mergefrom Xerosis cutis date May 2011 Refimprove date August 2010 File Xeroderma knuckles.jpg thumb 200px The surface of the knuckles of a hand with xerodermaXeroderma or xerodermia , derived from the Greek words for dry skin , is a condition involving the integumentary system , which in most cases can safely be treated with emollient s and or moisturizer s. Xeroderma occurs most commonly on the scalp , lower human leg legs , arm s, the knuckle s, the sides of the abdomen and thigh s. Symptoms most associated with xeroderma are scale dermatology scaling the visible peeling of the outer skin layer , itching and skin cracking . ref http www.wrongdiagnosis.com x xeroderma intro.htm Information and introductory article on wrongdianosis.com ref . Common causes Xeroderma is a very common condition. It happens more often in the winter where the cold air outside and the hot air inside creates a low relative humidity . This causes the skin to lose moisture and it may crack and peel. Bathing or hand washing too frequently, especially if one is using harsh soap s, may also contribute to xeroderma. Xeroderma can also be caused by a deficiency of vitamin A , vitamin D , systemic illness , severe sunburn , or some medication ref http www.medterms.com script main art.asp?articlekey 6038 Entry on medterms.com ref . Xeroderma can also be caused by choline inhibitor s. Detergents like washing powder and washing up liquid can also cause xeroderma. Prevention Use soap every other day to prevent dry skin. Use a pat towel technique when drying off to leave moisture on the skin. ref cite web last Lee first Doctor title Dry Skin Prevention url http doctorslee.com natural skin care accessdate 18 August 2011 ref Cure Rub emollients into the area which has xeroderma to cure it. To stop this area from getting worse cover it with a layer of petroleum jelly , which acts as a barrier to cracking. See also Xerodermapigmentosum Eczema Ichthyosis References Reflist Category Dermatologic terminology ... more details
A list of disease s in the English Wikipedia. DiseasesTOC X X chromosome, duplication Xq13 1 q21 1 X chromosome, monosomy Xp22 pter X chromosome, monosomy Xq28 X chromosome, trisomy Xp3 X chromosome, trisomy Xpter Xq13 X chromosome, trisomy Xq X chromosome, trisomy Xq25 X fragile site folic acid type Xa Xk Xanthic urolithiasis Xanthine oxydase deficiency Xanthinuria Xanthomatosis cerebrotendinous Xerocytosis, hereditary Xeroderma pigmentosum, type 1 Xeroderma pigmentosum, type 2 Xeroderma pigmentosum, type 3 Xeroderma pigmentosum, type 5 Xeroderma pigmentosum, type 6 Xeroderma pigmentosum, type 7 Xeroderma pigmentosum, variant type Xeroderma pigmentosum Xeroderma talipes enamel defects Xk aprosencephaly Xerophthalmia Xl X linked adrenal hypoplasia congenita X linked adrenoleukodystropy X linked alpha thalassemia mental retardation syndrome ATR X X linked dominant X linked ichthyosis X linked juvenile retinoschisis X linked juvenile retinoschisis X linked lymphoproliferative syndrome X linked mental retardation and macroorchidism X linked mental retardation associated with marXq2 X linked mental retardation Brooks type X linked mental retardation craniofacial abnormal microcephaly club X linked mental retardation De silva type X linked mental retardation Hamel type X linked mental retardation type Gustavson X linked mental retardation type Martinez X linked mental retardation type Raynaud X linked mental retardation type Schutz X linked mental retardation type Snyder X linked mental retardation type Wittner X linked mental retardation hypotonia X linked severe combined immunodeficiency X linked trait Xx Xy XX male syndrome XY Female XY gonadal agenesis syndrome DEFAULTSORT List Of Diseases X Category Lists of diseases X ... more details
PIBI D S syndrome is similar to BIDS syndrome , but also associated with photosensitivity , and in contrast to IBIDS syndrome , the ichthyosis is mild and not congential . ref name Fitz2 Freedberg, et al. 2003 . Fitzpatrick s Dermatology in General Medicine . 6th ed. . McGraw Hill. ISBN 0071380760. ref rp 501 Additionally, there is a relationship with xeroderma pigmentosum in that virtually all PIBI D S patients have a deficiency in the nucleotide excision repair of UV induced DNA damage that is indistinguishable from that of xeroderma pigmentosum group D. ref name Fitz2 rp 501 See also BIDS syndrome IBIDS syndrome Skin lesion List of cutaneous conditions References reflist Category Genodermatoses Genodermatoses stub ... more details
