Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: Annotated tables

Experimental Dermatology

Volumn 10, Issue 6, 2001, Pages 369-390

  Nakamura, M ^a   Sundberg, J P ^b   Paus, Ralf ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b JACKSON LABORATORY   (United States)

Author keywords

Hair cycle; Knockout; Sebaceous gland; Targeted mutant mice; Transgenic mouse

Indexed keywords

ALPHA CATENIN; BETA1 INTEGRIN; BONE MORPHOGENETIC PROTEIN 4; CATHEPSIN L; DISINTEGRIN; ENZYME; EPIDERMAL GROWTH FACTOR RECEPTOR; FIBROBLAST GROWTH FACTOR 10; FOLLISTATIN; GENE PRODUCT; HELIX LOOP HELIX PROTEIN; IMMUNOGLOBULIN KAPPA CHAIN; INHIBIN A; KERATINOCYTE GROWTH FACTOR; NERVE GROWTH FACTOR; NEUROTROPHIN 3; NOGGIN; PARATHYROID HORMONE RELATED PROTEIN; PLASMINOGEN ACTIVATOR INHIBITOR 1; PLATELET DERIVED GROWTH FACTOR; PROTEIN P75; SCATTER FACTOR; SOMATOMEDIN C; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR E2F; TRANSFORMING GROWTH FACTOR ALPHA; TRANSFORMING GROWTH FACTOR BETA1; TRANSFORMING GROWTH FACTOR BETA2; TUMOR NECROSIS FACTOR; UNINDEXED DRUG;

ANIMAL MODEL; COMPARATIVE STUDY; CYCLING; GENE ACTIVITY; GENE FUNCTION; GENE MUTATION; GENE SWITCHING; GENETIC ENGINEERING; HAIR DISEASE; HAIR FOLLICLE; HAIR GROWTH; IMMUNE DEFICIENCY; KNOCKOUT GENE; LABORATORY TEST; MOLECULAR BIOLOGY; MORPHOGENESIS; MOUSE; MUTAGENESIS; MUTANT; NONHUMAN; PHENOTYPE; REVIEW; SEBACEOUS GLAND; TRANSGENE;

ANIMALS; GENETIC ENGINEERING; HAIR FOLLICLE; MICE; MICE, KNOCKOUT; MICE, MUTANT STRAINS;

EID: 0035189491     PISSN: 09066705     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0625.2001.100601.x     Document Type: Review

References (293)

