41. Feasibility Of DNA Based Methods For Prenatal Diagnosis And Carrier Detection Of disease caused by a genetic deficiency of propionylCoA carboxylase (PCC) . an important role in genetic counselling in families with pcc deficiency. http://jmg.bmjjournals.com/cgi/content/full/36/5/412

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Abstract Full Text (PDF) Submit a response ... Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Muro, S Articles by Ugarte, M Related Collections Genetics J Med Genet 412-414 ( May ) Short report Feasibility of DNA based methods for prenatal diagnosis and carrier detection of propionic acidaemia S Muro a a a a P Briones b A Ribes b M Ugarte a a b Correspondence to: Dr Ugarte. Received 27 April 1998 Revised version accepted for publication 8 September 1998 Abstract Top Abstract Introduction Patients and methods Results and discussion References Propionic acidaemia (PA) is an autosomal recessive disease caused by a genetic deficiency of propionyl-CoA carboxylase (PCC). Defects in the PCCA and PCCB genes that code for the and subunits of PCC, respectively, are responsible for PA. A proband with PA

42. Archive Of Advisor Updates REMEDIATION OF SCIENCE PRECOLLEGE CURRICULUM (pcc) deficiency. On November 20,the Council on Academic Affairs (CAA) decided the following regarding pcc http://www.advising.eku.edu/archiveupdate/

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43. Hemophilia: Factor II (Prothrombin) Deficiency How do people get the acquired form of Factor II deficiency? Fresh frozenplasma; Prothrombin complex concentrates (pcc) containing prothrombin and http://www.hemophilia.ca/en/2.3.2.php

Other Factor Deficiencies Factor II Deficiency (Prothrombin Deficiency) Other Factor Deficiencies Factor II Deficiency (Prothrombin Deficiency) What is Factor II Deficiency? Are there different types of Factor II Deficiency? Is Factor II Deficiency common? How is Congenital Factor II Deficiency passed on? ... What treatments are available to control bleeding? What is Factor II Deficiency? Factor II (pronounced Factor 2) Deficiency is a bleeding disorder. It is due to one of two causes: a lower than normal amount of prothrombin in the blood or prothrombin which does not work properly. Prothrombin is a protein in the bloodstream, which is important in the clotting process. Factor Xa, another blood protein, changes prothrombin (Factor II) into thrombin. Thrombin, in turn, continues the coagulation chain reaction. Without prothrombin, the process breaks down. For more information on blood clotting, see "The clotting problem in Hemophilia" Are there different types of Factor II Deficiency? Yes, there are two different types. Congenital Factor II Deficiency - This is an hereditary condition. People are born with it.

44. Hemophilia A And B: Clotting Factor Concentrates plasmapheresisdonors, Surfaceactivated pcc, batch-controlled, Vapour heat, provinces under Special Access Program, Used to treat factor VII deficiency http://www.hemophilia.ca/en/2.1.8.php

Hemophilia A and B Clotting Factor Concentrates Hemophilia A and B Clotting Factor Concentrates Recombinant Factor VIII Plasma-Derived Factor VIII Recombinant Factor IX Plasma-Derived Factor IX ... Products to Treat Rare Factor Deficiencies Recombinant Factor VIII Product Generation* Albumin in cell culture Albumin as stabilizer Viral inactivation Availability Comments Helixate FS Manufactured by Bayer, Distributed by Aventis Behring Yes (human albumin) No (stabilized with sucrose) Solvent Detergent: TNBP/Polysorbate 80 Licensed, Provided on case-by-case basis Full-length factor VIII molecule, no von Willebrand factor Kogenate FS Manufactured and distributed by Bayer Yes (human albumin) No (stabilized with sucrose) Solvent Detergent: TNBP/Polysorbate 80 Licensed, Provided in all provinces Full-length factor VIII molecule, no von Willebrand factor Recombinate Manufactured and distributed by Baxter Yes (bovine albumin) Yes None Licensed, Provided in all provinces Full-length factor VIII molecule, no von Willebrand factor ReFacto Manufactured and distributed by Wyeth Yes (human albumin) No (stabilized with sucrose) Solvent Detergent: TNBP/Triton X 100 Licensed

45. Nutrition.org -- Sign In Page deficiency despite reduced activity of propionylCo A carboxylase (pcc)5 and In a subsequent study, mRNA levels for PC and pcc were not affected by http://www.nutrition.org/cgi/content/full/135/5/973

QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This item requires a subscription to Journal of Nutrition Online. Full Text Marginal Maternal Biotin Deficiency in CD-1 Mice Reduces Fetal Mass of Biotin-dependent... Sealey et al. J. Nutr.. This Article Abstract Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Sealey, W. M. Articles by Hansen, D. K. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password? Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 2 days for US$8.00 Pay for Admission - You may access all content in Journal of Nutrition Online (from the computer you are currently using) for 30 days for US$20.

