Angela M. Christiano - Publications

Affiliations: 
Columbia University, New York, NY 
Area:
Genetics, Cell Biology, Human Development

134 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Hasan Ali O, Yurchenko AA, Pavlova O, Sartori A, Bomze D, Higgins R, Ring SS, Hartmann F, Bühler D, Fritzsche FR, Jochum W, Navarini AA, Kim A, French LE, Dermitzakis E, ... Christiano AM, et al. Genomic profiling of late-onset basal cell carcinomas from two brothers with Naevoid Basal Cell Carcinoma Syndrome. Journal of the European Academy of Dermatology and Venereology : Jeadv. PMID 32564428 DOI: 10.1111/jdv.16767  0.32
2020 Vonica A, Bhat N, Phan K, Guo J, Iancu L, Weber JA, Karger A, Cain JW, Wang ECE, DeStefano GM, O'Donnell-Luria AH, Christiano AM, Riley B, Butler SJ, Luria V. Apcdd1 is a dual BMP/Wnt inhibitor in the developing nervous system and skin. Developmental Biology. PMID 32320685 DOI: 10.1016/j.ydbio.2020.03.015  0.36
2019 Jacków J, Guo Z, Hansen C, Abaci HE, Doucet YS, Shin JU, Hayashi R, DeLorenzo D, Kabata Y, Shinkuma S, Salas-Alanis JC, Christiano AM. CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells. Proceedings of the National Academy of Sciences of the United States of America. PMID 31818947 DOI: 10.1073/pnas.1907081116  0.48
2017 Wang EH, DeStefano GM, Patel AV, Drill E, Harel S, Cela C, Tavazoie M, Christiano AM. Identification of differentially expressed miRNAs in alopecia areata that target immune-regulatory pathways. Genes and Immunity. PMID 28300058 DOI: 10.1038/gene.2017.4  0.36
2016 Shinkuma S, Guo Z, Christiano AM. Site-specific genome editing for correction of induced pluripotent stem cells derived from dominant dystrophic epidermolysis bullosa. Proceedings of the National Academy of Sciences of the United States of America. PMID 27143720 DOI: 10.1073/pnas.1512028113  0.4
2015 Gledhill K, Guo Z, Umegaki-Arao N, Higgins CA, Itoh M, Christiano AM. Melanin Transfer in Human 3D Skin Equivalents Generated Exclusively from Induced Pluripotent Stem Cells. Plos One. 10: e0136713. PMID 26308443 DOI: 10.1371/journal.pone.0136713  0.4
2015 Geyer MB, Radhakrishnan K, Giller R, Umegaki N, Harel S, Kiuru M, Morel KD, LeBoeuf N, Kandel J, Bruckner A, Fabricatore S, Chen M, Woodley D, McGrath J, Baxter-Lowe L, ... ... Christiano AM, et al. Reduced Toxicity Conditioning and Allogeneic Hematopoietic Progenitor Cell Transplantation for Recessive Dystrophic Epidermolysis Bullosa. The Journal of Pediatrics. PMID 26148662 DOI: 10.1016/j.jpeds.2015.05.051  0.4
2015 Betz RC, Petukhova L, Ripke S, Huang H, Menelaou A, Redler S, Becker T, Heilmann S, Yamany T, Duvic M, Hordinsky M, Norris D, Price VH, Mackay-Wiggan J, de Jong A, ... ... Christiano AM, et al. Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci. Nature Communications. 6: 5966. PMID 25608926 DOI: 10.1038/ncomms6966  0.4
2015 Antonov NK, Kingsbery MY, Rohena LO, Lee TM, Christiano A, Garzon MC, Lauren CT. Early-onset heart failure, alopecia, and cutaneous abnormalities associated with a novel compound heterozygous mutation in desmoplakin. Pediatric Dermatology. 32: 102-8. PMID 25516398 DOI: 10.1111/pde.12484  0.4
2014 Umegaki-Arao N, Pasmooij AM, Itoh M, Cerise JE, Guo Z, Levy B, Gosty?ski A, Rothman LR, Jonkman MF, Christiano AM. Induced pluripotent stem cells from human revertant keratinocytes for the treatment of epidermolysis bullosa. Science Translational Medicine. 6: 264ra164. PMID 25429057 DOI: 10.1126/scitranslmed.3009342  0.4
2014 DeStefano GM, Christiano AM. The genetics of human skin disease. Cold Spring Harbor Perspectives in Medicine. 4. PMID 25274756 DOI: 10.1101/cshperspect.a015172  0.36
2014 Xing L, Dai Z, Jabbari A, Cerise JE, Higgins CA, Gong W, de Jong A, Harel S, DeStefano GM, Rothman L, Singh P, Petukhova L, Mackay-Wiggan J, Christiano AM, Clynes R. Alopecia areata is driven by cytotoxic T lymphocytes and is reversed by JAK inhibition. Nature Medicine. 20: 1043-9. PMID 25129481 DOI: 10.1038/nm.3645  0.4
2014 DeStefano GM, Kurban M, Anyane-Yeboa K, Dall'Armi C, Di Paolo G, Feenstra H, Silverberg N, Rohena L, López-Cepeda LD, Jobanputra V, Fantauzzo KA, Kiuru M, Tadin-Strapps M, Sobrino A, Vitebsky A, ... ... Christiano AM, et al. Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowth. Plos Genetics. 10: e1004333. PMID 24831815 DOI: 10.1371/journal.pgen.1004333  1
2014 Yesudian PD, Cabral RM, Ladusans E, Spinty S, Gibbs J, Fryer A, Christiano AM, Mendelsohn SS. Novel compound heterozygous mutations in the desmoplakin gene cause hair shaft abnormalities and culminate in lethal cardiomyopathy Clinical and Experimental Dermatology. 39: 506-508. PMID 24825141 DOI: 10.1111/ced.12329  0.4
2014 Xu J, Weng Z, Arumugam A, Tang X, Chaudhary SC, Li C, Christiano AM, Elmets CA, Bickers DR, Athar M. Hair follicle disruption facilitates pathogenesis to UVB-induced cutaneous inflammation and basal cell carcinoma development in Ptch(+/-) mice. The American Journal of Pathology. 184: 1529-40. PMID 24631180 DOI: 10.1016/j.ajpath.2014.01.013  0.32