The acronym XPG can refer to the following X Open Portability Guide , specifies the requirements for systems which are intended to be a Unix system, and a predecessor to the POSIX standard Xeroderma pigmentosum, complementation group G , a genetic disorder and a possible source of skin tumors XPG can be regarded as a protein involved in nucleotide excision repair .It is an endounclease involved in the damage specific incision of NER. disambig it XPG ... more details
XPC may refer to the following Pecheneg language , ISO 639 3 code xpc Shuttle Inc. Shuttle XPC , popular line of barebones computers and cases. SPEC XPC , the X Performance Characterization group working under the SPEC GPC group. XPC gene Xeroderma pigmentosum, complementation group C , a human gene xPC Target , a product from MathWorks disambig it XPC ... more details
DNA polymerase eta Pol is a eukaryotic DNA polymerase involved in the DNA repair Translesion synthesis DNA repair by translesion synthesis . The gene encoding DNA polymerase eta is POLH , also known as XPV, because loss of this gene results in the disease Xeroderma Pigmentosum Variant. Polymerase eta is particularly important for allowing accurate translesion synthesis of DNA damage resulting from ultraviolet radiation or UV. References refbegin http www.ncbi.nlm.nih.gov sites entrez?db gene&cmd retrieve&list uids 5429 refend Category DNA replication ... more details
Infobox Disease Name DeSanctis Cacchione syndrome Image Caption DiseasesDB 29880 ICD10 ICD9 ICDO OMIM 278800 MedlinePlus eMedicineSubj eMedicineTopic MeshID DeSanctis Cacchione syndrome is an extremely rare disorder characterized by the skin and eye symptoms of xeroderma pigmentosum XP occurring in association with microcephaly, progressive mental retardation, retarded growth and sexual development, deafness, choreoathetosis, ataxia and quadriparesis. ref name Bolognia cite book author Rapini, Ronald P. Bolognia, Jean L. Jorizzo, Joseph L. title Dermatology 2 Volume Set publisher Mosby location St. Louis year 2007 pages isbn 1 4160 2999 0 oclc doi accessdate ref Genetics In at least some case, the gene lesion involves a mutation in the Cockayne syndrome CSB gene. ref http hmg.oxfordjournals.org cgi content full 9 8 1171?view long&pmid 10767341 ref It can be associated with ERCC6 . ref name pmid10767341 cite journal author Colella S, Nardo T, Botta E, Lehmann AR, Stefanini M title Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis cacchione variant of xeroderma pigmentosum journal Hum. Mol. Genet. volume 9 issue 8 pages 1171 5 year 2000 month May pmid 10767341 doi 10.1093 hmg 9.8.1171 url http hmg.oxfordjournals.org cgi pmidlookup?view long&pmid 10767341 ref See also Xeroderma pigmentosum List of cutaneous conditions References reflist DNA repair deficiency disorder DEFAULTSORT Desanctis Cacchione Syndrome Category Genodermatoses Dermatology stub ... more details
PBB geneid 7508 Xerodermapigmentosum, complementation group C , also known as XPC , is a protein which in humans is encoded by the XPC gene . XPC is involved in the recognition of bulky DNA adducts in nucleotide excision repair . ref name entrez cite web title Entrez Gene XPC xerodermapigmentosum, complementation ... NER pathway. There are multiple components involved in the NER pathway, including Xerodermapigmentosum ... Clinical significance Mutations in this gene or some other NER components result in Xerodermapigmentosum ... January title Xerodermapigmentosum group C protein interacts physically and functionally with thymine ... F year 2001 month June title Centrosome protein centrin 2 caltractin 1 is part of the xerodermapigmentosum ... C, Maekawa T, Sugasawa K, Ohkuma Y, Hanaoka F year 2000 month March title The xerodermapigmentosum ... JC title A summary of mutations in the UV sensitive disorders xerodermapigmentosum, Cockayne syndrome ... R, Peterson C title Expression cloning of a human DNA repair gene involved in xerodermapigmentosum ... involved in xerodermapigmentosum group C journal Nature volume 359 issue 6390 pages 70 3 year 1992 pmid 1522891 doi 10.1038 359070a0 cite journal author Legerski RJ title Assignment of xerodermapigmentosum ..., Peterson CA, Legerski RJ title Characterization of molecular defects in xerodermapigmentosum group ... repair defect of xerodermapigmentosum cells of complementation groups A, B and C journal Gene Ther ... first5 A last6 Mezzina first6 M cite journal author Khan SG title Xerodermapigmentosum group C splice ... first9 Thomas D. cite journal author Yokoi M title The xerodermapigmentosum group C protein complex ... 