| 1 |
URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 1958).
|
| 2 |
Minoxidil FDA Label
|
| 3 |
Norepinephrine FDA Label
|
| 4 |
ClinicalTrials.gov (NCT03732807) PF-06651600 for the Treatment of Alopecia Areata (ALLEGRO-2b/3). U.S. National Institutes of Health.
|
| 5 |
ClinicalTrials.gov (NCT01359943) Efficacy, Safety and Tolerability of Secukinumab in Patients With Rheumatoid Arthritis Taking Methotrexate
|
| 6 |
Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
|
| 7 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800014482)
|
| 8 |
ClinicalTrials.gov (NCT03742518) A Study Evaluating the Efficacy and Safety of SM04554 Topical Solution in Male Subjects With Androgenetic Alopecia. U.S. National Institutes of Health.
|
| 9 |
ClinicalTrials.gov (NCT03946449) Study of ARO-AAT in Patients With Alpha-1 Antitrypsin Deficiency Associated Liver Disease (AATD). U.S. National Institutes of Health.
|
| 10 |
ClinicalTrials.gov (NCT01289574) Topical ASC-J9 Cream for Acne. U.S. National Institutes of Health.
|
| 11 |
ClinicalTrials.gov (NCT03594227) ATI-501 Oral Suspension Compared to Placebo in Subjects With Alopecia Areata, Alopecia Universalis or Alopecia Totalis. U.S. National Institutes of Health.
|
| 12 |
ClinicalTrials.gov (NCT03759340) ATI-502 Topical Solution for the Treatment of Alopecia Areata (AA), Alopecia Universalis (AU) and Alopecia Totalis (AT). U.S. National Institutes of Health.
|
| 13 |
ClinicalTrials.gov (NCT02590289) A Pharmacokinetic Study to Evaluate BBI-5000 Capsules and Food Effect in Healthy Adult Subjects. U.S. National Institutes of Health.
|
| 14 |
ClinicalTrials.gov (NCT03898479) Extension Study to Evaluate Safety and Efficacy of CTP-543 in Adults With Alopecia Areata. U.S. National Institutes of Health.
|
| 15 |
ClinicalTrials.gov (NCT03351322) ENERGI-F701 for Female Hair Loss Treatment. U.S. National Institutes of Health.
|
| 16 |
ClinicalTrials.gov (NCT00471510) Dose-Ranging Efficacy Study of Topical NEOSH101 to Treat Male Pattern Hair Loss. U.S. National Institutes of Health.
|
| 17 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800030641)
|
| 18 |
Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
|
| 19 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800025646)
|
| 20 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800019469)
|
| 21 |
Novel monoamine oxidase inhibitors: a patent review (2012 - 2014).Expert Opin Ther Pat. 2015 Jan;25(1):91-110.
|
| 22 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800005942)
|
| 23 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800013642)
|
| 24 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800028305)
|
| 25 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800009674)
|
| 26 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800008114)
|
| 27 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800007694)
|
| 28 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800008867)
|
| 29 |
Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800002834)
|
| 30 |
The ChEMBL database in 2017. Nucleic Acids Res. 2017 Jan 4;45(D1):D945-D954.
|
| 31 |
Targeting of CXXC5 by a Competing PeptideStimulates Hair Regrowth and Wound-Induced Hair Neogenesis.J Invest Dermatol. 2017 Nov;137(11):2260-2269. doi: 10.1016/j.jid.2017.04.038. Epub 2017 Jun 6.
|
| 32 |
Genetic prediction of male pattern baldness.PLoS Genet. 2017 Feb 14;13(2):e1006594. doi: 10.1371/journal.pgen.1006594. eCollection 2017 Feb.
|
| 33 |
PKA signaling drives reticularis differentiation and sexually dimorphic adrenal cortex renewal.JCI Insight. 2018 Jan 25;3(2):e98394. doi: 10.1172/jci.insight.98394. eCollection 2018 Jan 25.
|
| 34 |
Association of TLR4 (D299G, T399I), TLR9 -1486T>C, TIRAP S180L and TNF- promoter (-1031, -863, -857) polymorphisms with risk for systemic lupus erythematosus among South Indians.Lupus. 2015 Jan;24(1):50-7. doi: 10.1177/0961203314549792. Epub 2014 Sep 2.