2014 Furniss M, Higgins CA, Martinez-Mir A, Horev L, Petukhova L, Stanimirović A, Miljković J, Zlotogorski A, Christiano AM. Identification of distinct mutations in AAGAB in families with type 1 punctate palmoplantar keratoderma. The Journal of Investigative Dermatology. 134: 1749-52. PMID 24390136 DOI: 10.1038/jid.2014.4  0.4
2013 Shi Q, Duvic M, Osei JS, Hordinsky MK, Norris DA, Price VH, Amos CI, Christiano AM, Mendoza TR. Health-Related Quality of Life (HRQoL) in alopecia areata patients-a secondary analysis of the National Alopecia Areata Registry Data. The Journal of Investigative Dermatology. Symposium Proceedings / the Society For Investigative Dermatology, Inc. [and] European Society For Dermatological Research. 16: S49-50. PMID 24326555 DOI: 10.1038/jidsymp.2013.18  0.4
2013 Cabral RM, Kurban M, Rothman L, Wajid M, Shimomura Y, Petukhova L, Christiano AM. Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A gene. Journal of Human Genetics. 58: 566-7. PMID 23697977 DOI: 10.1038/jhg.2013.44  0.4
2013 DeStefano GM, Fantauzzo KA, Petukhova L, Kurban M, Tadin-Strapps M, Levy B, Warburton D, Cirulli ET, Han Y, Sun X, Shen Y, Shirazi M, Jobanputra V, Cepeda-Valdes R, Cesar Salas-Alanis J, ... Christiano AM, et al. Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis. Proceedings of the National Academy of Sciences of the United States of America. 110: 7790-5. PMID 23603273 DOI: 10.1073/pnas.1216412110  1
2012 Fantauzzo KA, Kurban M, Levy B, Christiano AM. Trps1 and its target gene Sox9 regulate epithelial proliferation in the developing hair follicle and are associated with hypertrichosis. Plos Genetics. 8: e1003002. PMID 23133399 DOI: 10.1371/journal.pgen.1003002  1
2012 Kim H, Casta A, Tang X, Luke CT, Kim AL, Bickers DR, Athar M, Christiano AM. Loss of hairless confers susceptibility to UVB-induced tumorigenesis via disruption of NF-kappaB signaling. Plos One. 7: e39691. PMID 22761871 DOI: 10.1371/journal.pone.0039691  0.32
2012 Ahmad RC, Kurban M, Christiano AM, Bruckner AL. Alopecia and generalized papular lesions in an adolescent female. Pediatric Dermatology. 29: 519-20. PMID 22758379 DOI: 10.1111/j.1525-1470.2011.01626.x  0.4
2012 Salas-Alanis JC, Cepeda-Valdes R, Mellerio JE, Christiano AM, Uitto J. Progress in epidermolysis bullosa: summary of a workshop in CILAD-2010*. International Journal of Dermatology. 51: 682-7. PMID 22607285 DOI: 10.1111/j.1365-4632.2011.05130.x  0.48
2012 Betz RC, Cabral RM, Christiano AM, Sprecher E. Unveiling the roots of monogenic genodermatoses: genotrichoses as a paradigm. The Journal of Investigative Dermatology. 132: 906-14. PMID 22170492 DOI: 10.1038/jid.2011.408  0.4
2012 Uitto J, Christiano AM, McLean WH, McGrath JA. Novel molecular therapies for heritable skin disorders. The Journal of Investigative Dermatology. 132: 820-8. PMID 22158553 DOI: 10.1038/jid.2011.389  0.4
2012 Fantauzzo KA, Christiano AM. Trps1 activates a network of secreted Wnt inhibitors and transcription factors crucial to vibrissa follicle morphogenesis. Development (Cambridge, England). 139: 203-14. PMID 22115758 DOI: 10.1242/dev.069971  1
2011 Salas-Alanis JC, Cepeda-Valdés R, González-Santos A, Amaya-Guerra M, Kurban M, Christiano AM. [Mutation in the ED1, Ala349Thr in a patient with X-linked hypohidrotic ectodermal dysplasia]. Revista MéDica De Chile. 139: 1601-4. PMID 22446708  0.48
2011 Salas-Alanis JC, Kurban M, Cepeda-Valdes R, Chavez-Alvarez S, Christiano AM, Bickers D. An unusual case of infiltrating basal cell carcinoma. Dermatologic Surgery : Official Publication For American Society For Dermatologic Surgery [Et Al.]. 37: 1316-8. PMID 21679275 DOI: 10.1111/j.1524-4725.2011.02080.x  0.48
2011 Fantauzzo KA, Christiano AM. There and back again: hair follicle stem cell dynamics. Cell Stem Cell. 8: 8-9. PMID 21211777 DOI: 10.1016/j.stem.2010.12.018  1
2011 Bi MY, Curry JL, Christiano AM, Hordinsky MK, Norris DA, Price VH, Duvic M. The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome. Journal of the American Academy of Dermatology. 64: 53-63. PMID 21036417 DOI: 10.1016/j.jaad.2009.12.056  0.4
2009 Bazzi H, Demehri S, Potter CS, Barber AG, Awgulewitsch A, Kopan R, Christiano AM. Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation. Differentiation; Research in Biological Diversity. 78: 292-300. PMID 19683850 DOI: 10.1016/j.diff.2009.06.004  0.4
2009 Richardson GD, Bazzi H, Fantauzzo KA, Waters JM, Crawford H, Hynd P, Christiano AM, Jahoda CA. KGF and EGF signalling block hair follicle induction and promote interfollicular epidermal fate in developing mouse skin. Development (Cambridge, England). 136: 2153-64. PMID 19474150 DOI: 10.1242/dev.031427  0.4
