Clipboard: Benign anomaly to malign dysplasia: Variable expression of lamin B receptor mutations in humans

Durgadas P Kasbekar1

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Clipboard: Benign anomaly to malign dysplasia: Variable expression of lamin B receptor mutations in humans

机译：剪贴板：良性异常到恶性发育不良：人类Lamin B受体突变的可变表达

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《Journal of biosciences》 |2004年第4期|共页
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Durgadas P Kasbekar1;
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1. Benign anomaly to malign dysplasia: Variable expression of lamin B receptor mutations in humans [J] . DURGADAS P KASBEKAR Journal of Biosciences . 2004,第4期

机译：良性异常导致恶性增生：人类中Lamin B受体突变的可变表达
2. Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly. [J] . Shultz LD, Lyons BL, Burzenski LM, Human Molecular Genetics . 2003,第1期

机译：小鼠鱼鳞病基因座处的突变位于lamin B受体基因内：这是人类Pelger-Huet异常的单一基因模型。
3. An Anadysplasia-Like, Spontaneously Remitting Spondylometaphyseal Dysplasia Secondary to Lamin B Receptor (LBR) Gene Mutations: Further Definition of the Phenotypic Heterogeneity of LBR-Bone Dysplasias [J] . Sobreira Nara, Modaff Peggy, Steel Gary, American journal of medical genetics, Part A . 2015,第1期

机译：继发于Lamin B受体（LBR）基因突变的发育不全，自发缓解的脊柱后凸发育不良：LBR骨发育异常的表型异质性的进一步定义
4. N-terminal mutations of the human estrogen receptor gene alter expression and function of its protein product [C] . Klaus Graumann, Wenke Feng, Alois Jungbauer, Asia-Pacific biochemical engineering conference;APBIOCHEC'97 . 1997

机译：人类雌激素受体基因的N端突变会改变其蛋白质产物的表达和功能
5. The effect of LMNA mutations on the lamin Ig-fold structure and muscle gene expression. [D] . Shrestha, Om Kumar. 2012

机译：LMNA突变对lamin Ig折叠结构和肌肉基因表达的影响。
6. An Anadysplasia-Like Spontaneously Remitting Spondylometaphyseal Dysplasia Secondary to Lamin B Receptor (LBR) Gene Mutations: Further Definition of the Phenotypic Heterogeneity of LBR-Bone Dysplasias [O] . Nara Sobreira, Peggy Modaff, Gary Steel, -1

机译：继发于Lamin B受体（LBR）基因突变的发育不全自发缓解的颈椎骨赘发育异常：LBR骨发育异常的表型异质性的进一步定义
7. Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly [O] . L. D. Shultz 2003

机译：小鼠ICHthyosis病毒源位的突变在Lamin B受体基因内：人类Pelger-hyet异常的单一基因模型

Clipboard: Benign anomaly to malign dysplasia: Variable expression of lamin B receptor mutations in humans

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