|
| 35 |
Association of AHSG with alopecia and mental retardation (APMR) syndrome. Hum Genet. 2017 Mar;136(3):287-296. doi: 10.1007/s00439-016-1756-5. Epub 2017 Jan 4.
|
| 36 |
HLA-DRB1 polymorphisms and alopecia areata disease risk: A systematic review and meta-analysis.Medicine (Baltimore). 2018 Aug;97(32):e11790. doi: 10.1097/MD.0000000000011790.
|
| 37 |
Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome.Genet Med. 2019 Sep;21(9):2025-2035. doi: 10.1038/s41436-019-0445-x. Epub 2019 Feb 6.
|
| 38 |
Identification and Characterizations of Novel, Selective Histone Methyltransferase SET7 Inhibitors by Scaffold Hopping- and 2D-Molecular Fingerprint-Based Similarity Search.Molecules. 2018 Mar 2;23(3):567. doi: 10.3390/molecules23030567.
|
| 39 |
Quality of life in patients with limited (1-3) brain metastases undergoing stereotactic or whole brain radiotherapy : Aprospective study of the DEGRO QoL working group.Strahlenther Onkol. 2020 Jan;196(1):48-57. doi: 10.1007/s00066-019-01506-w. Epub 2019 Aug 15.
|
| 40 |
T Cell Leukemia/Lymphoma 1A is essential for mouse epidermal keratinocytes proliferation promoted by insulin-like growth factor 1.PLoS One. 2018 Oct 4;13(10):e0204775. doi: 10.1371/journal.pone.0204775. eCollection 2018.
|
| 41 |
Methotrexate (MTX) pathway gene polymorphisms and their effects on MTX toxicity in Caucasian and African American patients with rheumatoid arthritis. J Rheumatol. 2008 Apr;35(4):572-9.
|
| 42 |
Polymorphic CAG Repeat Numbers in the Androgen Receptor Gene of Female Pattern Hair Loss in a Han Chinese Population.Dermatology. 2016;232(4):464-7. doi: 10.1159/000446648. Epub 2016 Jun 16.
|
| 43 |
Inducible in vivo silencing of Brd4 identifies potential toxicities of sustained BET protein inhibition.Cell Rep. 2014 Sep 25;8(6):1919-1929. doi: 10.1016/j.celrep.2014.08.025. Epub 2014 Sep 18.
|
| 44 |
CRF receptor antagonist astressin-B reverses and prevents alopecia in CRF over-expressing mice.PLoS One. 2011 Feb 16;6(2):e16377. doi: 10.1371/journal.pone.0016377.
|
| 45 |
Genetic variant association of PTPN22, CTLA4, IL2RA, as well as HLA frequencies in susceptibility to alopecia areata.Immunol Invest. 2018 Oct;47(7):666-679. doi: 10.1080/08820139.2018.1480032. Epub 2018 Jul 6.
|
| 46 |
Inhibition of triglyceride synthesis as a treatment strategy for obesity: lessons from DGAT1-deficient mice.Arterioscler Thromb Vasc Biol. 2005 Mar;25(3):482-6. doi: 10.1161/01.ATV.0000151874.81059.ad. Epub 2004 Nov 29.
|
| 47 |
Dickkopf-1 Expression in Androgenetic Alopecia and Alopecia Areata in Male Patients.Am J Dermatopathol. 2019 Feb;41(2):122-127. doi: 10.1097/DAD.0000000000001266.
|
| 48 |
Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes: potential importance of selectivity over dipeptidyl peptidases 8 and 9.Diabetes. 2005 Oct;54(10):2988-94. doi: 10.2337/diabetes.54.10.2988.
|
| 49 |
Desmoglein 3 anchors telogen hair in the follicle.J Cell Sci. 1998 Sep;111 ( Pt 17):2529-37. doi: 10.1242/jcs.111.17.2529.
|
| 50 |
Reduced penetrance in a family with X-linked dominant chondrodysplasia punctata.Eur J Med Genet. 2007 Sep-Oct;50(5):392-8. doi: 10.1016/j.ejmg.2007.05.004. Epub 2007 Jun 3.
|
| 51 |
Mandibulofacial dysostosis, severe lower eyelid coloboma, cleft palate, and alopecia: A new distinct form of mandibulofacial dysostosis or a severe form of Johnson-McMillin syndrome?.Am J Med Genet A. 2010 Jul;152A(7):1838-40. doi: 10.1002/ajmg.a.33477.
