Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse-Reference-Cited by-同舟云学术

Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse

Published:1998-10 Issue:2 Volume:20 Page:157-162
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Haque Muhammad Faiyaz ul,King Lily M.,Krakow Deborah,Cantor Rita M.,Rusiniak Michael E.,Swank Richard T.,Superti-Furga Andrea,Haque Sayedul,Abbas Hasan,Ahmad Wasim,Ahmad Mahmud,Cohn Daniel H.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1098_157.pdf

Reference42 articles.

1. Lipmann, F. Biological sulfate activation and transfer. Science 128, 575–580 (1958).

2. Elgavish, A., Smith, J.B., Pillion, D.J. & Meezan, E. Sulfate transport in human lung fibroblasts (IMR-90). J. Cell Physiol. 125, 243–250 ( 1985).

3. Markovich, D., Forgo, J., Stange, G., Biber, J. & Murer, H. Expression cloning of rat renal Na+/SO4(2-) cotransport . Proc. Natl Acad. Sci. USA VID>90, 8073– 8077 (1993).

4. Bissig, M., Hagenbuch, B., Stieger, B., Koller, T. & Meier, P.J. Functional expression cloning of the canalicular sulfate transport system of rat hepatocytes. J. Biol. Chem. 269, 3017–3021 (1994).

5. Hastbacka, J. et al. The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping. Cell 78, 1073–1087 ( 1994).

Cited by 186 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. SRY-Box Transcription Factor 9 regulates 3’-Phosphoadenosine 5’-Phosphosulfate Synthase 2 mRNA expression through derepression of the transcriptional repressor, CCAAT/enhancer-binding protein beta;2024-09-11

2. Solute Carrier Family 35 (SLC35)—An Overview and Recent Progress;Biologics;2024-08-15

3. Truncating variants in PAPSS2 gene: A cause of early prenatal onset brachyolmia?;Prenatal Diagnosis;2024-05-20

4. Integrative high-throughput enhancer surveying and functional verification divulges a YY2-condensed regulatory axis conferring risk for osteoporosis;Cell Genomics;2024-03

5. Bone Phenotype is Always Present; Androgen Excess is Less Frequently Seen in PAPSS2 Deficiency;Journal of Clinical Research in Pediatric Endocrinology;2023-12-12