2008 Fantauzzo KA, Tadin-Strapps M, You Y, Mentzer SE, Baumeister FA, Cianfarani S, Van Maldergem L, Warburton D, Sundberg JP, Christiano AM. A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice. Human Molecular Genetics. 17: 3539-51. PMID 18713754 DOI: 10.1093/hmg/ddn247  1
2008 Petukhova L, Sousa EC, Martinez-Mir A, Vitebsky A, Dos Santos LG, Shapiro L, Haynes C, Gordon D, Shimomura Y, Christiano AM. Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation. Genomics. 92: 273-8. PMID 18692127 DOI: 10.1016/j.ygeno.2008.06.009  0.4
2008 Owens P, Bazzi H, Engelking E, Han G, Christiano AM, Wang XJ. Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity. Developmental Biology. 322: 156-66. PMID 18692037 DOI: 10.1016/j.ydbio.2008.07.020  0.4
2008 Akman A, Masse M, Mihci E, Richard G, Christiano AM, Balle BJ, Ciftcioglu MA, Alpsoy E. Progressive symmetrical erythrokeratoderma: Report of a Turkish family and evaluation for loricrin and connexin gene mutations Clinical and Experimental Dermatology. 33: 582-584. PMID 18462442 DOI: 10.1111/j.1365-2230.2008.02728.x  0.4
2008 Engelhard A, Bauer RC, Casta A, Djabali K, Christiano AM. Ligand-independent regulation of the hairless promoter by vitamin D receptor. Photochemistry and Photobiology. 84: 515-21. PMID 18266815 DOI: 10.1111/j.1751-1097.2008.00301.x  0.32
2008 Fantauzzo KA, Bazzi H, Jahoda CA, Christiano AM. Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling. Gene Expression Patterns : Gep. 8: 51-7. PMID 18054290 DOI: 10.1016/j.modgep.2007.10.006  1
2008 Ishii Y, Wajid M, Bazzi H, Fantauzzo KA, Barber AG, Blaydon DC, Nam JS, Yoon JK, Kelsell DP, Christiano AM. Mutations in R-spondin 4 (RSPO4) underlie inherited anonychia. The Journal of Investigative Dermatology. 128: 867-70. PMID 17805348 DOI: 10.1038/sj.jid.5701078  1
2007 Michailidis E, Theos A, Zlotogorski A, Martinez-Mir A, Christiano AM. Atrichia with papular lesions resulting from novel compound heterozygous mutations in the human hairless gene. Pediatric Dermatology. 24: E79-82. PMID 17958788 DOI: 10.1111/j.1525-1470.2007.00448.x  0.4
2007 Bazzi H, Christiano AM. Broken hearts, woolly hair, and tattered skin: when desmosomal adhesion goes awry. Current Opinion in Cell Biology. 19: 515-20. PMID 17951043 DOI: 10.1016/j.ceb.2007.08.001  0.4
2007 Bazzi H, Fantauzzo KA, Richardson GD, Jahoda CA, Christiano AM. The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis. Developmental Biology. 305: 498-507. PMID 17397822 DOI: 10.1016/j.ydbio.2007.02.035  1
2007 Wajid M, Bazzi H, Rockey J, Lubetkin J, Zlotogorski A, Christiano AM. Localized autosomal recessive hypotrichosis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family. The Journal of Investigative Dermatology. 127: 1779-82. PMID 17392831 DOI: 10.1038/sj.jid.5700791  0.4
2007 Bazzi H, Fantauzzo KA, Richardson GD, Jahoda CA, Christiano AM. Transcriptional profiling of developing mouse epidermis reveals novel patterns of coordinated gene expression. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 236: 961-70. PMID 17330888 DOI: 10.1002/dvdy.21099  1
2007 Martinez-Mir A, Zlotogorski A, Gordon D, Petukhova L, Mo J, Gilliam TC, Londono D, Haynes C, Ott J, Hordinsky M, Nanova K, Norris D, Price V, Duvic M, Christiano AM. Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata. American Journal of Human Genetics. 80: 316-28. PMID 17236136 DOI: 10.1086/511442  0.4
2006 Ashoor G, Massé M, García Luciano LM, Sheffer R, Martinez-Mir A, Christiano AM, Zlotogorski A. A novel mutation in the 12(R)-lipoxygenase (ALOX12B) gene underlies nonbullous congenital ichthyosiform erythroderma. The British Journal of Dermatology. 155: 198-200. PMID 16792775 DOI: 10.1111/j.1365-2133.2006.07188.x  0.4
2006 Schaffer JV, Bazzi H, Vitebsky A, Witkiewicz A, Kovich OI, Kamino H, Shapiro LS, Amin SP, Orlow SJ, Christiano AM. Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions. The Journal of Investigative Dermatology. 126: 1286-91. PMID 16543896 DOI: 10.1038/sj.jid.5700237  0.4
2006 Bazzi H, Getz A, Mahoney MG, Ishida-Yamamoto A, Langbein L, Wahl JK, Christiano AM. Desmoglein 4 is expressed in highly differentiated keratinocytes and trichocytes in human epidermis and hair follicle. Differentiation; Research in Biological Diversity. 74: 129-40. PMID 16533311 DOI: 10.1111/j.1432-0436.2006.00061.x  0.4
2006 Mahoney MG, Hu Y, Brennan D, Bazzi H, Christiano AM, Wahl JK. Delineation of diversified desmoglein distribution in stratified squamous epithelia: implications in diseases. Experimental Dermatology. 15: 101-9. PMID 16433681 DOI: 10.1111/j.1600-0625.2006.00391.x  0.4
2006 Chuang GS, Martinez-Mir A, Engler DE, Gmyrek RF, Zlotogorski A, Christiano AM. Multiple cutaneous and uterine leiomyomata resulting from missense mutations in the fumarate hydratase gene Clinical and Experimental Dermatology. 31: 118-121. PMID 16309500 DOI: 10.1111/j.1365-2230.2005.01977.x  0.4