|
| 52 |
CD80CD86 deficiency disrupts regulatory CD4+FoxP3+T cell homoeostasis and induces autoimmune-like alopecia.Exp Dermatol. 2017 Nov;26(11):1053-1059. doi: 10.1111/exd.13371. Epub 2017 Jul 3.
|
| 53 |
Novel application of layered expression scanning for proteomic profiling of plucked hair follicles.Dermatology. 2005;210(4):273-8. doi: 10.1159/000084750.
|
| 54 |
The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome.Mol Biol Cell. 2011 Dec;22(24):4776-86. doi: 10.1091/mbc.E11-09-0778. Epub 2011 Oct 26.
|
| 55 |
GPRC5D is a target for the immunotherapy of multiple myeloma with rationally designed CAR T cells. Sci Transl Med. 2019 Mar 27;11(485):eaau7746.
|
| 56 |
Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease. Brain. 2015 Aug;138(Pt 8):2347-58. doi: 10.1093/brain/awv155. Epub 2015 Jun 10.
|
| 57 |
Single nucleotide polymorphisms in the promoter regions of Foxp3 and ICOSLG genes are associated with Alopecia areata.Clin Exp Med. 2014 Feb;14(1):91-7. doi: 10.1007/s10238-012-0224-3. Epub 2012 Nov 30.
|
| 58 |
Interleukin (IL) 31 induces in cynomolgus monkeys a rapid and intense itch response that can be inhibited by an IL-31 neutralizing antibody.J Eur Acad Dermatol Venereol. 2017 Jan;31(1):142-150. doi: 10.1111/jdv.13794. Epub 2016 Aug 8.
|
| 59 |
Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability.Eur J Hum Genet. 2016 Aug;24(8):1223-7. doi: 10.1038/ejhg.2015.260. Epub 2015 Dec 23.
|
| 60 |
Serum androgens and prostate-specific antigen levels in androgenetic alopecia: is there a difference between frontal and vertex baldness?.J Eur Acad Dermatol Venereol. 2018 Oct;32(10):1815-1818. doi: 10.1111/jdv.14758. Epub 2018 Jan 12.
|
| 61 |
A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia.Arch Dermatol Res. 2015 Nov;307(9):793-801. doi: 10.1007/s00403-015-1590-y. Epub 2015 Jul 7.
|
| 62 |
The -2T/C polymorphism in the adrenocorticotropin receptor gene affects stress perception of patients with alopecia areata.Int J Dermatol. 2013 Apr;52(4):441-5. doi: 10.1111/j.1365-4632.2012.05749.x. Epub 2012 Dec 11.
|
| 63 |
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.Exp Dermatol. 2017 Jun;26(6):536-541. doi: 10.1111/exd.13123. Epub 2017 Mar 23.
|
| 64 |
Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population.Gene. 2013 Nov 1;530(1):109-12. doi: 10.1016/j.gene.2013.08.016. Epub 2013 Aug 14.
|
| 65 |
Genetic evidence for the involvement of NOTCH4 in rheumatoid arthritis and alopecia areata.Immunol Lett. 2013 Feb;150(1-2):130-3. doi: 10.1016/j.imlet.2013.01.002. Epub 2013 Jan 11.
|
| 66 |
Gain-of-function variants in the ODC1 gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities.Am J Med Genet A. 2018 Dec;176(12):2554-2560. doi: 10.1002/ajmg.a.60677. Epub 2018 Nov 26.
|
| 67 |
Inflammatory and age-related pathologies in mice with ectopic expression of human PARP-1.Mech Ageing Dev. 2010 Jun;131(6):389-404. doi: 10.1016/j.mad.2010.05.005. Epub 2010 Jun 8.
|
| 68 |
Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.Nat Genet. 2019 Oct;51(10):1438-1441. doi: 10.1038/s41588-019-0498-4. Epub 2019 Sep 30.
|
| 69 |
Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA.J Med Genet. 2009 Feb;46(2):103-11. doi: 10.1136/jmg.2008.060905. Epub 2008 Oct 23.
|
| 70 |
Mapatumumab, an antibody targeting TRAIL-R1, in combination with paclitaxel and carboplatin in patients with advanced solid malignancies: results of a phase I and pharmacokinetic study.J Clin Oncol. 2009 Sep 10;27(26):4413-21. doi: 10.1200/JCO.2008.21.7422. Epub 2009 Aug 3.