1. Microinjection of a rabbit β-globin gene into zygotes and its subsequent expression in adult mice and their offspring
2. Rules and guidelines for genetic nomenclature in mice: Excerpted version. Committee on Standardized Genetic Nomenclature for Mice
3. 1 in the epidermis of transgenic mice
4. Sequence 5′ of the bovine keratin 5 gene direct tissue- and cell-type specific expression of a lacZ gene in the adult and during development
5. Expression of MK6a dominant-negative and C terminal mutant transgenes in mice has distinct phenotype consequences in the epidermis and hair follicle
6. Tissue-specific and differentiation-specific expression of a human k14 keratin gene in transgenic mice
7. Tissue- and stratum-specific expression of the human involucrin promoter in transgenic mice
8. Selective activation of the versican promoter by epithelial-mesenchymal interactions during har follicle development
9. A new role for neurotrophins: Involvement of brain derived neurotrophic factor and neurotrophin-4 in hair cycle control
10. Tissue specific regulation of the alpha-myosin heavy chain promoter in transgenic mice
11. Conditional gene expression in the epidermis of transgenic mice using the tetracycline-regulated transactivators tTA and rTA linked to the keratin 5 promoter
12. 1 in the epidermis
13. Temporal control of gene expression in transgenic mice by a tetracycline-responsive promoter
14. Doxycycline-mediated quantitative and tissue-specific control of gene expression in transgenic mice
15. Skin and its appendages: Normal anatomy and pathology of spontaneous, transgenic and targeted mouse mutations
16. Professional use of mutant mice in hair research
17. A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse
18. Genomewide, large-scale production of mutant mice by ENU mutagenesis
19. Introduction of a lacZ reporter gene into the mouse int-2 locus by homologous recombination
20. Conditional gene targeting
21. The magical touch: Genome targeting in epidermal stem cells induced by tamoxifen application to mouse skin
22. T2 recombinases
23. The product of the mouse nude locus, Whn, regulates the balance between epithelial cell growth and differentiation
24. Association between mouse nude gene expression and the initiation of epithelial terminal differentiation
25. Patterns of hairless (hr) gene expression in mouse hair follicle morphogenesis and cycling
26. The hairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
27. The role of the hairless (hr) gene in the regulation of hair follicle catagen transformation
28. Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humans
29. A novel serine protease overexpressed in the hair follicles of nude mice
30. Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of the nude skin phenotype
31. Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
32. FGF5 as a regulator of the hair growth cycle: Evidence from targeted and spontaneous mutations
33. Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation
34. TGFα deficiency results in hair follicle and eyue abnormalities in targeted and waved-1 mice
35. The mouse waved-2 phenotype results from a point mutation in the EGF receptor tyrosine kinase
36. Cathepsin L deficiency as molecular defect of furless: Hyperproliferation of keratinocytes and pertubation of hair follicle cycling
37. Mouse mutations as animal models and biomedical tools for dermamtological research
38. Gene-knockout mice with abnormal epidermal and hair follicular development
39. The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene
40. Conserved cysteine to serine mutation in tyrosinase is responsible for the classical albino mutation in laboratory mice
41. Molecular characterization of the mouse agouti locus
42. A comparehensive guide for the recognition and classification of distinct stages of hair follicle morphogenesis
43. Systematic approach to evaluation of mouse mutations with cutaneous appendage defects
44. Noggin is a mesenchymally derived stimulator on hair-follicle induction
45. The biology of hair follicles
46. A comprehensive guide for the accurate classification of murine hair follicles in distinct hair cycle stages
47. Controls of hair follicle cycling
48. Control of the hair cycle and hair diseases as cycling disorders
49. Transection level dictates the pattern of hair follicle sheath growth in vitro
50. Hair follicle biology, and sebaceous gland, and scarring alopecias
51. Targeting expression of keratinocyte growth factor to keratinocytes elicits striking changes in epithelial differentiation in transgenic mice
52. FGF10 acts as a major ligand for FGFF receptor 2 IIIb in mouse multi-organ development
53. The function of KGF in morphogenesis of epithelium and reepithelialization of wounds
54. Functional analysis of activins during mammalian development
