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28篇 您的检索式:作者名="POULAT F"
    题名 作者 年代 出处 被引量
1The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome显示文摘Pfeifer D Poulat F Holinski-Feder E 2000Genomics2000,63,1:1
2Nuclear localization of the testis determining gene product SRY显示文摘Poulat F Girard F Chevron M P 1995Cell Biol1995,128,:1
3Diversification pattern of the HMG and SOX family members during evolution 显示文摘Soullier S Jay P Poulat F 1999J Mol Evol1999,48,5:1
4Phosphorylation of an N - terminal motif enhances DNA - binding activity of the human SRY protein 显示文摘Desclozeaux M poulat F de Santa B P 1998Biological Chemistry1998,273,14:1
5The human testis determining factor SRY binds a nuclear factor containing PDZ protein interaction domains显示文摘Poulat F Barbara P S Desclozeaux M 1997Boil Chem1997,272,:1
6Serotonin innervation of the dorsal horn of the rat spinal cord: Light and electron microscopic immunocytochemical study显示文摘Marlier L Sandillon F Poulat P 1991Neurocytol1991,20,:1
7Expression and subcellular localization of SF -1, SOX9, WT1 and AMH proteins during early' human testieular development 显示文摘de Santa Barbara P Moniot B Poulat F 2000Dev Dyn2000,217,3:1
8Diversification pattern of the HMG and SOX family members during evolution显示文摘Soullier S Jay P Poulat F 1999J Mol Evo11999,48,5:1
9The human testis determining factor SRY binds a nuclear factor containing PDZprotein interaction domains 显示文摘Poulat F Santa Barbara P Desclozeaux M 1997J Biol Chem1997,272,11:1
10Diversification pattern of the HMG and SOX family members during evolution显示文摘Soullier S Jay P Poulat F 1999Mol Evolution1999,48,:1
11Phosphorylation of an N-terminal motif enhances DNA-binding activity of the human SRY protein 显示文摘Desclozeaux M Poulat F Santa Barbara P 1998J Biol Chem1998,273,14:1
12Characterization of two Spl binding sites of the human sex determining SRYpromoter 显示文摘Deselozeanx M Poulat F Santa Barbara P 1998Bioehim Biophys Acta1998,1397,3:1
13Phosphorylation of an N-terminal Motif Enhances DNA-binding Activity of the Human SRY Protein 显示文摘DESCLOZEAUX M POULAT F SANTA BARBARA P 1998J Biol Chem1998,273,14:1
14Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms显示文摘Klamt B Koziell A Poulat F 1998Hum Mol Genet1998,7,4:1
15Diversification pattern of the HMG and SOX family members during evolution 显示文摘Soullier S Jay P Poulat F 1999J Mol Evol1999,48,5:1
16Diversification pattern of the HMG and SOX family members during evolution显示文摘Soullier S Jay P Poulat F 1999J Mol Evol1999,48,5:1
17Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms显示文摘Klamt B Koziell A Poulat F 1998Hum Mol Genet1998,,7:1
18Serotonin innervation of the dorsal horn of the rat spinal cord:Light and electron microscopic immunocytochemical study显示文摘Marlier L Sandillon F Poulat P 1991Neurocytol1991,20,:1
19The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome显示文摘Pfeifer D Poulat F Holinski-Feder E 2000Genomics2000,63,1:1
20Expression and subcellular localization of SF-1, Sox9, WT1, and AMH proteins during early human testicular development显示文摘de Santa Barbara P Moniot B Poulat F 2000Dev Dyn2000,217,:1
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