|
| 71 |
Pharmacological Activation of Thermo-Transient Receptor Potential Vanilloid 3 Channels Inhibits Hair Growth by Inducing Cell Death of Hair Follicle Outer Root Sheath.J Pharmacol Exp Ther. 2019 Aug;370(2):299-307. doi: 10.1124/jpet.119.258087. Epub 2019 May 31.
|
| 72 |
A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients.Breast Cancer Res. 2013;15(5):R81. doi: 10.1186/bcr3475.
|
| 73 |
The sodium-dependent glucose cotransporter SLC5A11 as an autoimmune modifier gene in SLE.Tissue Antigens. 2008 Feb;71(2):114-26. doi: 10.1111/j.1399-0039.2007.00975.x. Epub 2007 Dec 6.
|
| 74 |
HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome.J Formos Med Assoc. 2019 Aug;118(8):1225-1231. doi: 10.1016/j.jfma.2019.04.013. Epub 2019 May 2.
|
| 75 |
Association of thiopurine methyltransferase status with azathioprine side effects in Chinese patients with systemic lupus erythematosus.Clin Rheumatol. 2014 Apr;33(4):499-503. doi: 10.1007/s10067-013-2441-x. Epub 2013 Dec 10.
|
| 76 |
Association of Autoimmune Regulator Gene Rs2075876 Variant, but Not Gene Expression with Alopecia Areata in Males: A Case-control Study.Immunol Invest. 2020 Feb;49(1-2):146-165. doi: 10.1080/08820139.2019.1671450. Epub 2019 Oct 11.
|
| 77 |
Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome.Clin Genet. 2016 Sep;90(3):263-9. doi: 10.1111/cge.12700. Epub 2016 Jan 19.
|
| 78 |
A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities.Arch Dermatol Res. 2012 Oct;304(8):679-81. doi: 10.1007/s00403-012-1244-2. Epub 2012 May 15.
|
| 79 |
Anti-SmD1 antibodies are associated with renal disorder, seizures, and pulmonary arterial hypertension in Chinese patients with active SLE.Sci Rep. 2017 Aug 8;7(1):7617. doi: 10.1038/s41598-017-08099-3.
|
| 80 |
Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs.Anim Genet. 2018 Aug;49(4):321-325. doi: 10.1111/age.12665. Epub 2018 Apr 19.
|
| 81 |
Risk of Depression after 5 Alpha Reductase Inhibitor Medication: Meta-Analysis.World J Mens Health. 2020 Oct;38(4):535-544. doi: 10.5534/wjmh.190046. Epub 2019 May 23.
|
| 82 |
Autophagy-related protein 12 associates with anti-apoptotic B cell lymphoma-2 to promote apoptosis in gentamicin-induced inner ear hair cell loss.Mol Med Rep. 2017 Jun;15(6):3819-3825. doi: 10.3892/mmr.2017.6458. Epub 2017 Apr 11.
|
| 83 |
Novel anti-aging gene NM_026333 contributes to proton-induced aging via NCX1-pathway.J Mol Cell Cardiol. 2018 Dec;125:174-184. doi: 10.1016/j.yjmcc.2018.10.021. Epub 2018 Oct 29.
|
| 84 |
Mechanical and Controlled PRP Injections in Patients Affected by Androgenetic Alopecia.J Vis Exp. 2018 Jan 27;(131):56406. doi: 10.3791/56406.
|
| 85 |
Cathepsin B as a potential cystatin M/E target in the mouse hair follicle.FASEB J. 2017 Oct;31(10):4286-4294. doi: 10.1096/fj.201700267R. Epub 2017 Jun 8.
|
| 86 |
Ectodysplasin-A2 induces apoptosis in cultured human hair follicle cells and promotes regression of hair follicles in mice.Biochem Biophys Res Commun. 2019 Dec 3;520(2):428-433. doi: 10.1016/j.bbrc.2019.10.031. Epub 2019 Oct 11.
|
| 87 |
Sox2 and FGF20 interact to regulate organ of Corti hair cell and supporting cell development in a spatially-graded manner.PLoS Genet. 2019 Jul 5;15(7):e1008254. doi: 10.1371/journal.pgen.1008254. eCollection 2019 Jul.
|
| 88 |
Zfp462 deficiency causes anxiety-like behaviors with excessive self-grooming in mice.Genes Brain Behav. 2017 Feb;16(2):296-307. doi: 10.1111/gbb.12339. Epub 2016 Oct 7.
