Search Results - "Clarkson, K B"
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P63 mutations are not a major cause of non-syndromic split hand/foot malformation
Published in Journal of medical genetics (01-01-2003)“…11 This gene spans 65 kb, contains 15 exons, and encodes six different protein isoforms using alternative splicing and two translational start sites. 22 P63…”
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2
Ischiospinal dysostosis with rib gaps and nephroblastomatosis
Published in Clinical dysmorphology (01-01-2001)“…Rib gaps, vertebral ossification defects, hypoplastic ischial bones and large kidneys were present in a newborn. A renal biopsy showed nephroblastomatosis …”
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3
Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals
Published in American journal of medical genetics (31-07-1995)“…Albright hereditary osteodystrophy (AHO) is a condition with characteristic physical findings (short stature, obesity, round face, brachydactyly) but variable…”
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4
Induced Fit and “Lock and Key” Recognition of 5 S RNA by Zinc Fingers of Transcription Factor IIIA
Published in Journal of molecular biology (17-03-2006)“…Transcription factor IIIA (TFIIIA) is a Cys 2His 2 zinc finger protein that regulates expression of the 5 S ribosomal RNA gene by binding specifically to the…”
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5
Induced fit and "lock and key" recognition of 5S RNA by zinc fingers of transcription factor IIIA
Published in Journal of molecular biology (17-03-2006)“…Transcription factor IIIA (TFIIIA) is a Cys2His2 zinc finger protein that regulates expression of the 5 S ribosomal RNA gene by binding specifically to the…”
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6
Myosin light chain kinase A is activated by cGMP-dependent and cGMP-independent pathways
Published in FEBS letters (03-04-2006)“…Stimulation of Dictyostelium cells with the chemoattractant cAMP results in transient phosphorylation of the myosin regulatory light chain (RLC). We show that…”
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