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Mapping pesticide mixtures to cancer risk at the country scale with spatial exposomics. [PDF]
Nat HealthHonles J +15 more
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Evidence that the limb bud ectoderm is required for survival of the underlying mesoderm
Developmental Biology, 2013 The limb forms from a bud of mesoderm encased in a hull of ectoderm that grows out from the flank of the embryo. Coordinated signaling between the limb mesoderm and ectoderm is critical for normal limb outgrowth and patterning.
Marian Fernandez-Teran +2 more
exaly +3 more sources
Transcription factors involved in lens development from the preplacodal ectoderm
Developmental Biology, 2012 Lens development is a stepwise process accompanied by the sequential activation of transcription factors. Transcription factor genes can be classified into three groups according to their functions: the first group comprises preplacodal genes, which are ...
Hajime Ogino +2 more
exaly +2 more sources
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American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2004
AbstractEctodermal dysplasias are a large group of heritable conditions characterized by congenital defects of one or more ectodermal structures and their appendages: hair (hypotrichosis, partial, or total alopecia), nails (dystrophic, hypertrophic, abnormally keratinized), teeth (enamel defect or absent), and sweat glands (hypoplastic or aplastic ...
Peter H, Itin, Susanna K, Fistarol
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AbstractEctodermal dysplasias are a large group of heritable conditions characterized by congenital defects of one or more ectodermal structures and their appendages: hair (hypotrichosis, partial, or total alopecia), nails (dystrophic, hypertrophic, abnormally keratinized), teeth (enamel defect or absent), and sweat glands (hypoplastic or aplastic ...
Peter H, Itin, Susanna K, Fistarol
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Dermatologic Clinics, 1987
In order to be considered an ectodermal dysplasia, a disorder should meet the following criteria: it must be congenital; it must be diffuse (not localized) and must involve the epidermis as well as at least one of its appendages; and it must not be progressive.
L M, Solomon, B, Cook, W, Klipfel
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In order to be considered an ectodermal dysplasia, a disorder should meet the following criteria: it must be congenital; it must be diffuse (not localized) and must involve the epidermis as well as at least one of its appendages; and it must not be progressive.
L M, Solomon, B, Cook, W, Klipfel
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Developmental Biology, 2007 Fgf8 signalling is known to play an important role during patterning of the first pharyngeal arch, setting up the oral region of the head and then defining the rostral and proximal domains of the arch.
Martyn T Cobourne +2 more
exaly +2 more sources
Dermatologica, 2009
Description of a patient presenting an hidrotic ectodermal dysplasia. Clinical signs were hypotrichosis, dystrophic nails, palmoplantar keratoderma, absence of teeth and hyperhidrosis.
G E, Pierard, D, Van Neste, B, Letot
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Description of a patient presenting an hidrotic ectodermal dysplasia. Clinical signs were hypotrichosis, dystrophic nails, palmoplantar keratoderma, absence of teeth and hyperhidrosis.
G E, Pierard, D, Van Neste, B, Letot
openaire +2 more sources
Acta Paediatrica, 1952
SummaryTwo case reports of ectodernial dysplasia in two females are presented. One case is believed to be the first reported with evidence of direct descent from mother to daughter. The other is a case of the mendelian dominant type. The submission is made that the anhydrotic type is not necessarily always a sex‐linked recessive manifestation in males ...
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SummaryTwo case reports of ectodernial dysplasia in two females are presented. One case is believed to be the first reported with evidence of direct descent from mother to daughter. The other is a case of the mendelian dominant type. The submission is made that the anhydrotic type is not necessarily always a sex‐linked recessive manifestation in males ...
openaire +2 more sources
Arthrogryposis and Ectodermal Dysplasia
Human Heredity, 1982Arthrogryposis, an unusual type of ectodermal dysplasia, growth retardation of prenatal onset, and diabetes mellitus were all present in the proposita and are unlikely to have arisen all independently. The combination of at least some of these abnormalities may represent a distinct syndrome.
G B, Côté +2 more
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