M A Crackower
Overview
Explore the profile of M A Crackower including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
973
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0
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Recent Articles
1.
Crackower M, Scherer S, Heng H, Tsui L
Mamm Genome
. 2016 Aug;
8(2):159-60.
PMID: 27518309
No abstract available.
2.
Sohal D, Nghiem M, Crackower M, Witt S, Kimball T, Tymitz K, et al.
Circ Res
. 2001 Jul;
89(1):20-5.
PMID: 11440973
The advent of conditional and tissue-specific recombination systems in gene-targeted or transgenic mice has permitted an assessment of single gene function in a temporally regulated and cell-specific manner. Here we...
3.
Bony C, Roche S, Shuichi U, Sasaki T, Crackower M, Penninger J, et al.
J Cell Biol
. 2001 Mar;
152(4):717-28.
PMID: 11266463
Purinergic stimulation of cardiomyocytes turns on a Src family tyrosine kinase-dependent pathway that stimulates PLCgamma and generates IP(3), a breakdown product of phosphatidylinositol 4,5-bisphosphate (PIP2). This signaling pathway closely regulates...
4.
Crackower M, Sinasac D, Lee J, Herbrick J, Tsui L, Scherer S
Cytogenet Cell Genet
. 2000 Mar;
87(3-4):197-8.
PMID: 10702666
No abstract available.
5.
Sinasac D, Crackower M, Lee J, Kobayashi K, Saheki T, Scherer S, et al.
Genomics
. 1999 Dec;
62(2):289-92.
PMID: 10610724
Citrullinemia is an autosomal recessive disease characterized by an argininosuccinate synthetase (ASS) deficiency. Adult-onset type II citrullinemia (CTLN2) is a form of the disease that is defined by a quantitative...
6.
Kobayashi K, Sinasac D, Iijima M, Boright A, Begum L, Lee J, et al.
Nat Genet
. 1999 Jun;
22(2):159-63.
PMID: 10369257
Citrullinaemia (CTLN) is an autosomal recessive disease caused by deficiency of argininosuccinate synthetase (ASS). Adult-onset type II citrullinaemia (CTLN2) is characterized by a liver-specific ASS deficiency with no abnormalities in...
7.
Crackower M, Sinasac D, Xia J, MOTOYAMA J, Prochazka M, Rommens J, et al.
Genomics
. 1999 Mar;
55(3):257-67.
PMID: 10049579
Cytoplasmic dynein is a large multisubunit microtubule-based motor protein, which mediates movement of numerous intracellular organelles. We report here the identification of the human homologue of cytoplasmic dynein intermediate chain...
8.
MOTOYAMA J, Heng H, Crackower M, Takabatake T, Takeshima K, Tsui L, et al.
Mech Dev
. 1998 Dec;
78(1-2):81-4.
PMID: 9858693
In Drosophila, patched encodes a negative regulator of Hedgehog signaling. Biochemical experiments have demonstrated that vertebrate patched homologues might function as a Sonic hedgehog (Shh) receptor. In mice, two patched...
9.
10.
Crackower M, MOTOYAMA J, Tsui L
Dev Biol
. 1998 Sep;
201(1):78-89.
PMID: 9733575
During vertebrate limb development the distal apex of the limb bud ectoderm is induced to form the apical ectodermal ridge (AER). The presence of the AER is required for the...