55. Mice carrying null mutations of the genes encoding insulin-like growth factor 1 (Igf-1) and type 1 IGF receptor (Igflr)
56. Overexpression of parathyroid hormone-related protein in the skin of transgenic mice interferes with hair follicle development
57. Disruption of the nuclear hormone receptor RORα in staggerer mice
58. Staggerer phenotype in retinoid-related orphan receptor alpha-deficient mice
59. The TGF-β2 isoform is both a required and sufficient inducer of murine hair follicle morphogenesis
60. Deregulated expression of E2F1 induces hyperplasia and cooperates with ras in skin tumor development
61. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
62. Development of several organs that require inductive epithelial-mesenchymal interactions in impaired in LEF-1 deficient mice
63. Ragged, a semidominant coat texture mutant in the house mouse
64. Opossum, a semi-dominant lethal mutation affecting hair and other characteristics of mice
65. BAC-mediated gene-dosage analysis reveals a role for Ziprol (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin
66. Hyperproliferation and defects in epithelial polarity upon conditional ablation of α-catenin in skin
67. IKK1-deficient mice exhibit abnormal development of skin and skeleton
68. Limb and skin abnormalities in mice lacking IKKα
69. Targeted mutation in β1,4-galactosyltransferase leads to pituitary insufficiency and neonatal lethality
70. Suprabasal integrin expression in the epidermis of transgenic mice results in developmental defects and a phenotype resembling psoriasis
71. Skin and hair follicle integrity is crucially dependent on β1 integrin expression on keratinocytes
72. Conditional ablation of β1 integrin in skin: Severe defects in epidermal proliferation, basement membrane formation, and hair follicle invagination
73. Directed expression of keratin 16 to the progenitor basal cells of transgenic mouse skin delays skin maturation
74. Mutation of the mouse klotho gene leads to a syndrome resembling ageing
75. Alterations in NF-κB function in transgenic epithelial tissue demonstrate a growth inhibitory role for NF-κB
76. Squamous cell carcinomas and increased apoptosis in skin with inhibited Rel/nuclear factor-κB signaling
77. Squamous epithelial proliferation induced by walleye dermal sarcoma retrovirus cyclin in transgenic mice
78. Zinc deficiency in murine milk underlies expression of the lethal-milk (lm) mutation
79. A novel gene involved in zinc transport is deficient in the lethal milk mouse
80. p63 is a p53 homologue required for limb and epidermal morphogenesis
81. p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development
82. Studies on an apparently new mutant, alopecia periodica, found in the mouse
83. Bald mice: Arthritic?
84. Fur deficient
85. Hair patches
86. The hook-tailed mouse
87. Long hair (1gh)
88. Abnormal development in the skin of the pupoid fetus (pflpf) mutant mouse: Abnormal keratinization, recovery of a normal phenotype, and relationship to the repeated epilation (ER) mutant mouse
89. Repeated epilation: A genetic epidermal syndrome in mice
90. Expression of a dominant negative mutant of epidermal growth factor receptor in the epidermis of transgenic mice elicits striking alterations in hair follicle development and skin structure
91. Targeted disruption of mouse EGF receptor: Effect of genetic background on mutant phenotype
92. Strain-dependent epithelial defects in mice lacking the EGF receptor
93. Epithelial immaturity and multiorgan failure in mice lacking epidermal growth factor receptor
94. Keratinocyte growth factor is required for hair development but not for wound healing
95. Multiple defects and perinatal death in mice deficient in follistatin
96. Overexpression of mouse follistatin causes reproductive defects in transgenic mice
97. Involvement of hepatocyte growth factor/scatter factor and Met receptor signaling in hair follicle morphogenesis and cycling
98. Insertion of Inhbb into the Inhba locus rescues the Inhba-null phenotype and reveals new activin functions
99. Increased vibrissa growth in transgenic mice expressing insulin-like growth factor 1
100. Overexpression of insulin-like growth factor-1 induces hyperplasia, dermal abnormalities, and spontaneous tumor formation in transgenic mice
101. Mice lacking nerve growth factor display perinatal loss of sensory and sympathetic neurons yet develop basal forebrain cholinergic neurons
102. Distinct roles for nerve growth factor and brain-derived neurotrophic factor in controlling the rate of hain follicle morphogenesis
103. A role for p75 neurotrophin receptor in the control of hair follicle morphogensis
104. Retardation of hair follicle development by the deletion of TrkC, high-affinity neurotrophin-3 receptor
