173 related articles for article (PubMed ID: 24898506)
81. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.
Wen Y; Liu Y; Xu Y; Zhao Y; Hua R; Wang K; Sun M; Li Y; Yang S; Zhang XJ; Kruse R; Cichon S; Betz RC; Nöthen MM; van Steensel MA; van Geel M; Steijlen PM; Hohl D; Huber M; Dunnill GS; Kennedy C; Messenger A; Munro CS; Terrinoni A; Hovnanian A; Bodemer C; de Prost Y; Paller AS; Irvine AD; Sinclair R; Green J; Shang D; Liu Q; Luo Y; Jiang L; Chen HD; Lo WH; McLean WH; He CD; Zhang X
Nat Genet; 2009 Feb; 41(2):228-33. PubMed ID: 19122663
[TBL] [Abstract][Full Text] [Related]
82. Hereditary hypotrichosis (Marie-Unna type) (two cases).
Hutchinson PE; Wells RS
Proc R Soc Med; 1975 Aug; 68(8):534-5. PubMed ID: 1202498
[No Abstract] [Full Text] [Related]
83. Autosomal recessive inheritance of atrichia congenita.
Cantú JM; Sánchez-Corona J; González-Mendoza A; Martínez y Martínez R; García-Cruz D
Clin Genet; 1980; 17(3):209-12. PubMed ID: 7363508
[TBL] [Abstract][Full Text] [Related]
84. In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosis.
Raza SI; Muhammad D; Jan A; Ali RH; Hassan M; Ahmad W; Rashid S
PLoS One; 2014; 9(8):e104756. PubMed ID: 25119526
[TBL] [Abstract][Full Text] [Related]
85. 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
Arch Dermatol Res; 2009 Jun; 301(5):391-3. PubMed ID: 18820939
[TBL] [Abstract][Full Text] [Related]
86. Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan.
Takeichi T; Tanahashi K; Taki T; Kono M; Sugiura K; Akiyama M
Br J Dermatol; 2017 Jul; 177(1):290-292. PubMed ID: 27641630
[No Abstract] [Full Text] [Related]
87. The alopecias associated with vitamin D-dependent rickets type IIA and with hairless gene mutations: a comparative clinical, histologic, and immunohistochemical study.
Bergman R; Schein-Goldshmid R; Hochberg Z; Ben-Izhak O; Sprecher E
Arch Dermatol; 2005 Mar; 141(3):343-51. PubMed ID: 15781675
[TBL] [Abstract][Full Text] [Related]
88. Value of dermoscopy for the diagnosis of monilethrix.
Baltazard T; Dhaille F; Chaby G; Lok C
Dermatol Online J; 2017 Jul; 23(7):. PubMed ID: 29469711
[TBL] [Abstract][Full Text] [Related]
89. Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair.
Horev L; Tosti A; Rosen I; Hershko K; Vincenzi C; Nanova K; Mali A; Potikha T; Zlotogorski A
J Am Acad Dermatol; 2009 Nov; 61(5):813-8. PubMed ID: 19766349
[TBL] [Abstract][Full Text] [Related]
90. Buschke-Ollendorff syndrome due to a novel LEMD3 mutation - an unusual case of alopecia.
Darr-Foit S; Schliemann S; Schulz S; Elsner P
J Dtsch Dermatol Ges; 2018 Mar; 16(3):348-349. PubMed ID: 29465813
[No Abstract] [Full Text] [Related]
91. Evidence for pseudodominant inheritance of atrichia with papular lesions.
Zlotogorski A; Martinez-Mir A; Green J; Lamdagger H; Panteleyevdagger AA; Sinclair R; Christiano AM
J Invest Dermatol; 2002 May; 118(5):881-6. PubMed ID: 11982769
[TBL] [Abstract][Full Text] [Related]
92. The molecular genetics of keratin disorders.
Smith F
Am J Clin Dermatol; 2003; 4(5):347-64. PubMed ID: 12688839
[TBL] [Abstract][Full Text] [Related]
93. Inherited Hairlessness: A Case Study of Familial Congenital Atrichia.
Tunuguntla MN; Mathew B; Quadri A; Movva S; Raghavan P; Rajpal S; Parmar MP; M M
Cureus; 2023 Apr; 15(4):e37608. PubMed ID: 37197112
[TBL] [Abstract][Full Text] [Related]
94. A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair.
Tariq M; Azhar A; Baig SM; Dahl N; Klar J
Sci Rep; 2012; 2():730. PubMed ID: 23066499
[TBL] [Abstract][Full Text] [Related]
95. Frameshift Sequence Variants in the Human Lipase-H Gene Causing Hypotrichosis.
Mehmood S; Shah SH; Jan A; Younus M; Ahmad F; Ayub M; Ahmad W
Pediatr Dermatol; 2016; 33(1):e40-2. PubMed ID: 26645693
[TBL] [Abstract][Full Text] [Related]
96. Primary cicatricial alopecia: Other lymphocytic primary cicatricial alopecias and neutrophilic and mixed primary cicatricial alopecias.
Bolduc C; Sperling LC; Shapiro J
J Am Acad Dermatol; 2016 Dec; 75(6):1101-1117. PubMed ID: 27846945
[TBL] [Abstract][Full Text] [Related]
97. APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex.
Shimomura Y; Agalliu D; Vonica A; Luria V; Wajid M; Baumer A; Belli S; Petukhova L; Schinzel A; Brivanlou AH; Barres BA; Christiano AM
Nature; 2010 Apr; 464(7291):1043-7. PubMed ID: 20393562
[TBL] [Abstract][Full Text] [Related]
98. Identification of a novel locus for Marie Unna hereditary hypotrichosis to a 17.5 cM interval at 1p21.1-1q21.3.
Yang S; Gao M; Cui Y; Yan KL; Ren YQ; Zhang GL; Wang PG; Xiao FL; Du WH; Liang YH; Sun LD; Xu SJ; Huang W; Zhang XJ
J Invest Dermatol; 2005 Oct; 125(4):711-4. PubMed ID: 16185270
[TBL] [Abstract][Full Text] [Related]
99. Alopecia, palmoplantar keratoderma, skin fragility and follicular hyperkeratoses due to compound heterozygous mutations in desmoplakin.
Tekin B; Yucelten D; Liu L; McGrath JA
Australas J Dermatol; 2017 Feb; 58(1):e17-e19. PubMed ID: 26303123
[TBL] [Abstract][Full Text] [Related]
100. Novel compound heterozygous nonsense mutations in the hairless gene causing atrichia with papular lesions.
Ashoor GG; Greenstein RM; Lam H; Martinez-Mir A; Zlotogorski A; Christiano AM
J Dermatol Sci; 2005 Oct; 40(1):29-33. PubMed ID: 16023329
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