2005 Martinez-Mir A, Zlotogorski A, Christiano AM. Search for susceptibility genes in alopecia areata. The Journal of Investigative Dermatology. Symposium Proceedings / the Society For Investigative Dermatology, Inc. [and] European Society For Dermatological Research. 10: 281-2. PMID 16402481 DOI: 10.1111/j.0022-202X.2005.10130_3.x  0.4
2005 Bazzi H, Martinez-Mir A, Kljuic A, Christiano AM. Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats. The Journal of Investigative Dermatology. Symposium Proceedings / the Society For Investigative Dermatology, Inc. [and] European Society For Dermatological Research. 10: 222-4. PMID 16382669 DOI: 10.1111/j.1087-0024.2005.10110.x  0.4
2005 Messenger AG, Bazzi H, Parslew R, Shapiro L, Christiano AM. A missense mutation in the cadherin interaction site of the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis. The Journal of Investigative Dermatology. 125: 1077-9. PMID 16297213 DOI: 10.1111/j.0022-202X.2005.23903.x  0.4
2005 Paradisi M, Massé M, Martinez-Mir A, Lam H, Pedicelli C, Christiano AM. Identification of a novel splice site mutation in the human hairless gene underlying atrichia with papular lesions. European Journal of Dermatology : Ejd. 15: 332-8. PMID 16172039  0.4
2005 Ashoor GG, Greenstein RM, Lam H, Martinez-Mir A, Zlotogorski A, Christiano AM. Novel compound heterozygous nonsense mutations in the hairless gene causing atrichia with papular lesions. Journal of Dermatological Science. 40: 29-33. PMID 16023329 DOI: 10.1016/j.jdermsci.2005.04.004  0.4
2005 Massé M, Martinez-Mir A, Lam H, Geraghty MT, Christiano AM. Identification of a recurrent mutation in the human hairless gene underlying atrichia with papular lesions Clinical and Experimental Dermatology. 30: 363-365. PMID 15953070 DOI: 10.1111/j.1365-2230.2005.01762.x  0.4
2005 Chuang GS, Martinez-Mir A, Geyer A, Engler DE, Glaser B, Cserhalmi-Friedman PB, Gordon D, Horev L, Lukash B, Herman E, Cid MP, Brenner S, Landau M, Sprecher E, Garcia Muret MP, ... Christiano AM, et al. Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata. Journal of the American Academy of Dermatology. 52: 410-6. PMID 15761418 DOI: 10.1016/j.jaad.2004.08.051  0.4
2005 Turkish AR, Henneberry AL, Cromley D, Padamsee M, Oelkers P, Bazzi H, Christiano AM, Billheimer JT, Sturley SL. Identification of two novel human acyl-CoA wax alcohol acyltransferases: members of the diacylglycerol acyltransferase 2 (DGAT2) gene superfamily. The Journal of Biological Chemistry. 280: 14755-64. PMID 15671038 DOI: 10.1074/jbc.M500025200  0.4
2005 Chan I, Wong T, Martinez-Mir A, Christiano AM, McGrath JA. Familial multiple cutaneous and uterine leiomyomas associated with papillary renal cell cancer. Clinical and Experimental Dermatology. 30: 75-8. PMID 15663510 DOI: 10.1111/j.1365-2230.2004.01675.x  0.4
2005 Nakabayashi K, Amann D, Ren Y, Saarialho-Kere U, Avidan N, Gentles S, MacDonald JR, Puffenberger EG, Christiano AM, Martinez-Mir A, Salas-Alanis JC, Rizzo R, Vamos E, Raams A, Les C, et al. Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy. American Journal of Human Genetics. 76: 510-6. PMID 15645389 DOI: 10.1086/428141  0.4
2004 Meyer B, Bazzi H, Zidek V, Musilova A, Pravenec M, Kurtz TW, Nurnberg P, Christiano AM. A spontaneous mutation in the desmoglein 4 gene underlies hypotrichosis in a new lanceolate hair rat model. Differentiation; Research in Biological Diversity. 72: 541-7. PMID 15617564 DOI: 10.1111/j.1432-0436.2004.07209007.x  0.4
2004 Bazzi H, Kljuic A, Christiano AM, Christiano AM, Panteleyev AA. Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo "hairless" rat. Differentiation; Research in Biological Diversity. 72: 450-64. PMID 15606503 DOI: 10.1111/j.1432-0436.2004.07208010.x  0.4
2004 Brennan D, Hu Y, Kljuic A, Choi Y, Joubeh S, Bashkin M, Wahl J, Fertala A, Pulkkinen L, Uitto J, Christiano AM, Panteleyev A, Mahoney MG. Differential structural properties and expression patterns suggest functional significance for multiple mouse desmoglein 1 isoforms. Differentiation; Research in Biological Diversity. 72: 434-49. PMID 15606502 DOI: 10.1111/j.1432-0436.2004.07208009.x  0.96
2004 Kljuic A, Bauer RC, Christiano AM. Genomic organization of mouse desmocollin genes reveals evolutionary conservation. Dna Sequence : the Journal of Dna Sequencing and Mapping. 15: 148-52. PMID 15346771  0.96
2004 Tadin-Strapps M, Warburton D, Baumeister FA, Fischer SG, Yonan J, Gilliam TC, Christiano AM. Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome. Cytogenetic and Genome Research. 107: 68-76. PMID 15305058 DOI: 10.1159/000079573  0.48
2004 Moss C, Martinez-Mir A, Lam H, Tadin-Strapps M, Kljuic A, Christiano AM. A recurrent intragenic deletion in the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis. The Journal of Investigative Dermatology. 123: 607-10. PMID 15304105 DOI: 10.1111/j.0022-202X.2004.23311.x  0.96
