Pages that link to "Q24595086"
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The following pages link to Gsh-4 encodes a LIM-type homeodomain, is expressed in the developing central nervous system and is required for early postnatal survival (Q24595086):
Displaying 50 items.
- Lhx9: a novel LIM-homeodomain gene expressed in the developing forebrain (Q22008639) (← links)
- The Nuclear LIM Domain Interactor NLI Mediates Homo- and Heterodimerization of LIM Domain Transcription Factors (Q24329116) (← links)
- Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4. (Q24536132) (← links)
- Developmental Aspects of Spinal Locomotor Function: Insights from Using the in vitro Mouse Spinal Cord Preparation (Q24656593) (← links)
- A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency (Q24658065) (← links)
- Structural Basis for Partial Redundancy in a Class of Transcription Factors, the LIM Homeodomain Proteins, in Neural Cell Type Specification (Q27675210) (← links)
- The LIM domain: regulation by association (Q28137861) (← links)
- Analysis of the human LHX3 neuroendocrine transcription factor gene and mapping to the subtelomeric region of chromosome 9 (Q28138625) (← links)
- Requirement for LIM homeobox gene Isl1 in motor neuron generation reveals a motor neuron-dependent step in interneuron differentiation (Q28273468) (← links)
- Independent requirement for ISL1 in formation of pancreatic mesenchyme and islet cells (Q28301584) (← links)
- Cyp1a2(-/-) null mutant mice develop normally but show deficient drug metabolism (Q28510829) (← links)
- Pax6 controls progenitor cell identity and neuronal fate in response to graded Shh signaling (Q28571762) (← links)
- Altered Forebrain and Hindbrain Development in Mice Mutant for theGsh-2Homeobox Gene (Q28588028) (← links)
- LIM homeodomain factors Lhx3 and Lhx4 assign subtype identities for motor neurons (Q28591209) (← links)
- Neonatal lethality associated with respiratory distress in mice lacking cytochrome P450 1A2 (Q28591646) (← links)
- Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development (Q28591652) (← links)
- Sim2 mutants have developmental defects not overlapping with those of Sim1 mutants (Q28863308) (← links)
- Biological effects of targeted inactivation of hepatocyte growth factor-like protein in mice (Q32106841) (← links)
- Genetic regulation of pituitary gland development in human and mouse (Q33590141) (← links)
- A model for the development of the hypothalamic-pituitary axis: transcribing the hypophysis (Q33636310) (← links)
- Early steps in pituitary organogenesis (Q33650524) (← links)
- Functions of LIM-homeobox genes. (Q33826742) (← links)
- Genetic defects of the growth hormone-insulin-like growth factor axis (Q33838238) (← links)
- cDNA cloning, chromosomal localization and expression pattern analysis of human LIM-homeobox gene LHX4. (Q34114038) (← links)
- A novel chromosomal translocation t(1;14)(q25;q32) in pre-B acute lymphoblastic leukemia involves the LIM homeodomain protein gene, Lhx4. (Q34138908) (← links)
- Lhx3 and Lhx4 suppress Kolmer-Agduhr interneuron characteristics within zebrafish axial motoneurons (Q34341831) (← links)
- P-Lim, a LIM homeodomain factor, is expressed during pituitary organ and cell commitment and synergizes with Pit-1. (Q34496854) (← links)
- Other transcription factors and hypopituitarism (Q34992939) (← links)
- Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia. (Q35441732) (← links)
- Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue (Q35587203) (← links)
- Novel Lethal Form of Congenital Hypopituitarism Associated With the First Recessive LHX4 Mutation (Q35680850) (← links)
- Roles of the LHX3 and LHX4 LIM-homeodomain factors in pituitary development. (Q35754081) (← links)
- Impaired platelet aggregation and sustained bleeding in mice lacking the fibrinogen motif bound by integrin alpha IIb beta 3. (Q35911430) (← links)
- Congenital adenohypophyseal hypoplasia associated with secondary hypothyroidism in a 2-week-old Portuguese water dog (Q35967707) (← links)
- A recessive mutation resulting in a disabling amino acid substitution (T194R) in the LHX3 homeodomain causes combined pituitary hormone deficiency. (Q35970431) (← links)
- LIM-homeodomain genes in mammalian development and human disease. (Q36196340) (← links)
- Three novel missense mutations within the LHX4 gene are associated with variable pituitary hormone deficiencies. (Q36494440) (← links)
- Knock-in mouse lines expressing either mitochondrial or microsomal CYP1A1: differing responses to dietary benzo[a]pyrene as proof of principle (Q37199118) (← links)
- ISL1-based LIM complexes control Slit2 transcription in developing cranial motor neurons. (Q37397243) (← links)
- Hox, Cdx, and anteroposterior patterning in the mouse embryo (Q37570835) (← links)
- Pituitary transcription factors in the aetiology of combined pituitary hormone deficiency (Q37852201) (← links)
- The role of homeodomain transcription factors in heritable pituitary disease (Q37905532) (← links)
- Administration of factor XIII B subunit increased plasma factor XIII A subunit levels in factor XIII B subunit knock-out mice (Q39752484) (← links)
- Review: borders, patterns, and distinctive families of homeodomains (Q40503601) (← links)
- Microarray analysis of novel cell lines representing two stages of metanephric mesenchyme differentiation (Q40750408) (← links)
- Patterning cascades in the neural tube. Neural development. (Q41110651) (← links)
- Structure and Function of LIM Domains (Q41662734) (← links)
- DeLIMiting development (Q41721616) (← links)
- A coding SNP of LHX4 gene is associated with body weight and body length in bovine (Q42614850) (← links)
- Developmental restriction of the LIM homeodomain transcription factor Islet-1 expression to cholinergic neurons in the rat striatum (Q43574474) (← links)