|
| 89 |
Preclinical evidence that the PPAR modulator, N-Acetyl-GED-0507-34-Levo, may protect human hair follicle epithelial stem cells against lichen planopilaris-associated damage.J Eur Acad Dermatol Venereol. 2020 Apr;34(4):e195-e197. doi: 10.1111/jdv.16114. Epub 2020 Feb 5.
|
| 90 |
A second KRT71 allele in curly coated dogs.Anim Genet. 2019 Feb;50(1):97-100. doi: 10.1111/age.12743. Epub 2018 Nov 15.
|
| 91 |
Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families. Hum Genet. 2011 Apr;129(4):419-24. doi: 10.1007/s00439-010-0938-9. Epub 2010 Dec 28.
|
| 92 |
Disruption of Ninjurin1 Leads to Repetitive and Anxiety-Like Behaviors in Mice.Mol Neurobiol. 2017 Nov;54(9):7353-7368. doi: 10.1007/s12035-016-0207-6. Epub 2016 Nov 5.
|
| 93 |
Severe thiopurine-induced leukocytopenia and hair loss in Japanese patients with defective NUDT15 variant: Retrospective case-control study.J Dermatol. 2018 Oct;45(10):1160-1165. doi: 10.1111/1346-8138.14588. Epub 2018 Aug 13.
|
| 94 |
Abnormalities of hair structure and skin histology derived from CRISPR/Cas9-based knockout of phospholipase C-delta 1 in mice.J Transl Med. 2018 May 25;16(1):141. doi: 10.1186/s12967-018-1512-9.
|
| 95 |
A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions.Hum Genet. 2019 May;138(5):535-539. doi: 10.1007/s00439-019-02005-9. Epub 2019 Mar 29.
|
| 96 |
Alkaline Ceramidase 1 Protects Mice from Premature Hair Loss by Maintaining the Homeostasis of Hair Follicle Stem Cells.Stem Cell Reports. 2017 Nov 14;9(5):1488-1500. doi: 10.1016/j.stemcr.2017.09.015. Epub 2017 Oct 19.
|
| 97 |
Clinical evaluation of a novel fractional radiofrequency device for hair growth: Fractional radiofrequency for hair growth stimulation.Dermatol Ther. 2018 May;31(3):e12590. doi: 10.1111/dth.12590. Epub 2018 Jan 15.
|
| 98 |
Hyperlipidemia and cutaneous abnormalities in transgenic mice overexpressing human apolipoprotein C1.J Clin Invest. 1998 Jan 1;101(1):145-52. doi: 10.1172/JCI791.
|
| 99 |
Selective ablation of Ctip2/Bcl11b in epidermal keratinocytes triggers atopic dermatitis-like skin inflammatory responses in adult mice.PLoS One. 2012;7(12):e51262. doi: 10.1371/journal.pone.0051262. Epub 2012 Dec 20.
|
| 100 |
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.FASEB J. 2010 Sep;24(9):3416-26. doi: 10.1096/fj.10-155622. Epub 2010 May 6.
|
| 101 |
Zebrafish Models for the Mechanosensory Hair Cell Dysfunction in Usher Syndrome 3 Reveal That Clarin-1 Is an Essential Hair Bundle Protein.J Neurosci. 2015 Jul 15;35(28):10188-201. doi: 10.1523/JNEUROSCI.1096-15.2015.
|
| 102 |
CtBP1 overexpression in keratinocytes perturbs skin homeostasis.J Invest Dermatol. 2014 May;134(5):1323-1331. doi: 10.1038/jid.2013.504. Epub 2013 Nov 26.
|
| 103 |
Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss.Br J Dermatol. 2012 Jun;166(6):1314-8. doi: 10.1111/j.1365-2133.2012.10877.x.
|
| 104 |
Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia.PLoS One. 2018 Oct 29;13(10):e0205775. doi: 10.1371/journal.pone.0205775. eCollection 2018.
|
| 105 |
Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata.Int J Immunogenet. 2006 Dec;33(6):393-5. doi: 10.1111/j.1744-313X.2006.00633.x.
|
| 106 |
Increased pachyonychia congenita severity in patients with concurrent keratin and filaggrin mutations.Br J Dermatol. 2009 Dec;161(6):1391-5. doi: 10.1111/j.1365-2133.2009.09471.x. Epub 2009 Sep 28.
