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| Research lectures arranged in alphabetical order by the first surname listed |
|
Patterns
of creb and phospo-creb expression during murine hair follicle
development and cycling |
| Circadian
clock genes are expressed in human hair follicles M. Akram, S. Müller-Röver, J. Bull, C. Chronnell, I. McKay, M. Philpott, London, UK (F 6) |
| A
gene for hypotrichosis simplex of the scalp maps to chromosome
6p21.3 1R. Betz, 2Y-A. Lee, 3A. Bygum, 3F. Brandrup, 4A. Bernal, 4J. Toribio, 4J. Alvarez, 1G.Kukuk, 3H. Ibsen, 3H. Rasmussen, 5T.F. Wienker, 2A. Reis, 1P. Propping, 6R. Kruse, 1S. Cichon,1M. Nöthen, 1Bonn, 2Berlin, 6 Düsseldorf, Germany; 3Odense, Denmark; 4 Compostela, Spain (F 20) |
| Histopathology
features of a canine syndrome characterised by alopecia and
abnormality of steroidogenesis 1,2R. Cerundolo, 2D.H. Lloyd, 3J.R. Rest, 1Naples, Italy; 2 London, 3Cambridge, UK (F 12) |
| Enhanced
expression of SRY and SOX9 genes in balding scalp of men with
androgenetic alopecia 1WenChieh Chen, 2Ren-Yu Tsai, 1Wen-Chuan Hsieh, 1Tainan, 2Taipei, Taiwan (F 26) |
|
A
comparison of two rodent models for the assessment of potassium
channel openers on hair growth in vivo |
| Pili
annulati: new hair shaft and follicle findings with pedigree
analysis in 3 families 1K.A. Feldmann, 2D.A.R. de Berker, 1H. Wolff, 3D.J.P. Ferguson, 4M.R. Pittelkow, 3R.P.R. Dawber, 1Munich, Germany; 2Bristol, 3Oxford, UK; 4Rochester, USA (F 28) |
| Human
nude-ity exposed: a nonsense mutation in the WHN gene underlies
congenital alopecia and nail dystrophy with severeT-cell immunodeficiency
1J.Frank, 2C. Pignata, 2L. Gaetaniello, 2N. Pozzi, 3A.M. Christiano, 1Aachen, Germany; 2Naples, Italy; 3New York, USA (F 23) |
| The
role of FAS and FAS ligand in alopecia areata of C3H/HeJ mice 1P. Freyschmidt-Paul, 1K.McElwee, 2V. Botchkarev, 3J.P. Sundberg, 1R. Happle, 1R. Hoffmann, 1Marburg, Germany; 2Boston, 3Bar Harbor, USA (F 16) |
| Passive
transfer of IgG from horses with alopecia areata-like hair loss 1S.H. Gardner, 2T. Olivry, 1N.J. Lindsey, and 1D.J. Tobin, 1Bradford, UK; 2Raleigh, USA (F 18) |
| Red
scalp syndrome R. Grimalt, L. Lacueva, G. Hausmann, J. Ferrando, Barcelona, Spain (F 11) |
|
Monilethrix:
Mutational hotspot in the helix termination motif of the human
hair basic keratin 6 |
|
Expression
of pro-opiomelanocortin-derived peptides in hair follicle
melanocytes is inversely correlated with pigmentation level |
| The
X-linked gene defect of adrenoleukodystrophy is involved in
androgenetic alopecia 1A. König, 1R. Happle, 1E. Tchitcherina, 1J.R. Schaefer, 2P. Sokolowski, 2W. Köhler, 1R. Hoffmann, 1Marburg, 2Wermsdorf, Germany (F 27) |
| Androgenetic
alopecia: relationship to genetic variability in the human hairless
gene 1R. Kruse, 2A.M. Hillmer, 2S. Cichon, 3F. Macciardi, 2M.M. Nöthen, 1Düsseldorf, 2Bonn, Germany; 3Toronto, Canada (F 25) |
| Characterizing
C3H/HeJ mice with apparent resistance to alopecia areata onset 1K.J. McElwee, 2M. Zöller, 1E. Wenzel, 1P. Freyschmidt-Paul, 3J.P. Sundberg, 1R. Hoffmann, 1Marburg, 2Heidelberg, Germany; 3Bar Harbor, USA (F 17) |
| Steroid
sulfatase is primarily expressed within the dermal papilla of
human hair follicles: a new pharmaceutical target for the treatment
of androgenetic alopecia? 1S. Niiyama, 2A. Rot, 2A. Billich, 1R. Hoffmann, 1Marburg, Germany; 2 Vienna, Austria (F 7) |
|
Mechanisms
of action of minoxidil as a hair growth stimulator: Open questions,
hypothetical concepts |
|
Neurotransmitters,
neuropeptides and neurotrophins as regulators of murine hair
follicle morphogenesis and cycling |
| Defolliculated:
A hair cycle mouse mutant which loses its pelage follicles completely 1R.M. Porter, 2J. Reichelt, 1D.P. Lunny, 1E.B. Lane, 3C.A.B. Jahoda ,2T. M. Magin, 1Dundee, 3Durham, UK; 2Bonn, Germany (F 13) |
| Histology
and hormonal activity in senescent thinning in males 1V.H. Price, 2M.E. Sawaya, 3J. Headington, 4M.K. Kibarian, 1San Francisco, 2Miami, 3Ann Arbor, 4Washington, USA (F 8) |
| Localization
of the gene for hypotrichosis congenita Marie Unna - linkage
analysis and contig construction 1M. Van Steensel, 1M. Van Geel, 2F. J. Smith, 2C. M. Colema, 2W.H.I. McLean, 2P. M. Steijlen, 1Nijmegen, The Netherlands; 2Dundee, UK (F 19) |
| Alopecia
areata-like hair loss in C3H/HeJ mice: a complex polygenic autoimmune
disease 1J.P. Sundberg, 2E. Levin, 2K.McElwee, 3L.E. King, 1G. Cox, 1G. Churchill, 1Bar Harbor, 3Nashville, USA; 2Marburg, Germany (F 15) |
|
Interleukin-1
gene cluster polymorphisms in alopecia areata: strong association
of IL-1RN and IL-1L1 genotypes with severe disease an early
age at onset |
|
Cathepsin
l is important for catagen progression, entry into anagen
and the formation of the inner root sheath and telogen club
hair |
|
Identification
of two new mutations in the gene responsible for the tricho-rhino-phalangeal
syndrome type I |
| Postmenopausal
frontal fibrosing alopecia: 20 cases V. Vaisse, B. Matard, P. Assouly, C. Jouannique, P. Reygagne, Paris, France (F 9) |
| Congenital
atrichia in a Palestinian patient resulting from a mutation
in the human hairless gene 1A. Zlotogorski, 2A.M. Christiano, 1Jerusalem, Israel; 2New York, USA (F 24) |