46. Nutrition.org -- Sign In Page Biotin deficiency was induced experimentally by feeding an eggwhite diet for 28 d . Decreased activity of pcc in lymphocytes was shown to be a sensitive http://www.nutrition.org/cgi/content/full/135/1/42

QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This item requires a subscription to Journal of Nutrition Online. Full Text Biotin Deficiency Reduces Expression of SLC19A3, a Potential Biotin Transporter,... Vlasova et al. J. Nutr.. This Article Abstract Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Vlasova, T. I. Articles by Mock, D. M. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password? Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 2 days for US$8.00 Pay for Admission - You may access all content in Journal of Nutrition Online (from the computer you are currently using) for 30 days for US$20.

47. Microarray Analysis Of The Genome Wide Response To Iron Deficiency And Iron Reco pcc 6803 was used to identify genes that were transcriptionally regulated Fe deficiency results in a variety of physiological and morphological changes http://www.biology.purdue.edu/people/faculty/sherman/ShermanLab/MicroarrayAnalys

J. Microarray Analysis of the Genome Wide Response to Iron Deficiency and Iron Reconstitution. Plant Phys 03 1.) Summary A full-genome microarray of the (oxy)photosynthetic cyanobacterium Synechocystis 2.) Introduction Prochlorococcus sp. Chl a2/b2 light-harvesting protein (Ting et al., 2002). Many other changes are associated with Fe deficiency in cyanobacteria and cells continue to grow, although the growth rate is somewhat lower and the cells are smaller. The addition of Fe to the cultures can reverse these changes, and cells return to normal within 18 to 24 h after the addition of Fe (Sherman and Sherman, 1983; Riethman et al., 1988). Microarray technology permits an assay of global gene expression patterns under a variety of experimental conditions. These arrays are particularly efficient in organisms for which the entire genome has been sequenced, such as Synechocystis sp. PCC 6803, which is now thought to have 3,264 genes (Kaneko et al., 1996; see Cyanobase at http://www.kazusa.or.jp/cyano/cyano.html). Microarrays have been developed for many systems, including for bacteria such as Escherichia coli (Richmond et al., 1999; Tao et al., 1999; Arfin et al., 2000) and for plants such as

48. Biotin synthetase deficiency, and the isolated deficiencies of PC, pcc and MCC.Marginal states of biotin deficiency may develop during normal pregnancy and in http://www.eagle-min.com/faq/faq86.htm

Toll Free 1 888 441 4184 SupraLife Online Shopping cart Shopping Cart Full Spectrum Specialized ... Sports Our Family Bio-lumin Supralife Youngevity COLLOIDAL MINERALS BIOTIN Deficiencies : Severe deficiency causes 1) thinning of hair, loss of hair color, and eventual complete loss of hair; 2) a scaly, red rash distributed around the openings of the eyes, nose, mouth, and perineal area; and 3) central nervous system abnormalities such as depression, lethargy, hallucinations, and paresthesias. In infants, the neurologic findings include hypotonia, lethargy, and developmental delay as well as a peculiar withdrawn behavior. In patients on total or near total intravenous feeding, an unusual distribution of facial fat coupled with the rash and hair loss produces a distinct appearance called "biotin deficiency facies." Clinical uses : Biotin is routinely provided to individuals receiving total intravenous feeding and is incorporated into almost all nutritionally complete dietary supplements and infant formulas. In larger doses, biotin is also used to treat inborn errors of metabolism such as biotinidase deficiency, holocarboxylase synthetase deficiency, and the isolated deficiencies of PC, PCC and MCC. Marginal states of biotin deficiency may develop during normal pregnancy and in patients taking medications such as anticonvulsants that accelerate the rate of biotin breakdown. Diet recommendations The Estimated Safe and Adequate Daily Dietary Intakes are:

49. JGI Synechococcus Elongatus Home The freshwater cyanobacterium Synechococcus elongatus pcc 7942 holds a iron deficiency induction of the idiA gene of Synechococcus elongatus pcc 7942. http://genome.jgi-psf.org/finished_microbes/synel/synel.home.html

