Detalhe da pesquisa
1.
Characterization of a cDNA encoding the 55 kDa B regulatory subunit of Arabidopsis protein phosphatase 2A.
Plant Mol Biol
; 28(2): 257-66, 1995 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-7599311
2.
Characterization of DNA sequences encoding a novel isoform of the 55 kDa B regulatory subunit of the type 2A protein serine/threonine phosphatase of Arabidopsis thaliana.
Plant Mol Biol
; 31(2): 419-27, 1996 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-8756607
3.
Molecular characterization of the B' regulatory subunit gene family of Arabidopsis protein phosphatase 2A.
Eur J Biochem
; 260(1): 127-36, 1999 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-10091592
4.
The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats.
Hum Mol Genet
; 7(11): 1661-9, 1998 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-9736768
5.
Molecular cloning and characterization of TRPC5 (HTRP5), the human homologue of a mouse brain receptor-activated capacitative Ca2+ entry channel.
Genomics
; 60(3): 330-40, 1999 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-10493832
6.
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects.
Hum Mol Genet
; 7(8): 1327-32, 1998 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-9668176
7.
Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in Tabby mice.
Hum Mol Genet
; 10(26): 2973-81, 2001 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-11751679
8.
The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains.
Proc Natl Acad Sci U S A
; 94(24): 13069-74, 1997 Nov 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-9371801