2004 Tadin-Strapps M, Warburton D, Salas-Alanis JC, Lopez-Cepeda LD, Christiano AM. Fishing for new genes in skin biology: impact of cytogenetics on gene discovery. Clinical Genetics. 66: 94-106. PMID 15253757 DOI: 10.1111/j.0009-9163.2004.00301.x  0.48
2004 Chuang GS, Martinez-Mir A, Yu HS, Sung FY, Chuang RY, Cserhalmi-Friedman PB, Christiano AM. A novel missense mutation in the COL7A1 gene underlies epidermolysis bullosa pruriginosa Clinical and Experimental Dermatology. 29: 304-307. PMID 15115517 DOI: 10.1111/j.1365-2230.2004.01495.x  0.4
2004 Jahoda CA, Kljuic A, O'Shaughnessy R, Crossley N, Whitehouse CJ, Robinson M, Reynolds AJ, Demarchez M, Porter RM, Shapiro L, Christiano AM. The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene. Genomics. 83: 747-56. PMID 15081105 DOI: 10.1016/j.ygeno.2003.11.015  0.96
2003 Martinez-Mir A, Zlotogorski A, Londono D, Gordon D, Grunn A, Uribe E, Horev L, Ruiz IM, Davalos NO, Alayan O, Liu J, Gilliam TC, Salas-Alanis JC, Christiano AM. Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24. Journal of Medical Genetics. 40: 872-8. PMID 14684683 DOI: 10.1136/jmg.40.12.872  0.48
2003 Martinez-Mir A, Glaser B, Chuang GS, Horev L, Waldman A, Engler DE, Gordon D, Spelman LJ, Hatzibougias I, Green J, Christiano AM, Zlotogorski A. Germline Fumarate Hydratase Mutations in Families with Multiple Cutaneous and Uterine Leiomyomata Journal of Investigative Dermatology. 121: 741-744. PMID 14632190 DOI: 10.1046/j.1523-1747.2003.12499.x  0.4
2003 Paradisi M, Chuang GS, Angelo C, Pedicelli C, Martinez-Mir A, Christiano AM. Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene Clinical and Experimental Dermatology. 28: 535-538. PMID 12950347 DOI: 10.1046/j.1365-2230.2003.01333.x  0.4
2003 Kljuic A, Gilead L, Martinez-Mir A, Frank J, Christiano AM, Zlotogorski A. A nonsense mutation in the desmoglein 1 gene underlies striate keratoderma. Experimental Dermatology. 12: 523-7. PMID 12930313  0.96
2003 Lavker RM, Sun TT, Oshima H, Barrandon Y, Akiyama M, Ferraris C, Chevalier G, Favier B, Jahoda CA, Dhouailly D, Panteleyev AA, Christiano AM. Hair follicle stem cells. The Journal of Investigative Dermatology. Symposium Proceedings / the Society For Investigative Dermatology, Inc. [and] European Society For Dermatological Research. 8: 28-38. PMID 12894992 DOI: 10.1046/j.1523-1747.2003.12169.x  0.4
2003 Paller AS, Varigos G, Metzker A, Bauer RC, Opie J, Martinez-Mir A, Christiano AM, Zlotogorski A. Compound heterozygous mutations in the hairless gene in atrichia with papular lesions. The Journal of Investigative Dermatology. 121: 430-2. PMID 12880440 DOI: 10.1046/j.1523-1747.2003.12370.x  0.4
2003 Tadin-Strapps M, Salas-Alanis JC, Moreno L, Warburton D, Martinez-Mir A, Christiano AM. Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked trait. Clinical Genetics. 63: 418-22. PMID 12752576  0.48
2003 Kljuic A, Bazzi H, Sundberg JP, Martinez-Mir A, O'Shaughnessy R, Mahoney MG, Levy M, Montagutelli X, Ahmad W, Aita VM, Gordon D, Uitto J, Whiting D, Ott J, Fischer S, ... ... Christiano AM, et al. Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell. 113: 249-60. PMID 12705872 DOI: 10.1016/S0092-8674(03)00273-3  0.96
2003 Djabali K, Panteleyev AA, Lalin T, Garzon MC, Longley BJ, Bickers DR, Zlotogorski A, Christiano AM. Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix. Clinical and Experimental Dermatology. 28: 206-10. PMID 12653715 DOI: 10.1046/j.1365-2230.2003.01196.x  0.4
2003 Kljuic A, Christiano AM. A novel mouse desmosomal cadherin family member, desmoglein 1 gamma. Experimental Dermatology. 12: 20-9. PMID 12631243  0.96
2003 Horev L, Waran Lalin T, Martinez-Mir A, Bagheri BA, Tadin-Strapps M, Schneiderman PI, Grossman ME, Bickers DR, Christiano AM. Identification of mutations in the COL7A1 gene in a proband with mild recessive dystrophic epidermolysis bullosa and aortic insufficiency. Clinical and Experimental Dermatology. 28: 80-4. PMID 12558638  0.48
2002 Martinez-Mir A, Liu J, Gordon D, Weiner MS, Ahmad W, Fine JD, Ott J, Gilliam TC, Christiano AM. EB simplex superficialis resulting from a mutation in the type VII collagen gene. The Journal of Investigative Dermatology. 118: 547-9. PMID 11874498 DOI: 10.1046/j.0022-202x.2001.01702.x  0.4
2002 Ahmad W, Ratterree MS, Panteleyev AA, Aita VM, Sundberg JP, Christiano AM. Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene. Laboratory Animals. 36: 61-7. PMID 11831740 DOI: 10.1258/0023677021911777  0.4
2001 Cserhalmi-Friedman PB, Garzon MC, Guzman E, Martinez-Mir A, Chung WK, Anyane-Yeboa K, Christiano AM. Maternal germline mosaicism in dominant dystrophic epidermolysis bullosa. The Journal of Investigative Dermatology. 117: 1327-8. PMID 11710955 DOI: 10.1046/j.0022-202x.2001.01558.x  0.4