105. Neurotrophin-3 involvement in the regulation of hair follicle morphogenesis
106. Roles for PDGF-A and sonic hedgehog in development of mesenchymal components of the hair follicle
107. Sonic hedgehog signaling is essential for hair development
108. Essential role for sonic hedgehog during hair follicle morphogenesis
109. Waved: An autosomal recessive coat from character in the mouse
110. Transgenic mice provide new insights into the role of TGF-α during epidermal development and differentiation
111. Cachexia and graft-vs.-host-disease-type skin changes in keratin promoter-driven TNF α transgenic mice
112. Hair defects and pup loss in mice with targeted deletion of the first cut repeat domain of the Cux/CDP homeoprotein gene
113. Defective trophoblast function in mice with a targeted mutation of Ets2
114. The sonic hedgehog target gene Gli2 plays a pivotal role in hair follicle development
115. Epidermal dysplasia and abnormal hair follicles in transgenic mice overexpressing homeobox gene Msx-2
116. Lymphoid enhancer factor 1 directs hair follicle patterning and epithelial cell fate
117. An essential role for ectodomain shedding in mammalian development
118. Mottled, a sex-modified lethal in the house mouse
119. Threshold phenomena versus cell heredity in the manifestation of sex-linked genes in mammals
120. Molecular basis of the brindled mouse mutant (Mo(br)): A murine model of Menkes disease
121. Atp7a-dappled
122. Production of normal macular mouse chimeras - The presence of critical tissue in the macular mutant mouse, a model of Menkes' kinky hair disease
123. The tortoise shell house mouse
124. Mo
125. The genetics of a new hair deficiency, furless, in the house mouse
126. Transgenic mouse lines with ectopic expression of α-1,3-galactosyltransferase: Production and characteristics
127. De novo hair follicle morphogenesis and hair tumors in mice expressing a truncated β-catenin in skin
128. Targeted expression of activated erbB-2 to the epidermis of transgenic mice elicits striking developmental abnormalities in the epidermis and hair follicles
129. Expression of the integrin-linked kinase (ILK) in mouse skin
130. Role of Gab1 in heart, placenta, and skin development and growth factor- and cytokine-induced extracellular signal-regulated kinase mitogen-activated protein kinase activation
131. Skin abnormalities in mice transgenic for plasminogen activator inhibitor 1: Implications for the regulation of desquamation and follicular neogenesis by plasminogen activator enzymes
132. Caracul, a dominant mutation
133. Directional caracul, Ca
134. Congenital progressive hydronephrosis in mice: A new recessive mutation
135. Crimpy (cpy) a new recessive hair mutation on Chromosome 15 of the mouse
136. Curly-whiskers and its linkage with tail-kinks in linkage group II of the mouse
137. New mutation
138. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities
139. Two new hair mutants, rough and frizzy, in the house mouse
140. "Glabrous" a new hair deficient mutant in the house mouse
141. Retarded hair growth (rhg)
142. Scabby
143. Scruffy, Scr, a new mutation on distal Chr 6
144. Hair growth in mouse mutants affecting coat texture
145. Waved alopecia
146. Waved coat (Wc)
147. Wavy fur (Wf)
148. Selective suppression of CD44 in keratinocytes of mice bearing an antisense CD44 transgene driven by a tissue-specific promoter disrupts hyaluronate metabolism in the skin and impairs keratinocyte proliferation
149. Transgenic mice as a model to study the role of TGF-β-related molecules in hair follicles
150. The angora locus (go) in the mouse. Hair morphology, duration of growth cycle and site of action
151. Angora
152. Analysis of the angora-Y gene expression
153. New roles for glial cell line-derived neutrophic factor and neurturin: Involvement in hair cycle control
154. A role for p75 neutrophin receptor in the control of apoptosis-driven hair follicle regression
155. A new role for neutrophin-3. Involvement in the regulation of hair follicle regression (catagen)
156. Skin abnormalities generated by temporally controlled RXRα mutations in mouse epidermis
157. 1 in vivo
158. Control of hair growth and follicle size by VEGF-mediated angiogenesis
159. Evaluation of keratinocyte proliferation and differentiation in vitamin D receptor knockout mice
160. Mice lacking the vitamin D receptor exhibit impaired bone formation, uterine hypoplasia and growth retardation after weaning
161. Targeted ablation of the vitamin D receptor: An animal model of vitamin D-dependent rickets type II with alopecia
162. WNT signaling in the control of hair growth and structure
163. Role of endogenous retrovirus as mutagens: The hairless mutation of mice
164. Hairless mice
165. Towards defining the pathogenesis of the Hairless phenotype
166. Hr←ba→-bald
