-
1
-
-
0027241314
-
Alopecia universalis as a single abnormality in an inbred Pakistani kindred
-
Ahmad M., Abbas H., Ul Haque S. Alopecia universalis as a single abnormality in an inbred Pakistani kindred. Am. J. Med. Genet. 46:1993;369-371.
-
(1993)
Am. J. Med. Genet.
, vol.46
, pp. 369-371
-
-
Ahmad, M.1
Abbas, H.2
Ul Haque, S.3
-
2
-
-
6844265562
-
Alopecia universalis associated with a mutation in the human hairless gene
-
Ahmad W., Ul Haque M. F., Brancolini V., Tsou H. C., Ul Haque S., Lam H., Aita V. M., Owen J., deBlaquiere M., Frank J., Cserhalmi-Friedman P. B., Leask A., McGrath J. A., Peacocke M., Ahmad M., Ott J., Christiano A. M. Alopecia universalis associated with a mutation in the human hairless gene. Science. 279:1998a;720-724.
-
(1998)
Science
, vol.279
, pp. 720-724
-
-
Ahmad, W.1
Ul Haque, M.F.2
Brancolini, V.3
Tsou, H.C.4
Ul Haque, S.5
Lam, H.6
Aita, V.M.7
Owen, J.8
Deblaquiere, M.9
Frank, J.10
Cserhalmi-Friedman, P.B.11
Leask, A.12
McGrath, J.A.13
Peacocke, M.14
Ahmad, M.15
Ott, J.16
Christiano, A.M.17
-
3
-
-
0032231885
-
A missense mutation in the zinc-finger domain of the human hairless gene underlines congenital atrichia in a family of Irish travelers
-
Ahmad W., Irvine A. D., Lam H., Buckley C., Bingham E. A., Panteleyev A. A., Ahmad M., McGrath J. A., Christiano A. M. A missense mutation in the zinc-finger domain of the human hairless gene underlines congenital atrichia in a family of Irish travelers. Am. J. Hum. Genet. 63:1998b;984-991.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 984-991
-
-
Ahmad, W.1
Irvine, A.D.2
Lam, H.3
Buckley, C.4
Bingham, E.A.5
Panteleyev, A.A.6
Ahmad, M.7
McGrath, J.A.8
Christiano, A.M.9
-
6
-
-
0028031305
-
Structure and expression of the hairless gene of mice
-
Cachon-Gonzalez M. B., Fenner S., Coffin J. M., Moran C., Best S., Stoye J. P. Structure and expression of the hairless gene of mice. Proc. Natl. Acad. Sci. USA. 91:1994;7717-7721.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 7717-7721
-
-
Cachon-Gonzalez, M.B.1
Fenner, S.2
Coffin, J.M.3
Moran, C.4
Best, S.5
Stoye, J.P.6
-
7
-
-
0018879771
-
Autosomal recessive inheritance of atrichia congenita
-
Cantu J. M., Sanchez-Corona J., Gonzalez-Mendoza A., Martinez Y., Martinez R., Garcia-Cruz D. Autosomal recessive inheritance of atrichia congenita. Clin. Genet. 17:1980;209-212.
-
(1980)
Clin. Genet.
, vol.17
, pp. 209-212
-
-
Cantu, J.M.1
Sanchez-Corona, J.2
Gonzalez-Mendoza, A.3
Martinez, Y.4
Martinez, R.5
Garcia-Cruz, D.6
-
8
-
-
0025313294
-
Label retaining cells reside in the bulge area of pilosebaceous unit: Implications for follicular stem cells, hair cycle, and skin carcinogenesis
-
Costarelis G., Sun T.-T., Lavker R. M. Label retaining cells reside in the bulge area of pilosebaceous unit: Implications for follicular stem cells, hair cycle, and skin carcinogenesis. Cell. 61:1990;1329-1337.
-
(1990)
Cell
, vol.61
, pp. 1329-1337
-
-
Costarelis, G.1
Sun, T.-T.2
Lavker, R.M.3
-
9
-
-
0001004631
-
Zur kenntnis der kongenitale hypotrichosis
-
Fredrich H. C. Zur kenntnis der kongenitale hypotrichosis. Dermatol. Wochenschr. 121:1950;408-410.