2001 Frank J, Jugert FK, Merk HF, Kalka K, Goerz G, Anderson K, Bickers DR, Poh-Fitzpatrick MB, Christiano AM. A spectrum of novel mutations in the protoporphyrinogen oxidase gene in 13 families with variegate porphyria. The Journal of Investigative Dermatology. 116: 821-3. PMID 11348478 DOI: 10.1046/J.1523-1747.2001.01308.X  0.32
2001 Cserhalmi-Friedman PB, Frank JA, Ahmad W, Panteleyev AA, Aita VM, Christiano AM. Structural analysis reflects the evolutionary relationship between the human desmocollin gene family members. Experimental Dermatology. 10: 95-9. PMID 11260247 DOI: 10.1034/j.1600-0625.2001.010002095.x  0.4
2001 Frank J, Cserhalmi-Friedman PB, Ahmad W, Panteleyev AA, Aita VM, Christiano AM. Characterization of the desmosomal cadherin gene family: genomic organization of two desmoglein genes on human chromosome 18q12. Experimental Dermatology. 10: 90-4. PMID 11260246 DOI: 10.1034/j.1600-0625.2001.010002090.x  0.4
2001 Frank J, Aita VM, Ahmad W, Lam H, Wolff C, Christiano AM. Identification of a founder mutation in the protoporphyrinogen oxidase gene in variegate porphyria patients from chile. Human Heredity. 51: 160-8. PMID 11173967 DOI: 10.1159/000053337  0.4
2001 Cserhalmi-Friedman PB, Olson PF, Koch M, Champliaud MF, Brunken WJ, Burgeson RE, Christiano AM. Structural analysis and mutation detection strategy for the human LAMC3 gene. Biochemical and Biophysical Research Communications. 280: 39-44. PMID 11162474 DOI: 10.1006/bbrc.2000.4086  0.4
2001 Pignata C, Gaetaniello L, Masci AM, Frank J, Christiano A, Matrecano E, Racioppi L. Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation of immunologic reconstitution after bone marrow transplantation. Blood. 97: 880-5. PMID 11159512 DOI: 10.1182/blood.V97.4.880  0.4
2000 Packer AI, Jane-Wit D, McLean L, Panteleyev AA, Christiano AM, Wolgemuth DJ. Hoxa4 expression in developing mouse hair follicles and skin. Mechanisms of Development. 99: 153-7. PMID 11091084 DOI: 10.1016/S0925-4773(00)00471-8  0.4
2000 Aita VM, Zlotogorski A, Christiano AM. Settling the score on hairless [1] (multiple letters) Journal of Investigative Dermatology. 115: 761-764. PMID 10998157 DOI: 10.1046/j.1523-1747.2000.00124.x  0.4
2000 Cserhalmi-Friedman PB, Squeo R, Gordon D, Garzon M, Schneiderman P, Grossman ME, Christiano AM. Epidermolytic hyperkeratosis in a Hispanic family resulting from a mutation in the keratin 1 gene. Clinical and Experimental Dermatology. 25: 241-3. PMID 10844506 DOI: 10.1046/j.1365-2230.2000.00625.x  0.32
2000 Fine JD, Eady RA, Bauer EA, Briggaman RA, Bruckner-Tuderman L, Christiano A, Heagerty A, Hintner H, Jonkman MF, McGrath J, McGuire J, Moshell A, Shimizu H, Tadini G, Uitto J. Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa. Journal of the American Academy of Dermatology. 42: 1051-66. PMID 10827412 DOI: 10.1067/mjd.2000.106369  0.4
2000 Aita VM, Ahmad W, Panteleyev AA, Kozlowska U, Kozlowska A, Gilliam TC, Jablonska S, Christiano AM. A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions. Experimental Dermatology. 9: 157-62. PMID 10772391 DOI: 10.1034/j.1600-0625.2000.009002157.x  0.4
2000 Panteleyev AA, Christiano AM, O'Brien TG, Sundberg JP. Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions Experimental Dermatology. 9: 146-151. PMID 10772389 DOI: 10.1034/j.1600-0625.2000.009002146.x  0.4
1999 Ahmad W, Panteleyev AA, Christiano AM. The molecular basis of congenital atrichia in humans and mice: mutations in the hairless gene. The Journal of Investigative Dermatology. Symposium Proceedings / the Society For Investigative Dermatology, Inc. [and] European Society For Dermatological Research. 4: 240-3. PMID 10674375 DOI: 10.1038/SJ.JIDSP.5640220  0.4
1999 Green KJ, Guy SG, Cserhalmi-Friedman PB, McLean WH, Christiano AM, Wagner RM. Analysis of the desmoplakin gene reveals striking conservation with other members of the plakin family of cytolinkers. Experimental Dermatology. 8: 462-70. PMID 10597135 DOI: 10.1111/J.1600-0625.1999.TB00304.X  0.4
1999 Szabó Z, Levi-Minzi SA, Christiano AM, Struminger C, Stoneking M, Batzer MA, Boyd CD. Sequential loss of two neighboring exons of the tropoelastin gene during primate evolution Journal of Molecular Evolution. 49: 664-671. PMID 10552047 DOI: 10.1007/PL00006587  0.4
1999 Christiano AM, Crollick J, Pincus S, Uitto J. Squamous cell carcinoma in a family with dominant dystrophic epidermolysis bullosa: a molecular genetic study. Experimental Dermatology. 8: 146-52. PMID 10232408 DOI: 10.1111/J.1600-0625.1999.TB00364.X  0.4
1999 Frank J, Pignata C, Panteleyev AA, Prowse DM, Baden H, Weiner L, Gaetaniello L, Ahmad W, Pozzi N, Cserhalmi-Friedman PB, Aita VM, Uyttendaele H, Gordon D, Ott J, Brissette JL, ... Christiano AM, et al. Exposing the human nude phenotype [4] Nature. 398: 473-474. PMID 10206641 DOI: 10.1038/18997  0.4
