THE POLYCYSTIC KIDNEY-DISEASE-1 GENE ENCODES A 14-KB TRANSCRIPT AND LIES WITHIN A DUPLICATED REGION ON CHROMOSOME-16

THE POLYCYSTIC KIDNEY-DISEASE-1 GENE ENCODES A 14-KB TRANSCRIPT AND LIES WITHIN A DUPLICATED REGION ON CHROMOSOME-16

ग्रंथसूची विवरण
मुख्य लेखकों:	Ward, C, Peral, B, Hughes, J, Thomas, S, Gamble, V, Maccarthy, A, Sloanestanley, J, Buckle, V, Kearney, L, Higgs, D, Ratcliffe, P, Harris, P, Roelfsema, J, Spruit, L, Saris, J, Dauwerse, H, Peters, D, Breuning, M, Nellist, M, Brookcarter, P, Maheshwar, M, Cordeiro, I, Santos, H, Cabral, P, Sampson, J
स्वरूप:	Journal article
प्रकाशित:	1994

समान संसाधन

A large duplicated area in the polycystic kidney disease 1 (PKD1) region of chromosome 16 is prone to rearrangement.
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प्रकाशित: (1994)

A LARGE DUPLICATED AREA ON THE PROXIMAL EDGE OF THE POLYCYSTIC KIDNEY-DISEASE-1 (PKDI) REGION IS PRONE TO REARRANGEMENT
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Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16.
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प्रकाशित: (1991)

Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster.
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Long-Read High-Throughput Sequencing (HTS) Revealed That the Sf-Rhabdovirus X<sup>+</sup> Genome Contains a 3.7 kb Internal Duplication
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RAPID GENETIC-ANALYSIS OF POLYCYSTIC KIDNEY DISEASE-1 (PKD1) FAMILIES WITH A CLOSELY LINKED, HIGHLY POLYMORPHIC MICROSATELLITE
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Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite marker.
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Duplication of Foot*
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Independent recombination events between the duplicated human alpha globin genes; implications for their concerted evolution.
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Breakup of a homeobox cluster after genome duplication in teleosts.
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Duplication resolves conflict
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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.
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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
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Molecular mechanisms of immune regulation by the receptors CD5 and CD6
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T cell costimulation by CD6 is dependent on bivalent binding of a GADS/SLP-76 complex
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A sequence conserved between CD5 and CD6 binds an FERM domain and exerts a restraint on T‐cell activation
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Horizontal transfer, not duplication, drives the expansion of protein families in prokaryotes.
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Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects.
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Isolation of 3.5-kb Fragments on Magnetic Solid Supports
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A new acro-osteolysis syndrome caused by duplications including PTHLH.
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Agarose Gel Analysis of 15–40-kb PCR Amplimers
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