167. Four dominant autosomal mutations affecting skin and hair development in the mouse
168. "Rhino", an allele of hairless in the house mouse
169. Insertional mutation of the hairless locus on mouse chromosome
170. Keratinocyte-specific ablation of Stat3 exhibits impaired skin remodeling, but does not affect skin morphogenesis
171. Longevity, stress response, and cancer in aging telomerase-deficient mice
172. Intercellular adhesion molecule-1 and hair follicle regression
173. Plakoglobin suppresses epithelial proliferation and hair growth in vivo
174. Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair
175. Targeted disruption of Bcl-2αβ in mice: Occurrence of gray hair, polycystic kidney disease, and lymphocytopenia
176. Bcl-2 deficiency in mice leads to pleiotrophic abnormalities: Accelerated lymphoid cell death in thymus and spleen, polycystic kidney, hair hypopigmentation, and distorted small intestine
177. Accelerated disappearance of melanocytes in bcl-2-deficient mice
178. Overexpression of bcl-2 protects from ultravioletl B-induced apoptosis but promotes hair follicle regression and chemotherapy-induced alopecia
179. Manipulation of outer root sheath cell survival perturbs the hair-growth cycle
180. Expression of E6 and E7 papillomavirus oncogenes in the outer root sheath of hair follicles extends the growth phase and bypasses resting at telogen
181. Adrenocortical dysplasia: A mouse model system for adrenocortical insufficiency
182. Alopecia, a dominant mutation in the house mouse
183. A new hairless mutant in the house mouse
184. Influence de l'alopecie sur quelques caracteristiques biometriques de la souris
185. Frl
186. Four dominant autosomal mutations affecting skin and hair development in the mouse
187. A single-gene antagonism between mother and fetus in the mouse
188. Hairy ears, Eh
189. Juvenile bare (jb)
190. Koala, a dominant mutation
191. Hereditary hair loss in the tufted mutant of the house mouse
192. Interleukin 6: Insights to its function in skin by overexpression in transgenic mice
193. Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle
194. Targeted overexpression of Notch1 in the hair follicle leads to defects in inner root sheat differentiation and dysregulation of hair cycling
195. Activation of the Notch pathway in the hair cortex leads to aberrant differentiation of the adjacent hair-shaft layers
196. "Nude", a new hairless gene with pleiotropic effects in the mouse
197. J)
198. Y strain
199. Two genetically separable steps in the differentiation of thymic epithelium
200. Ectopic expression of the nude gene induces hyperproliferation and defects in differentiation: Implications for the self-renewal of cutaneous epithelia
201. Rescue of the hairless phenotype in nude mice by transgenic insertion of the wild-type Hfh11 genomic locus
202. Hoxc13 mutant mice lack external hair
203. The ovo gene required for cuticle formation and oogenesis in flies is involved in hair formation and spermatogenesis in mice
204. Bare-patches, a new sex-linked gene in the mouse, associated with a high production of XO females. I. A preliminary report of breeding experiments
205. The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase
206. Striated, a new sex-linked gene in the house mouse
207. Increased frequency of spontaneous skin tumors in transgenic mice which overexpress ornithine decarboxylase
208. Modulation of murine hair follicle function by alterations in ornithine decarboxylase activity
209. Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
210. Normalization of hair growth in sparse fur-abnormal skin and hair (SPF-ASH) mice by introduction of the rat ornithine transcarbamylase (OTC) gene
211. Abnormal ornithine carbamoyltransferase in mice having the sparse-fur mutation
212. A new allele of the sparse fur gene in the mouse
213. Urokinase-type plasminogen activator and its receptor synergize to promote pathogenic proteolysis
214. Targeted disruption of the pemphigus vulgaris antigen (desmoglein 3) gene in mice causes loss of keratinocyte cell adhesion with a phenotype similar to pemphigus vulgaris
215. Desmoglein 3 anchors telogen hair in the follicle
216. Balding (bal)
217. Vesicle formation and follicular root sheath separation in mice homozygous for deleterious alleles at the balding (bal) locus
218. The spontaneous balding and desmoglein 3 null mutations: Mouse models for pemphigus vulgaris
219. A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy
220. Genetic disorders of keratin: Are scarring alopeceas a sub-set?
221. Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation
222. Cyclic hair-loss and regrowth in transgenic mice overexpressing an intermediate filament gene
223. 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata
224. Td-tattered
225. Targeted expression of SV40 T antigen in the hair follicle of transgenic mice produces an aberrant hair phenotype
