Literature DB >> 24361867

To grow or not to grow: hair morphogenesis and human genetic hair disorders.

Olivier Duverger1, Maria I Morasso2.   

Abstract

Mouse models have greatly helped in elucidating the molecular mechanisms involved in hair formation and regeneration. Recent publications have reviewed the genes involved in mouse hair development based on the phenotype of transgenic, knockout and mutant animal models. While much of this information has been instrumental in determining molecular aspects of human hair development and cycling, mice exhibit a specific pattern of hair morphogenesis and hair distribution throughout the body that cannot be directly correlated to human hair. In this mini-review, we discuss specific aspects of human hair follicle development and present an up-to-date summary of human genetic disorders associated with abnormalities in hair follicle morphogenesis, structure or regeneration. Published by Elsevier Ltd.

Entities:  

Keywords:  Alopecia; Genetic disorders; Hair follicle; Morphogenesis; Shaft differentiation

Mesh:

Year:  2013        PMID: 24361867      PMCID: PMC3988237          DOI: 10.1016/j.semcdb.2013.12.006

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  85 in total

1.  Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome.

Authors:  S Chavanas; C Bodemer; A Rochat; D Hamel-Teillac; M Ali; A D Irvine; J L Bonafé; J Wilkinson; A Taïeb; Y Barrandon; J I Harper; Y de Prost; A Hovnanian
Journal:  Nat Genet       Date:  2000-06       Impact factor: 38.330

2.  Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia.

Authors:  K Suzuki; D Hu; T Bustos; J Zlotogora; A Richieri-Costa; J A Helms; R A Spritz
Journal:  Nat Genet       Date:  2000-08       Impact factor: 38.330

3.  Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I.

Authors:  P Momeni; G Glöckner; O Schmidt; D von Holtum; B Albrecht; G Gillessen-Kaesbach; R Hennekam; P Meinecke; B Zabel; A Rosenthal; B Horsthemke; H J Lüdecke
Journal:  Nat Genet       Date:  2000-01       Impact factor: 38.330

4.  Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

Authors:  G McKoy; N Protonotarios; A Crosby; A Tsatsopoulou; A Anastasakis; A Coonar; M Norman; C Baboonian; S Jeffery; W J McKenna
Journal:  Lancet       Date:  2000-06-17       Impact factor: 79.321

5.  Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome.

Authors:  J Celli; P Duijf; B C Hamel; M Bamshad; B Kramer; A P Smits; R Newbury-Ecob; R C Hennekam; G Van Buggenhout; A van Haeringen; C G Woods; A J van Essen; R de Waal; G Vriend; D A Haber; A Yang; F McKeon; H G Brunner; H van Bokhoven
Journal:  Cell       Date:  1999-10-15       Impact factor: 41.582

6.  Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex.

Authors:  Sandra M Pasternack; Melanie Refke; Elham Paknia; Hans Christian Hennies; Thomas Franz; Niklas Schäfer; Alan Fryer; Maurice van Steensel; Elizabeth Sweeney; Miquel Just; Clemens Grimm; Roland Kruse; Carlos Ferrándiz; Markus M Nöthen; Utz Fischer; Regina C Betz
Journal:  Am J Hum Genet       Date:  2012-12-13       Impact factor: 11.025

Review 7.  Mesenchymal-epithelial interactions during hair follicle morphogenesis and cycling.

Authors:  Rachel Sennett; Michael Rendl
Journal:  Semin Cell Dev Biol       Date:  2012-08-31       Impact factor: 7.727

8.  Mutations in ANTXR1 cause GAPO syndrome.

Authors:  Viktor Stránecký; Alexander Hoischen; Hana Hartmannová; Maha S Zaki; Amit Chaudhary; Enrique Zudaire; Lenka Nosková; Veronika Barešová; Anna Přistoupilová; Kateřina Hodaňová; Jana Sovová; Helena Hůlková; Lenka Piherová; Jayne Y Hehir-Kwa; Deepthi de Silva; Manouri P Senanayake; Sameh Farrag; Jiří Zeman; Pavel Martásek; Alice Baxová; Hanan H Afifi; Brad St Croix; Han G Brunner; Samia Temtamy; Stanislav Kmoch
Journal:  Am J Hum Genet       Date:  2013-04-18       Impact factor: 11.025

9.  Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis.

