Skeletal dysplasias with increased bone density: Evolution of molecular pathogenesis in the last century (English)
- New search for: Aggarwal, Shagun
- New search for: Aggarwal, Shagun
In:
Gene
;
528
, 1
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41-45
;
2013
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ISSN:
- Article (Journal) / Electronic Resource
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Title:Skeletal dysplasias with increased bone density: Evolution of molecular pathogenesis in the last century
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Contributors:Aggarwal, Shagun ( author )
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Published in:Gene ; 528, 1 ; 41-45
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Publisher:
- New search for: Elsevier B.V.
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Publication date:2013-01-01
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Size:5 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:TCIRG1 , T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3 [Homo sapiens] , SLC29A3 , solute carrier family 29 (nucleoside transporters), member 3 [Homo sapiens] , SOST , sclerostin [Homo sapiens] , LRP5 , low density lipoprotein receptor-related protein 5 [Homo sapiens] , RANKL , receptor activator of nuclear factor kappa B ligand [Homo Sapiens] , CA2 , carbonic anhydrase II [Homo sapiens] , CLCN7 , chloride channel, voltage-sensitive 7 [Homo sapiens] , OSTM1 , osteopetrosis associated transmembrane protein 1 [Homo sapiens] , PLEKHM1 , pleckstrin homology domain containing, family M (with RUN domain) member 1 [Homo sapiens] , FERMT3 , fermitin family member 3 [Homo sapiens] , RANK , receptor activator of NF-KB [Homo Sapiens] , NEMO , NF-kappa-B essential modulator [Homo sapiens] , SNX10 , sorting nexin 10 [Homo sapiens] , ANKH , ankylosis, progressive homolog (mouse) [Homo sapiens] , TGFB1 , transforming growth factor, beta 1 [Homo sapiens] , WTX , Wilms tumor gene on the X chromosome protein [Homo sapiens] , LEMD3 , LEM domain containing 3 [Homo sapiens] , AD , Autosomal dominant , AR , Autosomal recessive , SKD , Skeletal dysplasia , Osteopetrosis , Increased bone density , Genetics , History
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Source:
Table of contents – Volume 528, Issue 1
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1
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Introduction to the Special Issue Historical Medical Genetics: Skeletal DisordersDr. Murgatroyd, Christopher et al. | 2013
- 2
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Hereditary premature closure of a coronal suture in the Abraham Lincoln familyFishman, Ronald S. et al. | 2013
- 7
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The skeleton in the closetKaplan, Frederick S. et al. | 2013
- 12
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Is LB1 diseased or modern? A review of the proposed pathologiesvan Heteren, Anneke H. et al. | 2013
- 21
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Aberrant and alternative splicing in skeletal system diseaseFan, Xin / Tang, Liling et al. | 2013
- 27
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Evolutionary anthropology and genes: Investigating the genetics of human evolution from excavated skeletal remainsAnastasiou, Evilena / Mitchell, Piers D. et al. | 2013
- 33
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Palaeopathology and genes: Investigating the genetics of infectious diseases in excavated human skeletal remains and mummies from past populationsAnastasiou, Evilena / Mitchell, Piers D. et al. | 2013
- 41
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Skeletal dysplasias with increased bone density: Evolution of molecular pathogenesis in the last centuryAggarwal, Shagun et al. | 2013
- 46
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The “Gout of the Medici”: Making the modern diagnosis using paleopathologyFornaciari, Gino / Giuffra, Valentina et al. | 2013
- 51
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A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: Additional support for a CHD locus at distal 13q34 regionYang, Yi-Feng / Ai, Qi / Huang, Can / Chen, Jin-Lan / Wang, Jian / Xie, Li / Zhang, Wei-Zhi / Yang, Jin-Fu / Tan, Zhi-Ping et al. | 2013
- 55
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The smallest of the smallHall, Judith G. et al. | 2013
- iv
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Editorial Board| 2013