2 caltractin 1 is part of the xerodermapigmentosum group C complex that initiates global genome nucleotide ... xp GeneReviews NIH NCBI UW entry on XerodermaPigmentosum The PBB Controls template provides controls ... C title Purification and cloning of a nucleotide excision repair complex involving the xerodermapigmentosum group C protein and a human homologue of yeast RAD23 journal EMBO J. volume 13 issue 8 ... more details
CM, Prakash S, Prakash L title hRAD30 mutations in the variant form of xerodermapigmentosum journal ... significance Xerodermapigmentosum XP is an autosomal recessive human disease characterized by sunlight ... UW entry on XerodermaPigmentosum Further reading refbegin 2 PBB Further reading citations cite journal author Masutani C, Kusumoto R, Yamada A, et al. title The XPV xerodermapigmentosum variant gene ... hRAD30 mutations in the variant form of xerodermapigmentosum journal Science volume 285 issue 5425 ... of defective translesion synthesis and UV light sensitivity in xerodermapigmentosum variant cells ... Xerodermapigmentosum variant heterozygotes show reduced levels of recovery of replicative DNA synthesis ... Molecular analysis of mutations in DNA polymerase in xerodermapigmentosum variant patients journal ... in somatic hypermutation determined by analysis of mutations in a patient with xerodermapigmentosum ... switch recombination. ref name entrez Mutations in this gene result in XPV, a variant type of xerodermapigmentosum . ref name pmid12405351 cite journal author Stary A, Sarasin A title Molecular mechanisms ... T, Hanaoka F title Genomic structure, chromosomal localization and identification of mutations in the xerodermapigmentosum variant XPV gene journal Oncogene volume 19 issue 41 pages 4721 8 year 2000 ... Limoli CL, Giedzinski E, Bonner WM, Cleaver JE title UV induced replication arrest in the xerodermapigmentosum variant leads to DNA double strand breaks, H2AX formation, and Mre11 relocalization ... more details
Unreferenced stub auto yes date December 2009 Excision endonuclease , also known as excinuclease or UV Specific Endonuclease , is a nuclease enzyme which excises a fragment of nucleotides during DNA repair . The excinuclease cuts out a fragment by hydrolyzing two phosphodiester bonds, one on either side of the lesion in the DNA. This process is part of nucleotide excision repair , a mechanism that can fix specific damages to the DNA in the G1 phase of the eukaryotic cell cycle . Such damages can include the thymine dimers created by UV rays. A deficiency of excinuclease occurs in a rare autosomal recessive disease called xeroderma pigmentosum . Diagnosis of this disease is done by measuring the enzyme s level in white blood cells in a blood sample. Symptoms in children include extreme ultraviolet UV sensitivity, excessive freckle freckling , multiple skin cancer s and corneal ulcer ations. Typically, these symptoms are seen during a child s first sun exposure. Citation needed date November 2009 Category DNA repair Enzyme stub ca escinucleasa es escinucleasa ... more details
group 5 xerodermapigmentosum, complementation group G is involved in excision repair of UV induced ... in the UV sensitive disorders xerodermapigmentosum, Cockayne syndrome, and trichothiodystrophy ... the DNA repair gene XPG in a xerodermapigmentosum group G patient journal Hum. Mol. Genet. volume ..., Sung P, Prakash L, Prakash S title Human xerodermapigmentosum group G gene encodes a DNA endonuclease .... title Complementation of the DNA repair defect in xerodermapigmentosum group G cells by a human ... DNA repair protein, Xerodermapigmentosum type G, in the nucleus journal Proc. Natl. Acad. Sci ... in Cockayne syndrome patients from xerodermapigmentosum group G implications for a second XPG ... links http www.ncbi.nlm.nih.gov bookshelf br.fcgi?book gene&part xp GeneReviews NIH NCBI UW entry on XerodermaPigmentosum Further reading refbegin 2 PBB Further reading citations cite journal author ... Y, Saito T, et al. title An ERCC5 gene with homology to yeast RAD2 is involved in group G xerodermapigmentosum journal Mutat. Res. volume 314 issue 2 pages 167 75 year 1994 pmid 7510366 doi cite ... 10.1038 363182a0 cite journal author O Donovan A, Wood RD title Identical defects in DNA repair in xerodermapigmentosum group G and rodent ERCC group 5 journal Nature volume 363 issue 6425 pages 185 ... more details