Authors:  Gina M DeStefano; Katherine A Fantauzzo; Lynn Petukhova; Mazen Kurban; Marija Tadin-Strapps; Brynn Levy; Dorothy Warburton; Elizabeth T Cirulli; Yujun Han; Xiaoyun Sun; Yufeng Shen; Maryam Shirazi; Vaidehi Jobanputra; Rodrigo Cepeda-Valdes; Julio Cesar Salas-Alanis; Angela M Christiano
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-19       Impact factor: 11.205

10.  Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium.

Authors:  A Smahi; G Courtois; P Vabres; S Yamaoka; S Heuertz; A Munnich; A Israël; N S Heiss; S M Klauck; P Kioschis; S Wiemann; A Poustka; T Esposito; T Bardaro; F Gianfrancesco; A Ciccodicola; M D'Urso; H Woffendin; T Jakins; D Donnai; H Stewart; S J Kenwrick; S Aradhya; T Yamagata; M Levy; R A Lewis; D L Nelson
Journal:  Nature       Date:  2000-05-25       Impact factor: 49.962

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  19 in total

1.  Hair keratin mutations in tooth enamel increase dental decay risk.

Authors:  Olivier Duverger; Takahiro Ohara; John R Shaffer; Danielle Donahue; Patricia Zerfas; Andrew Dullnig; Christopher Crecelius; Elia Beniash; Mary L Marazita; Maria I Morasso
Journal:  J Clin Invest       Date:  2014-10-27       Impact factor: 14.808

Review 2.  Keratins as components of the enamel organic matrix.

Authors:  Olivier Duverger; Elia Beniash; Maria I Morasso
Journal:  Matrix Biol       Date:  2015-12-17       Impact factor: 11.583

3.  Whole blood transcriptome profiling identifies candidate genes associated with alopecia in male giant pandas (Ailuropoda melanoleuca).

Authors:  Haibo Shen; Caiwu Li; Ming He; Yan Huang; Jing Wang; Jing Luo; Minglei Wang; Bisong Yue; Xiuyue Zhang
Journal:  BMC Genomics       Date:  2022-04-12       Impact factor: 3.969

Review 4.  Generation and characterization of hair-bearing skin organoids from human pluripotent stem cells.

Authors:  Wouter H van der Valk; Sara A Serdy; CiCi Deakin; Jiyoon Lee; Jin Kim; Anh Phuong Le; Karl R Koehler
Journal:  Nat Protoc       Date:  2022-03-23       Impact factor: 17.021

5.  Foxp1 Regulates the Proliferation of Hair Follicle Stem Cells in Response to Oxidative Stress during Hair Cycling.

Authors:  Jianzhi Zhao; Hanjun Li; Rujiang Zhou; Gang Ma; Joseph D Dekker; Haley O Tucker; Zhengju Yao; Xizhi Guo
Journal:  PLoS One       Date:  2015-07-14       Impact factor: 3.240

6.  Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22.

Authors:  Shukai Yuan; Feifei Li; Qingyong Meng; Yiqiang Zhao; Lei Chen; Hongquan Zhang; Lixiang Xue; Xiuqing Zhang; Christopher Lengner; Zhengquan Yu
Journal:  PLoS Genet       Date:  2015-05-28       Impact factor: 5.917

7.  Integrated Analysis of the Roles of Long Noncoding RNA and Coding RNA Expression in Sheep (Ovis aries) Skin during Initiation of Secondary Hair Follicle.

Authors:  Yaojing Yue; Tingting Guo; Chao Yuan; Jianbin Liu; Jian Guo; Ruilin Feng; Chune Niu; Xiaoping Sun; Bohui Yang
Journal:  PLoS One       Date:  2016-06-08       Impact factor: 3.240

8.  A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits.

Authors:  Sunduimijid Bolormaa; Andrew A Swan; Paul Stothard; Majid Khansefid; Nasir Moghaddar; Naomi Duijvesteijn; Julius H J van der Werf; Hans D Daetwyler; Iona M MacLeod
Journal:  Genet Sel Evol       Date:  2021-07-08       Impact factor: 4.297

9.  Hair follicle characteristics as early marker of Type 2 Diabetes.

Authors:  J Jaime Miranda; Alvaro Taype-Rondan; Jose Carlos Tapia; Maria Gabriela Gastanadui-Gonzalez; Ricardo Roman-Carpio
Journal:  Med Hypotheses       Date:  2016-08-16       Impact factor: 4.411

10.  "Cold" X5 Hairlaser™ used to treat male androgenic alopecia and hair growth: an uncontrolled pilot study.

Authors:  Kenneth Blum; David Han; Margaret A Madigan; Raquel Lohmann; Eric R Braverman
Journal:  BMC Res Notes       Date:  2014-02-24
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