BLAST Download Annotation Info ... HELP! Photo: L.A. Sherman and D.M. Sherman, Purdue University The freshwater cyanobacterium Synechococcus elongatus PCC 7942 holds a special place in the development of cyanobacterial molecular genetics. It was this isolate, previously known as Anacystis nidulans R2, that was the first cyanobacterium demonstrated to be reliably transformable by exogenously added DNA (32). Over the decades, many genetic tools have been developed for S. elongatus , and applied to other transformable cyanobacteria (1, 9, 16). Strain PCC 7942 is very closely related to, and considered the same species as, PCC 6301, which is the type strain for S. elongatus (13) and the first accession in the Pasteur Culture Collection (http://www.pasteur.fr/recherche/banques/PCC/). It is an obligate photoautotroph (13), with a genome of approximately 2.7 Mb (15). Two plasmids (approximately 8 and 46 kb) have been sequenced entirely (GenBank accessions S89470 and AF441790, respectively). S. elongatus

50. Australian Centre For Control Of Iodine Deficiency Disorders The Tibet IDD Elimination Project Coordinating Committee (pcc) hosted the delegation.On behalf of the pcc, Professor Eastman, Chairman of the pcc, http://www.icpmr.gov.au/accidd/news/02may.htm

Tibet Delegation visit to ICPMR On April 27, the seven member Tibetan People's Congress delegation, headed by Mr. Gya Tso Deputy Director of the Standing Committee of People's Congress, Tibet Autonomous Region, visited the ICPMR. The Tibet IDD Elimination Project Coordinating Committee (PCC) hosted the delegation. On behalf of the PCC, Professor Eastman, Chairman of the PCC, welcomed the delegation and gave a brief presentation on the Tibet IDD Elimination Project. Mr Gya Tso said it was like I am sitting in a meeting in Lhasa," as all we have talked about here has been related to the development of Tibet and the health of the Tibetan people. We would like to have more countries like Australia to help Tibet and more people like Professor Eastman and others from ICPMR to care for the Tibetan people." Mr Garry Nehl, recently retired former MHR for Cowper and Deputy Speaker of the Federal Parliament, and Dr Bernie Amos, former Director General of the NSW Department of Health, member of the PCC and consultant to ACCIDD attended the meeting.

51. PCCB - Propionyl-CoA Carboxylase Beta Chain, Mitochondrial Precursor Inherited deficiency of pcc due to mutations in either the pccA or the pccB generesults in propionic acidemia (PA), a clinically heterogeneous disorder http://www.pdg.cnb.uam.es/UniPub/iHOP/gg/90850.html

We report 24 novel PA mutations, nine affecting the PCCA gene and 15 affecting the PCCB gene. Abstract-9722924 Two PstI RFLPs in the PCCB gene on the long arm of chromosome 3 Abstract-5808342 Affected patients may have mutations of either the PCCA or PCCB gene. Abstract-9002936 An enzyme deficiency can result from mutations in either PCCA or PCCB Abstract-10418797 Overview of mutations in the PCCA and PCCB genes causing propionic acidemia. Abstract-8286627 Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemia. Abstract-10418797 PCC consists of two subunits, alpha and beta, encoded by the PCCA and PCCB genes, respectively. Abstract-8412544 The alpha- and beta-subunits of the enzyme are encoded by the PCCA and PCCB genes, respectively. Abstract-6636369 PCC is composed of two subunits, alpha and beta, encoded by the PCCA and PCCB genes, respectively. Abstract-1757511 Sequence analyses showed that accC and accB are co-transcribed and that pccB is transcribed separately.

52. Blackwell Synergy - Cookie Absent Severe factor X (FX) deficiency is one of the severest inherited coagulation A dose of 40 iµ/kg of pcc twice weekly or every 10 d has been suggested to http://www.blackwell-synergy.com/doi/abs/10.1046/j.1365-2141.2002.03932.x

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53. Portal Toolkit Invalid Site URL the effect of sperm protamine deficiency on sperm pcc formation postICSI . deficiency affects fertilization rate and possibly prones sperm to pcc http://ppv.ovid.com/pt/re/andr/abstract.00000536-200406000-00001.htm

Sorry, the URL specified, http://ppv.ovid.com:80/pt/re/andr/abstract.00000536-200406000-00001.htm , is invalid. To go to site for "OvidPPV" please click here http://ppv.ovid.com To go to site for "Andrologia" please click here http://www.lwwonline.com To go to the LWW Online site, please click here http://www.lwwonline.com Thank you

54. Effect Of Boron Deficiency On Photosynthesis And Reductant Sources And Their Rel Nitrogenase activity of Anabaena pcc 7119 is inhibited under conditions of After 24 to 48 hours of boron deficiency, reductions in photosynthetic O2 http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1062550

