Literature DB >> 17095700

Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH.

Anastasiya Kazantseva1, Andrey Goltsov, Rena Zinchenko, Anastasia P Grigorenko, Anna V Abrukova, Yuri K Moliaka, Alexander G Kirillov, Zhiru Guo, Stephen Lyle, Evgeny K Ginter, Evgeny I Rogaev.   

Abstract

The molecular mechanisms controlling human hair growth and scalp hair loss are poorly understood. By screening about 350,000 individuals in two populations from the Volga-Ural region of Russia, we identified a gene mutation in families who show an inherited form of hair loss and a hair growth defect. Affected individuals were homozygous for a deletion in the LIPH gene on chromosome 3q27, caused by short interspersed nuclear element-retrotransposon-mediated recombination. The LIPH gene is expressed in hair follicles and encodes a phospholipase called lipase H (alternatively known as membrane-associated phosphatidic acid-selective phospholipase A1alpha), an enzyme that regulates the production of bioactive lipids. These results suggest that lipase H participates in hair growth and development.

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Year:  2006        PMID: 17095700     DOI: 10.1126/science.1133276

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  53 in total

1.  Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families.

Authors:  Naveed Wasif; Syed Kamran ul-Hassan Naqvi; Sulman Basit; Nadir Ali; Muhammad Ansar; Wasim Ahmad
Journal:  Hum Genet       Date:  2010-12-28       Impact factor: 4.132

2.  Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex.

Authors:  Maria-Teresa Romano; Aylar Tafazzoli; Maximilian Mattern; Sugirthan Sivalingam; Sabrina Wolf; Alexander Rupp; Holger Thiele; Janine Altmüller; Peter Nürnberg; Jürgen Ellwanger; Reto Gambon; Alessandra Baumer; Nicolai Kohlschmidt; Dieter Metze; Stefan Holdenrieder; Ralf Paus; Dieter Lütjohann; Jorge Frank; Matthias Geyer; Marta Bertolini; Pavlos Kokordelis; Regina C Betz
Journal:  Am J Hum Genet       Date:  2018-10-25       Impact factor: 11.025

3.  Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene.

Authors:  Yutaka Shimomura; Maria C Garzon; Leonard Kristal; Lawrence Shapiro; Angela M Christiano
Journal:  Exp Dermatol       Date:  2008-09-18       Impact factor: 3.960

4.  Isolation and culture of adult epithelial stem cells from human skin.

Authors:  Zhiru Guo; Kyle Draheim; Stephen Lyle
Journal:  J Vis Exp       Date:  2011-03-31       Impact factor: 1.355

5.  Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.

Authors:  Yutaka Shimomura; Muhammad Wajid; Lynn Petukhova; Mazen Kurban; Angela M Christiano
Journal:  Am J Hum Genet       Date:  2010-03-25       Impact factor: 11.025

6.  Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome.

Authors:  Huijun Wang; Aytaj Humbatova; Yuanxiang Liu; Wen Qin; Mingyang Lee; Nicole Cesarato; Fanny Kortüm; Sheetal Kumar; Maria Teresa Romano; Shangzhi Dai; Ran Mo; Sugirthan Sivalingam; Susanne Motameny; Yuan Wu; Xiaopeng Wang; Xinwu Niu; Songmei Geng; Dorothea Bornholdt; Peter M Kroisel; Gianluca Tadini; Scott D Walter; Fabian Hauck; Katta M Girisha; Anne-Marie Calza; Armand Bottani; Janine Altmüller; Andreas Buness; Shuxia Yang; Xiujuan Sun; Lin Ma; Kerstin Kutsche; Karl-Heinz Grzeschik; Regina C Betz; Zhimiao Lin
Journal:  Am J Hum Genet       Date:  2020-06-03       Impact factor: 11.025

7.  Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect.

Authors:  Elena A Bliznetz; Svetlana M Tverskaya; Rena A Zinchenko; Anna V Abrukova; Ekaterina N Savaskina; Maxim V Nikulin; Alexander G Kirillov; Evgeny K Ginter; Alexander V Polyakov
Journal:  Eur J Hum Genet       Date:  2009-01-28       Impact factor: 4.246

8.  Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3.

Authors:  Gul Naz; Ghazanfar Ali; Syed Kamran-ul-Hassan Naqvi; Zahid Azeem; Wasim Ahmad
Journal:  Hum Genet       Date:  2010-04       Impact factor: 4.132

9.  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 10.  Aiming drug discovery at lysophosphatidic acid targets.

Authors:  Gabor Tigyi
Journal:  Br J Pharmacol       Date:  2010-09       Impact factor: 8.739

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