PBB geneid 2071 XPB XerodermaPigmentosum B is an Adenosine triphosphate ATP dependent human DNA helicase that is a part of the TFIIH transcription factor complex. Structure The 3D structure of the archeael homologue of XPB has been solved by X ray crystallography by Dr. John Tainer and his group at The Scripps Research Institute . ref cite journal author Fan L, Arvai A, Cooper P, Iwai S, Hanaoka F, Tainer J title Conserved XPB core structure and motifs for DNA unwinding implications for pathway selection of transcription or excision repair journal Mol Cell volume 22 issue 1 pages 27 37 year 2006 pmid 16600867 doi 10.1016 j.molcel.2006.02.017 ref Function XPB plays a significant role in normal ... complementation groups, XPA XPG, leads to a number of genetic disorders such as XerodermaPigmentosum ... The xerodermapigmentosum group C protein complex XPC HR23B plays an important role in the recruitment ... Jan. title The BCR ABL oncoprotein potentially interacts with the xerodermapigmentosum group B protein ... . ref name pmid15220921 ref name pmid9118947 See also Xerodermapigmentosum, complementation group ... disorders xerodermapigmentosum, Cockayne syndrome, and trichothiodystrophy. journal Hum. Mutat .... title Localization of the xerodermapigmentosum group B correcting gene ERCC3 to human chromosome 2q21 ... XPBC ERCC 3 gene involved in DNA repair disorders xerodermapigmentosum and Cockayne s syndrome ... in the human repair disorders xerodermapigmentosum and Cockayne s syndrome. journal Cell volume ... van Vuuren AJ, Vermeulen W, Ma L, et al. title Correction of xerodermapigmentosum repair defect ... within xerodermapigmentosum associated with mutations in the DNA repair and transcription ... 1918172 cite journal author Scott RJ, Itin P, Kleijer WJ, et al. title Xerodermapigmentosum Cockayne ... transcription factor TFIIH of xerodermapigmentosum group B affects both DNA repair and transcription ... xp GeneReviews NIH NCBI UW entry on XerodermaPigmentosum MeshName XPBC ERCC 3 protein The PBB Controls ... more details
JC title A summary of mutations in the UV sensitive disorders xerodermapigmentosum, Cockayne syndrome ... Molecular basis of group A xerodermapigmentosum a missense mutation and two deletions located in a zinc ... mutation of the XPAC gene as causes of group A xerodermapigmentosum journal Mutat. Res ... Mutational analysis of the structure and function of the xerodermapigmentosum group A complementing ... author Satokata I title Characterization of a splicing mutation in group A xerodermapigmentosum ... XPAC xerodermapigmentosum group A complementing gene journal J. Biol. Chem. volume 266 issue ... author Tanaka K title Analysis of a human DNA excision repair gene involved in group A xerodermapigmentosum ... of xerodermapigmentosum group A gene journal Jpn. J. Hum. Genet. volume 38 issue 1 pages 1 14 ... bookshelf br.fcgi?book gene&part xp GeneReviews NIH NCBI UW entry on XerodermaPigmentosum ... more details
wiktionary XP may refer to Windows XP , an operating system by Microsoft Microsoft Office XP Office XP , a Microsoft Office version Chi Rho Chi Rho are the Greek letters that form the Labarum, or the first two letters of Christ in Greek Athlon Athlon XP MP Athlon XP , a line of central processing units by AMD Cross platform X looks like a saltire cross and is often used to replace this word or its synonyms in abbreviations An emoticon expressing disgust, general discontentedness, sticking one s tongue out a more forceful version of P , or being dead . The X represents wincing or crossed out eyes, while the P represents a mouth with a tongue sticking out. Experience point s, in a role playing game, representation of a character s advancement and improvement in skills Extreme Programming , a software engineering methodology Xeroderma pigmentosum , a rare genetic disorder Xtra Airways IATA code In theoretical linguistics , any kind of a phrase, such as a noun phrase NP , an adjectival phrase AP , a prepositional phrase PP etc. XP complexity class disambiguation zh min nan XP bg XP cs XP da XP de XP es XP fa XP fr XP ko XP it XP he XP sw XP nl XP ja XP pl XP pt XP ru XP fi XP sv XP th XP uk XP zh XP ... more details
