The LIM homeodomain transcription factor Isl1 was investigated in mouse thyroid organogenesis. All progenitor cells of the midline thyroid diverticulum and lateral primordia (ultimobranchial bodies) expressed Isl1. This pattern persisted until the growing anlagen fused at embryonic day (E) 13.5. In Isl1 null mutants thyroid progenitors expressing Nkx2.1 and Pax8 were readily specified in the anterior endoderm but the size of the thyroid rudiment was reduced. In late development, only immature C-cells expressed Isl1. In the adult gland the number of Isl1+ cells was small compared with cells expressing calcitonin. Analysis of microarray profiles indicated a higher level of Isl1 expression in medullary thyroid carcinomas than in tumors derived...
Congenital hypothyroidism (CH) affects 1 in 3000 children and is the major cause of treatable mental...
Congenital Hypothyroidism (CH) is commonly due to structural defects of thyroid gland, collectively ...
Congenital Hypothyroidism (CH) is commonly due to structural defects of thyroid gland, collectively ...
The LIM homeodomain transcription factor Isl1 was investigated in mouse thyroid organogenesis. All p...
Notch signalling plays an important role in endocrine development, through its target gene Hes1. Hes...
The human insulin gene enhancer-binding protein islet-1 (ISL1) is a transcription factor involved in...
CONTEXT:Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000- 4...
Notch signalling plays an important role in endocrine development, through its target gene Hes1. Hes...
The human insulin gene enhancer-binding protein islet-1 (ISL1) is a transcription factor involved in...
CONTEXT:Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000- 4...
CONTEXT:Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000- 4...
The thyroid gland located in the anterior neck consists of two main cell types. First, the follicula...
BACKGROUND: Islet 1 (ISL1), a LIM-homeodomain transcription factor is essential for promoting pancre...
CONTEXT:Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000- 4...
The LIM homeodomain protein Islet-1 (Isl1), one of the earliest markers for motor neuron differentia...
Congenital hypothyroidism (CH) affects 1 in 3000 children and is the major cause of treatable mental...
Congenital Hypothyroidism (CH) is commonly due to structural defects of thyroid gland, collectively ...
Congenital Hypothyroidism (CH) is commonly due to structural defects of thyroid gland, collectively ...
The LIM homeodomain transcription factor Isl1 was investigated in mouse thyroid organogenesis. All p...
Notch signalling plays an important role in endocrine development, through its target gene Hes1. Hes...
The human insulin gene enhancer-binding protein islet-1 (ISL1) is a transcription factor involved in...
CONTEXT:Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000- 4...
Notch signalling plays an important role in endocrine development, through its target gene Hes1. Hes...
The human insulin gene enhancer-binding protein islet-1 (ISL1) is a transcription factor involved in...
CONTEXT:Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000- 4...
CONTEXT:Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000- 4...
The thyroid gland located in the anterior neck consists of two main cell types. First, the follicula...
BACKGROUND: Islet 1 (ISL1), a LIM-homeodomain transcription factor is essential for promoting pancre...
CONTEXT:Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000- 4...
The LIM homeodomain protein Islet-1 (Isl1), one of the earliest markers for motor neuron differentia...
Congenital hypothyroidism (CH) affects 1 in 3000 children and is the major cause of treatable mental...
Congenital Hypothyroidism (CH) is commonly due to structural defects of thyroid gland, collectively ...
Congenital Hypothyroidism (CH) is commonly due to structural defects of thyroid gland, collectively ...