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1-Acyldihydroxyacetone-phosphate reductase (Ayr1p) of the yeast Saccharomyces cerevisiae encoded by the open reading frame YIL124w is a major component of lipid particles
1-Acyldihydroxyacetone-phosphate reductase (Ayr1p) of the yeast Saccharomyces cerevisiae encoded by the open reading frame YIL124w is a major component of lipid particles
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1-Acyldihydroxyacetone-phosphate reductase (Ayr1p) of the yeast Saccharomyces cerevisiae encoded by the open reading frame YIL124w is a major component of lipid particles

Athenstaedt, K ; Daum, G

The Journal of biological chemistry, 2000-01, Vol.275 (1), p.235-240 [Periódico revisado por pares]

United States

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2
1,2-Dibromo-3-chloropropane (DBCP) is positive for sex-linked recessive lethals, heritable translocations and chromosome loss in Drosophila
1,2-Dibromo-3-chloropropane (DBCP) is positive for sex-linked recessive lethals, heritable translocations and chromosome loss in Drosophila
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1,2-Dibromo-3-chloropropane (DBCP) is positive for sex-linked recessive lethals, heritable translocations and chromosome loss in Drosophila

Zimmering, S.

Mutation research. Mutation research letters, 1983-01, Vol.119 (3), p.287-288 [Periódico revisado por pares]

Elsevier B.V

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3
1,25-dihydroxyvitamin D3 and its receptor inhibit the chenodeoxycholic acid-dependent transactivation by farnesoid X receptor
1,25-dihydroxyvitamin D3 and its receptor inhibit the chenodeoxycholic acid-dependent transactivation by farnesoid X receptor
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1,25-dihydroxyvitamin D3 and its receptor inhibit the chenodeoxycholic acid-dependent transactivation by farnesoid X receptor

Honjo, Yumiko ; Sasaki, Shigekazu ; Kobayashi, Yoshimasa ; Misawa, Hiroko ; Nakamura, Hirotoshi

Journal of endocrinology, 2006-03, Vol.188 (3), p.635-643 [Periódico revisado por pares]

Colchester: BioScientifica

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4
1,25-Dihydroxyvitamin D3 Controls a Cohort of Vitamin D Receptor Target Genes in the Proximal Intestine That Is Enriched for Calcium-regulating Components
1,25-Dihydroxyvitamin D3 Controls a Cohort of Vitamin D Receptor Target Genes in the Proximal Intestine That Is Enriched for Calcium-regulating Components
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1,25-Dihydroxyvitamin D3 Controls a Cohort of Vitamin D Receptor Target Genes in the Proximal Intestine That Is Enriched for Calcium-regulating Components

Lee, Seong Min ; Riley, Erin M. ; Meyer, Mark B. ; Benkusky, Nancy A. ; Plum, Lori A. ; DeLuca, Hector F. ; Pike, J. Wesley

The Journal of biological chemistry, 2015-07, Vol.290 (29), p.18199-18215 [Periódico revisado por pares]

United States: Elsevier Inc

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5
1,25-Dihydroxyvitamin D3 Down-regulation of PHEX Gene Expression Is Mediated by Apparent Repression of a 110 kDa Transfactor That Binds to a Polyadenine Element in the Promoter
1,25-Dihydroxyvitamin D3 Down-regulation of PHEX Gene Expression Is Mediated by Apparent Repression of a 110 kDa Transfactor That Binds to a Polyadenine Element in the Promoter
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1,25-Dihydroxyvitamin D3 Down-regulation of PHEX Gene Expression Is Mediated by Apparent Repression of a 110 kDa Transfactor That Binds to a Polyadenine Element in the Promoter

Hines, Eric R ; Kolek, Olga I ; Jones, Marci D ; Serey, Samantha H ; Sirjani, Nafisseh B ; Kiela, Pawel R ; Jurutka, Peter W ; Haussler, Mark R ; Collins, James F ; Ghishan, Fayez K

The Journal of biological chemistry, 2004-11, Vol.279 (45), p.46406-46414 [Periódico revisado por pares]