with xerodermapigmentosum and 4 . ref OMIM 610756 Cerebrooculofacioskeletal Syndrome 2 COFS2 br OMIM 278780 XerodermaPigmentosum, Complementation Group G XPG br OMIM 610758 Cerebrooculofacioskeletal .... Xerodermapigmentosum Cockayne syndrome XP CS occurs when an individual also suffers from xerodermapigmentosum, another DNA repair disease. Some symptoms of each disease are expressed. Genetics ... more details
Infobox book series name Moonlight Bay Trilogy author Dean Koontz language English genre Horror fiction Horror publisher Cemetery Dance Publications , Bantam Books Bantam Publishing The Moonlight Bay Trilogy is a proposed trilogy of three novels by Dean Koontz . They revolve around the mysterious events in Moonlight Bay that are investigated by the main character Christopher Snow , who suffers from the genetic disorder Xeroderma pigmentosum . Only the first two books have been released. The books in the trilogy are Fear Nothing , 1998 , ISBN 0 7472 5832 5 Paperback , ISBN 0 553 10664 3 Hardback Seize the Night , 1999 , ISBN 0 7472 5833 3 Paperback , ISBN 0 553 10665 1 Hardback Ride the Storm novel Ride the Storm Tentative title , TBA According to a January 14, 2000 interview with Bookreporter.com, Dean Koontz was quoted as saying I m half way through Ride the Storm , the third Christopher Snow story, but another book will appear between False Memory and Ride . As of 2003, Koontz was still reportedly halfway through Ride the Storm. ref name teenreads http www.teenreads.com authors au koontz dean.asp Interview with Dean Koontz , teenreads.com, 2003 ref Footnotes reflist Category Novel series Category Upcoming books fr Trilogie de Moonlight Bay ... more details
. 2003 Jan 15 97 2 425 40. ref XPC, XPE DDB2 NER GGR type ref Lehmann AR, McGibbon D, Stefanini M. Xerodermapigmentosum. Orphanet J Rare Dis. 2011 Nov 1 6 70. ref skin cancer melanoma and Non melanoma skin cancer non melanoma ref Lehmann AR, McGibbon D, Stefanini M. Xerodermapigmentosum. Orphanet ... AR, McGibbon D, Stefanini M. Xerodermapigmentosum. Orphanet J Rare Dis. 2011 Nov 1 6 70. ref skin .... Xerodermapigmentosum. Orphanet J Rare Dis. 2011 Nov 1 6 70. ref XPV POLH TLS ref Lehmann AR, McGibbon D, Stefanini M. Xerodermapigmentosum. Orphanet J Rare Dis. 2011 Nov 1 6 70. ref skin cancer melanoma and non melanoma ref Lehmann AR, McGibbon D, Stefanini M. Xerodermapigmentosum. Orphanet J Rare ... genes give rise to Fanconi anemia XPC xeroderma pigmentosa C XPE DDB2 DNA damage binding protein 2, the smaller subunit of a heterodimeric protein implicated in the etiology of xerodermapigmentosum group E XPA, XPB, XPD, XPF, XPG mutations in any of these 4 genes give rise to xeroderma pigmentosa XPV POLH mutation in polymerase H gives rise to xeroderma pigmentosa hMSH2, hMSH6, hMLH1, hPMS2 ... more details
, Harcourt SA, et al. title Molecular and cellular analysis of the DNA repair defect in a patient in xerodermapigmentosum complementation group D who has the clinical features of xerodermapigmentosum ... A summary of mutations in the UV sensitive disorders xerodermapigmentosum, Cockayne syndrome, and trichothiodystrophy ... gene&part xp GeneReviews NIH NCBI UW entry on XerodermaPigmentosum MeshName ERCC2 Protein The PBB ... 10.1002 SICI 1098 1004 1999 14 1 9 AID HUMU2 3.0.CO 2 6 cite journal author Lehmann AR title The xerodermapigmentosum group D XPD gene one gene, two functions, three diseases. journal Genes Dev. volume ... more details
al. title Xerodermapigmentosum group C protein complex is the initiator of global genome nucleotide ... pmc 139241 cite journal author Shimizu Y, Iwai S, Hanaoka F, Sugasawa K title Xerodermapigmentosum ... repair by damage induced and RAD23 dependent stabilization of xerodermapigmentosum group C protein ... Araki M, Masutani C, Takemura M, et al. title Centrosome protein centrin 2 caltractin 1 is part of the xerodermapigmentosum group C complex that initiates global genome nucleotide excision repair journal ... more details
