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research PRC 2 preserves intestinal progenitors and restricts secretory lineage commitment

75 citations , September 2016 in “EMBO journal”

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

research Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix

20 citations , December 1999 in “Journal of Investigative Dermatology”

Mutations in the hHb6 gene cause the hair disorder monilethrix.

research Onset of Keratin 17 Expression Coincides with the Definition of Major Epithelial Lineages during Skin Development

318 citations , October 1998 in “The Journal of Cell Biology”

Keratin 17 is important for skin development and may help define skin cell types.

research An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15

15 citations , January 1991 in “Mammalian Genome”

research Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene

45 citations , January 2010 in “Journal of Veterinary Medical Science”

A gene mutation causes curly hair and hair loss in rats.

research STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity

65 citations , September 2014 in “Orphanet Journal of Rare Diseases”

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

research ATP-dependent chromatin remodeling during mammalian development

182 citations , August 2016 in “Development”

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

research Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes

4 citations , January 2017 in “Journal of pediatric endocrinology & metabolism/Journal of pediatric endocrinology and metabolism”

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Functional Mapping of the Mouse Hairless Gene Promoter Region

research Functional mapping of the mouse hairlessi> gene promoter region

January 2018 in “bioRxiv (Cold Spring Harbor Laboratory)”

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

research 1313 Fzd2 controls multiple aspects of epidermal development through distinct signaling mechanisms
1 citations , April 2018 in “Journal of Investigative Dermatology”

Fzd2 is important for skin and hair development through various signaling ways.

research Generation of a Novel Inducible and Dermal Papilla‐Specific Wif1‐CreERi> Knock‐In Mouse Line for Hair Follicle Research
May 2025 in “Experimental Dermatology”

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

research A CLE14 Signalling Cascade Promotes Arabidopsis Root Hair Elongation
3 citations , May 2025 in “Plant Cell & Environment”

CLE14 peptide promotes root hair growth in Arabidopsis.

research MYB30 and ETHYLENE INSENEITIVE3 antagonistically regulate root hair growth and phosphorus uptake under phosphate deficiency in Arabidopsis
16 citations , April 2021 in “Plant Signaling & Behavior”

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

research Novel splice site mutation in the LIPHi> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
9 citations , February 2018 in “The Journal of Dermatology”

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

research BUZZi>: an essential gene for postinitiation root hair growth and a mediator of root architecture in Brachypodium distachyoni>
July 2023 in “New phytologist”

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

research 549 Temporary cell cycle arrest in human scalp hair follicles and their epithelial stem cells by ALRN-6924: A novel strategy to selectively protect p53-wildtype cells against paclitaxel-induced alopecia
1 citations , November 2022 in “Journal of Investigative Dermatology”

ALRN-6924 may prevent hair loss caused by chemotherapy.

research Novel RNF113Ai> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
January 2026 in “American Journal of Medical Genetics Part A”

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

research Androgen receptor inhibits the hair follicle induction potential of dermal papilla cells by binding with Tcf4 at the A574 binding site
4 citations , May 2022 in “Genes & Diseases”

research The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
35 citations , April 2008 in “Journal of Biological Chemistry”

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

research Keratin 17 null mice exhibit age- and strain-dependent alopecia
122 citations , June 2002 in “Genes & Development”

Keratin 17 is crucial for early hair strength and cell survival.

research [Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix].
2 citations , April 2008 in “PubMed”

A gene mutation causes monilethrix in a Chinese family.

research Co-Expression Pattern of Artemis Serine 516 Phosphorylation with Indicators Involving in Differentiation, Proliferation and Apoptosis of Human Anagen Hair Follicles: An Immunofluorescence Double-Staining Study
January 2023 in “Frontiers in bioscience”

Artemis protein may help control hair growth and health by influencing cell processes.

research Co-operation between follicular ornithine decarboxylase and v-Ha-ras induces spontaneous papillomas and malignant conversion in transgenic skin
88 citations , August 1998 in “Carcinogenesis”

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

research Heterozygous KRT32i> variant is responsible for autosomal dominant loose anagen hair syndrome
May 2025

A KRT32 gene variant causes loose anagen hair syndrome.

research First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
October 2007 in “Clinical Biochemistry”

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

research 1358 PRC1 fine-tunes gene repression and activation to safeguard skin epithelium development and stem cell specification
1 citations , April 2018 in “Journal of Investigative Dermatology”

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

research AP-1 and TGFß cooperativity drives non-canonical Hedgehog signaling in resistant basal cell carcinoma
60 citations , October 2020 in “Nature Communications”

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

research NUDT15i>,FTOi>, andRUNX1i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases
40 citations , January 2017 in “Intestinal Research”

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

research Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
August 2025 in “American Journal of Case Reports”

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

research A homozygous nonsense mutation identified in COL7A1i> in a family with autosomal recessive dystrophic epidermolysis bullosa
September 2024 in “Journal of Medicine and Life”

A specific gene mutation causes a severe skin disorder in a family.

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Search:

Research

research PRC 2 preserves intestinal progenitors and restricts secretory lineage commitment

research Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix

research Onset of Keratin 17 Expression Coincides with the Definition of Major Epithelial Lineages during Skin Development

research An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15

research Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene

research STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity

research ATP-dependent chromatin remodeling during mammalian development

research Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes

research Functional mapping of the mouse hairlessi> gene promoter region

research 1313 Fzd2 controls multiple aspects of epidermal development through distinct signaling mechanisms

research Generation of a Novel Inducible and Dermal Papilla‐Specific Wif1‐CreERi> Knock‐In Mouse Line for Hair Follicle Research

research A CLE14 Signalling Cascade Promotes Arabidopsis Root Hair Elongation

research MYB30 and ETHYLENE INSENEITIVE3 antagonistically regulate root hair growth and phosphorus uptake under phosphate deficiency in Arabidopsis

research Novel splice site mutation in the LIPHi> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review

research BUZZi>: an essential gene for postinitiation root hair growth and a mediator of root architecture in Brachypodium distachyoni>

research 549 Temporary cell cycle arrest in human scalp hair follicles and their epithelial stem cells by ALRN-6924: A novel strategy to selectively protect p53-wildtype cells against paclitaxel-induced alopecia

research Novel RNF113Ai> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother

research Androgen receptor inhibits the hair follicle induction potential of dermal papilla cells by binding with Tcf4 at the A574 binding site

research The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes

research Keratin 17 null mice exhibit age- and strain-dependent alopecia

research [Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix].

research Co-Expression Pattern of Artemis Serine 516 Phosphorylation with Indicators Involving in Differentiation, Proliferation and Apoptosis of Human Anagen Hair Follicles: An Immunofluorescence Double-Staining Study

research Co-operation between follicular ornithine decarboxylase and v-Ha-ras induces spontaneous papillomas and malignant conversion in transgenic skin

research Heterozygous KRT32i> variant is responsible for autosomal dominant loose anagen hair syndrome

research First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy

research 1358 PRC1 fine-tunes gene repression and activation to safeguard skin epithelium development and stem cell specification

research AP-1 and TGFß cooperativity drives non-canonical Hedgehog signaling in resistant basal cell carcinoma

research NUDT15i>,FTOi>, andRUNX1i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases

research Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report

research A homozygous nonsense mutation identified in COL7A1i> in a family with autosomal recessive dystrophic epidermolysis bullosa