-
(1950)
Dermatol. Wochenschr.
, vol.121
, pp. 408-410
-
-
Fredrich, H.C.1
-
10
-
-
0026571418
-
The secret life of the hair follicle
-
Hardy M. The secret life of the hair follicle. Trends Genet. 8:1992;55-61.
-
(1992)
Trends Genet.
, vol.8
, pp. 55-61
-
-
Hardy, M.1
-
11
-
-
0030986236
-
A signature motif in transcriptional co-activators mediates binding to nuclear receptors
-
Heery D. M., Kalkhoven E., Hoare S., Parker M. G. A signature motif in transcriptional co-activators mediates binding to nuclear receptors. Nature. 387:1997;733-736.
-
(1997)
Nature
, vol.387
, pp. 733-736
-
-
Heery, D.M.1
Kalkhoven, E.2
Hoare, S.3
Parker, M.G.4
-
12
-
-
0025790483
-
Analysis of a murine male germ cell-specific transcript that encodes a putative zinc finger protein
-
Hoog C., Schalling M., Grunder-Brundell E., Daneholt B. Analysis of a murine male germ cell-specific transcript that encodes a putative zinc finger protein. Mol. Reprod. Dev. 30:1991;173-181.
-
(1991)
Mol. Reprod. Dev.
, vol.30
, pp. 173-181
-
-
Hoog, C.1
Schalling, M.2
Grunder-Brundell, E.3
Daneholt, B.4
-
13
-
-
0008912369
-
Ein beitrag zur hypotrichosis congenita
-
Landes E., Langer I. Ein beitrag zur hypotrichosis congenita. Hautzart. 7:1956;413-415.
-
(1956)
Hautzart
, vol.7
, pp. 413-415
-
-
Landes, E.1
Langer, I.2
-
14
-
-
0028876893
-
Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor
-
Lee J. W., Choi H.-S., Gyuris J., Brent R., Moore D. D. Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor. Mol. Endocrinol. 9:1995;243-254.
-
(1995)
Mol. Endocrinol.
, vol.9
, pp. 243-254
-
-
Lee, J.W.1
Choi, H.-S.2
Gyuris, J.3
Brent, R.4
Moore, D.D.5
-
15
-
-
0029835707
-
Defects in RNA splicing and the consequence of shortened translational reading frames
-
Maquat L. E. Defects in RNA splicing and the consequence of shortened translational reading frames. Am. J. Hum. Genet. 59:1996;279-286.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 279-286
-
-
Maquat, L.E.1
-
16
-
-
0002720466
-
The skin of hairless mice. The formation of cysts and the distribution of lipids
-
Montagna W., Chase H. B., Melaragno H. P. The skin of hairless mice. The formation of cysts and the distribution of lipids. J. Invest. Dermatol. 19:1952;83-94.
-
(1952)
J. Invest. Dermatol.
, vol.19
, pp. 83-94
-
-
Montagna, W.1
Chase, H.B.2
Melaragno, H.P.3
-
17
-
-
17344370417
-
A gene for autosomal congenital alopecia maps to chromosome 8p21-22
-
Nothen M. M., Cichon S., Vogt I. R., Hemmer S., Kruse R., Knapp M., Holler T., Ul Haque M. F., Ul Haque S., Propping P., Ahmad M., Rietschel M. A gene for autosomal congenital alopecia maps to chromosome 8p21-22. Am. J. Hum. Genet. 62:1998;386-390.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 386-390
-
-
Nothen, M.M.1
Cichon, S.2
Vogt, I.R.3
Hemmer, S.4
Kruse, R.5
Knapp, M.6
Holler, T.7
Ul Haque, M.F.8
Ul Haque, S.9
Propping, P.10
Ahmad, M.11
Rietschel, M.12
-
19
-
-
0031808638
-
Towards defining the pathogenesis of the hairless phenotype
-
Panteleyev A. A., van der Veen C., Rosenbach T., Muller-Rover S., Sokolov V. E., Paus R. Towards defining the pathogenesis of the hairless phenotype. J. Invest. Dermatol. 110:1998b;903-907.
