and therapy (08.11.2018)
Published in AIDS research and therapy (08.11.2018)
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Journal Article
Detection and quantification of gene expression in environmental bacteriology
SHARKEY, Freddie H, BANAT, Ibrahim M, MARCHANT, Roger
Published in Applied and environmental microbiology (01.07.2004)
Published in Applied and environmental microbiology (01.07.2004)
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Journal Article
Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?
Li, Feng, Shen, Yiping, Köhler, Udo, Sharkey, Freddie H, Menon, Deepa, Coulleaux, Laurence, Malan, Valérie, Rio, Marlène, McMullan, Dominic J, Cox, H, Fagan, Kerry A, Gaunt, Lorraine, Metcalfe, Kay, Heinrich, Uwe, Hislop, Gordon, Maye, Una, Sutcliffe, Maxine, Wu, Bai-Lin, Thiel, Brian D, Mulchandani, Surabhi, Conlin, Laura K, Spinner, Nancy B, Murphy, Kathleen M, Batista, Denise A.S
Published in European journal of medical genetics (01.03.2010)
Published in European journal of medical genetics (01.03.2010)
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Journal Article
The degradation of n-hexadecane in soil by thermophilic geobacilli
Marchant, Roger, Sharkey, Freddie H., Banat, Ibrahim M., Rahman, Thahira J., Perfumo, Amedea
Published in FEMS microbiology ecology (01.04.2006)
Published in FEMS microbiology ecology (01.04.2006)
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Journal Article
The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2
Nazaryan, Lusine, Stefanou, Eunice G, Hansen, Claus, Kosyakova, Nadezda, Bak, Mads, Sharkey, Freddie H, Mantziou, Theodora, Papanastasiou, Anastasios D, Velissariou, Voula, Liehr, Thomas, Syrrou, Maria, Tommerup, Niels
Published in European journal of human genetics : EJHG (01.03.2014)
Published in European journal of human genetics : EJHG (01.03.2014)
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Journal Article
De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay
McMahon, Colin J, Breathnach, Colm, Betts, David R, Sharkey, Freddie H, Greally, Marie T
Published in American journal of medical genetics. Part A (01.05.2015)
Published in American journal of medical genetics. Part A (01.05.2015)
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Journal Article
Complex Segmental Duplications Mediate a Recurrent dup(X)(p11.22-p11.23) Associated with Mental Retardation, Speech Delay, and EEG Anomalies in Males and Females
Giorda, Roberto, Bonaglia, M. Clara, Beri, Silvana, Fichera, Marco, Novara, Francesca, Magini, Pamela, Urquhart, Jill, Sharkey, Freddie H., Zucca, Claudio, Grasso, Rita, Marelli, Susan, Castiglia, Lucia, Di Benedetto, Daniela, Musumeci, Sebastiano A., Vitello, Girolamo A., Failla, Pinella, Reitano, Santina, Avola, Emanuela, Bisulli, Francesca, Tinuper, Paolo, Mastrangelo, Massimo, Fiocchi, Isabella, Spaccini, Luigina, Torniero, Claudia, Fontana, Elena, Lynch, Sally Ann, Clayton-Smith, Jill, Black, Graeme, Jonveaux, Philippe, Leheup, Bruno, Seri, Marco, Romano, Corrado, Bernardina, Bernardo dalla, Zuffardi, Orsetta
Published in American journal of human genetics (11.09.2009)
Published in American journal of human genetics (11.09.2009)
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Journal Article
Characterization of a 8q21.11 Microdeletion Syndrome Associated with Intellectual Disability and a Recognizable Phenotype
Palomares, María, Delicado, Alicia, Mansilla, Elena, de Torres, María Luisa, Vallespín, Elena, Fernandez, Luis, Martinez-Glez, Victor, García-Miñaur, Sixto, Nevado, Julián, Simarro, Fernando Santos, Ruiz-Perez, Victor L., Lynch, Sally Ann, Sharkey, Freddie H., Thuresson, Ann-Charlotte, Annerén, Göran, Belligni, Elga F., Martínez-Fernández, María Luisa, Bermejo, Eva, Nowakowska, Beata, Kutkowska-Kazmierczak, Anna, Bocian, Ewa, Obersztyn, Ewa, Martínez-Frías, María Luisa, Hennekam, Raoul C.M., Lapunzina, Pablo
Published in American journal of human genetics (12.08.2011)
Published in American journal of human genetics (12.08.2011)
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Journal Article
Mutations in SOX2 cause anophthalmia–esophageal–genital (AEG) syndrome
Williamson, Kathleen A., Hever, Ann M., Rainger, Joe, Rogers, R. Curtis, Magee, Alex, Fiedler, Zdenek, Keng, Wee Teik, Sharkey, Freddie H., McGill, Niolette, Hill, Clare J., Schneider, Adele, Messina, Mario, Turnpenny, Peter D., Fantes, Judy A., van Heyningen, Veronica, FitzPatrick, David R.
Published in Human molecular genetics (15.06.2006)
Published in Human molecular genetics (15.06.2006)
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Journal Article
Quantitative effects of carbohydrates and aromatic amino acids on Clostridium botulinum toxin gene expression using a rapid competitive RT/PCR assay
Sharkey, Freddie H, Dooley, James S, Haylock, Richard W
Published in Journal of molecular microbiology and biotechnology (01.01.2005)
Published in Journal of molecular microbiology and biotechnology (01.01.2005)
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Journal Article
17q21.31 Microdeletion Syndrome: Further Expanding the Clinical Phenotype
Sharkey, F.H., Morrison, N., Murray, R., Iremonger, J., Stephen, J., Maher, E., Tolmie, J., Jackson, A.P.
Published in Cytogenetic and genome research (01.01.2009)
Published in Cytogenetic and genome research (01.01.2009)
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Journal Article
Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting
Goobie, S., Knijnenburg, J., FitzPatrick, D., Sharkey, F.H., Lionel, A.C., Marshall, C.R., Azam, T., Shago, M., Chong, K., Mendoza-Londono, R., den Hollander, N.S., Ruivenkamp, C., Maher, E., Tanke, H.J., Szuhai, K., Wintle, R.F., Scherer, S.W.
Published in Cytogenetic and genome research (01.01.2008)
Published in Cytogenetic and genome research (01.01.2008)
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Journal Article