1998 Rouan F, Pulkkinen L, Jonkman MF, Bauer JW, Cserhalmi-Friedman PB, Christiano AM, Uitto J. Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: implications for genetic counseling. The Journal of Investigative Dermatology. 111: 1210-3. PMID 9856843 DOI: 10.1046/j.1523-1747.1998.00422.x  0.4
1998 Ahmad W, Panteleyev AA, Sundberg JP, Christiano AM. Molecular basis for the rhino (hr(rh-8J)) phenotype: A nonsense mutation in the mouse hairless gene Genomics. 53: 383-386. PMID 9799606 DOI: 10.1006/geno.1998.5495  0.4
1998 Ahmad W, Brancolini V, Ul Haque MF, Lam H, Ul Haque S, Haider M, Maimon A, Aita VM, Owen J, Brown D, Zegarelli DJ, Ahmad M, Ott J, Christiano AM. A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1 [2] American Journal of Human Genetics. 62: 987-991. PMID 9529357 DOI: 10.1086/301799  0.4
1997 Christiano AM, Fine JD, Uitto J. Genetic basis of dominantly inherited transient bullous dermolysis of the newborn: a splice site mutation in the type VII collagen gene. The Journal of Investigative Dermatology. 109: 811-4. PMID 9406826 DOI: 10.1111/1523-1747.ep12341013  0.4
1997 Hovnanian A, Rochat A, Bodemer C, Petit E, Rivers CA, Prost C, Fraitag S, Christiano AM, Uitto J, Lathrop M, Barrandon Y, De Prost Y. Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation American Journal of Human Genetics. 61: 599-610. PMID 9326325 DOI: 10.1086/515495  0.4
1997 Christiano AM, Pulkkinen L, McGrath JA, Uitto J. Mutation-based prenatal diagnosis of Herlitz junctional epidermolysis bullosa. Prenatal Diagnosis. 17: 343-54. PMID 9160387 DOI: 10.1002/(SICI)1097-0223(199704)17:4<343::AID-PD73>3.0.CO;2-7  0.4
1997 Darling TN, McGrath JA, Yee C, Gatalica B, Hametner R, Bauer JW, Pohla-Gubo G, Christiano AM, Uitto J, Hintner H, Yancey KB. Premature termination codons are present on both alleles of the bullous pemphigoid antigen 2/ Type XVII collagen gene in five Austrian families with generalized atrophic benign epidermolysis bullosa Journal of Investigative Dermatology. 108: 463-468. PMID 9077475 DOI: 10.1111/1523-1747.ep12289718  0.4
1997 McGrath JA, Hawk JL, Graham RM, Christiano AM. Lack of the R59W South African founder effect mutation in protoporphyrinogen oxidase in a British patient with homozygous variegate porphyria. The British Journal of Dermatology. 136: 292. PMID 9068758 DOI: 10.1111/j.1365-2133.1997.tb14923.x  0.4
1997 Lam H, Dragan L, Tsou HC, Merk H, Peacocke M, Goerz G, Sassa S, Poh-Fitzpatrick M, Bickers DR, Christiano AM. Molecular basis of variegate porphyria: a de novo insertion mutation in the protoporphyrinogen oxidase gene. Human Genetics. 99: 126-9. PMID 9003509 DOI: 10.1007/s004390050325  0.32
1996 Kivirikko S, McGrath JA, Pulkkinen L, Uitto J, Christiano AM. Mutational hotspots in the LAMB3 gene in the lethal (Herlitz) type of junctional epidermolysis bullosa. Human Molecular Genetics. 5: 231-7. PMID 8824879 DOI: 10.1093/hmg/5.2.231  0.4
1996 Dunnill MG, McGrath JA, Richards AJ, Christiano AM, Uitto J, Pope FM, Eady RA. Clinicopathological correlations of compound heterozygous COL7A1 mutations in recessive dystrophic epidermolysis bullosa. The Journal of Investigative Dermatology. 107: 171-7. PMID 8757758 DOI: 10.1111/1523-1747.ep12329570  0.4
1996 McLean WH, Pulkkinen L, Smith FJ, Rugg EL, Lane EB, Bullrich F, Burgeson RE, Amano S, Hudson DL, Owaribe K, McGrath JA, McMillan JR, Eady RA, Leigh IM, Christiano AM, et al. Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization. Genes & Development. 10: 1724-35. PMID 8698233 DOI: 10.1101/gad.10.14.1724  0.4
1996 Maestrini E, Monaco AP, McGrath JA, Ishida-Yamamoto A, Camisa C, Hovnanian A, Weeks DE, Lathrop M, Uitto J, Christiano AM. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Nature Genetics. 13: 70-7. PMID 8673107 DOI: 10.1038/ng0596-70  0.4
1996 McGarth JA, Christiano AM, Pulkkinen L, Eady RA, Uitto J. Compound heterozygosity for nonsense ans missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosa. The Journal of Investigative Dermatology. 106: 1157-9. PMID 8618058 DOI: 10.1111/1523-1747.ep12340210  0.4
1996 McGrath JA, Kivirikko S, Ciatti S, Moss C, Christiano AM, Uitto J. A recurrent homozygous nonsense mutation within the LAMA3 gene as a cause of Herlitz junctional epidermolysis bullosa in patients of Pakistani ancestry: evidence for a founder effect. The Journal of Investigative Dermatology. 106: 781-4. PMID 8618022 DOI: 10.1111/1523-1747.ep12346349  0.4
1996 Christiano AM, McGrath JA, Uitto J. Influence of the second COL7A1 mutation in determining the phenotypic severity of recessive dystrophic epidermolysis bullosa. The Journal of Investigative Dermatology. 106: 766-70. PMID 8618018 DOI: 10.1111/1523-1747.ep12345814  0.4