55. European Journal Of Gastroenterology & Hepatology - UserLogin However, pcc substitution for bleeding in liver deficiency has not been generallyaccepted, as pccs were considered to have a higher risk for http://www.eurojgh.com/pt/re/ejgh/fulltext.00042737-200301000-00004.htm

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56. Journal Of Pediatric Hematology Oncology - UserLogin Hereditary prothrombin (factor II) deficiency is one of the rarest human The pcc Bebulin® VH was chosen for several reasons it has a relatively high http://www.jpho-online.com/pt/re/jpho/fulltext.00043426-200408000-00003.htm

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57. Rare Pediatric Disease Database A deficiency in the pcc enzyme results in the inability to break down proteinsthat contain the amino acids methionine, threonine, isoleucine, and valine. http://www.madisonsfoundation.org/content/3/1/display.asp?did=278

58. Entrez PubMed Microarray analysis of the genomewide response to iron deficiency and iron pcc 6803 was used to identify genes that were transcriptionally regulated by http://genomebiology.com/pubmed/12913140

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59. Walking Tours In Ireland human growth hormone deficiency http//humangroth-hormone.eblan.pcc.jp/ .pcc.jp/athlete_growth_hormone_human.html human growth hormone deficiency http://www.comfortfeet.com/walking-tours-articles/archives/walking-tours-in-irel

@import url( /images/graphics_files/style.css ); Comfortable shoes Podiatrist Shoes Walking Tours Selectivebrands ... Oscar Thompson Shoes Float through your day Love Comfort Shoes? Chat with comfort experts Contact Information ComfortFeet.com 1240 Johnson Ferry Place Suite A-10 Marietta, Ga 30068 CONTACT US BY USING CHAT Links Syndicate this site (XML) Historic New Orleans Walking Tours - Main - London Walking Tours Walking Tours In Ireland Ireland: the very name conjures images of rolling green hills and panoramic vistas. The visitor’s challenge isn’t to find Ireland’s beauty, or to enjoy the visit: the challenge is to fit all its most fascinating, interesting, and historical sites into one action-packed adventure. With walking tours, you get the best of everything: the best sites, the best views, all planned by the people who know Ireland best. http://www.joycesireland.co.uk/ is one of the most versatile tour groups, and is perfect for the first-time traveler. It offers a number of tours, and integrates walking, hiking, and mini-coach shuttles to show you the up close and personal Ireland. And the tours are so specialized, they are tailored specifically to your interests. Whether you will embrace the melding of Irish architecture and landscape with the Causeway, Cliffs, and Castles tour, or opt for the unspoiled views of the Hidden Ireland or Undiscovered Ireland tours, you will be as impressed with the professionalism of the guides as you are with the scenery. While showing you the beauty of both the traveled path and road rarely taken, Joyce’s Ireland offers superb accommodations, in all kinds of uniquely Irish Bed and Breakfasts, cottages, sometimes even castles! Just take a look at the site, and you’ll get incredibly detailed information about prospective tours, including daily itineraries, distances, and even vivid, detailed pictures of actual tour sites and points of interest. These tours are perfect for anyone wanting to get more out of their Irish journey without the hassle of making plans or the uncertainty of where to go or what to do.

60. Anticoagulation Protocols The use of pcc may be sanctioned by the oncall haematology SpR. Family historyof VTE + Protein C deficiency or Factor V Leiden (homozygote) or http://static.oxfordradcliffe.net/med/guidelines/coagulation.html

Anticoagulation Protocols Page Contents Surgery Management of Bleeding Prothrombin Complex Concentrates Anticoagulation Use ... Back to top Indication Duration Antiphospholipid Syndrome (Arterial thrombosis) ­ seek advice 2.5 (2.0 ­ 3.0) or 3.5 (3.0 ­ 4.0) Consider long-term Antiphospholipid Syndrome (Venous Thrombosis) Consider long-term Arterial Thromboembolism Discuss with haematologist Atrial Fibrillation Long Term Calf DVT 3 months Cardiomyopathy Long Term Cardioversion Mechanical Prosthetic Heart Valve (MHV) Long Term Mural Thrombosis 3 months Proximal DVT 6 months* Pulmonary Embolus (PE) 6 months Recurrence of venous thromboembolism (when no longer on an oral anticoagulants) Consider long-term Recurrence of venous thromboembolism (whilst on oral anticoagulants) Consider long-term Table 1. Oral anticoagulation duration and INR range guidelines.

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