Literature DB >> 22581323

Lymphohematopoietic licence: sterol C-14 reductase activity of lamin B receptor (Lbr) is essential for neutrophil differentiation.

Durgadas P Kasbekar1.   

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Year:  2012        PMID: 22581323     DOI: 10.1007/s12038-012-9203-9

Source DB:  PubMed          Journal:  J Biosci        ISSN: 0250-5991            Impact factor:   1.826


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  12 in total

1.  Lamin B receptor regulates the growth and maturation of myeloid progenitors via its sterol reductase domain: implications for cholesterol biosynthesis in regulating myelopoiesis.

Authors:  Gayathri Subramanian; Pulkit Chaudhury; Krishnakumar Malu; Samantha Fowler; Rahul Manmode; Deepali Gotur; Monika Zwerger; David Ryan; Rita Roberti; Peter Gaines
Journal:  J Immunol       Date:  2011-12-02       Impact factor: 5.422

2.  Lymphohematopoietic progenitors immortalized by a retroviral vector harboring a dominant-negative retinoic acid receptor can recapitulate lymphoid, myeloid, and erythroid development.

Authors:  S Tsai; S Bartelmez; E Sitnicka; S Collins
Journal:  Genes Dev       Date:  1994-12-01       Impact factor: 11.361

3.  The sterol C-14 reductase encoded by the Neurospora crassa erg-3 gene: essential charged and polar residues identified by site-specific mutagenesis.

Authors:  A Prakash; D P Kasbekar
Journal:  Mol Genet Genomics       Date:  2001-10-16       Impact factor: 3.291

4.  The erg-3 (sterol delta14,15-reductase) gene of Neurospora crassa: generation of null mutants by repeat-induced point mutation and complementation by proteins chimeric for human lamin B receptor sequences.

Authors:  A Prakash; S Sengupta; K Aparna; D P Kasbekar
Journal:  Microbiology       Date:  1999-06       Impact factor: 2.777

5.  Genes encoding chimeras of Neurospora crassa erg-3 and human TM7SF2 proteins fail to complement Neurospora and yeast sterol C-14 reductase mutants.

Authors:  A Prakash; Durgadas P Kasbekar
Journal:  J Biosci       Date:  2002-03       Impact factor: 1.826

6.  Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene.

Authors:  Hans R Waterham; Janet Koster; Petra Mooyer; Gerard van Noort Gv; Richard I Kelley; William R Wilcox; Ronald J A Wanders; Raoul C M Hennekam; Jan C Oosterwijk
Journal:  Am J Hum Genet       Date:  2003-02-28       Impact factor: 11.025

7.  Disruption of the gene encoding 3beta-hydroxysterol Delta-reductase (Tm7sf2) in mice does not impair cholesterol biosynthesis.

Authors:  Anna M Bennati; Gianluca Schiavoni; Sebastian Franken; Danilo Piobbico; Maria A Della Fazia; Donatella Caruso; Emma De Fabiani; Laura Benedetti; Maria G Cusella De Angelis; Volkmar Gieselmann; Giuseppe Servillo; Tommaso Beccari; Rita Roberti
Journal:  FEBS J       Date:  2008-09-10       Impact factor: 5.542

8.  Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly.

Authors:  Leonard D Shultz; Bonnie L Lyons; Lisa M Burzenski; Bruce Gott; Rebecca Samuels; Peter A Schweitzer; Christine Dreger; Harald Herrmann; Vera Kalscheuer; Ada L Olins; Donald E Olins; Karl Sperling; Katrin Hoffmann
Journal:  Hum Mol Genet       Date:  2003-01-01       Impact factor: 6.150

9.  Mouse neutrophils lacking lamin B-receptor expression exhibit aberrant development and lack critical functional responses.

Authors:  Peter Gaines; Chiung W Tien; Ada L Olins; Donald E Olins; Leonard D Shultz; Lisa Carney; Nancy Berliner
Journal:  Exp Hematol       Date:  2008-06-11       Impact factor: 3.084

10.  Sterol dependent regulation of human TM7SF2 gene expression: role of the encoded 3beta-hydroxysterol Delta14-reductase in human cholesterol biosynthesis.

Authors:  Anna Maria Bennati; Marilena Castelli; Maria Agnese Della Fazia; Tommaso Beccari; Donatella Caruso; Giuseppe Servillo; Rita Roberti
Journal:  Biochim Biophys Acta       Date:  2006-05-19
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