|
| 107 |
De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature.Eur J Med Genet. 2012 Feb;55(2):117-9. doi: 10.1016/j.ejmg.2011.11.004. Epub 2011 Dec 2.
|
| 108 |
Genomic imprinting: an obsession with depilatory mice.Curr Biol. 2011 Apr 12;21(7):R257-9. doi: 10.1016/j.cub.2011.02.027.
|
| 109 |
Genetic association of HLA-DQB1 and HLA-DRB1 polymorphisms with alopecia areata in the Italian population.Br J Dermatol. 2011 Oct;165(4):823-7. doi: 10.1111/j.1365-2133.2011.10466.x. Epub 2011 Sep 15.
|
| 110 |
Genetic analysis of the interleukin-1 receptor antagonist and its homologue IL-1L1 in alopecia areata: strong severity association and possible gene interaction.Eur J Immunogenet. 2002 Feb;29(1):25-30. doi: 10.1046/j.1365-2370.2002.00271.x.
|
| 111 |
Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A LIPH mutation.Br J Dermatol. 2017 Jan;176(1):138-144. doi: 10.1111/bjd.14836. Epub 2016 Dec 19.
|
| 112 |
Novel MBTPS2 missense mutation causes a keratosis follicularis spinulosa decalvans phenotype: mutation update and review of the literature.Clin Exp Dermatol. 2016 Oct;41(7):757-60. doi: 10.1111/ced.12889.
|
| 113 |
Structure and polymorphism of the human gene for the interferon-induced p78 protein (MX1): evidence of association with alopecia areata in the Down syndrome region.Hum Genet. 2000 Jun;106(6):639-45. doi: 10.1007/s004390000318.
|
| 114 |
The human orthologue of murine Mpzl3 with predicted adhesive and immune functions is a potential candidate gene for immune-related hereditary hair loss.Exp Dermatol. 2009 Mar;18(3):261-3. doi: 10.1111/j.1600-0625.2008.00797.x. Epub 2008 Oct 22.
|
| 115 |
Treatment and prevention of chemotherapy-induced alopecia with PTH-CBD, a collagen-targeted parathyroid hormone analog, in a non-depilated mouse model.Anticancer Drugs. 2014 Jan;25(1):30-8. doi: 10.1097/CAD.0b013e3283650bff.
|
| 116 |
Prevention of chemotherapy-induced alopecia by the anti-death FNK protein.Life Sci. 2008 Jan 16;82(3-4):218-25. doi: 10.1016/j.lfs.2007.11.011. Epub 2007 Dec 3.
|
| 117 |
The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata: A meta-analysis of case-control studies.Medicine (Baltimore). 2019 May;98(20):e15448. doi: 10.1097/MD.0000000000015448.
|
| 118 |
ANE syndrome caused by mutated RBM28 gene: a novel etiology of combined pituitary hormone deficiency.Eur J Endocrinol. 2010 Jun;162(6):1021-5. doi: 10.1530/EJE-10-0077. Epub 2010 Mar 15.
|
| 119 |
HLA-DQA1*0301-associated susceptibility for autoimmune polyglandular syndrome type II and III.Horm Metab Res. 2003 Feb;35(2):120-4. doi: 10.1055/s-2003-39059.
|
| 120 |
Risk genotypes in folate-dependent enzymes and their association with methotrexate-related side effects in rheumatoid arthritis.Arthritis Rheum. 2006 Feb;54(2):607-12. doi: 10.1002/art.21573.
|
| 121 |
Molecular and cellular basis of obsessive-compulsive disorder-like behaviors: emerging view from mouse models.Curr Opin Neurol. 2011 Apr;24(2):114-8. doi: 10.1097/WCO.0b013e32834451fb.
|
| 122 |
Novel STAMBP mutation and additional findings in an Arabic family.Am J Med Genet A. 2015 Apr;167A(4):805-9. doi: 10.1002/ajmg.a.36782. Epub 2015 Feb 18.
|
| 123 |
Disruption of Supv3L1 damages the skin and causes sarcopenia, loss of fat, and death.Mamm Genome. 2009 Feb;20(2):92-108. doi: 10.1007/s00335-008-9168-z. Epub 2009 Jan 15.
|
| 124 |
Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency.J Allergy Clin Immunol. 2014 Dec;134(6):1354-1364.e6. doi: 10.1016/j.jaci.2014.07.019. Epub 2014 Aug 28.
|
|
|
|
|
|
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