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Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease.
J Invest Dermatol. 2007 Nov;127(11):2539-43. doi: 10.1038/sj.jid.5700915. Epub 2007 Jun 21.
J Invest Dermatol. 2007.
PMID: 17581619
Free article.
Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata.
Pforr J, Blaumeiser B, Becker T, Freudenberg-Hua Y, Hanneken S, Eigelshoven S, Cuyt I, De Weert J, Lambert J, Kruse R, Nöthen MM, Betz RC.
Pforr J, et al.
Tissue Antigens. 2006 Jul;68(1):58-61. doi: 10.1111/j.1399-0039.2006.00598.x.
Tissue Antigens. 2006.
PMID: 16774540
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Identification of mutations in the human hairless gene in two new families with congenital atrichia.
Betz RC, Indelman M, Pforr J, Schreiner F, Bauer R, Bergman R, Lentze MJ, Nöthen MM, Cichon S, Sprecher E.
Betz RC, et al. Among authors: pforr j.
Arch Dermatol Res. 2007 Jun;299(3):157-61. doi: 10.1007/s00403-007-0747-8. Epub 2007 Mar 20.
Arch Dermatol Res. 2007.
PMID: 17372750
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A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp.
Dávalos NO, García-Vargas A, Pforr J, Dávalos IP, Picos-Cárdenas VJ, García-Cruz D, Kruse R, Figuera LE, Nöthen MM, Betz RC.
Dávalos NO, et al. Among authors: pforr j.
Br J Dermatol. 2005 Dec;153(6):1216-9. doi: 10.1111/j.1365-2133.2005.06958.x.
Br J Dermatol. 2005.
PMID: 16307662
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A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families.
Nahum S, Pasternack SM, Pforr J, Indelman M, Wollnik B, Bergman R, Nöthen MM, König A, Khamaysi Z, Betz RC, Sprecher E.
Nahum S, et al. Among authors: pforr j.
Arch Dermatol Res. 2009 Jun;301(5):391-3. doi: 10.1007/s00403-008-0903-9. Epub 2008 Sep 27.
Arch Dermatol Res. 2009.
PMID: 18820939
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Comprehensive comparison between azacytidine and decitabine treatment in an acute myeloid leukemia cell line.
Aumer T, Gremmelmaier CB, Runtsch LS, Pforr JC, Yeşiltaç GN, Kaiser S, Traube FR.
Aumer T, et al. Among authors: pforr jc.
Clin Epigenetics. 2022 Sep 11;14(1):113. doi: 10.1186/s13148-022-01329-0.
Clin Epigenetics. 2022.
PMID: 36089606
Free PMC article.
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Symptom Science: Omics Supports Common Biological Underpinnings Across Symptoms.
McCall MK, Stanfill AG, Skrovanek E, Pforr JR, Wesmiller SW, Conley YP.
McCall MK, et al. Among authors: pforr jr.
Biol Res Nurs. 2018 Mar;20(2):183-191. doi: 10.1177/1099800417751069. Epub 2018 Jan 11.
Biol Res Nurs. 2018.
PMID: 29325450
Free PMC article.
Review.
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