-
(1998)
J. Invest. Dermatol.
, vol.110
, pp. 903-907
-
-
Panteleyev, A.A.1
Van Der Veen, C.2
Rosenbach, T.3
Muller-Rover, S.4
Sokolov, V.E.5
Paus, R.6
-
20
-
-
0000436267
-
Pathobiology of the hairless phenotype: Dysregulation of hair follicle apoptosis and topobiology during the initiation of follicle cycling
-
Panteleyev A. A., Botchkareva N. V., van der Veen C., Christiano A. M., Paus R. Pathobiology of the hairless phenotype: Dysregulation of hair follicle apoptosis and topobiology during the initiation of follicle cycling. J. Invest. Dermatol. 110:1998c.
-
(1998)
J. Invest. Dermatol.
, vol.110
-
-
Panteleyev, A.A.1
Botchkareva, N.V.2
Van Der Veen, C.3
Christiano, A.M.4
Paus, R.5
-
21
-
-
0031763056
-
Molecular and functional aspects of the hairless (hr
-
Panteleyev A. A., Paus R., Ahmad W., Sundberg J. P., Christiano A. M. Molecular and functional aspects of the hairless (hr. Exp. Dermatol. 7:1998d;249-267.
-
(1998)
Exp. Dermatol.
, vol.7
, pp. 249-267
-
-
Panteleyev, A.A.1
Paus, R.2
Ahmad, W.3
Sundberg, J.P.4
Christiano, A.M.5
-
22
-
-
0028267236
-
Location of stem cells in human hair follicles by clonal analysis
-
Rochat A., Kobayashi K., Barrandon Y. Location of stem cells in human hair follicles by clonal analysis. Cell. 76:1994;1063-1073.
-
(1994)
Cell
, vol.76
, pp. 1063-1073
-
-
Rochat, A.1
Kobayashi, K.2
Barrandon, Y.3
-
25
-
-
0001474913
-
Hairless mouse, HRS/J hr/hr
-
T. C. Jones, U. Mohr, & R. D. Hunt. Heidelberg: Springer-Verlag
-
Sundberg J. P., Dunstan R. W., Compton J. G. Hairless mouse, HRS/J hr/hr. Jones T. C., Mohr U., Hunt R. D. Monographs on Pathology of Laboratory Animals. Integument and Mammary Glands. 1989;192-197 Springer-Verlag, Heidelberg.
-
(1989)
Monographs on Pathology of Laboratory Animals. Integument and Mammary Glands
, pp. 192-197
-
-
Sundberg, J.P.1
Dunstan, R.W.2
Compton, J.G.3
-
26
-
-
0029848197
-
Thyroid hormone-responsive genes in developing cerebellum include a novel synaptotagmin and a hairless homolog
-
Thompson C. C. Thyroid hormone-responsive genes in developing cerebellum include a novel synaptotagmin and a hairless homolog. J. Neurosci. 16:1996;7832-7840.
-
(1996)
J. Neurosci.
, vol.16
, pp. 7832-7840
-
-
Thompson, C.C.1
-
27
-
-
0030737945
-
The product of a thyroid hormone-responsive gene interacts with thyroid hormone receptors
-
Thompson C. C., Bottcher M. C. The product of a thyroid hormone-responsive gene interacts with thyroid hormone receptors. Proc. Natl. Acad. Sci. USA. 94:1997;8527-8532.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 8527-8532
-
-
Thompson, C.C.1
Bottcher, M.C.2
-
28
-
-
0031723522
-
Congenital atrichia in five Arab Palestinian families resulting in a mutation in the human hairless gene
-
Zlotogorski A., Ahmad W., Christiano A. M. Congenital atrichia in five Arab Palestinian families resulting in a mutation in the human hairless gene. Hum. Genet. 103:1998;400-404.
-
(1998)
Hum. Genet.
, vol.103
, pp. 400-404
-
-
Zlotogorski, A.1
Ahmad, W.2
Christiano, A.M.3
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