United States: American Society for Biochemistry and Molecular Biology

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6
1.5 kb direct repeat sequence flanks the suppressor of forked gene at the euchromatin-heterochromatin boundary of the Drosophila melanogaster X chromosome
1.5 kb direct repeat sequence flanks the suppressor of forked gene at the euchromatin-heterochromatin boundary of the Drosophila melanogaster X chromosome
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1.5 kb direct repeat sequence flanks the suppressor of forked gene at the euchromatin-heterochromatin boundary of the Drosophila melanogaster X chromosome

Tudor, M ; Mitchelson, A ; O'Hare, K

Genetical Research, 1996, Vol.68 (3), p.191-202

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7
1.5Mb deletion of chromosome 4p16.3 associated with postnatal growth delay, psychomotor impairment, epilepsy, impulsive behavior and asynchronous skeletal development
1.5Mb deletion of chromosome 4p16.3 associated with postnatal growth delay, psychomotor impairment, epilepsy, impulsive behavior and asynchronous skeletal development
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1.5Mb deletion of chromosome 4p16.3 associated with postnatal growth delay, psychomotor impairment, epilepsy, impulsive behavior and asynchronous skeletal development

Misceo, D. ; Barøy, T. ; Helle, J.R. ; Braaten, Ø. ; Fannemel, M. ; Frengen, E.

Gene, 2012-10, Vol.507 (1), p.85-91 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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8
1.8-Mb-reduced Streptomyces clavuligerus genome: relevance for secondary metabolism and differentiation
1.8-Mb-reduced Streptomyces clavuligerus genome: relevance for secondary metabolism and differentiation
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1.8-Mb-reduced Streptomyces clavuligerus genome: relevance for secondary metabolism and differentiation

Álvarez-Álvarez, R ; Rodríguez-García, A ; Martínez-Burgo, Y ; Robles-Reglero, V ; Santamarta, I ; Pérez-Redondo, R ; Martín, J. F ; Liras, P

Applied microbiology and biotechnology, 2014-03, Vol.98 (5), p.2183-2195 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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9
A 0.5-Mbp deletion on bovine chromosome 23 is a strong candidate for stillbirth in Nordic Red cattle
A 0.5-Mbp deletion on bovine chromosome 23 is a strong candidate for stillbirth in Nordic Red cattle
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A 0.5-Mbp deletion on bovine chromosome 23 is a strong candidate for stillbirth in Nordic Red cattle

Sahana, Goutam ; Iso-Touru, Terhi ; Wu, Xiaoping ; Nielsen, Ulrik Sander ; de Koning, Dirk-Jan ; Lund, Mogens Sandø ; Vilkki, Johanna ; Guldbrandtsen, Bernt

Genetics selection evolution (Paris), 2016-04, Vol.48 (1), p.35-35, Article 35 [Periódico revisado por pares]

France: BioMed Central

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10
A 1.1 Million Base Pair X-Chromosomal Deletion Covering the PDHA1 and CDKL5 Genes in a Female Patient with West Syndrome and Pyruvate Oxidation Deficiency
A 1.1 Million Base Pair X-Chromosomal Deletion Covering the PDHA1 and CDKL5 Genes in a Female Patient with West Syndrome and Pyruvate Oxidation Deficiency
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A 1.1 Million Base Pair X-Chromosomal Deletion Covering the PDHA1 and CDKL5 Genes in a Female Patient with West Syndrome and Pyruvate Oxidation Deficiency

Mayr, Johannes A. ; Koch, Johannes ; Fauth, Christine ; Zimmermann, Franz A. ; Rauscher, Christian ; Zschocke, Johannes ; Sperl, Wolfgang

Neuropediatrics, 2012-06, Vol.43 (3), p.130-134 [Periódico revisado por pares]

333 Seventh Avenue, New York, NY 10001, USA: Thieme Medical Publishers

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Deste Autor:

  1. Kulikowski, L
  2. Silva, L
  3. Bicudo, L
  4. Pereira, C
  5. Rosenberg, C

Neste Assunto:

  1. Science & Technology
  2. Life Sciences & Biomedicine
  3. Gene Deletion
  4. Humans
  5. Animals

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.