1996 Christiano AM, D'Alessio M, Paradisi M, Angelo C, Mazzanti C, Puddu P, Uitto J. A Common Insertion Mutation in COL7A1 in Two Italian Families with Recessive Dystrophie Epidermolysis Bullosa Journal of Investigative Dermatology. 106: 679-684. PMID 8618004 DOI: 10.1111/1523-1747.ep12345508  0.4
1996 Shimizu H, McGrath JA, Christiano AM, Nishikawa T, Uitto J. Molecular basis of recessive dystrophic epidermolysis bullosa: Genotype/phenotype correlation in a case of moderate clinical severity Journal of Investigative Dermatology. 106: 119-124. PMID 8592061 DOI: 10.1111/1523-1747.ep12329600  0.4
1995 Mauch JC, Sandberg LB, Roos PJ, Jimenez F, Christiano AM, Deak SB, Boyd CD. Extensive alternate exon usage at the 5' end of the sheep tropoelastin gene. Matrix Biology : Journal of the International Society For Matrix Biology. 14: 635-41. PMID 9057813 DOI: 10.1016/S0945-053X(05)80027-7  0.4
1995 Marinkovich MP, Meneguzzi G, Burgeson RE, Blanchet-Bardon C, Holbrook KA, Smith LT, Christiano AM, Ortonne JP. Prenatal diagnosis of Herlitz junctional epidermolysis bullosa by amniocentesis. Prenatal Diagnosis. 15: 1027-34. PMID 8606881 DOI: 10.1002/pd.1970151107  0.4
1995 Olson TM, Michels VV, Urban Z, Csiszar K, Christiano AM, Driscoll DJ, Feldt RH, Boyd CD, Thibodeau SN. A 30 kb deletion within the elastin gene results in familial supravalvular aortic stenosis. Human Molecular Genetics. 4: 1677-9. PMID 8541862 DOI: 10.1093/hmg/4.9.1677  0.4
1995 Pulkkinen L, Gerecke DR, Christiano AM, Wagman DW, Burgeson RE, Uitto J. Cloning of the beta 3 chain gene (LAMB3) of human laminin 5, a candidate gene in junctional epidermolysis bullosa. Genomics. 25: 192-8. PMID 7774918 DOI: 10.1016/0888-7543(95)80125-6  0.4
1995 Pulkkinen L, McGrath JA, Christiano AM, Uitto J. Detection of sequence variants in the gene encoding the β3 chain of laminin 5 (LAMB3) Human Mutation. 6: 77-84. PMID 7550237 DOI: 10.1002/humu.1380060115  0.4
1995 Anton-Lamprecht I, McGrath JA, Christiano AM, Uitto J. Mutations in the laminin 5 LAMB3 gene in generalized atrophic benign epidermolysis bullosa [3] Journal of Investigative Dermatology. 105: 856-857. PMID 7490484 DOI: 10.1111/1523-1747.ep12326697  0.4
1994 Lebwohl M, Neldner K, Pope FM, De Paepe A, Christiano AM, Boyd CD, Uitto J, McKusick VA. Classification of pseudoxanthoma elasticum: report of a consensus conference. Journal of the American Academy of Dermatology. 30: 103-7. PMID 8277008 DOI: 10.1016/S0190-9622(08)81894-4  0.4
1994 Pulkkinen L, Christiano AM, Gerecke D, Wagman DW, Burgeson RE, Pittelkow MR, Uitto J. A homozygous nonsense mutation in the beta 3 chain gene of laminin 5 (LAMB3) in Herlitz junctional epidermolysis bullosa. Genomics. 24: 357-60. PMID 7698759 DOI: 10.1006/geno.1994.1627  0.4
1993 Lapiere JC, Woodley DT, Parente MG, Iwasaki T, Wynn KC, Christiano AM, Uitto J. Epitope mapping of type VII collagen. Identification of discrete peptide sequences recognized by sera from patients with acquired epidermolysis bullosa. The Journal of Clinical Investigation. 92: 1831-9. PMID 7691888 DOI: 10.1172/JCI116774  0.4
1992 Ryynänen J, Sollberg S, Parente MG, Chung LC, Christiano AM, Uitto J. Type VII collagen gene expression by cultured human cells and in fetal skin. Abundant mRNA and protein levels in epidermal keratinocytes. The Journal of Clinical Investigation. 89: 163-8. PMID 1729268 DOI: 10.1172/JCI115557  0.4
1992 Christiano AM, Lebwohl MG, Boyd CD, Uitto J. Workshop on pseudoxanthoma elasticum: Molecular biology and pathology of the elastic fibers. Jefferson Medical College, Philadelphia, Pennsylvania, June 10, 1992 Journal of Investigative Dermatology. 99: 660-663. PMID 1431233 DOI: 10.1111/1523-1747.ep12668156  0.4
1991 Tromp G, Christiano A, Goldstein N, Indik Z, Boyd C, Rosenbloom J, Deak S, Prockop D, Kuivaniemi H. A to G polymorphism in ELN gene Nucleic Acids Research. 19: 4314. PMID 1871001 DOI: 10.1093/nar/19.15.4314-a  0.4
1991 Uitto J, Christiano AM, Kahari VM, Bashir MM, Rosenbloom J. Molecular biology and pathology of human elastin Biochemical Society Transactions. 19: 824-829. PMID 1794566 DOI: 10.1042/bst0190824  0.4
1991 Boyd CD, Christiano AM, Pierce RA, Stolle CA, Deak SB. Mammalian tropoelastin: Multiple domains of the protein define an evolutionarily divergent amino acid sequence Matrix. 11: 235-241. PMID 1656173 DOI: 10.1016/S0934-8832(11)80230-1  0.4
1987 Bowcock AM, Hebert JM, Christiano AM, Wijsman E, Cavalli-Sforza LL, Boyd CD. The pro alpha 1 (Iv) collagen gene is linked to the d13s3 locus at the distal end of human chromosome 13q Cytogenetic and Genome Research. 45: 234-236. PMID 2891465 DOI: 10.1159/000132460  0.4
1986 Boyd CD, Weliky K, Toth-Fejel S, Deak SB, Christiano AM, Mackenzie JW, Sandell LJ, Tryggvason K, Magenis E. The single copy gene coding for human α1 (IV) procollagen is located at the terminal end of the long arm of chromosome 13 Human Genetics. 74: 121-125. PMID 3770740 DOI: 10.1007/BF00282074  0.4
Show low-probability matches.