Infobox Book See Wikipedia WikiProject Novels or Wikipedia WikiProject Books name Ride the Storm orig title translator image image caption author Dean Koontz cover artist country United States language English language English series Moonlight Bay Trilogy genre Suspense , Mystery novel publisher release date media type pages isbn preceded by Seize the Night novel Seize the Night followed by Ride the Storm will be the final book in the Moonlight Bay Trilogy , to be written by New York Times best selling author Dean Koontz . The book is the third installment featuring Christopher Snow, a young man who suffers from the rare but real disease called XP xeroderma pigmentosum . Book one, Fear Nothing , was released in 1998, and book two, Seize the Night , was released in 1999. According to a January 14, 2000 interview with Bookreporter.com, Dean Koontz was quoted as saying I m half way through Ride the Storm , the third Christopher Snow story, but another book will appear between False Memory and Ride . As of 2003, Koontz was still halfway through Ride the Storm . ref name teenreads http www.teenreads.com authors au koontz dean.asp Interview with Koontz , teenreads.com, 2003. ref In a Frequently Asked Questions pamphlet delivered with Koontz official email newsletter Useless News , Koontz writes The third Chris Snow novel after FEAR NOTHING and SEIZE THE NIGHT will be written, God willing, but has been delayed because other ideas demand attention first. RIDE THE STORM, the third Snow, has been cooking for a long time, but it s a delicate dish to develop. Citation needed date December 2010 Footnotes reflist Dean Koontz state collapsed Category Novel series Category Thriller novels Category Novels by Dean Koontz Category Upcoming books thriller novel stub ... more details
protein centrin 2 caltractin 1 is part of the xerodermapigmentosum group C complex that initiates ... 2 caltractin 1 is part of the xerodermapigmentosum group C complex that initiates global genome ... author Popescu A, Miron S, Blouquit Y, et al. title Xerodermapigmentosum group C protein possesses ... E, et al. title Centrin 2 stimulates nucleotide excision repair by interacting with xerodermapigmentosum group C protein. journal Mol. Cell. Biol. volume 25 issue 13 pages 5664 74 year 2005 pmid ... more details
activity causes the repair defect in the patients with xerodermapigmentosum complementation group ... author Chu G, Chang E title Xerodermapigmentosum group E cells lack a nuclear factor that binds ... Correction of the DNA repair defect in xerodermapigmentosum group E by injection of a DNA damage ... Characterization of a human DNA damage binding protein implicated in xerodermapigmentosum E. journal ... in xerodermapigmentosum group E cells. journal Mutat. Res. volume 362 issue 1 pages 105 17 year 1996 pmid 8538642 doi cite journal author Nichols AF, Ong P, Linn S title Mutations specific to the xerodermapigmentosum group E Ddb phenotype. journal J. Biol. Chem. volume 271 issue 40 pages 24317 ... more details
xerodermapigmentosum, Cockayne syndrome, and trichothiodystrophy journal Hum. Mutat. volume 14 issue ... mutage 8.3.199 cite journal author Sijbers AM, de Laat WL, Ariza RR, et al. title Xerodermapigmentosum ... Characterization of molecular defects in xerodermapigmentosum group F in relation to its clinically ... Defining the function of xerodermapigmentosum group F protein in psoralen interstrand cross link ... br.fcgi?book gene&part xp GeneReviews NIH NCBI UW entry on XerodermaPigmentosum PDB Gallery ... more details
P, Linn S title Mutations specific to the xerodermapigmentosum group E Ddb phenotype. journal J. Biol ... p53 Binds and activates the xerodermapigmentosum DDB2 gene in humans but not mice. journal Mol ... bookshelf br.fcgi?book gene&part xp GeneReviews NIH NCBI UW entry on XerodermaPigmentosum ... more details
Europe Xerodermapigmentosum, Cockayne syndrome and trichothiodystrophy journal DNA Repair ... syndrome and xerodermapigmentosum display symptoms dominated by vulnerability to cancer, whereas ... url http linkinghub.elsevier.com retrieve pii S1568 7864 08 00042 6 ref Werner syndrome Xerodermapigmentosum DNA repair defects distinguished from accelerated aging Most of the DNA repair deficiency ... more details
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