Literature DB >> 16265785

Carbonic anhydrase type II deficiency.

Roel J Bolt1, Janneke M B Wennink, Jonathan I M L Verbeke, Gul N Shah, William S Sly, Arend Bökenkamp.   

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Year:  2005        PMID： 16265785

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN： 0272-6386            Impact factor:   8.860


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  6 in total

1.  Two novel CAII mutations causing carbonic anhydrase II deficiency syndrome in two unrelated Chinese families.

Authors:  Qianqian Pang; Xuan Qi; Yan Jiang; Ou Wang; Mei Li; Xiaoping Xing; Jin Dong; Weibo Xia
Journal:  Metab Brain Dis       Date:  2015-02-27       Impact factor: 3.584

2.  Molecular biology of bone remodelling.

Authors:  Nadia Rucci
Journal:  Clin Cases Miner Bone Metab       Date:  2008-01

3.  A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis.

Authors:  Nesrin Besbas; Markus Draaken; Michael Ludwig; Ozgur Deren; Diclehan Orhan; Yelda Bilginer; Fatih Ozaltin
Journal:  Eur J Pediatr       Date:  2009-02-24       Impact factor: 3.183

Review 4.  Proximal renal tubular acidosis: a not so rare disorder of multiple etiologies.

Authors:  Syed K Haque; Gema Ariceta; Daniel Batlle
Journal:  Nephrol Dial Transplant       Date:  2012-12       Impact factor: 5.992

5.  A single nucleotide polymorphism in kidney anion exchanger 1 gene is associated with incomplete type 1 renal tubular acidosis.

Authors:  Takumi Takeuchi; Mami Hattori-Kato; Yumiko Okuno; Atsushi Kanatani; Masayoshi Zaitsu; Koji Mikami
Journal:  Sci Rep       Date:  2016-10-21       Impact factor: 4.379

6.  Carbonic Anhydrase III Promotes Cell Migration and Epithelial-Mesenchymal Transition in Oral Squamous Cell Carcinoma.

Authors:  Yin-Hung Chu; Chun-Wen Su; Yih-Shou Hsieh; Pei-Ni Chen; Chiao-Wen Lin; Shun-Fa Yang
Journal:  Cells       Date:  2020-03-13       Impact factor: 6.600
  6 in total

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