226. Atrichosis
227. "Bare," a new hairless mutant in the mouse-genetics and histology
228. A new mutant causing hairloss in the DBA/1/Lac colony
229. Varieties of hairless-like mutant mice
230. Depilated (dep), a mutant gene that affects the coat of the mouse and acts in the epidermis
231. Skin exfoliation and purulent conjunctivitis in a new mutant - The exfoliative mouse
232. Fr-frizzy
233. The hair of fuzzy mice
234. Frowzy, fz
235. Fuzzy tail (fzt)
236. Inheritance of hair constrictions in mice
237. Two new mutations
238. Harlequin ichthyosis (ichq): A juvenile lethal mouse mutation with ichthyosiform dermatitis
239. Ichthyosis, a new recessive mutant in the house mouse
240. Juvenile depilation (jd): A new hair loss mutation in the mouse
241. Lanceolate hair (lah): A recessive mouse mutation with alopecia and abnormal hair
242. Lanceolate hair-J (lahJ). A mouse model for human hair disorders
243. The keratin defect and hair-cycle of a new mutant (matted) in the house-mouse
244. Über den Hautzyclus einer Spontannmutante (Nackig) mit mangelhafter Haarkeratinisierung bei der Maus
245. Nackt (nkt), a new hair loss mutation of the mouse with associated CD4 deficiency
246. The external expression and comparative dermal histology of hereditary hairlessness in mammals
247. New mutations causing sterility restricted to the male in rats and mice
248. Rex: A dominant autosomal monogenic coat texture character in the mouse
249. Re
250. Rough Coat
251. Rough fur (ruf)
252. Scant hair (sch)
253. Close linkage between genes which cause hairlessness in the mouse
254. Sparse coat, spc.
255. Thin fur, a recessive mutant on chromosome 17 of the mouse
256. Uncv (uncovered): A new mutation causing hairloss on mouse chromosome 11
257. Neue Mutationen und Koppelungsgruppen bei der Hausmaus
258. Dermatopathological studies on skin lesions of MRL mice
259. Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis
260. Transgenic mice expressing IFN-γ in the epidermis have eczema, hair hypopigmentation, and hair loss
261. Inflammatory skin disease in transgenic mice that express high levels of interleukin 1α in basal epidermis
262. Lymphocyte infiltration of the skin in transgenic mice carrying the human interleukin-2 gene
263. Motheaten, an immunodeficient mutant of the mouse. I. Genetics and pathology
264. Mutations at the murine motheaten locus are within the hematopoietic cell protein-tyrosine phosphatase (Hcph) gene
265. Motheaten and viable motheaten mice have mutations in the haematopoietic cell phosphatase gene
266. Viable motheaten, a new allele at the motheaten locus. I. Pathology
267. Inactivation of the integrin β6 subunit gene reveals a role of epithelial integrins in regulating inflammation in the lung and skin
268. A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice
269. Mice lacking the transcription factor Re1B develop T cell-dependent skin lesions similar to human atopic dermatitis
270. Increased expression of type 2 cytokines in chronic proliferative dermatitis (cpdm) mutant mice and resolution of inflammation following treatment with IL-12
271. Development and progression of psoriasiform dermatitis and systemic lesions in the flaky skin (fsn) mouse mutant
272. The initiation and development of the hair follicle population in tabby mice
273. The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains
274. Cloning of Tabby, the murine homolog of the human EDA gene: Evidence for a membrane-associated protein with a short collagenous domain
275. New mutation, an allele of Tabby
276. A recurrent mutation of the Tabby locus?
277. Hair follicle initiation in reciprocal recombinations of downless homozygote and heterozygote mouse tail epidermis and dermis
278. Mutations in the human homologue of mouse all cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia
279. Involvement of a novel Tnf receptor homologue in hair follicle induction
280. The teeth of the sleek mouse
281. Hereditary absence of sebaceous glands in the mouse
282. Scd1 is expressed in sebaceous glands and is disrupted in the asebia mouse
283. Asebia-J is known to be very close to ru on Chr 19
284. ab2J): A new allele and a model for scarring alopecia
285. In the absence of the low density lipoprotein receptor, human apolipoprotein C1 overexpression in transgenic mice inhibits the hepatic uptake of very low density lipoproteins via a receptor-associated protein-sensitive pathway
286. Hyperlipidemia and cutaneous abnormalities in transgenic mice overexpressing human apolipoprotein C1
287. Bareskin (Bsk)
288. The genetics and development of "crinkled", a new mutant in the mouse
289. IL-7 overexpression in transgenic mouse keratinocytes causes a lymphoproliferative skin disease dominated by intermediate TCR cells