Scott, Hamish Steele

 
 
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2005

Scientific Articles

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Meiotic and epigenetic defects in Dnmt3L-knockout mouse spermatogenesisWebster, K. E.; O'Bryan, M. K.; Fletcher, Stephen; Crewther, P. E.; ... Scott, Hamish Steele

2001

Scientific Articles

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A cSNP map and database for human chromosome 21Deutsch, Samuel; Iseli, C.; Bucher, P.; Antonarakis, Stylianos; Scott, Hamish Steele
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APECED mutations in the autoimmune regulator (AIRE) geneHeino, M.; Peterson, P.; Kudoh, J.; Shimizu, N.; ... Krohn, K.
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Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesiaBartoloni, Lucia; Blouin, Jean-Louis; Maiti, A. K.; Sainsbury, A.; ... Antonarakis, Stylianos
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Differential gene expression studies to explore the molecular pathophysiology of Down syndromeAntonarakis, Stylianos; Lyle, Robert; Chrast, R.; Scott, Hamish Steele;
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Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafnessScott, Hamish Steele; Kudoh, J.; Wattenhofer, M.; Shibuya, K.; ... Antonarakis, Stylianos
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Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domainsWattenhofer, M.; Shibuya, K.; Kudoh, J.; Lyle, Robert; ... Scott, Hamish Steele
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Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafnessMasmoudi, S.; Antonarakis, Stylianos; Schwede, T.; Ghorbel, A. M.; ... Guipponi, Michel
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Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafnessBen-Yosef, T.; Wattenhofer, M.; Riazuddin, S.; Ahmed, Z. M.; ... Morell, R. J.

2000

Scientific Articles

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C21orf5, a novel human chromosome 21 gene, has a Caenorhabditis elegans ortholog (pad-1) required for embryonic patterningGuipponi, Michel; Brunschwig, K.; Chamoun, Z.; Scott, Hamish Steele; ... Antonarakis, Stylianos
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Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiencyBartoloni, Lucia; Wattenhofer, M.; Kudoh, J.; Berry, A.; ... Antonarakis, Stylianos
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Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat proteinMichaud, J.; Kudoh, J.; Berry, A.; Bonne-Tamir, B.; ... Scott, Hamish Steele
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Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene familyAapola, Ulla; Kawasaki, K.; Scott, Hamish Steele; Ollila, J.; ... Peterson, P.
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Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndromeChrast, R.; Scott, Hamish Steele; Madani, Rime; Huber, L.; ... Antonarakis, Stylianos
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Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3Scott, Hamish Steele; Antonarakis, Stylianos; Mittaz, L.; Lalioti, M. D.; ... Gal, A.
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Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the regionBerry, A.; Scott, Hamish Steele; Kudoh, J.; Talior, I.; ... Bonne-Tamir, B.
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RNA and protein expression of the murine autoimmune regulator gene (Aire) in normal, RelB-deficient and in NOD mouseHeino, M.; Peterson, P.; Sillanpaa, N.; Guerin, S.; ... Krohn, K. J.
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The autoimmune regulator protein has transcriptional transactivating properties and interacts with the common coactivator CREB-binding proteinPitkanen, J.; Doucas, V.; Sternsdorf, T.; Nakajima, T.; ... Peterson, P.
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The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normalsChrast, R.; Scott, Hamish Steele; Papasavvas, M. P.; Rossier, Colette; ... Antonarakis, Stylianos

1999

Scientific Articles

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A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and YChen, H.; Rossier, Colette; Morris, Michael Andréw; Scott, Hamish Steele; ... Antonarakis, Stylianos
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Altered spacing of promoter elements due to the dodecamer repeat expansion contributes to reduced expression of the cystatin B gene in EPM1Lalioti, M. D.; Scott, Hamish Steele; Antonarakis, Stylianos;
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Autoimmune regulator is expressed in the cells regulating immune tolerance in thymus medullaHeino, M.; Peterson, P.; Kudoh, J.; Nagamine, K.; ... Krohn, K.
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Isolation and characterization of the mouse Aire geneMittaz, L.; Rossier, Colette; Heino, M.; Peterson, P.; ... Scott, Hamish Steele
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Linearization and purification of BAC DNA for the development of transgenic miceChrast, R.; Scott, Hamish Steele; Antonarakis, Stylianos;
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Mutation analyses of North American APS-1 patientsHeino, M.; Scott, Hamish Steele; Chen, Q.; Peterson, P.; ... Krohn, K.
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Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1)Roessler, E.; Mittaz, L.; Du, Y.; Scott, Hamish Steele; ... Antonarakis, Stylianos
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The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutationsRadhakrishna, U.; Bornholdt, D.; Scott, Hamish Steele; Patel, U. C.; ... Antonarakis, Stylianos

1998

Scientific Articles

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A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patientsRosatelli, M. C.; Meloni, A.; Devoto, M.; Cao, A.; ... Antonarakis, Stylianos
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A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onsetLalioti, M. D.; Scott, Hamish Steele; Genton, P.; Grid, D.; ... Antonarakis, Stylianos
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APECED: a monogenic autoimmune disease providing new clues to self-tolerancePeterson, P.; Nagamine, K.; Scott, Hamish Steele; Heino, M.; ... Krohn, K. J.
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Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysisScott, Hamish Steele; Kyriakou, D. S.; Peterson, P.; Heino, M.; ... Antonarakis, Stylianos
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Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different originsScott, Hamish Steele; Heino, M.; Peterson, P.; Mittaz, L.; ... Antonarakis, Stylianos
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Construction of a 2.5-Mb integrated physical and gene map of distal 21q22.3Lapenta, V.; Sossi, V.; Gosset, P.; Vayssettes, C.; ... Brahe, C.
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Genomic structure, sequence, and refined mapping of the human intersectin gene (ITSN), which encompasses 250 kb on chromosome 21q22.1-->q22.2Guipponi, Michel; Scott, Hamish Steele; Hattori, M.; Ishii, K.; ... Antonarakis, Stylianos
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Identification and characterization of a novel cyclic nucleotide phosphodiesterase gene (PDE9A) that maps to 21q22.3: alternative splicing of mRNA transcripts, genomic structure and sequenceGuipponi, Michel; Scott, Hamish Steele; Kudoh, J.; Kawasaki, K.; ... Antonarakis, Stylianos
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Identification and characterization of two putative human arginine methyltransferases (HRMT1L1 and HRMT1L2)Scott, Hamish Steele; Antonarakis, Stylianos; Lalioti, M. D.; Rossier, Colette; ... Henry, M. F.
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Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneityMehenni, H.; Gehrig, Corinne; Nezu, J.; Oku, A.; ... Antonarakis, Stylianos
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Two isoforms of a human intersectin (ITSN) protein are produced by brain-specific alternative splicing in a stop codonGuipponi, Michel; Scott, Hamish Steele; Chen, H.; Schebesta, A.; ... Antonarakis, Stylianos
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